V. V. Zakusov Research Institute of Pharmacology, Moscow, Russia.
Bull Exp Biol Med. 2022 May;173(1):37-40. doi: 10.1007/s10517-022-05488-1. Epub 2022 May 27.
A low-molecular-weight nerve growth factor mimetic, compound GK-2 (bis-(N-monosuccinyl- L-glutamyl-L-lysine)hexamethylenediamide) that previously demonstrated antidiabetic activity in rats with streptozotocin-induced type 2 diabetes mellitus was studied on the model of diabetic neuropathy. It was found that in 8 weeks after diabetes mellitus development, untreated diabetic rats demonstrated impaired tactile sensitivity in von Frey test, while GK-2 therapy (7.5 mg/kg orally for 28 days) restored this parameter. The decrease of tactile sensitivity in diabetic neuropathy closely correlated with the severity of hyperglycemia (r=0.76). Our findings are consistent with the concept on the role of glucose toxicity and nerve growth factor deficiency in the pathogenesis of diabetic neuropathy and attest to feasibility of further studies of nerve growth factor mimetic GK-2 as a potential treatment for diabetes and diabetic neuropathy.
一种低分子量神经生长因子模拟物,化合物 GK-2(双-(N-单琥珀酰-L-谷氨酰-L-赖氨酸)六亚甲基二胺),先前在链脲佐菌素诱导的 2 型糖尿病大鼠中表现出抗糖尿病活性,在糖尿病神经病变模型上进行了研究。研究发现,在糖尿病发展 8 周后,未经治疗的糖尿病大鼠在 von Frey 试验中触觉敏感性受损,而 GK-2 治疗(口服 7.5mg/kg,持续 28 天)恢复了这一参数。糖尿病神经病变中触觉敏感性的降低与高血糖的严重程度密切相关(r=0.76)。我们的发现与葡萄糖毒性和神经生长因子缺乏在糖尿病神经病变发病机制中的作用的概念一致,并证明进一步研究神经生长因子模拟物 GK-2 作为治疗糖尿病和糖尿病神经病变的潜在治疗方法是可行的。