Histopathological Study of Evening Primrose Oil Effects on Experimental Diabetic Neuropathy

被引:16
作者
Omran, Ola M. [1 ,2 ]
机构
[1] Assiut Univ Hosp, Fac Med, Dept Pathol, Assiut, Egypt
[2] Ohio State Univ, Dept Pathol 4166, Columbus, OH 43210 USA
关键词
Diabetic polyneuropathy; evening primrose oil; experimental study; sciatic nerve; streptozotocin; OXIDATIVE STRESS; C-PEPTIDE; NERVE; RATS; COMPLICATIONS; REGENERATION; GROWTH; ACID; REPLACEMENT; ANTIOXIDANT;
D O I
10.3109/01913123.2012.662268
中图分类号
TH742 [显微镜];
学科分类号
080401 [精密仪器及机械];
摘要
Diabetic polyneuropathy is a serious complication of diabetes mellitus and the most frequent neuropathy worldwide. Aim: This study was designed to investigate the possible beneficial effects of evening primrose oil (EPO) on histopathological changes of sciatic nerves in streptozotocin-induced diabetic rats. Materials and methods: The rats were randomly allotted into three experimental groups: A (control), B (diabetic untreated), and C (diabetic treated with EPO); each group contained 10 animals. Groups B and C received streptozotocin (STZ) to induce diabetes. The rats in group C were given EPO for 2 weeks after 6 weeks of STZ injection. Blood and tissue samples were obtained for biochemical and histopathological investigation. Results: STZ-treated diabetic rats showed reduction of the size of islets of Langerhans, fatty degeneration in the pancreatic acini with dilation, irregularity, and increased thickness of blood vessels. Electron micrography of sciatic nerves of diabetic rats showed multiple vaculations and partial separation of myelinated nerve fibers with axonal atrophy, endoneural edema, and increased collagen fibers. Compared with diabetic rats, EPO induced partial recovery from diabetes-induced pancreatic and nerve damage. Conclusions: Histologic evaluation of the tissues in diabetic animals treated with EPO showed fewer morphologic alterations with significant decrease of myelin breakdown. Furthermore, the ultrastructural features of axons showed partial improvement. It is believed that further preclinical research into the utility of EPO may indicate its usefulness as a potential treatment on peripheral neuropathy in STZ-induced diabetic rats.
引用
收藏
页码:222 / 227
页数:6
相关论文
共 40 条
[1]
Interleukin-6 attenuates the development of experimental diabetes-related neuropathy [J].
Andriambeloson, E ;
Baillet, C ;
Vitte, PA ;
Garotta, G ;
Dreano, M ;
Callizot, N .
NEUROPATHOLOGY, 2006, 26 (01) :32-42
[2]
Nerve regeneration in diabetic neuropathy [J].
Apfel, SC .
DIABETES OBESITY & METABOLISM, 1999, 1 (01) :3-11
[3]
Prevention of incipient diabetic nephropathy by high-dose thiamine and benfotiamine [J].
Babaei-Jadidi, R ;
Karachalias, N ;
Ahmed, N ;
Battah, S ;
Thornalley, PJ .
DIABETES, 2003, 52 (08) :2110-2120
[4]
Protective effects of ferulic acid on hyperlipidemic diabetic rats [J].
Balasubashini, MS ;
Rukkumani, R ;
Menon, VP .
ACTA DIABETOLOGICA, 2003, 40 (03) :118-122
[5]
ROLE OF OXIDATIVE STRESS IN DEVELOPMENT OF COMPLICATIONS IN DIABETES [J].
BAYNES, JW .
DIABETES, 1991, 40 (04) :405-412
[6]
ON THE PROTECTION AGAINST ALLOXAN DIABETES BY HEXOSES [J].
BHATTACHARYA, G .
SCIENCE, 1954, 120 (3125) :841-843
[7]
Metabolic and vascular factors in the pathogenesis of diabetic neuropathy [J].
Cameron, NE ;
Cotter, MA .
DIABETES, 1997, 46 :S31-S37
[8]
CARTER JP, 1988, FOOD TECHNOL-CHICAGO, V42, P72
[9]
Diabetes-induced myelin abnormalities are associated with an altered lipid pattern: protective effects of LXR activation [J].
Cermenati, Gaia ;
Abbiati, Federico ;
Cermenati, Solei ;
Brioschi, Elisabetta ;
Volonterio, Alessandro ;
Cavaletti, Guido ;
Saez, Enrique ;
De Fabiani, Emma ;
Crestani, Maurizio ;
Garcia-Segura, Luis M. ;
Melcangi, Roberto C. ;
Caruso, Donatella ;
Mitro, Nico .
JOURNAL OF LIPID RESEARCH, 2012, 53 (02) :300-310
[10]
Role of growth factors in the development of diabetic complications [J].
Chiarelli, F ;
Santilli, F ;
Mohn, A .
HORMONE RESEARCH, 2000, 53 (02) :53-67