Korean J Intern Med.
1999 Jul;14(2):34-40.
Effect of cilostazol on the neuropathies of streptozotocin-induced diabetic
rats
- Affiliations
-
- 1Division of Endocrinology & Metabolism, Department of Internal Medicine, Endocrine Research Institute, Kyung Hee University School of Medicine, Seoul, Korea.
- 2Department of Applied Biology, College of Life Resource Science, Dongguk University, Seoul, Korea.
Abstract
OBJECTIVES
This study examined the effect of cilostazol, a potent
phosphodiesterase inhibitor, on the progression of neuropathies associated with
streptozotocin-induced diabetes mellitus in Sprague-Dawley rats. METHODS: Eight
weeks after streptozotocin treatment, a pelleted diet containing 0.03%
cilostazol (15 mg/kg body weight) was given for four weeks. Body weight, blood
glucose level, motor nerve conduction velocity (MNCV), myelinated fiber density
and size distribution of sciatic nerves were compared between age-matched normal
rats (Group 1), control diabetic rats (Group 2) and cilostazol-treated diabetic
rats (Group 3). RESULTS: Body weight was significantly reduced and blood glucose
level was significantly increased in diabetic rats (Group 2 and 3) compared to
normal rats. MNCV and cAMP content of sciatic nerves were significantly reduced
in diabetic rats 12 weeks after streptozotocin treatment. Myelinated fiber size
and density were also significantly reduced, and thickening of the capillary
walls and duplication of the basement membranes of the endoneural vessels were
observed in the diabetic rats. Whereas both body weight and blood glucose level
of Group 3 did not differ significantly from those of Group 2, cilostazol
treatment significantly increased MNCV and cAMP content of sciatic nerves in
Group 3 but not to the levels observed in Group 1. MNCV positively correlated
with cAMP content of sciatic nerves (r = 0.86; p < 0.001). Cilostazol treatment
not only restored myelinated fiber density and size distribution but reversed
some of the vascular abnormalities. CONCLUSION: These findings suggest that a
reduced cAMP content in motor nerves may be involved in the development of
diabetic neuropathy, and that cilostazol may prevent the progression of diabetic
neuropathy by restoring functional impairment and morphological changes of
peripheral nerves.