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首页> 外文期刊>The European Journal of Neuroscience >The cAMP response element-binding protein in the bed nucleus of the stria terminalis modulates the formalin-induced pain behavior in the female rat.
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The cAMP response element-binding protein in the bed nucleus of the stria terminalis modulates the formalin-induced pain behavior in the female rat.

机译:末端纹状体床核中的cAMP反应元件结合蛋白调节雌性大鼠中福尔马林引起的疼痛行为。

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Abstract Differences in male and female responses to pain are widely recognized in many species, including humans, but the cerebral mechanisms that generate these responses are unknown. Using the formalin test, we confirmed that proestrus female rats showed nociceptive behavior, modulated by estrogen that was distinct from male rats, particularly during the interphase period. We then explored the brain areas, which were involved in the female pattern of nociceptive behavior. We found that, after a formalin injection and at the time corresponding to the behavioral interphase, the number of phosphorylated cAMP response element-binding protein (pCREB)-immunoreactive neurons observed by immunocytochemistry increased in the dorsolateral division of the bed nucleus of the stria terminalis (BSTLD) in female but not male rats. There were no significant sex differences in pCREB expression following formalin in any region other than the BSTLD. The increased pCREB in female rats was eliminated after an ovariectomy and restored with 17beta-estradiol treatment. Neither an orchidectomy nor 17beta-estradiol treatment affected the pCREB response in male rats. The increase in pCREB expression in the BSTLD in female rats after formalin injection was confirmed with immunoblotting. To determine the role of CREB in the BSTLD, adenovirus-mediated expression of a dominant-negative form of CREB (mCREB) was carried out. The nociceptive behavior during interphase was significantly attenuated by injection of virus carrying mCREB into the BSTLD in female rats but not in male rats. These results suggest a novel role for CREB in the BSTLD as a modulator of the pain response in a female-specific, estrogen-dependent manner.
机译:摘要男性和女性对疼痛的反应差异在包括人类在内的许多物种中得到了广泛认可,但是产生这些反应的大脑机制尚不清楚。使用福尔马林测试,我们证实雌激素的发情期雌鼠表现出伤害性行为,受雌激素调节的行为与雄性大鼠不同,尤其是在相间期。然后,我们探索了大脑区域,这些区域参与了伤害性行为的女性模式。我们发现,在福尔马林注射后和行为相间相符的时间,通过免疫细胞化学观察到的磷酸化的cAMP反应元件结合蛋白(pCREB)-免疫反应性神经元的数量在纹状体终末床核的背外侧分中增加了(BSTLD)在雌性而非雄性大鼠中。福尔马林注射后,除BSTLD以外的任何区域,pCREB表达均无明显性别差异。卵巢切除术后消除雌性大鼠中增加的pCREB,并用17β-雌二醇治疗恢复。兰花切除术和17β-雌二醇治疗均不影响雄性大鼠的pCREB反应。免疫印迹证实了福尔马林注射后雌性大鼠BSTLD中pCREB表达的增加。为了确定CREB在BSTLD中的作用,进行了腺病毒介导的CREB显性阴性形式(mCREB)的表达。在雌性大鼠中,通过向BSTLD中注射携带mCREB的病毒可以显着减弱间期的伤害感受,而雄性大鼠则没有。这些结果表明,CREB在BSTLD中以女性特异性,雌激素依赖性方式作为疼痛反应的调节剂发挥了新的作用。

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