首页> 外文期刊>Behavioural Brain Research: An International Journal >Candesartan improves memory decline in mice: involvement of AT1 receptors in memory deficit induced by intracerebral streptozotocin.
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Candesartan improves memory decline in mice: involvement of AT1 receptors in memory deficit induced by intracerebral streptozotocin.

机译:坎地沙坦可改善小鼠的记忆力减退:AT1受体参与脑内链脲佐菌素诱导的记忆力减退。

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The Renin-angiotensin system, besides blood pressure regulation, affects learning and memory as evidenced by improvement of cognition in hypertensive patients being treated with AT1 receptor blockers like candesartan. The present study examined the influence of candesartan on memory impairment induced by intracerebral streptozotocin (IC STZ 0.5 mg/kg) in mice. Candesartan (0.05 mg/kg and 0.1 mg/kg, i.p.) was given for 14 days following IC STZ administration. The dose of 0.1 mg/kg significantly improved latency period in passive avoidance test. Further, treatment with 0.1 mg/kg candesartan for 14 days significantly improved spatial memory in mice in water maze test also. In another group, after memory impairment in mice following IC STZ administration, memory improving effect of a 7 days treatment with 0.1 mg/kg candesartan lasted only for 3 subsequent days in water maze task. IC STZ increased oxidative stress but pretreatment with 0.1 mg/kg candesartan decreased oxidative stress as indicated by a decrease in MDA and increase in GSH. Further, candesartan decreased free radicals as evidenced by flow cytometry. IC STZ affected cholinergic system also by increasing acetylcholine esterase activity that was restored by pretreatment with 0.1 mg/kg candesartan. Locomotor activity and serum glucose level remained unaffected by candesartan treatment. These results suggest that AT1 receptors play a facilitatory role in STZ induced memory deficit and corroborate number of human studies that AT1 receptor blockers can be used therapeutically against cognitive decline in hypertensive patients.
机译:肾素-血管紧张素系统除调节血压外,还影响学习和记忆,这是通过接受坎地沙坦等AT1受体阻滞剂治疗的高血压患者认知能力的改善所证明的。本研究检查了坎地沙坦对小鼠脑内链脲佐菌素(IC STZ 0.5 mg / kg)诱导的记忆障碍的影响。在IC STZ给药后14天给予坎地沙坦(0.05mg / kg和0.1mg / kg,腹膜内)。 0.1 mg / kg的剂量可显着改善被动回避测试的潜伏期。此外,在水迷宫测试中,用0.1 mg / kg坎地沙坦治疗14天也显着改善了小鼠的空间记忆。在另一组中,IC STZ给药后小鼠记忆力减退后,在水迷宫任务中,用0.1 mg / kg坎地沙坦治疗7天的记忆力改善作用仅持续了3天。 IC STZ可增加氧化应激,但0.1 mg / kg坎地沙坦预处理可降低氧化应激,如MDA降低和GSH升高所表明。此外,坎地沙坦减少了自由基,如流式细胞术所证明的。 IC STZ还通过增加乙酰胆碱酯酶活性来影响胆碱能系统,该活性可通过用0.1 mg / kg坎地沙坦预处理来恢复。运动活性和血清葡萄糖水平不受坎地沙坦治疗的影响。这些结果表明,AT1受体在STZ诱导的记忆缺陷中起促进作用,并证实了许多关于AT1受体阻滞剂可用于治疗高血压患者认知功能下降的研究。

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