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首页> 外文期刊>Molecular pharmacology. >Gastrin-releasing peptide mediates photic entrainable signals to dorsal subsets of suprachiasmatic nucleus via induction of Period gene in mice.
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Gastrin-releasing peptide mediates photic entrainable signals to dorsal subsets of suprachiasmatic nucleus via induction of Period gene in mice.

机译:释放胃泌素的肽通过在小鼠中诱导Period基因而将光合夹带的信号介导至视交叉上核的背侧子集。

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摘要

The suprachiasmatic nucleus (SCN), locus of the central circadian clock, consists of two neuronal populations (i.e., a light-recipient ventral SCN subpopulation directly entrained by light and a dorsal SCN subpopulation with an autonomous oscillatory function possessing an indirect or weak light response). However, the mechanism underlying the transmission of photic signals from the ventral to dorsal SCN remains unclear. Because gastrin-releasing peptide (GRP), expressed mainly in the ventral SCN, exerts phase-shifting actions, loss of the GRP receptor intuitively implies a reduction of photic information from the ventral to dorsal SCN. Therefore, using GRP receptor-deficient mice, we examined the involvement of GRP and the GRP receptor in light- and GRP-induced entrainment by the assessment of behavioral rhythm and induction of mousePeriod (mPer) gene in the SCN, which is believed to be a critical for photic entrainment. Administration of GRP during nighttime dose dependently produced a phase delay of behavior in wild-type but not GRP receptor-deficient mice. This phase-shift by GRP was closely associated with induction of mPer1 and mPer2 mRNA as well as c-Fos protein in the dorsal portion of the SCN, where the GRP receptor was also expressed abundantly. Both the light-induced phase shift in behavior and the induction of mPer mRNA and c-Fos protein in the dorsal SCN were attenuated in GRP receptor-deficient mice. Our present studies suggest that GRP neurons in the retinorecipient ventral area of the SCN convey the photic entrainable signals from the ventral SCN to the dorsal SCN via induction of the mPer gene.
机译:上生物钟(SCN)是中央昼夜节律的所在地,由两个神经元种群组成(即,一个直接受光夹带的轻受体腹侧SCN亚群和一个具有自主振荡功能的背侧SCN亚群,具有间接或弱光响应)。然而,光信号从腹侧到背侧SCN的传输机制尚不清楚。因为主要在腹侧SCN中表达的胃泌素释放肽(GRP)发挥相移作用,所以GRP受体的丧失直观上意味着从腹侧SCN到背侧SCN的光信息减少。因此,我们使用GRP受体缺陷型小鼠,通过评估SCN的行为节律和mousePeriod(mPer)基因的诱导,研究了GRP和GRP受体在光和GRP诱导的夹带中的参与。对光合带至关重要。夜间剂量的GRP给药可在野生型小鼠中产生阶段性行为延迟,但在GRP受体缺陷型小鼠中则不会。 GRP的这种相移与SCN背侧部分mPer1和mPer2 mRNA以及c-Fos蛋白的诱导密切相关,在该区域中GRP受体也大量表达。在GRP受体缺陷型小鼠中,光诱导的行为相移以及背侧SCN中mPer mRNA和c-Fos蛋白的诱导均减弱。我们目前的研究表明,在SCN的视网膜受体腹侧区域的GRP神经元通过mPer基因的诱导将光合的信号从腹侧SCN传递到背侧SCN。

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