首页> 外文期刊>Entomological Science >D2-like dopamine receptors mediate regulation of pupal diapause in Chinese oak silkmoth Antheraea pernyi
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D2-like dopamine receptors mediate regulation of pupal diapause in Chinese oak silkmoth Antheraea pernyi

机译:D2样多巴胺受体介导中国栎蚕mo蚕di滞育的调节

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The present study investigated the pharmacological properties of dopamine receptors that functioned in the termination of pupal diapause in the Chinese oak silkmoth, Antheraea pernyi (Lepidoptera: Saturniidae). Dopamine receptors are classified according to their structure and function into two subfamilies as D1- and D2-like receptors. D1-like receptors activate, whereas D2-like receptors inhibit, adenylate cyclase. We examined the effects of agonists and antagonists selective for D1- and D2-like receptors on the diapause state. As A.pernyi is a long-day species, pupal diapause is maintained during short days and can be terminated by exposure to a long-day photoperiod. The D2-like receptor-selective agonist quinpirole delayed the timing of adult emergence under long days, and the D2-receptor-selective antagonist sulpiride terminated pupal diapause even under a short-day photoperiod. The D1-like receptor-selective agonist and antagonist, SKF-38393 and SCH-23390, respectively, caused no significant effects on diapause pupae. These results suggest that not D1- but D2-like receptors mediated diapause regulation in A.pernyi. This dopamine pathway appeared to block the termination of pupal diapause. Furthermore, the actions of the cAMP analog 8-CPT-cAMP and dopamine receptor antagonists upon diapause pupae were similar, which supports the notion that D2-like receptors involved in diapause of this insect prevent adenylate cyclase from producing cAMP like vertebrate D2-like receptors. Taken together, our findings suggest that dopamine blocked diapause termination through D2-like receptors that inhibited adenylate cyclase in A.pernyi. During short days under which diapause was maintained in pupae, the dopaminergic mechanism might be stimulated to suppress cAMP levels in cells regulating diapause.
机译:本研究调查了在中国栎蚕蛾(Antheraea pernyi,鳞翅目:Saturniidae))滞育中起作用的多巴胺受体的药理特性。多巴胺受体根据其结构和功能分为两个亚家族,即D1和D2类受体。 D1样受体激活,而D2样受体抑制腺苷酸环化酶。我们研究了对滞育状态选择性激动剂和拮抗剂对D1和D2样受体选择性的影响。由于pernyi是一种长日种​​,,的滞育在短时间内得以维持,并且可以通过暴露于长期的光周期而终止。 D2样受体选择性激动剂喹吡罗延长了成年人在长日内出苗的时间,而D2受体选择性拮抗剂舒必利即使在短期光照下也能终止小儿滞育。 D1样受体选择性激动剂和拮抗剂SKF-38393和SCH-23390分别对滞育p没有明显影响。这些结果表明,不是D1而是D2样受体介导了pernyi的滞育调节。该多巴胺途径似乎阻止the滞育的终止。此外,cAMP类似物8-CPT-cAMP和多巴胺受体拮抗剂对滞育p的作用相似,这支持了这种昆虫滞育中涉及的D2样受体阻止腺苷酸环化酶像脊椎动物D2样受体一样产生cAMP的观点。 。综上所述,我们的研究结果表明,多巴胺可通过抑制A.pernyi中腺苷酸环化酶的D2样受体阻断滞育终止。在short保持滞育的短时间内,可能会刺激多巴胺能机制抑制调节滞育的细胞中的cAMP水平。

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