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Distribution, Morphological Characterization, and Resiniferatoxin-Susceptibility of Sensory Neurons That Innervate Rat Perirenal Adipose Tissue.
Liu, Bo-Xun; Qiu, Ming; Zong, Peng-Yu; Chen, Xu-Guan; Zhao, Kun; Li, Yong; Li, Peng; Sun, Wei; Kong, Xiang-Qing.
Afiliación
  • Liu BX; Department of Cardiology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Qiu M; Department of Cardiology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Zong PY; Department of Cardiology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Chen XG; Department of Cardiology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Zhao K; Department of Cardiology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Li Y; Department of Cardiology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Li P; Department of Cardiology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Sun W; Department of Cardiology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Kong XQ; Department of Cardiology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Front Neuroanat ; 13: 29, 2019.
Article en En | MEDLINE | ID: mdl-30930754
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Neuroanat Año: 2019 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Neuroanat Año: 2019 Tipo del documento: Article País de afiliación: China
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