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支配大鼠肾周脂肪组织的感觉神经元的分布、形态学特征及对树脂毒素的敏感性

Distribution, Morphological Characterization, and Resiniferatoxin-Susceptibility of Sensory Neurons That Innervate Rat Perirenal Adipose Tissue.

作者信息

Liu Bo-Xun, Qiu Ming, Zong Peng-Yu, Chen Xu-Guan, Zhao Kun, Li Yong, Li Peng, Sun Wei, Kong Xiang-Qing

机构信息

Department of Cardiology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

出版信息

Front Neuroanat. 2019 Mar 14;13:29. doi: 10.3389/fnana.2019.00029. eCollection 2019.

Abstract

Perirenal adipose tissue (PrAT) is a visceral adipose tissue involved in the pathogenesis of obesity and cardiovascular diseases via neural pathways. However, the origins, morphological characterization, and resiniferatoxin (RTX)-susceptibility of sensory neurons that innervate rat PrAT are yet unclear. Using neural tracing, an injection of DiI (1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate) into PrAT revealed that sensory neurons that innervate PrAT reside in T9-L3 dorsal root ganglia (DRG). Peak labeling occurred in T13 and L1 DRGs. Two distinct peaks were observed in cross-sectional areas of the labeled soma, and the mean cross-sectional area was 717.1 ± 27.7 μm2. Immunofluorescence staining for transient receptor potential cation channel subfamily V member 1 (TRPV1) separated DiI-positive neurons into three subpopulations: small TRPV1-negative, small TRPV1-positive, and large TRPV1-negative. Furthermore, the injection of RTX into PrAT reduced labeled cells by 36.7% where TRPV1-positive cells were the main target of RTX denervation. These novel findings provide a structural basis for future TRPV1-dependent and TRPV1-independent studies on the sensory innervation of PrAT, which may be of interest for future therapeutic obesity treatment and intervention.

摘要

肾周脂肪组织(PrAT)是一种内脏脂肪组织,可通过神经通路参与肥胖症和心血管疾病的发病机制。然而,支配大鼠PrAT的感觉神经元的起源、形态特征和对树脂毒素(RTX)的敏感性尚不清楚。利用神经追踪技术,向PrAT注射碘化二苯并咪唑(DiI,1,1'-二辛基-3,3,3',3'-四甲基吲哚羰花青高氯酸盐)显示,支配PrAT的感觉神经元位于T9-L3背根神经节(DRG)。在T13和L1 DRG中出现了标记峰值。在标记的胞体横截面积中观察到两个不同的峰值,平均横截面积为717.1±27.7μm²。对瞬时受体电位阳离子通道亚家族V成员1(TRPV1)进行免疫荧光染色,将DiI阳性神经元分为三个亚群:小的TRPV1阴性、小的TRPV1阳性和大的TRPV1阴性。此外,向PrAT注射RTX使标记细胞减少了36.7%,其中TRPV1阳性细胞是RTX去神经支配的主要靶点。这些新发现为未来关于PrAT感觉神经支配的TRPV1依赖性和TRPV1非依赖性研究提供了结构基础,这可能对未来肥胖症的治疗和干预具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77b/6427091/8a8cd418c39d/fnana-13-00029-g001.jpg

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