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Effect of thioperamide on modified forced swimming test-induced oxidative stress in mice.

机译:硫代过酰胺对改良的强迫游泳试验诱导的小鼠氧化应激的影响。

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This study was designed i) to investigate the role of histamine H3-receptor ligands on mouse modified forced swimming test, a method that distinguishes the catecholaminergic behaviour with that of serotonergic compounds and ii) to evaluate the role of free radicals in mediation of such effects. Swiss strain albino mice were treated with different doses of histamine H3-receptor antagonist thioperamide (3.75, 7.5 and 15 mg/kg intraperitoneally) and agonist (R)-alpha-methylhistamine (5 microg intracerebroventricularly). The climbing, swimming and immobility times were recorded for 6 min. Immediately after modified forced swimming test, the animals were sacrificed and parameters of oxidative stress were assessed in the brain by measuring the thiobarbituric acid reactive substance (TBARS), glutathione (GSH) and catalase levels. Thioperamide (7.5 and 15 mg/kg intraperitoneally) dose-dependently decreased immobility time and increased swimming time but not climbing time. The behaviour of mice treated with (R)-alpha-methylhistamine was similar to that of control mice. A significant reduction in GSH and an increase in catalase levels were observed in brains of mice exposed to modified forced swimming test. Thioperamide pretreatment dose-dependently reversed such an alteration in oxidative stress parameters. (R)-alpha-methylhistamine caused a reversal of altered catalase but not GSH levels. Thioperamide shows antidepressant effects in the modified forced swimming test and causes a reversal of the test-induced oxidative stress indicating its antioxidant potential. The antidepressant effect of thioperamide appears to be mediated via serotonergic and/or antioxidant mechanisms.
机译:本研究旨在:i)研究组胺H3受体配体在小鼠改良的强迫游泳试验中的作用,该方法可区分儿茶酚胺能行为与血清素能化合物的行为,以及ii)评估自由基在介导此类作用中的作用。用不同剂量的组胺H3受体拮抗剂硫代过酰胺(3.75、7.5和15 mg / kg腹膜内)和激动剂(R)-α-甲基组胺(脑室内5微克)治疗瑞士品系白化病小鼠。记录6分钟的攀登,游泳和不动时间。经过改良的强迫游泳试验后,立即处死动物,并通过测量硫代巴比妥酸反应性物质(TBARS),谷胱甘肽(GSH)和过氧化氢酶水平来评估大脑中的氧化应激参数。硫哌酰胺(腹膜内注射浓度为7.5和15 mg / kg)剂量依赖性地减少了固定时间,增加了游泳时间,但没有增加爬山时间。用(R)-α-甲基组胺治疗的小鼠的行为与对照小鼠相似。在接受改良强迫游泳试验的小鼠的大脑中,GSH显着降低,过氧化氢酶水平升高。硫代酰胺预处理剂量依赖性地逆转了氧化应激参数的这种改变。 (R)-α-甲基组胺可逆转过氧化氢酶,但不会逆转GSH水平。硫哌丁胺在改良的强迫游泳试验中显示出抗抑郁作用,并引起试验诱导的氧化应激逆转,表明其抗氧化能力。硫代过酰胺的抗抑郁作用似乎是通过血清素能和/或抗氧化剂机制介导的。

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