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Diabetes, Vol 41, Issue 7 872-878, Copyright © 1992 by American Diabetes Association
Enhanced glucose tolerance in spontaneously hypertensive rats. Pancreatic beta-cell hyperfunction with normal insulin sensitivity
TA Buchanan, JH Youn, VM Campese and GF Sipos
Department of Medicine, University of Southern California Medical School, Los Angeles.
We used intravenous glucose tolerance tests in vivo and 3-O-methylglucose
transport into skeletal muscle in vitro to assess glucose tolerance,
pancreatic beta-cell function, and insulin action in 9- to 11-wk-old
spontaneously hypertensive rats (SHR) and age-matched normotensive Wistar
Kyoto rats (WKY). Body weight was slightly higher in the WKY (P less than
0.001), while blood pressure was elevated in the SHR (P less than 0.001).
Insulin responses to intravenous glucose after 4 or 12 h of fasting in SHR
were 2-3 times the responses of WKY rats (P less than 0.001). The greater
insulin responses in SHR were associated with accelerated glucose
disappearance P less than 0.001 vs. WKY rats). A direct correlation (r =
0.49, P less than 0.05) between the peak plasma insulin responses to
glucose and Kg values in SHR suggested that the exaggerated insulin
responses contributed to the accelerated glucose disappearance in that
group. 3-O-methylglucose transport rates into epitrochlearis muscles in
vitro did not differ significantly between SHR and WKY groups in the
absence of insulin (P less than 0.2) or in the presence of insulin at
physiological (600 pM, P greater than 0.4) or pharmacological (120,000 pM,
P greater than 0.9) concentrations. Thus, compared with WKY rats, SHR had
exaggerated insulin responses to glucose, similar insulin-mediated glucose
transport into skeletal muscle, and enhanced glucose tolerance. Our
findings indicate that young, hypertensive SHR have hyperfunction of
pancreatic beta-cells that is unrelated to insulin resistance. The
resultant nutrient-stimulated hyperinsulinemia could play a role in the
development or maintenance of elevated blood pressure in SHR.

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Copyright © 1992 by the American Diabetes Association.
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