Cocaine- and Amphetamine-Regulated Transcript Peptide in the Central Nervous System of the Gecko, Hemidactylus leschenaultii: Molecular Characterization, Neuroanatomical Organization, and Regulation by Neuropeptide Y

IF 2.3 4区 医学 Q3 NEUROSCIENCES
Omprakash Singh, Sumela Basu, Abhinav Srivastava, Dipti R. Pradhan, Pallabi Dandapat, Chandramohan Bathrachalam, Praful S. Singru
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引用次数: 0

Abstract

Neuropeptide cocaine- and amphetamine-regulated transcript (CART) is widely expressed in the brains of teleosts, amphibians, birds, and mammals and has emerged as a conserved regulator of energy balance across these vertebrate phyla. However, as yet, there is no information on CART in the reptilian brain. We characterized the cDNA encoding CART and mapped CART-containing elements in the brain of gecko, Hemidactylus leschenaultii (hl) using a specific anti-CART antiserum. We report a 683-bp hlcart transcript containing a 336-bp open reading frame, which encodes a putative 111-amino acid hl-preproCART. The 89-amino acid hl-proCART generated from hl-preproCART produced two putative bioactive hl-CART-peptides. These bioactive CART-peptides were > 93% similar with those in rats/humans. Although reverse transcription-polymerase chain reaction (RT-PCR) detected hlcart-transcript in the brain, CART-containing neurons/fibers were widely distributed in the telencephalon, diencephalon, mesencephalon, rhombencephalon, spinal cord, and retina. The mitral cells in olfactory bulb, neurons in the paraventricular, periventricular, arcuate (Arc), Edinger–Westphal, and brainstem nuclei were intensely CART-positive. In view of antagonistic roles of neuropeptide Y (NPY) and CART in energy balance in the framework of mammalian hypothalamus, we probed CART–NPY interaction in the hypothalamus of H. leschenaultii. Double immunofluorescence showed a dense NPY-innervation of Arc CART neurons. Ex vivo hypothalamic slices treated with NPY/NPY-Y1-receptor agonist significantly reduced hlcart-mRNA levels in the Arc-containing tissues and CART-ir in the dorsal-Arc. However, CART-ir in ventral-Arc was unaffected. NPY via Y1-receptors may regulate energy balance by inhibiting dArc CART neurons. This study on CART in a reptilian brain fills the current void in literature and underscores the conserved feature of the neuropeptide across the entire vertebrate phyla.

Abstract Image

壁虎 Hemidactylus leschenaultii 中枢神经系统中的可卡因和苯丙胺调节转录肽:分子特征、神经解剖组织和神经肽 Y 的调控。
神经肽可卡因和苯丙胺调节转录物(CART)在远足类、两栖类、鸟类和哺乳类动物的大脑中广泛表达,并已成为这些脊椎动物门类中能量平衡的保守调节因子。然而,目前还没有爬行动物大脑中 CART 的相关信息。我们鉴定了编码 CART 的 cDNA,并使用特异性抗 CART 抗血清绘制了壁虎 Hemidactylus leschenaultii(hl)大脑中含有 CART 的元素。我们报告了一个 683 bp 的 hlcart 转录本,其中包含一个 336 bp 的开放阅读框,它编码一个假定的 111 氨基酸 hl-preproCART。由 hl-preproCART 生成的 89 氨基酸 hl-proCART 产生了两种假定的生物活性 hl-CART-肽。这些具有生物活性的CART肽与大鼠/人类体内的CART肽相似度大于93%。虽然逆转录聚合酶链反应(RT-PCR)在大脑中检测到了hlcart转录本,但含CART的神经元/纤维广泛分布于端脑、间脑、间脑、菱形脑、脊髓和视网膜。嗅球的有丝分裂细胞、脑室旁、脑室周围、弓状(Arc)、艾丁格-韦斯特脑和脑干核中的神经元呈强 CART 阳性。鉴于神经肽 Y(NPY)和 CART 在哺乳动物下丘脑框架内能量平衡中的拮抗作用,我们探究了 H. leschenaultii 下丘脑中 CART-NPY 的相互作用。双重免疫荧光显示弧CART神经元有密集的NPY神经支配。用NPY/NPY-Y1-受体激动剂处理的体外下丘脑切片可显著降低含弧组织中的hlcart-mRNA水平和背弧组织中的CART-ir水平。然而,腹侧弧的CART-ir不受影响。NPY通过Y1-受体可能会抑制dArc CART神经元,从而调节能量平衡。这项关于爬行动物大脑中 CART 的研究填补了目前的文献空白,并强调了该神经肽在整个脊椎动物门中的保守性。
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来源期刊
CiteScore
5.80
自引率
8.00%
发文量
158
审稿时长
3-6 weeks
期刊介绍: Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states. Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se. JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.
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