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Diabetes, Vol 48, Issue 10 2090-2095, Copyright © 1999 by American Diabetes Association
A protein kinase C-beta-selective inhibitor ameliorates neural dysfunction in streptozotocin-induced diabetic rats
J Nakamura, K Kato, Y Hamada, M Nakayama, S Chaya, E Nakashima, K Naruse, Y Kasuya, R Mizubayashi, K Miwa, Y Yasuda, H Kamiya, K Ienaga, F Sakakibara, N Koh and N Hotta
Third Department of Internal Medicine, Nagoya University School of Medicine, Japan. jiro@tsuru.med.nagoya-u.ac.jp
Increased protein kinase C (PKC) activity has been implicated in the
pathogenesis of diabetic retinopathy and nephropathy. However, the role of
PKC in diabetic neuropathy remains unclear. The present study was conducted
to compare the effect of PKC inhibition by a PKC-beta-selective inhibitor,
LY333531 (LY), on diabetic nerve dysfunction with that of an aldose
reductase inhibitor, NZ-314 (NZ). Streptozotocin-induced diabetic rats were
treated with or without LY and/or NZ for 4 weeks, and motor nerve
conduction velocity (MNCV), coefficient of variation of R-R interval
(CVR-R), sciatic nerve blood flow (SNBF), peak latencies of oscillatory
potentials on electroretinogram, PKC activities in membranous and cytosolic
fractions of sciatic nerves, and polyol contents in the tail nerves were
measured. Untreated diabetic rats demonstrated delayed MNCV, decreased
CVR-R, reduced SNBF, and prolonged peak latencies of oscillatory
potentials. Treatment with LY as well as NZ prevented all these deficits in
diabetic rats. There were no significant differences in PKC activities in
membranous or cytosolic fractions of sciatic nerves between normal and
diabetic rats. Treatment with neither LY nor NZ altered PKC activities.
Nerve myo-inositol depletion in diabetic rats was ameliorated not only by
NZ, but also by LY. These observations suggest that inhibition of PKC-beta
by LY may have a beneficial effect in preventing the development of
diabetic nerve dysfunction, and that this effect may be mediated through
its action on the endoneurial micro-vasculature.

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Copyright © 1999 by the American Diabetes Association.
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