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首页> 外文期刊>Life sciences >Antagonism of morphine-induced antinociception by tetrandrine is dependent on serotonergic mechanisms.
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Antagonism of morphine-induced antinociception by tetrandrine is dependent on serotonergic mechanisms.

机译:粉防己碱对吗啡诱导的抗伤害感受的拮抗作用取决于血清素能机制。

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'Tetrandrine (TET), a non-specific calcium antagonist, inhibited morphine-induced antinociception in the tail-flick test in mice. This study was undertaken to assess the mechanism of the antagonism of morphine-induced antinociception by TET. Morphine-induced antinociception was prevented by pretreatment with TET in the tail-flick but not in the tail-pinch tests carried out in mice and this antagonism was abolished by pretreatment of a serotonin precursor, 5-hydroxytryptophan (5-HTP), but not by the pretreatment of a noradrenaline precursor, L-dihydroxyphenylalanine (L-DOPA), in the tail-flick test. These results indicate that serotonergic mechanisms are involved in the antagonism of morphine-induced antinociception by TET. On the other hand, the development of morphine-induced analgesic tolerance was not prevented by TET. This result, in agreement with other reports, also indicates the possible dissociation of morphine analgesic effect from its tolerance-inducing effect. In addition, TET suppressed the 5-hydroxytryptamine (5-HT)-induced head twtch response. This result provides additional evidence that TET may modulate serotonergic function and the antagonism of morphine-induced antinociception by TET is dependent on serotonergic mechanisms.
机译:老鼠在甩尾试验中,一种非特异性钙拮抗药-粉防己碱(TET)抑制了吗啡诱导的镇痛作用。进行这项研究以评估TET对吗啡诱导的镇痛作用的拮抗作用机理。吗啡诱导的镇痛作用在小鼠的甩尾试验中通过TET预处理得以预防,但在小鼠进行的尾巴捏捏试验中并未阻止,并且通过5-羟色胺前体5-羟色氨酸(5-HTP)的预处理消除了这种拮抗作用,但并没有在甩尾试验中对去甲肾上腺素前体L-二羟基苯丙氨酸(L-DOPA)进行了预处理。这些结果表明血清素能机制参与了TET对吗啡诱导的抗伤害感受的拮抗作用。另一方面,TET不能阻止吗啡诱导的镇痛耐受性的发展。该结果与其他报道一致,也表明吗啡镇痛作用可能与其耐受诱导作用分离。此外,TET抑制了5-羟色胺(5-HT)诱导的头部twtch反应。该结果提供了另外的证据,即TET可以调节血清素能功能,并且TET对吗啡诱导的抗伤害感受的拮抗作用取决于血清素能机制。

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