Pechlivanova D, Petrov K, Grozdanov P, Nenchovska Z, Tchekalarova J, Stoynev A
a Institute of Neurobiology, Bulgarian Academy of Sciences, 23 Acad. G. Bonchev Str., 1113 Sofia, Bulgaria.
b Department of Pathophysiology, Medical University-Sofia, 1 Georgi Sofiiski Str., 1431 Sofia, Bulgaria.
Can J Physiol Pharmacol. 2018 May;96(5):471-478. doi: 10.1139/cjpp-2017-0428. Epub 2017 Oct 13.
Cumulative data suggest the significant role of the renin-angiotensin system in the development of the pathological consequences of diabetes mellitus (DM). Newly synthesized AT2 receptor agonists gained importance as a target for creating new antihypertensives. The aim of the present work was to study the effects of peptide AT2 agonist novokinin, infused intracerebroventricularly, on the consequences of the streptozotocin-induced type 1 DM (T1DM) in Wistar rats. Food and water consumption, body mass, urine excretion (metabolic cages), motor activity (open-field test), anxiety (elevated plus maze), nociception (paw pressure analgesimeter test), spatial memory (T-maze alternation test), and plasma levels of glucose and corticosterone (ELISA) were assessed 2 weeks after the T1DM induction. Novokinin increased water and food consumption, as well as urine output, and reduced mass gain in the control rats. Diabetic rats demonstrated hyperalgesia, increased level of plasma corticosterone, decreased motor and exploratory activity, and impaired spatial memory. Novokinin infusion increased water intake, diuresis, and mortality rate, decreased food intake, exacerbated diabetes-induced hyperalgesia, and provoked anxiety-like behavior but improved spatial memory in diabetic rats. These initial data suggest that angiotensin AT2 receptors participate in the pathogenesis of T1DM-induced complications in the function of the nervous system.
累积数据表明肾素 - 血管紧张素系统在糖尿病(DM)病理后果的发展中起重要作用。新合成的AT2受体激动剂作为新型抗高血压药物的靶点变得越来越重要。本研究的目的是研究脑室内注射肽类AT2激动剂诺沃基宁对链脲佐菌素诱导的Wistar大鼠1型糖尿病(T1DM)后果的影响。在诱导T1DM两周后,评估食物和水的消耗量、体重、尿液排泄(代谢笼)、运动活动(旷场试验)、焦虑(高架十字迷宫)、痛觉感受(爪压镇痛仪试验)、空间记忆(T迷宫交替试验)以及血浆葡萄糖和皮质酮水平(酶联免疫吸附测定)。诺沃基宁增加了对照大鼠的水和食物消耗量以及尿量,并减少了体重增加。糖尿病大鼠表现出痛觉过敏、血浆皮质酮水平升高、运动和探索活动减少以及空间记忆受损。注射诺沃基宁增加了糖尿病大鼠的水摄入量、利尿和死亡率,减少了食物摄入量,加剧了糖尿病诱导的痛觉过敏,并引发了焦虑样行为,但改善了空间记忆。这些初步数据表明,血管紧张素AT2受体参与了T1DM诱导的神经系统功能并发症的发病机制。