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氯沙坦对 Wistar 和自发性高血压大鼠 2 型糖尿病诱导的一些并发症的保护作用。

Protective effects of losartan on some type 2 diabetes mellitus-induced complications in Wistar and spontaneously hypertensive rats.

机构信息

Institute of Neurobiology, Bulgarian Academy of Sciences, Acad. G. Bonchev Str., Bl. 23, 1113, Sofia, Bulgaria.

Institute of Microbiology, Bulgarian Academy of Sciences, Acad. G. Bonchev Str., Bl. 23, 1113, Sofia, Bulgaria.

出版信息

Metab Brain Dis. 2020 Mar;35(3):527-538. doi: 10.1007/s11011-020-00534-1. Epub 2020 Jan 29.

Abstract

Diabetes mellitus type 2 (T2DM) is characterized by resistance of insulin receptors and/or inadequate insulin secretion resulting in metabolic and structural complications including vascular diseases, arterial hypertension and different behavioral alterations. We aimed to study the effects of the antihypertensive angiotensin AT1 receptor antagonist losartan on the T2DM-induced changes of exploratory behavior, anxiety, nociception and short term memory in normotensive Wistar and spontaneously hypertensive rats (SHRs). The experimental model of T2DM induced by a combination of high fat diet and streptozotocin, decreased exploratory activity and increased the level of carbonylated proteins in selected brain structures in both strains; as well it increased corticosterone level, pain threshold, anxiety-like behavior, and decline short term memory only in SHRs. Losartan treatment alleviated some of the T2DM- induced metabolic complications, abolished the T2DM-induced hypo activity, and normalized the corticosterone level, carbonylated proteins in brain, nociception and memory. Losartan did not exert effect on the anxiety behavior in both strains. We showed that T2DM exerted more pronounced negative effects on the rats with comorbid hypertension as compared to normotensive rats. Overall effects on the studied behavioral parameters are related to decreased exploration of the new environment, increased anxiety-like behavior, and decline in short-term memory. The systemic sub-chronic treatment with an angiotensin AT1 receptor antagonist losartan ameliorated most of these complications.

摘要

2 型糖尿病(T2DM)的特征是胰岛素受体的抵抗和/或胰岛素分泌不足,导致代谢和结构并发症,包括血管疾病、动脉高血压和不同的行为改变。我们旨在研究抗高血压血管紧张素 AT1 受体拮抗剂氯沙坦对正常血压 Wistar 大鼠和自发性高血压大鼠(SHR)中 T2DM 诱导的探索行为、焦虑、痛觉和短期记忆变化的影响。由高脂肪饮食和链脲佐菌素联合诱导的 T2DM 实验模型降低了两种品系的探索性活动,并增加了选定脑结构中羰基化蛋白的水平;同时,它还增加了皮质酮水平、疼痛阈值、焦虑样行为,并仅在 SHR 中降低了短期记忆。氯沙坦治疗缓解了 T2DM 引起的一些代谢并发症,消除了 T2DM 引起的低活性,并使皮质酮水平、大脑中的羰基化蛋白、痛觉和记忆正常化。氯沙坦对两种品系的焦虑行为均无影响。我们表明,与正常血压大鼠相比,T2DM 对合并高血压的大鼠产生了更明显的负面影响。对所研究的行为参数的总体影响与探索新环境的减少、焦虑样行为的增加和短期记忆的下降有关。用血管紧张素 AT1 受体拮抗剂氯沙坦进行系统的亚慢性治疗改善了这些并发症中的大多数。

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