Skip to main content
  • More from ADA
    • Diabetes Care
    • Clinical Diabetes
    • Diabetes Spectrum
    • ADA Standards of Medical Care in Diabetes
    • ADA Scientific Sessions Abstracts
    • BMJ Open Diabetes Research & Care
  • Subscribe
  • Log in
  • My Cart
  • Follow ada on Twitter
  • RSS
  • Visit ada on Facebook
Diabetes

Advanced Search

Main menu

  • Home
  • Current
    • Current Issue
    • Online Ahead of Print
    • ADA Scientific Sessions Abstracts
  • Browse
    • By Topic
    • Issue Archive
    • Saved Searches
    • ADA Scientific Sessions Abstracts
    • Diabetes COVID-19 Article Collection
    • Diabetes Symposium 2020
  • Info
    • About the Journal
    • About the Editors
    • ADA Journal Policies
    • Instructions for Authors
    • Guidance for Reviewers
  • Reprints/Reuse
  • Advertising
  • Subscriptions
    • Individual Subscriptions
    • Institutional Subscriptions and Site Licenses
    • Access Institutional Usage Reports
    • Purchase Single Issues
  • Alerts
    • E­mail Alerts
    • RSS Feeds
  • Podcasts
    • Diabetes Core Update
    • Special Podcast Series: Therapeutic Inertia
    • Special Podcast Series: Influenza Podcasts
    • Special Podcast Series: SGLT2 Inhibitors
    • Special Podcast Series: COVID-19
  • Submit
    • Submit a Manuscript
    • Submit Cover Art
    • ADA Journal Policies
    • Instructions for Authors
    • ADA Peer Review
  • More from ADA
    • Diabetes Care
    • Clinical Diabetes
    • Diabetes Spectrum
    • ADA Standards of Medical Care in Diabetes
    • ADA Scientific Sessions Abstracts
    • BMJ Open Diabetes Research & Care

User menu

  • Subscribe
  • Log in
  • My Cart

Search

  • Advanced search
Diabetes
  • Home
  • Current
    • Current Issue
    • Online Ahead of Print
    • ADA Scientific Sessions Abstracts
  • Browse
    • By Topic
    • Issue Archive
    • Saved Searches
    • ADA Scientific Sessions Abstracts
    • Diabetes COVID-19 Article Collection
    • Diabetes Symposium 2020
  • Info
    • About the Journal
    • About the Editors
    • ADA Journal Policies
    • Instructions for Authors
    • Guidance for Reviewers
  • Reprints/Reuse
  • Advertising
  • Subscriptions
    • Individual Subscriptions
    • Institutional Subscriptions and Site Licenses
    • Access Institutional Usage Reports
    • Purchase Single Issues
  • Alerts
    • E­mail Alerts
    • RSS Feeds
  • Podcasts
    • Diabetes Core Update
    • Special Podcast Series: Therapeutic Inertia
    • Special Podcast Series: Influenza Podcasts
    • Special Podcast Series: SGLT2 Inhibitors
    • Special Podcast Series: COVID-19
  • Submit
    • Submit a Manuscript
    • Submit Cover Art
    • ADA Journal Policies
    • Instructions for Authors
    • ADA Peer Review
Original Article

Effect of Endogenous GLP-1 on Insulin Secretion in Type 2 Diabetes

  1. Marzieh Salehi1,
  2. Benedict Aulinger1,
  3. Ronald L. Prigeon2 and
  4. David A. D'Alessio1
  1. 1University of Cincinnati, Department of Internal Medicine, Cincinnati, Ohio; and
  2. 2University of Maryland, Department of Medicine, Division of Gerontology, Baltimore, Maryland.
  1. Corresponding author: Marzieh Salehi, salehim{at}uc.edu.
Diabetes 2010 Jun; 59(6): 1330-1337. https://doi.org/10.2337/db09-1253
PreviousNext
  • Article
  • Figures & Tables
  • Info & Metrics
  • PDF
Loading

Abstract

OBJECTIVE The incretins glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) account for up to 60% of postprandial insulin release in healthy people. Previous studies showed a reduced incretin effect in patients with type 2 diabetes but a robust response to exogenous GLP-1. The primary goal of this study was to determine whether endogenous GLP-1 regulates insulin secretion in type 2 diabetes.

METHODS Twelve patients with well-controlled type 2 diabetes and eight matched nondiabetic subjects consumed a breakfast meal containing d-xylose during fixed hyperglycemia at 5 mmol/l above fasting levels. Studies were repeated, once with infusion of the GLP-1 receptor antagonist, exendin-(9–39) (Ex-9), and once with saline.

RESULTS The relative increase in insulin secretion after meal ingestion was comparable in diabetic and nondiabetic groups (44 ± 4% vs. 47 ± 7%). Blocking the action of GLP-1 suppressed postprandial insulin secretion similarly in the diabetic and nondiabetic subjects (25 ± 4% vs. 27 ± 8%). However, Ex-9 also reduced the insulin response to intravenous glucose (25 ± 5% vs. 26 ± 7%; diabetic vs. nondiabetic subjects), when plasma GLP-1 levels were undetectable. The appearance of postprandial ingested d-xylose in the blood was not affected by Ex-9.

CONCLUSIONS These findings indicate that in patients with well-controlled diabetes, the relative effects of enteral stimuli and endogenous GLP-1 to enhance insulin release are retained and comparable with those in nondiabetic subjects. Surprisingly, GLP-1 receptor signaling promotes glucose-stimulated insulin secretion independent of the mode of glucose entry. Based on rates of d-xylose absorption, GLP-1 receptor blockade did not affect gastric emptying of a solid meal.

Glucagon-like peptide 1 (GLP-1) is a gut-brain peptide that is a major component of the incretin effect and is essential for normal glucose tolerance (1). Based on studies in which synthetic GLP-1, or GLP-1 receptor (GLP-1r) agonists, is administered to humans, GLP-1 has a broad range of actions that promote glucose homeostasis, including stimulating insulin secretion (2), suppressing glucagon release (3–4), delaying gastric emptying (5), and increasing hepatic glucose balance (6–7). Importantly, and unlike other insulinotropic gut peptides, the effects of GLP-1 on glucose metabolism are retained in people with diabetes (8–10). This has led to the development of novel therapeutic compounds for use in diabetic patients that are based on GLP-1r signaling (11).

The physiologic role of GLP-1 in individuals with diabetes has not been determined. However, there are several reasons to question whether the GLP-1 system is fully functional in this patient group. First, there is some evidence that GLP-1 secretion in response to meal ingestion in type 2 diabetes is impaired (12–15), although this finding has not been uniform (16–17). Second, the sensitivity of insulin secretion to exogenous GLP-1 is reduced in diabetic individuals (18). Finally, it has long been believed that the augmentation of glucose-stimulated insulin secretion during enteral glucose absorption, the incretin effect, is severely attenuated in type 2 diabetes, implying that incretins such as GLP-1 are not normally active in this group of subjects.

In this study, we tested the hypothesis that the effect of endogenous GLP-1 to promote insulin secretion after meal ingestion is reduced in people with diabetes. Diabetic subjects and age- and weight-matched nondiabetic subjects were studied with and without infusion of the specific GLP-1r antagonist, exendin-(9–39) (Ex-9), during fixed hyperglycemia before and after a breakfast meal.

RESEARCH DESIGN AND METHODS

Subjects.

Twelve subjects with established type 2 diabetes (five females and seven males) and eight age- and BMI-matched nondiabetic subjects (six females and two males) were studied on two separate days (Table 1). All subjects were weight stable for 3 months prior to the experiments. Diabetic patients had good glycemic control with a mean A1C level of 6.3 ± 0.1% (range 5.9–7.6%). Normal glucose tolerance was confirmed in the nondiabetic subjects by a 2-h venous plasma glucose level of <7.8 mmol/l after a 75-g oral glucose tolerance test. The control subjects had no family history of type 2 diabetes, were free of any chronic medical conditions such as coronary artery disease, uncontrolled dyslipidemia, or hypertension, and received no medications for any of these conditions. The studies were approved by the institutional review board of the University of Cincinnati, and all participants provided written informed consent prior to the studies.

View this table:
  • View inline
  • View popup
TABLE 1

Characteristics of the study participants

Peptides.

Synthetic exendin-(9–39) (Clinalfa; Merck Biosciences AG, Läufelfingen, Switzerland) was greater than 95% pure, sterile, and free of pyrogens. Lyophilized peptide was prepared in 0.25% human serum albumin on the day of study. The use of synthetic Ex-9 is approved under the U.S. Food and Drug Administration Investigational New Drug 65,837.

Experimental procedures.

Subjects were instructed to consume greater than 200 g of carbohydrate for 3 days before each visit and not to engage in vigorous physical activity. Subjects with diabetes withheld their oral antidiabetic medication for 3 days before each study. They were admitted to the General Clinical Research Center at Cincinnati Children's Hospital on separate occasions after an overnight fast. Intravenous catheters were placed in each forearm for the withdrawal of blood and the infusion of glucose and Ex-9; the arm used for blood sampling was continuously warmed using a heating pad to arterialize the venous blood. After removal of fasting blood samples, a primed continuous infusion of 20% glucose was started to achieve and maintain a target blood glucose concentration of 5 mmol/l greater than fasting levels (19). At 30 min, subjects received either 1) an intravenous bolus of synthetic Ex-9 (7,500 pmol/kg) for 1 min followed by a continuous infusion (750 pmol/kg/min) for the remainder of the study, or 2) saline, as a control (19). The order of the infusions was balanced so that half the subjects received saline or Ex-9 as their first infusion, and the two experiments were separated by an interval of at least 1 week. At 90 min, subjects consumed a mixed nutrient breakfast (300 kcal with a calorie distribution of 40% carbohydrate, 20% protein, and 40% fat) consisting of scrambled eggs, English muffin, margarine, chocolate pudding mixed with 10 g d-xylose, and milk that was eaten within 10 min. Subjects were instructed to consume the pudding in the middle of the meal. The rate of intravenous glucose infusion was adjusted to maintain the blood glucose at the target rate throughout the meal and for the remainder of the study. Blood samples were drawn at −10, −5, 0, 15, 30, 45, 60, 70, 75, 80, 85, 90, 95,100, 105, 110, 120, 130, 140, 150, 160, 170, 180, 190, 200, 210, 220, 230, 240, 250, 255, 260, 265, and 270 min; the plasma was separated within 60 min of blood withdrawal and stored at −80°C until assay. Blood samples were collected in tubes containing heparin, 50 mmol/l EDTA, and 500 kallikrein inhibitory units per milliliter of aprotinin.

Assays.

Blood glucose concentrations were determined by a glucose oxidase method using a glucose analyzer (YSI 2300 STAT Plus; Yellow Springs Instruments, Yellow Springs, OH). Insulin, glucagon, total GLP-1, and C-peptide were measured by radioimmunoassays as described previously (19). d-xylose was measured by colorimetric assay (20), and total glucose-dependent insulinotropic polypeptide (GIP) was measured by ELISA (Linco Research, St. Charles, MO).

Calculations and analysis.

Insulin secretion rates (ISRs) were derived from plasma C-peptide concentrations using deconvolution with population estimates of C-peptide clearance (21–22). Fasting concentrations of blood glucose, hormones, and ISR were taken as the mean of the three samples drawn at −10, −5, and 0 min. Preprandial insulin secretory responses were computed as the mean increments above fasting values of ISR from 60 to 90 min; these were used to determine the responses to intravenous glucose–induced hyperglycemia. Postprandial insulin secretory responses were calculated as the mean increments above the 60–90 min values of ISR from 95 to 270 min. This measure of postprandial insulin secretion reflects the augmentation of ISR, beyond 5 mmol/l hyperglycemia, by meal-induced stimuli, and has been used previously as a surrogate for the incretin effect (23–25). The d-xylose, GLP-1, and GIP concentrations from 80 to 90 min were taken as baseline, and levels after meal consumption (95–270 min for d-xylose and GLP-1; 95–240 min for GIP) were used to compute postprandial areas under the curve (AUC) above baseline. The glucagon levels from 80 to 90 min (preprandial) were compared with fasting as well as values of glucagon from 250 to 260 min. The stability of the glucose clamps was computed as the mean of coefficients of variation for each study from 60 to 270 min. The reproducibility of the clamps was computed as the difference in mean glucose from 60 to 270 for each subject.

The contribution of endogenous GLP-1 to insulin secretion was determined by comparing the mean values of ISR for each subject during infusion of saline or Ex-9. Separate comparisons were made for the preprandial and postprandial periods.

The parameters obtained from each subject in the two studies and from the diabetic and nondiabetic groups were compared using one- and two-way ANOVA with repeated measures. Spearman correlation was used to seek relationships between measured outcomes and subject characteristics such as A1C, and paired t test was used to compare measured variables within each study. Data are presented as the mean ± SEM.

RESULTS

Fasting glucose was significantly higher in the diabetic than in the nondiabetic subjects (P < 0.001), but fasting insulin and C-peptide concentrations were comparable, and the values for each subject were similar on the days of the saline and Ex-9 studies (Table 2). Blood glucose concentrations were raised by ∼5 mmol/l from fasting values to hyperglycemic levels from 60 to 270 min that were comparable during the Ex-9 and saline studies (Fig. 1, Table 2). The average clamped glucose levels (60–270 min) for nondiabetic subjects during the saline and Ex-9 studies were 9.3 ± 0.2 and 9.3 ± 0.2 mmol/l, respectively, with a mean difference of 0.02 ± 0.03 mmol/l. For the diabetic subjects, the mean glucose concentrations (60–270 min) were 12.0 ± 0.4 and 12.1 ± 0.4 mmol/l for the control and Ex-9 clamps, respectively, and the mean difference was 0.09 ± 0.07 mmol/l. The average coefficient of variation of the glucose concentrations during the hyperglycemic clamp control studies was 4.4 ± 0.4% for the nondiabetic and 4.9 ± 0.5% for the diabetic subjects.

View this table:
  • View inline
  • View popup
TABLE 2

Effect of meal ingestion during hyperglycemic clamp on β-cell hormonal response and gastrointestinal peptides in studies with and without intravenous Ex-9 in subjects with and without diabetes

FIG. 1.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIG. 1.

Blood glucose concentrations and glucose infusion rates during intravenous-meal clamps with Ex-9 or saline infusions in nondiabetic (left) and diabetic (right) subjects. Data are presented as mean ± SEM.

The glucose infusion rates needed to reach target glycemia were higher in the nondiabetic compared with diabetic subjects during the preprandial (60–90 min; P < 0.01) and postprandial (95–270 min; P < 0.05) periods. Infusion of Ex-9 was associated with a significant reduction of the glucose infusion rates necessary to maintain target glycemia from 60 to 90 min in both groups (P < 0.05 for both comparisons). After ingestion of the breakfast meal, the glucose infusion rate was initially reduced in some subjects to compensate for glucose influx from the gut, but was significantly higher than preprandial infusions by the end of the study (Fig. 1, Table 2).

In both the diabetic and nondiabetic groups, β-cell secretion rose in response to intravenous glucose administration to a plateau from 60 to 90 min (Fig. 2, Table 2); preprandial insulin, C-peptide, and ISR were greater in the nondiabetic than the diabetic group (P < 0.05). Among the diabetic subjects, there were significant inverse correlations between the preprandial insulin secretory response and fasting glucose (r = −0.7, P < 0.01) and A1C (r = −0.8, P < 0.05). Compared with the study with saline infusion, GLP-1r blockade with Ex-9 caused a significant reduction of insulin secretion before meal ingestion (60–90 min), as indicated by significantly lower mean values of insulin, C-peptide, and ISR (Table 2). The GLP-1 effect on intravenous glucose–stimulated insulin secretion, taken as the percentage difference in mean ISR from 60 to 90 min with and without Ex-9, was 25 ± 5% in diabetic subjects and 26 ± 7% in the nondiabetic group (Fig. 3).

FIG. 2.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIG. 2.

β-cell secretion in response to hyperglycemia and meal ingestion with and without Ex-9 infusion. Plasma insulin concentrations (A) and insulin secretion rates (B) for nondiabetic (left) and diabetic (right) subjects. Data are presented as mean ± SEM.

FIG. 3.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIG. 3.

The contribution of GLP-1 to preprandial and postprandial insulin secretion. The percentage reduction of insulin secretion rates by Ex-9 is shown for the preprandial (60–90 min) and postprandial (95–270 min) periods in the nondiabetic (black bars) and diabetic (gray bars) groups. Data are presented as mean ± SEM.

After meal consumption (95–270 min), β-cell secretion increased significantly over preprandial (60–90 min) values in both the nondiabetic (P < 0.01) and diabetic (P < 0.05) subjects; although the absolute responses were significantly lower in the diabetic group (P < 0.05; Fig. 2, Table 2). Among the diabetic subjects, there were significant inverse correlations between postprandial insulin secretory responses and A1C (r = −0.6, P < 0.05). During the saline infusion study, meal ingestion significantly enhanced ISR, by 47 ± 7% in the nondiabetic and 44 ± 4% for diabetic subjects, above preprandial ISR. During the Ex-9 infusion, postprandial ISR was 44 ± 6% and 45 ± 4% higher than preprandial ISR in the nondiabetic and diabetic groups, respectively. Blocking endogenous GLP-1 with Ex-9 diminished postprandial ISR by 27 ± 8% in nondiabetic and 25 ± 4% in diabetic subjects, compared with the studies with saline infusion (Fig. 3).

Fasting glucagon concentrations in the diabetic subjects were similar during the saline and Ex-9 studies (Table 2). During both the saline and Ex-9 infusions, the hyperglycemic clamp suppressed glucagon levels from 80 to 90 min (P < 0.05). Glucagon values at the conclusion of the experiments remained suppressed during the saline infusion, but were significantly higher when Ex-9 was given (P < 0.05). In nondiabetic subjects, plasma glucagon concentrations decreased slightly, but not significantly, between the fasting and preprandial periods, and did not change further after the meal, with either saline or Ex-9.

Plasma concentrations of d-xylose increased steadily after meal intake and peaked at 60 min after meal consumption in both diabetic and nondiabetic subjects during both saline and Ex-9 studies (Fig. 4). The area under plasma d-xylose curve in the studies with saline and Ex-9 infusion, respectively, were 105 ± 8.2 and 102 ± 9.1 mmol/l/min in diabetic and 71 ± 8.5 and 70 ± 8 mmol/l/min in nondiabetic subjects, indicating that GLP-1 receptor blockade had minimal effects on the passage of d-xylose from the stomach to the intestine. d-xylose AUC was significantly greater in the diabetic compared with the nondiabetic group (P < 0.05).

FIG. 4.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIG. 4.

Postprandial concentrations of d-xylose (A), GIP (B), and GLP-1 (C) in nondiabetic (left) and diabetic (right) subjects. Data are presented as mean ± SEM.

Fasting plasma GIP levels were comparable before meal ingestion in the studies with saline and Ex-9 infusion in the diabetic (16 ± 1 and 16 ± 2 pmol/l) and nondiabetic (20 ± 1 and 20 ± 2 pmol/l) subjects. In both the nondiabetic and diabetic groups, meal consumption caused a similar rise of GIP concentrations in the saline and Ex-9 studies (Fig. 4, Table 2), suggesting that GLP-1r blockade had no effect on GIP secretion. The GIP response was significantly greater in the diabetic compared with nondiabetic group (P < 0.05). Fasting plasma GLP-1 were not different in the diabetic (3.6 ± 0.3 and 3.6 ± 0.2 pmol/l) and nondiabetic (3.1 ± 0.1 and 3.0 ± 0.0 pmol/l) groups, during the saline and Ex-9 studies, but levels were undetectable in ∼80% of the subjects. Plasma GLP-1 increased after meal ingestion in both groups (Fig. 4, Table 2), and Ex-9 infusion significantly increased these responses in the nondiabetic and diabetic subjects (P < 0.05).

Subjects tolerated the experiments without notable problems, and there were no adverse events associated with Ex-9 infusion.

DISCUSSION

The current study investigated the role of endogenous GLP-1 on islet hormone secretion and gastric emptying in patients with type 2 diabetes. Although previous studies have demonstrated that diabetic patients respond to pharmacologic amounts of GLP-1, the effect of endogenous GLP-1 has not been previously demonstrated. Our results indicate that in diabetic subjects with good glycemic control, there is an enhancement of glucose-stimulated insulin secretion after meal ingestion that is similar on a relative basis to nondiabetic individuals. Moreover, the impact of GLP-1r blockade was also comparable in the groups, indicating that endogenous GLP-1 contributes significantly to postprandial insulin secretion in diabetic subjects. Surprisingly, GLP-1r blockade reduced insulin secretion in response to intravenous glucose alone, and the magnitude of this effect was as great as that on postprandial β-cell responses. Gastric emptying, as reflected by d-xylose uptake, was not affected by blocking GLP-1r. These findings support an important physiologic role for GLP-1 to amplify glucose-stimulated insulin secretion, and demonstrate that this effect is retained in at least a subset of type 2 diabetic patients.

Our group and others (4,19,26–27) have previously used Ex-9 to demonstrate the effects of GLP-1r signaling in human subjects. In our previous report, we demonstrated that doses of Ex-9 identical to those used in the present study were effective for blocking supraphysiologic infusions of GLP-1 nearly completely, and for reducing postprandial insulin secretion by ∼30%. Although no one has established definitively a dose of Ex-9 beyond which no further inhibition of GLP-1 action can be detected, based on previously published results (4,19,26) we believe that the dose used in this study was near maximal for what can be achieved in an acute infusion.

The classic method for determining the incretin effect is a 2-day method with an oral glucose tolerance test on day 1 followed on day 2 by an intravenous glucose infusion isoglycemic to arterialized venous glucose levels after glucose ingestion (28). Using this method, Nauck et al. demonstrated a severe impairment of the incretin effect in subjects with type 2 diabetes (29), a much cited finding that has been very influential in shaping the understanding of enteroinsular physiology. We elected to use an alternative method, the hyperglycemic clamp-meal test, as a means of comparing the relative increase in insulin secretion when carbohydrate is absorbed enterally, because the test can be performed in a single morning, reducing day-to-day variability and the time commitment of research subjects. Variations of this method have been used previously by a number of investigators (23–25). Our preliminary data for normal glucose-tolerant subjects demonstrate that the estimation of the incretin effect using the 1-day and 2-day methods is comparable with a strong and significant within-subject correlation (30). In the present study, we used a mixed nutrient meal as the enteral stimulus during the hyperglycemic clamp to assess the nutrient, incretin, and neural responses activated by typical food consumption. We targeted the clamp as 5 mmol/l above fasting glucose to achieve levels that were slightly greater than what we expected as a result of meal ingestion alone. Overall, this design permitted a measure of the enhancement of insulin secretion by meal ingestion, and the GLP-1 component of it. Without further validation, this measure cannot be equated to the classically derived incretin effect, although we believe that the two methods assess similar physiologic processes.

In contrast to what was described originally by Nauck et al. (29), and confirmed in more recent studies (13), the cohort of diabetic subjects described here had a comparable degree of meal enhancement of insulin secretion to the nondiabetic group. Although β-cell secretion was clearly abnormal in diabetic compared with the nondiabetic subjects, relative to the ISR or plasma insulin levels achieved during stimulation with intravenous glucose alone, meal ingestion caused equivalent augmentation in the diabetic and nondiabetic groups (Table 2). This finding is consistent with the results reported by Perley and Kipnis more than three decades ago (31), showing that obese subjects with mild type 2 diabetes had preserved stimulation of insulin secretion by alimentary factors relative to nondiabetic control subjects. In contrast to the findings of Nauck et al. (29), the plasma GIP responses were increased in our diabetic compared with nondiabetic subjects. Increased GIP secretion has been reported previously in some studies of diabetic subjects (reviewed in [32]). Although an increased effect of GIP could account for a bigger augmentation of insulin secretion by meal ingestion in our diabetic subjects, most previous studies indicate that GIP has very modest effects on insulin secretion in type 2 diabetes (8).

Just as the relative increase of ISR with meal ingestion was similar in the diabetic and nondiabetic subjects, so too was the contribution of GLP-1 action to postprandial β-cell responses. Based on the effects of Ex-9, GLP-1 accounted for ∼25% of the insulin response to the mixed meal at a fixed level of hyperglycemia. This is consistent with what we reported recently as the GLP-1 effect in healthy lean subjects during an oral glucose tolerance test (19). The finding of intact effects of GLP-1 in the diabetic group was unexpected, in that previous work had indicated that type 2 diabetic subjects have a blunted response to exogenous GLP-1 infused to supraphysiologic levels (18). Although there was a weak trend toward the diabetic group having a greater postprandial GLP-1 response, there was considerable heterogeneity in the AUC among the subjects and no correlation between this measure and insulin secretion or the magnitude of insulin suppression by GLP-1 receptor blockade. These results suggest that circulating GLP-1 may not be a good predictor of the physiologic response to endogenous peptide.

The most surprising finding in this study was that Ex-9 diminished insulin secretion in response to intravenous glucose–induced hyperglycemia before meal consumption, at a time when circulatory levels of GLP-1 were often undetectable. In fact, the relative effect of GLP-1r blockade on preprandial and postprandial ISR was nearly identical. These findings indicate that GLP-1r effects on the β-cell are not restricted to the potentiation of insulin secretion after enteral nutrient absorption when circulating levels of GLP-1 increase. It is important to note that in previous studies blockade of the GLP-1 receptor did not affect fasting plasma insulin levels (4,27,33), but that Schirra et al. noted a reduction in plasma insulin, similar to what we describe here, during a hyperglycemic clamp when Ex-9 was infused (27). Thus, when considered together, the current evidence supports a role for GLP-1r signaling to potentiate glucose-stimulated but not basal insulin secretion in humans. This is consistent with studies in mice with engineered deletion of the GLP-1r gene in which similar degrees of glucose intolerance have been described to both oral and intraperitoneal glucose challenges (34), conditions with elevated and basal plasma GLP-1 levels, respectively. The mechanism whereby Ex-9 affects insulin secretion in the absence of elevated circulating levels of GLP-1 is unclear. However, recent studies raise the possibility of neural (35–36) and paracrine (37) modes of GLP-1 signaling, either of which could be affected by GLP-1r blockade. In addition, in vitro work suggests that Ex-9 can act as an inverse agonist in isolated mouse islets (38). Overall, our findings fit with an expanded model of β-cell regulation by GLP-1 that stretches beyond endocrine effects after eating.

Although several investigators have suggested that the predominant effect of GLP-1 on glucose control is based on its effect on gastric emptying (39–40), this conjecture is based on the results of studies using exogenous administration of GLP-1. Given the identical pattern of postprandial plasma d-xylose in our subjects with and without Ex-9, endogenous GLP-1 has no detectable effect on the rate of passage of nutrients from the stomach to the intestine. Appearance of ingested d-xylose followed a similar time course in diabetic and nondiabetic subjects, but d-xylose reached higher concentrations in the diabetic group, suggesting more rapid gastric emptying in patients with early or mild diabetes, compatible with previous reports (41–42). The lack of effect of Ex-9 to alter d-xylose appearance is similar to what we have reported previously in studies with GLP-1 blockade in healthy humans and nonhuman primates given liquid glucose solution (19,33). We have extended these findings in this study by using a solid meal, and our data stand against an important physiologic role for GLP-1 in the regulation of prandial gastric motility in humans. However, Deane et al. have recently published evidence that endogenous GLP-1 delays gastric emptying in healthy subjects after a solid carbohydrate meal (43). Because these investigators used scintigraphy, the gold standard for measuring gastric emptying, our findings must be interpreted cautiously. Nonetheless, our results are consistent with a recent report that gastric emptying in diabetic patients was not affected by administration of a dipeptidyl peptidase-4 inhibitor that enhanced endogenous GLP-1 by threefold (44).

In previous studies, we and others (4,19) have found that infusion of Ex-9 during oral or intestinal glucose administration increases postprandial plasma glucagon, supporting an important role for GLP-1 to regulate the α-cell. This effect was seen here, but only in the diabetic group. The diabetic subjects had equivalent suppression of glucagon in response to intravenous glucose during the Ex-9 and control experiments, but after the meal there was a significant rise in plasma levels when the GLP-1r was blocked. Interestingly, we did not see this latter effect in the nondiabetic subjects. Although this outcome could indicate differential regulation of prandial α-cell secretion in diabetes, this conclusion needs more rigorous confirmation.

In summary, we report here that administration of Ex-9 reduces insulin secretion proportionately in response to intravenous glucose and enteral stimuli, and that this effect is similar in diabetic and nondiabetic subjects. These findings indicate that the effect of endogenous GLP-1 on postprandial insulin release is preserved in patients with well-controlled type 2 diabetes. Moreover, GLP-1r signaling is important for stimulated insulin secretion independent of the mode of glucose entry. Based on these results, it appears that the function of the enteroinsular axis is intact, at least in some people with type 2 diabetes, and that the role of endogenous GLP-1 to regulate islet function is not mediated entirely by an endocrine mechanism.

ACKNOWLEDGMENTS

These studies were supported by grants from the National Institutes of Health, DK-57900 (D.A.D.) and M01-RR-08084 (Cincinnati Children's Hospital General Clinical Research Center), and the Medical Research Service of the Department of the Veterans Administration.

No potential conflicts of interest relevant to this article were reported.

Parts of this study were presented in abstract form at the 67th Scientific Sessions of the American Diabetes Association, Chicago, Illinois, 22–26 June 2007.

We thank Kay Ellis, Clinton Elfers, Ron Bitner, and Brianne Paxton for their technical support and Suzanne Summers, R.D., for assistance with the design and preparation of test meals. We also thank the nursing staff from Clinical Research Center of Cincinnati Children's Hospital for their expert technical assistance.

Footnotes

  • The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

  • Received August 26, 2009.
  • Accepted February 24, 2010.
  • © 2010 by the American Diabetes Association.

Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.

REFERENCES

  1. ↵
    1. Drucker DJ
    : The biology of incretin hormones. Cell Metab 2006; 3: 153–165
    OpenUrlCrossRefPubMedWeb of Science
  2. ↵
    1. Kreymann B,
    2. Williams G,
    3. Ghatei MA,
    4. Bloom SR
    : Glucagon-like peptide-1 7–36: a physiological incretin in man. Lancet 1987; 2: 1300–1304
    OpenUrlCrossRefPubMedWeb of Science
  3. ↵
    1. Creutzfeldt WO,
    2. Kleine N,
    3. Willms B,
    4. Orskov C,
    5. Holst JJ,
    6. Nauck MA
    : Glucagonostatic actions and reduction of fasting hyperglycemia by exogenous glucagon-like peptide I(7–36) amide in type I diabetic patients. Diabetes Care 1996; 19: 580–586
    OpenUrlAbstract/FREE Full Text
  4. ↵
    1. Schirra J,
    2. Nicolaus M,
    3. Roggel R,
    4. Katschinski M,
    5. Storr M,
    6. Woerle HJ,
    7. Göke B
    : Endogenous glucagon-like peptide 1 controls endocrine pancreatic secretion and antro-pyloro-duodenal motility in humans. Gut 2006; 55: 243–251
    OpenUrlAbstract/FREE Full Text
  5. ↵
    1. Delgado-Aros S,
    2. Kim DY,
    3. Burton DD,
    4. Thomforde GM,
    5. Stephens D,
    6. Brinkmann BH,
    7. Vella A,
    8. Camilleri M
    : Effect of GLP-1 on gastric volume, emptying, maximum volume ingested, and postprandial symptoms in humans. Am J Physiol Gastrointest Liver Physiol 2002; 282: G424–G431
    OpenUrlAbstract/FREE Full Text
  6. ↵
    1. Prigeon RL,
    2. Quddusi S,
    3. Paty B,
    4. D'Alessio DA
    : Suppression of glucose production by GLP-1 independent of islet hormones: a novel extrapancreatic effect. Am J Physiol Endocrinol Metab 2003; 285: E701–E707
    OpenUrlAbstract/FREE Full Text
  7. ↵
    1. Dardevet D,
    2. Moore MC,
    3. Neal D,
    4. DiCostanzo CA,
    5. Snead W,
    6. Cherrington AD
    : Insulin-independent effects of GLP-1 on canine liver glucose metabolism: duration of infusion and involvement of hepatoportal region. Am J Physiol Endocrinol Metab 2004; 287: E75–E81
    OpenUrlAbstract/FREE Full Text
  8. ↵
    1. Nauck MA,
    2. Heimesaat MM,
    3. Orskov C,
    4. Holst JJ,
    5. Ebert R,
    6. Creutzfeldt W
    : Preserved incretin activity of glucagon-like peptide 1 [7–36 amide] but not of synthetic human gastric inhibitory polypeptide in patients with type-2 diabetes mellitus. J Clin Invest 1993; 91: 301–307
    OpenUrlCrossRefPubMedWeb of Science
  9. ↵
    1. Nauck MA,
    2. Kleine N,
    3. Orskov C,
    4. Holst JJ,
    5. Willms B,
    6. Creutzfeldt W
    : Normalization of fasting hyperglycaemia by exogenous glucagon-like peptide 1 (7–36 amide) in type 2 (non-insulin-dependent) diabetic patients. Diabetologia 1993; 36: 741–744
    OpenUrlCrossRefPubMedWeb of Science
  10. ↵
    1. Rachman J,
    2. Gribble FM,
    3. Barrow BA,
    4. Levy JC,
    5. Buchanan KD,
    6. Turner RC
    : Normalization of insulin responses to glucose by overnight infusion of glucagon-like peptide 1 (7–36) amide in patients with NIDDM. Diabetes 1996; 45: 1524–1530
    OpenUrlAbstract/FREE Full Text
  11. ↵
    1. Ahrén B,
    2. Schmitz O
    : GLP-1 receptor agonists and DPP-4 inhibitors in the treatment of type 2 diabetes. Horm Metab Res 2004; 36: 867–876
    OpenUrlCrossRefPubMedWeb of Science
  12. ↵
    1. Vilsbøll T,
    2. Krarup T,
    3. Deacon CF,
    4. Madsbad S,
    5. Holst JJ
    : Reduced postprandial concentrations of intact biologically active glucagon-like peptide 1 in type 2 diabetic patients. Diabetes 2001; 50: 609–613
    OpenUrlAbstract/FREE Full Text
  13. ↵
    1. Muscelli E,
    2. Mari A,
    3. Casolaro A,
    4. Camastra S,
    5. Seghieri G,
    6. Gastaldelli A,
    7. Holst JJ,
    8. Ferrannini E
    : Separate impact of obesity and glucose tolerance on the incretin effect in normal subjects and type 2 diabetic patients. Diabetes 2008; 57: 1340–1348
    OpenUrlAbstract/FREE Full Text
  14. ↵
    1. Toft-Nielsen MB,
    2. Damholt MB,
    3. Madsbad S,
    4. Hilsted LM,
    5. Hughes TE,
    6. Michelsen BK,
    7. Holst JJ
    : Determinants of the impaired secretion of glucagon-like peptide-1 in type 2 diabetic patients. J Clin Endocrinol Metab 2001; 86: 3717–3723
    OpenUrlCrossRefPubMedWeb of Science
  15. ↵
    1. Rask E,
    2. Olsson T,
    3. Söderberg S,
    4. Johnson O,
    5. Seckl J,
    6. Holst JJ,
    7. Ahrén B
    : Northern Sweden Monitoring of Trends and Determinants in Cardiovascular Disease (MONICA). Impaired incretin response after a mixed meal is associated with insulin resistance in nondiabetic men. Diabetes Care 2001; 24: 1640–1645
    OpenUrlAbstract/FREE Full Text
  16. ↵
    1. Vollmer K,
    2. Holst JJ,
    3. Baller B,
    4. Ellrichmann M,
    5. Nauck MA,
    6. Schmidt WE,
    7. Meier JJ
    : Predictors of incretin concentrations in subjects with normal, impaired, and diabetic glucose tolerance. Diabetes 2008; 57: 678–687
    OpenUrlAbstract/FREE Full Text
  17. ↵
    1. Meier JJ,
    2. Nauck MA
    : Is secretion of glucagon-like peptide-1 reduced in type 2 diabetes mellitus? Nat Clin Pract Endocrinol Metab 2008; 4: 606–607
    OpenUrlCrossRefPubMedWeb of Science
  18. ↵
    1. Kjems LL,
    2. Holst JJ,
    3. Vølund A,
    4. Madsbad S
    : The influence of GLP-1 on glucose-stimulated insulin secretion: effects on beta-cell sensitivity in type 2 and nondiabetic subjects. Diabetes 2003; 52: 380–386
    OpenUrlAbstract/FREE Full Text
  19. ↵
    1. Salehi M,
    2. Vahl TP,
    3. D'Alessio DA
    : Regulation of islet hormone release and gastric emptying by endogenous glucagon-like peptide 1 after glucose ingestion. J Clin Endocrinol Metab 2008; 93: 4909–4916
    OpenUrlCrossRefPubMedWeb of Science
  20. ↵
    1. Eberts TJ,
    2. Sample RH,
    3. Glick MR,
    4. Ellis GH
    : A simplified, colorimetric micromethod for xylose in serum or urine, with phloroglucinol. Clin Chem 1979; 25: 1440–1443
    OpenUrlAbstract/FREE Full Text
  21. ↵
    1. Van Cauter E,
    2. Mestrez F,
    3. Sturis J,
    4. Polonsky KS
    : Estimation of insulin secretion rates from C-peptide levels. Comparison of individual and standard kinetic parameters for C-peptide clearance. Diabetes 1992; 41: 368–377
    OpenUrlAbstract/FREE Full Text
  22. ↵
    1. Tillil H,
    2. Shapiro ET,
    3. Miller MA,
    4. Karrison T,
    5. Frank BH,
    6. Galloway JA,
    7. Rubenstein AH,
    8. Polonsky KS
    : Dose-dependent effects of oral and intravenous glucose on insulin secretion and clearance in normal humans. Am J Physiol 1988; 254: E349–E357
    OpenUrlPubMed
  23. ↵
    1. Andersen DK,
    2. Elahi D,
    3. Brown JC,
    4. Tobin JD,
    5. Andres R
    : Oral glucose augmentation of insulin secretion. Interactions of gastric inhibitory polypeptide with ambient glucose and insulin levels. J Clin Invest 1978; 62: 152–161
    OpenUrlCrossRefPubMedWeb of Science
  24. ↵
    1. Ferrannini E,
    2. Katz LD,
    3. Glickman MG,
    4. Defronzo RA
    : Influence of combined intravenous and oral glucose administration on splanchnic glucose uptake in man. Clin Physiol 1990; 10: 527–538
    OpenUrlCrossRefPubMed
  25. ↵
    1. Henchoz E,
    2. D'Alessio DA,
    3. Gillet M,
    4. Halkic N,
    5. Matzinger O,
    6. Goy JJ,
    7. Chioléro R,
    8. Tappy L,
    9. Schneiter P
    : Impaired insulin response after oral but not intravenous glucose in heart- and liver-transplant recipients. Transplantation 2003; 76: 923–929
    OpenUrlCrossRefPubMed
  26. ↵
    1. Edwards CM,
    2. Todd JF,
    3. Mahmoudi M,
    4. Wang Z,
    5. Wang RM,
    6. Ghatei MA,
    7. Bloom SR
    : Glucagon-like peptide 1 has a physiological role in the control of postprandial glucose in humans: studies with the antagonist exendin 9–39. Diabetes 1999; 48: 86–93
    OpenUrlAbstract
  27. ↵
    1. Schirra J,
    2. Sturm K,
    3. Leicht P,
    4. Arnold R,
    5. Göke B,
    6. Katschinski M
    : Exendin(9–39)amide is an antagonist of glucagon-like peptide-1(7–36)amide in humans. J Clin Invest 1998; 101: 1421–1430
    OpenUrlCrossRefPubMedWeb of Science
  28. ↵
    1. Nauck MA,
    2. Homberger E,
    3. Siegel EG,
    4. Allen RC,
    5. Eaton RP,
    6. Ebert R,
    7. Creutzfeldt W
    : Incretin effects of increasing glucose loads in man calculated from venous insulin and C-peptide responses. J Clin Endocrinol Metab 1986; 63: 492–498
    OpenUrlCrossRefPubMedWeb of Science
  29. ↵
    1. Nauck M,
    2. Stöckmann F,
    3. Ebert R,
    4. Creutzfeldt W
    : Reduced incretin effect in type 2 (non-insulin-dependent) diabetes. Diabetologia 1986; 29: 46–52
    OpenUrlCrossRefPubMedWeb of Science
  30. ↵
    1. Tong J,
    2. Aulinger B,
    3. Salehi M,
    4. D'Alessio DA
    : Comparison of one- and two-day methods for measuring the incretin effect. Poster presented at 69th Scientific Sessions of The American Diabetes Association, June 2009, New Orleans, Louisiana
  31. ↵
    1. Perley MJ,
    2. Kipnis DM
    : Plasma insulin responses to oral and intravenous glucose: studies in normal and diabetic subjects. J Clin Invest 1967; 46: 1954–1962
    OpenUrlCrossRefPubMedWeb of Science
  32. ↵
    1. Ebert R,
    2. Creutzfeldt W
    : Gastrointestinal peptides and insulin secretion. Diabetes Metab Rev 1987; 3: 1–26
    OpenUrlPubMed
  33. ↵
    1. D'Alessio DA,
    2. Vogel R,
    3. Prigeon R,
    4. Laschansky E,
    5. Koerker D,
    6. Eng J,
    7. Ensinck JW
    : Elimination of the action of glucagon-like peptide 1 causes an impairment of glucose tolerance after nutrient ingestion by healthy baboons. J Clin Invest 1996; 97: 133–138
    OpenUrlCrossRefPubMedWeb of Science
  34. ↵
    1. Baggio L,
    2. Kieffer TJ,
    3. Drucker DJ
    : Glucagon-like peptide-1, but not glucose-dependent insulinotropic peptide, regulates fasting glycemia and nonenteral glucose clearance in mice. Endocrinology 2000; 141: 3703–3709
    OpenUrlCrossRefPubMedWeb of Science
  35. ↵
    1. Vahl TP,
    2. Tauchi M,
    3. Durler TS,
    4. Elfers EE,
    5. Fernandes TM,
    6. Bitner RD,
    7. Ellis KS,
    8. Woods SC,
    9. Seeley RJ,
    10. Herman JP,
    11. D'Alessio DA
    : Glucagon-like peptide-1 (GLP-1) receptors expressed on nerve terminals in the portal vein mediate the effects of endogenous GLP-1 on glucose tolerance in rats. Endocrinology 2007; 148: 4965–4973
    OpenUrlCrossRefPubMedWeb of Science
  36. ↵
    1. Sandoval DA,
    2. Bagnol D,
    3. Woods SC,
    4. D'Alessio DA,
    5. Seeley RJ
    : Arcuate glucagon-like peptide 1 receptors regulate glucose homeostasis but not food intake. Diabetes 2008; 57: 2046–2054
    OpenUrlAbstract/FREE Full Text
  37. ↵
    1. Masur K,
    2. Tibaduiza EC,
    3. Chen C,
    4. Ligon B,
    5. Beinborn M
    : Basal receptor activation by locally produced glucagon-like peptide-1 contributes to maintaining beta-cell function. Mol Endocrinol 2005; 19: 1373–1382
    OpenUrlCrossRefPubMedWeb of Science
  38. ↵
    1. Serre V,
    2. Dolci W,
    3. Schaerer E,
    4. Scrocchi L,
    5. Drucker D,
    6. Efrat S,
    7. Thorens B
    : Exendin-(9–39) is an inverse agonist of the murine glucagon-like peptide-1 receptor: implications for basal intracellular cyclic adenosine 3′,5′-monophosphate levels and beta-cell glucose competence. Endocrinology 1998; 139: 4448–4454
    OpenUrlCrossRefPubMedWeb of Science
  39. ↵
    1. Nauck MA
    : Is glucagon-like peptide 1 an incretin hormone? Diabetologia 1999; 42: 373–379
    OpenUrlCrossRefPubMedWeb of Science
  40. ↵
    1. Nauck MA,
    2. Niedereichholz U,
    3. Ettler R,
    4. Holst JJ,
    5. Orskov C,
    6. Ritzel R,
    7. Schmiegel WH
    : Glucagon-like peptide 1 inhibition of gastric emptying outweighs its insulinotropic effects in healthy humans. Am J Physiol 1997; 273: E981–E988
    OpenUrlPubMedWeb of Science
  41. ↵
    1. Schwartz JG,
    2. Green GM,
    3. Guan D,
    4. McMahan CA,
    5. Phillips WT
    : Rapid gastric emptying of a solid pancake meal in type II diabetic patients. Diabetes Care 1996; 19: 468–471
    OpenUrlAbstract/FREE Full Text
  42. ↵
    1. Bertin E,
    2. Schneider N,
    3. Abdelli N,
    4. Wampach H,
    5. Cadiot G,
    6. Loboguerrero A,
    7. Leutenegger M,
    8. Liehn JC,
    9. Thiefin G
    : Gastric emptying is accelerated in obese type 2 diabetic patients without autonomic neuropathy. Diabete Metab 2001; 27: 357–364
    OpenUrlPubMed
  43. ↵
    1. Deane AM,
    2. Nguyen NQ,
    3. Stevens JE,
    4. Fraser RJ,
    5. Holloway RH,
    6. Besanko LK,
    7. Burgstad C,
    8. Jones KL,
    9. Chapman MJ,
    10. Rayner CK,
    11. Horowitz M
    : Endogenous glucagon-like peptide-1 slows gastric emptying in healthy subjects, attenuating postprandial glycemia. J Clin Endocrinol Metab 2010; 95: 215–221
    OpenUrlCrossRefPubMed
  44. ↵
    1. Vella A,
    2. Bock G,
    3. Giesler PD,
    4. Burton DB,
    5. Serra DB,
    6. Saylan ML,
    7. Dunning BE,
    8. Foley JE,
    9. Rizza RA,
    10. Camilleri M
    : Effects of dipeptidyl peptidase-4 inhibition on gastrointestinal function, meal appearance, and glucose metabolism in type 2 diabetes. Diabetes 2007; 56: 1475–1480
    OpenUrlAbstract/FREE Full Text
PreviousNext
Back to top

In this Issue

June 2010, 59(6)
  • Table of Contents
  • Index by Author
Sign up to receive current issue alerts
View Selected Citations (0)
Print
Download PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for your interest in spreading the word about Diabetes.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Effect of Endogenous GLP-1 on Insulin Secretion in Type 2 Diabetes
(Your Name) has forwarded a page to you from Diabetes
(Your Name) thought you would like to see this page from the Diabetes web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Citation Tools
Effect of Endogenous GLP-1 on Insulin Secretion in Type 2 Diabetes
Marzieh Salehi, Benedict Aulinger, Ronald L. Prigeon, David A. D'Alessio
Diabetes Jun 2010, 59 (6) 1330-1337; DOI: 10.2337/db09-1253

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Add to Selected Citations
Share

Effect of Endogenous GLP-1 on Insulin Secretion in Type 2 Diabetes
Marzieh Salehi, Benedict Aulinger, Ronald L. Prigeon, David A. D'Alessio
Diabetes Jun 2010, 59 (6) 1330-1337; DOI: 10.2337/db09-1253
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • RESEARCH DESIGN AND METHODS
    • RESULTS
    • DISCUSSION
    • ACKNOWLEDGMENTS
    • Footnotes
    • REFERENCES
  • Figures & Tables
  • Info & Metrics
  • PDF

Related Articles

Cited By...

More in this TOC Section

Original Article

  • An Update on the Molecular Actions of Fenofibrate and Its Clinical Effects on Diabetic Retinopathy and Other Microvascular End Points in Patients With Diabetes
  • Loss of Prohibitin Induces Mitochondrial Damages Altering β-Cell Function and Survival and Is Responsible for Gradual Diabetes Development
  • Cbl-b Is a Critical Regulator of Macrophage Activation Associated With Obesity-Induced Insulin Resistance in Mice
Show more Original Article

Metabolism

  • Ncor2/PPARα-Dependent Upregulation of MCUb in the Type 2 Diabetic Heart Impacts Cardiac Metabolic Flexibility and Function
  • Role of the Neutral Amino Acid Transporter SLC7A10 in Adipocyte Lipid Storage, Obesity, and Insulin Resistance
  • Heme Oxygenase-1 Regulates Ferrous Iron and Foxo1 in Control of Hepatic Gluconeogenesis
Show more Metabolism

Similar Articles

Navigate

  • Current Issue
  • Online Ahead of Print
  • Scientific Sessions Abstracts
  • Collections
  • Archives
  • Submit
  • Subscribe
  • Email Alerts
  • RSS Feeds

More Information

  • About the Journal
  • Instructions for Authors
  • Journal Policies
  • Reprints and Permissions
  • Advertising
  • Privacy Policy: ADA Journals
  • Copyright Notice/Public Access Policy
  • Contact Us

Other ADA Resources

  • Diabetes Care
  • Clinical Diabetes
  • Diabetes Spectrum
  • Scientific Sessions Abstracts
  • Standards of Medical Care in Diabetes
  • BMJ Open - Diabetes Research & Care
  • Professional Books
  • Diabetes Forecast

 

  • DiabetesJournals.org
  • Diabetes Core Update
  • ADA's DiabetesPro
  • ADA Member Directory
  • Diabetes.org

© 2021 by the American Diabetes Association. Diabetes Print ISSN: 0012-1797, Online ISSN: 1939-327X.