Kelany Mohamed Elsayed, Hakami Tahir M, Omar Adel H, Abdallah Mohamed A
Department of Clinical Pharmacology, Faculty of Medicine, Jazan University, Jazan, Saudi Arabia.
Pharmacology. 2016;98(5-6):242-250. doi: 10.1159/000448043. Epub 2016 Jul 23.
The present study evaluated the effects of sitagliptin-insulin against type 2 diabetes mellitus with neuropathy in rats and possible neuroprotective mechanisms.
Diabetes was induced in 32 adult male albino rats by 6-week high-fat high-sugar diet followed by streptozotocin 30 mg/kg intraperitoneal injection. For 4 weeks thereafter, diabetic rats were divided into 4 groups, each group receiving one of the following daily: vehicle (untreated diabetic), insulin 10 IU/kg SC, sitagliptin 30 mg/kg PO or sitagliptin-insulin. We assessed systolic blood pressure (SBP), blood glucose, serum insulin and advanced glycation end-products (AGEs), thermal hyperalgesia and sciatic nerve tumor necrosis factor-alpha (TNF-α), superoxide dismutase (SOD) and malondialdehyde (MDA) and sciatic histopathology.
Compared to untreated and insulin-treated groups, sitagliptin decreased SBP, serum AGEs and sciatic MDA and TNF-α, and increased serum insulin and sciatic SOD, but insulin decreased blood glucose more. Sitagliptin-insulin (greater than sitagliptin or insulin alone) superiorly decreased and increased the above respective parameters, and ameliorated hyperalgesia and sciatic histopathological changes, but was similar to insulin in decreasing blood glucose, and similar to sitagliptin in rising serum insulin.
Sitagliptin-insulin combination produced hypoglycemic and neuroprotective effect and ameliorated hyperalgesia, oxidative stress and inflammation more than either drug alone. This combination might have clinical efficacy in uncontrolled type 2 diabetes with neuropathy.
本研究评估了西他列汀 - 胰岛素对大鼠2型糖尿病伴神经病变的影响及可能的神经保护机制。
32只成年雄性白化大鼠通过6周高脂高糖饮食诱导糖尿病,随后腹腔注射30mg/kg链脲佐菌素。此后4周,将糖尿病大鼠分为4组,每组每天接受以下一种处理:赋形剂(未治疗的糖尿病大鼠)、10IU/kg皮下注射胰岛素、30mg/kg口服西他列汀或西他列汀 - 胰岛素。我们评估了收缩压(SBP)、血糖、血清胰岛素和晚期糖基化终产物(AGEs)、热痛觉过敏以及坐骨神经肿瘤坏死因子 -α(TNF -α)、超氧化物歧化酶(SOD)和丙二醛(MDA),并进行了坐骨神经组织病理学检查。
与未治疗组和胰岛素治疗组相比,西他列汀降低了SBP、血清AGEs以及坐骨神经的MDA和TNF -α,并增加了血清胰岛素和坐骨神经SOD,但胰岛素降低血糖的效果更明显。西他列汀 - 胰岛素(比单独使用西他列汀或胰岛素效果更好)更显著地降低和增加了上述相应参数,并改善了痛觉过敏和坐骨神经组织病理学变化,但在降低血糖方面与胰岛素相似,在升高血清胰岛素方面与西他列汀相似。
西他列汀 - 胰岛素联合用药产生了降血糖和神经保护作用,并且比单独使用任何一种药物更能改善痛觉过敏、氧化应激和炎症。这种联合用药可能对未控制的2型糖尿病伴神经病变具有临床疗效。