NEUROTROPIN PREVENTS NEUROPSYCHOLOGICAL ABNORMALITIES AND ADP-INDUCED HYPERAGGREGABILITY IN RATS WITH STREPTOZOTOCIN-INDUCED DIABETES

被引:5
作者
HOTTA, N
KOH, N
SAKAKIBARA, F
NAKAMURA, J
HARA, T
YAMADA, H
HAMADA, Y
TAKEUCHI, N
机构
[1] The Third Department of Internal Medicine, Nagoya University School of Medicine, Showa-ku, Nagoya, 466
关键词
STREPTOZOTOCIN-INDUCED DIABETES; MOTOR NERVE CONDUCTION VELOCITY; SCIATIC NERVE BLOOD FLOW; PLATELET AGGREGATION; SORBITOL NEUROTROPIN;
D O I
10.1016/0024-3205(95)02203-U
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
Neurotropin, a non-proteinaceous extract from the inflamed dermis of rabbits inoculated with vaccinia virus, was administered for 8 weeks to rats with streptozotocin-induced diabetes. The physiological and biochemical changes of the nerves were studied as well as ADP-induced platelet aggregation. Neurotropin improved the caudal motor nerve conduction velocity, R-R variability, sciatic nerve blood flow, and platelet hyperaggregability in diabetic rats, despite having no effect on sorbitol and fructose accumulation or myoinositol depletion in the sciatic nerve. The correlation between nerve conduction velocity, R-R variability, nerve blood how, and platelet aggregation were significant between each two parameters (p < 0.0001). Thus, the mechanism of action of neurotropin differed from that of aldose reductase inhibitors. These findings suggest that vascular factors may play an important role in the development of diabetic neuropathy, and that neurotropin may be useful for the treatment of this condition.
引用
收藏
页码:2101 / 2111
页数:11
相关论文
共 52 条
[1]
NERVE GROWTH-FACTOR PREVENTS EXPERIMENTAL CISPLATIN NEUROPATHY [J].
APFEL, SC ;
AREZZO, JC ;
LIPSON, L ;
KESSLER, JA .
ANNALS OF NEUROLOGY, 1992, 31 (01) :76-80
[2]
ADENOSINE DIPHOSPHATE-INDUCED PLATELET AGGREGATION IN SUSPENSIONS OF WASHED RABBIT PLATELETS [J].
ARDLIE, NG ;
PACKHAM, MA ;
MUSTARD, JF .
BRITISH JOURNAL OF HAEMATOLOGY, 1970, 19 (01) :7-&
[3]
ACUTE ENDOTHELIAL SWELLING IS INDUCED IN ENDONEURIAL MICROVESSELS BY ISCHEMIA [J].
BENSTEAD, TJ ;
SANGALANG, VE ;
DYCK, PJ .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1990, 99 (01) :37-49
[4]
Bergmeyer H. U., 1974, METHOD ENZYMAT AN, V3, P1323
[5]
Bernt E., 1974, METHOD ENZYMAT AN, P1304
[6]
RELATIONSHIP OF ENDONEURIAL CAPILLARY ABNORMALITIES TO TYPE AND SEVERITY OF DIABETIC POLYNEUROPATHY [J].
BRITLAND, ST ;
YOUNG, RJ ;
SHARMA, AK ;
CLARKE, BF .
DIABETES, 1990, 39 (08) :909-913
[7]
POTENTIAL THERAPEUTIC APPROACHES TO THE TREATMENT OR PREVENTION OF DIABETIC NEUROPATHY - EVIDENCE FROM EXPERIMENTAL STUDIES [J].
CAMERON, NE ;
COTTER, MA .
DIABETIC MEDICINE, 1993, 10 (07) :593-605
[8]
POLYOL PATHWAY IN AORTA - REGULATION BY HORMONES [J].
CLEMENTS, RS ;
MORRISON, AD ;
WINEGRAD, AI .
SCIENCE, 1969, 166 (3908) :1007-&
[9]
COLWELL JA, 1976, DIABETES, V25, P826
[10]
FIBER LOSS IS PRIMARY AND MULTIFOCAL IN SURAL NERVES IN DIABETIC POLYNEUROPATHY [J].
DYCK, PJ ;
LAIS, A ;
KARNES, JL ;
OBRIEN, P ;
RIZZA, R .
ANNALS OF NEUROLOGY, 1986, 19 (05) :425-439