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慢性丙酸睾酮补充可能会激活大脑中的 Nrf2-ARE 通路,并改善老年大鼠的行为。

Chronic testosterone propionate supplement could activated the Nrf2-ARE pathway in the brain and ameliorated the behaviors of aged rats.

机构信息

Department of Neurobiology, Hebei Medical University, Shijiazhuang, Hebei 050017, PR China.

出版信息

Behav Brain Res. 2013 Sep 1;252:388-95. doi: 10.1016/j.bbr.2013.05.063. Epub 2013 Jun 10.

Abstract

Aging is usually associated with a progressive disruption of the redox balance leading to recurrent damage resulting from oxidative stress. Oxidative stress resulting from excessive free-radical release is likely implicated in the initiation and progression of motor behavior disorders. Therefore, antioxidant therapies have received considerable attention in motor behavior defects treatment. The nuclear factor erythroid 2-related factor 2 (Nrf2) binds to antioxidant response element (ARE) to induce antioxidant and phase II detoxification enzymes under conditions of oxidative stress, which reduces oxidative stress and accumulation of toxic metabolites. Testosterone has many physiological and behavioral effects throughout the lifespan and shown to affect motor behavior in adult male rats and gonadectomized rats. However, whether Nrf2-ARE pathway is activated after testosterone administration has not been studied in aged rats. The tilting-plane test and the horizontal-wire test as well as the oxidative stress parameters, the expression of Nrf2, heme oxygenase-1 (HO-1) and NAD(P)H: quinone oxidoreductase-1 (NQO1) and the number of tyrosine hydroxylase immunoreactive (TH-ir) cells in brain were examined in aged rats following chronic subcutaneous injections of testosterone propionate (TP). Our study showed that chronic TP supplement significantly ameliorated the decline of balancing reactions and muscular strength associated with aging. Oxidative stress parameters were ameliorate, the expression of Nrf2, HO-1 and NQO1 at protein or gene levels and the number of TH-ir cells significantly increased in substantia nigra or caudate putamen after TP treatment in aged rats. Our findings demonstrated that chronic TP treatment activated Nrf2-ARE pathway may influence the maintenance of the balancing reactions and muscular strength and reduce TH-ir cells death in aged rats. Therefore, TP supplement have shown for therapeutic strategies in the treatment and modification of motor behavior disorders.

摘要

衰老是与氧化应激导致的反复损伤相关的氧化还原平衡的渐进性破坏。过量自由基释放导致的氧化应激可能与运动行为障碍的发生和进展有关。因此,抗氧化治疗在运动行为缺陷的治疗中受到了广泛关注。核因子红细胞 2 相关因子 2(Nrf2)在氧化应激条件下与抗氧化反应元件(ARE)结合,诱导抗氧化和 II 相解毒酶,从而减少氧化应激和有毒代谢物的积累。睾酮在整个生命周期中具有许多生理和行为作用,并显示出对成年雄性大鼠和去势大鼠的运动行为的影响。然而,睾酮给药后 Nrf2-ARE 途径是否被激活尚未在老年大鼠中研究过。倾斜平面试验和水平丝试验以及氧化应激参数、Nrf2、血红素加氧酶-1(HO-1)和 NAD(P)H:醌氧化还原酶-1(NQO1)的表达以及脑内酪氨酸羟化酶免疫反应性(TH-ir)细胞的数量在接受丙酸睾酮(TP)慢性皮下注射的老年大鼠中进行了检查。我们的研究表明,慢性 TP 补充显著改善了与衰老相关的平衡反应和肌肉力量的下降。氧化应激参数得到改善,Nrf2、HO-1 和 NQO1 的表达在蛋白或基因水平上以及 TH-ir 细胞的数量在 TP 治疗后明显增加。我们的研究结果表明,慢性 TP 治疗激活 Nrf2-ARE 途径可能影响老年大鼠平衡反应和肌肉力量的维持,并减少 TH-ir 细胞的死亡。因此,TP 补充已显示出治疗和改善运动行为障碍的治疗策略。

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