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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Chronic treatment with celecoxib reverses chronic unpredictable stress-induced depressive-like behavior via reducing cyclooxygenase-2 expression in rat brain.
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Chronic treatment with celecoxib reverses chronic unpredictable stress-induced depressive-like behavior via reducing cyclooxygenase-2 expression in rat brain.

机译:塞来昔布的慢性治疗通过减少大鼠脑中环氧合酶2的表达来逆转慢性不可预测的应激诱导的抑郁样行为。

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Recent clinical trails reported that adjunctive cyclooxygenase (COX)-2 inhibition with celecoxib is beneficial in treating depression. However, another clinical study showed celecoxib did not have inhibitory effect of COX-2 in human brain when given at a therapeutic dose. Therefore, whether celecoxib is exerting its influence through COX inhibition or by some other mechanism remains unclear. The present study further investigated the effect of celecoxib on COX-2 expression, prostaglandin E(2) (PGE2, a major COX-2-mediated inflammatory mediator) concentration and the depressive-like behaviors in rats. Celecoxib was administrated by oral gavage to naive rats (16 mg/kg) or stressed rats (2, 8, 16 mg/kg, respectively) for 21 days, or to stressed rats for a single dose (16 mg/kg). The results showed that 21 days chronic unpredictable stress induced depressive-like behaviors and increased the COX-2 expression and PGE2 concentration in rat brain. Chronic treatments with celecoxib alleviated the depressive-like behavior and reversed the levels of COX-2 expression and PGE2 concentration in stressed rat in a dose-dependent manner. Celecoxib also improved the emotional state and decreased COX-2 expression and PGE2 concentration in naive rats. In addition, a single dose of celecoxib treatment reversed COX-2 expression and PGE2 concentration, but didn't alter the depressive-like behavior in stressed rat. These results suggest that COX-2 enzyme might play a key role in pathophysiology of depression. Furthermore, these data indicate that chronic celecoxib treatment reverse chronic unpredictable stress-induced depressive-like behavior might via reducing COX-2 enzyme in brain, and the selective COX-2 inhibitors could be developed as potential remedies for the management of depression.
机译:最近的临床研究表明,塞来昔布抑制辅助环氧合酶(COX)-2有助于治疗抑郁症。但是,另一项临床研究表明,以治疗剂量给予塞来昔布对人脑没有COX-2的抑制作用。因此,尚不清楚塞来昔布是通过抑制COX还是通过其他机制发挥作用。本研究进一步研究了塞来昔布对大鼠COX-2表达,前列腺素E(2)(PGE2,一种主要的COX-2介导的炎性介质)浓度和抑郁样行为的影响。通过口服管饲法将塞来昔布给予未治疗的大鼠(16 mg / kg)或应激的大鼠(分别为2、8、16 mg / kg),持续21天,或给药至应激的大鼠,单剂量(16 mg / kg)。结果表明,21天的慢性不可预知的应激会诱发抑郁样行为,并增加大鼠大脑中COX-2表达和PGE2的浓度。塞来昔布的慢性治疗以剂量依赖的方式减轻了应激大鼠的抑郁样行为并逆转了COX-2表达和PGE2浓度。塞来昔布还可以改善幼稚大鼠的情绪状态,并降低其COX-2表达和PGE2浓度。此外,单剂量塞来昔布治疗可逆转COX-2表达和PGE2浓度,但并未改变应激大鼠的抑郁样行为。这些结果表明,COX-2酶可能在抑郁症的病理生理中起关键作用。此外,这些数据表明,慢性塞来昔布治疗可能通过减少脑中的COX-2酶逆转慢性不可预知的应激诱导的抑郁样行为,并且选择性COX-2抑制剂可作为治疗抑郁症的潜在药物。

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