Kumar Sokindra, Arun K H S, Kaul Chaman L, Sharma Shyam S
Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Sec-67, SAS Nagar, Punjab-160062, India.
Neurol Res. 2005 Jan;27(1):60-6. doi: 10.1179/016164105X18278.
This study examined the effects of chronic administration of adenosine and CGS 21680 hydrochloride (adenosine A(2A) receptor agonist) on motor nerve conduction velocity (MNCV), nerve blood flow (NBF) and histology of sciatic nerve in animal model of diabetic neuropathy. Adenosinergic agents were administered for 2 weeks after 6 weeks of streptozotocin-induced (50 mg/kg i.p.) diabetes in male Sprague-Dawley rats. Significant reduction in sciatic MNCV and NBF were observed after 8 weeks in diabetic animals in comparison with control (non diabetic) rats. Adenosine (10 mg/kg, i.p.) significantly improved sciatic MNCV and NBF in diabetic rats. The protective effect of adenosine on MNCV and NBF was completely reversed by theophylline (50 mg/kg, i.p.), a non-selective adenosine receptor antagonist, suggesting that the adenosine effect was mediated via adenosinergic receptors. CGS 21680 (0.1 mg/kg, i.p.) significantly improved NBF; however, MNCV was not significantly improved in diabetic rats. At a dose of 1 mg/kg, neither MNCV nor NBF was improved by CGS 21680 in diabetic rats. ZM 241385 (adenosine A(2A) receptor antagonist) prevented the effect of CGS 21680 (0.1 mg/kg, i.p.). Histological changes observed in sciatic nerve were partially improved by the adenosinergic agents in diabetic rats. Results of the present study, suggest the potential of adenosinergic agents in the therapy of diabetic neuropathy.
本研究在糖尿病性神经病变动物模型中,检测了长期给予腺苷和盐酸CGS 21680(腺苷A(2A)受体激动剂)对运动神经传导速度(MNCV)、神经血流(NBF)以及坐骨神经组织学的影响。在雄性Sprague-Dawley大鼠经链脲佐菌素(50 mg/kg腹腔注射)诱导糖尿病6周后,给予腺苷能药物2周。与对照(非糖尿病)大鼠相比,糖尿病动物在8周后坐骨神经的MNCV和NBF显著降低。腺苷(10 mg/kg腹腔注射)可显著改善糖尿病大鼠的坐骨神经MNCV和NBF。非选择性腺苷受体拮抗剂茶碱(50 mg/kg腹腔注射)可完全逆转腺苷对MNCV和NBF的保护作用,提示腺苷的作用是通过腺苷能受体介导的。CGS 21680(0.1 mg/kg腹腔注射)可显著改善NBF;然而,糖尿病大鼠的MNCV未得到显著改善。在1 mg/kg剂量时,CGS 21680对糖尿病大鼠的MNCV和NBF均无改善作用。ZM 241385(腺苷A(2A)受体拮抗剂)可阻断CGS 21680(0.1 mg/kg腹腔注射)的作用。糖尿病大鼠坐骨神经的组织学变化经腺苷能药物部分改善。本研究结果提示腺苷能药物在糖尿病性神经病变治疗中的潜力。