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

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 uncl...

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Main Authors: Bo-Xun Liu (Author), Ming Qiu (Author), Peng-Yu Zong (Author), Xu-Guan Chen (Author), Kun Zhao (Author), Yong Li (Author), Peng Li (Author), Wei Sun (Author), Xiang-Qing Kong (Author)
Format: Book
Published: Frontiers Media S.A., 2019-03-01T00:00:00Z.
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100 1 0 |a Bo-Xun Liu  |e author 
700 1 0 |a Ming Qiu  |e author 
700 1 0 |a Peng-Yu Zong  |e author 
700 1 0 |a Xu-Guan Chen  |e author 
700 1 0 |a Kun Zhao  |e author 
700 1 0 |a Yong Li  |e author 
700 1 0 |a Peng Li  |e author 
700 1 0 |a Wei Sun  |e author 
700 1 0 |a Xiang-Qing Kong  |e author 
245 0 0 |a Distribution, Morphological Characterization, and Resiniferatoxin-Susceptibility of Sensory Neurons That Innervate Rat Perirenal Adipose Tissue 
260 |b Frontiers Media S.A.,   |c 2019-03-01T00:00:00Z. 
500 |a 1662-5129 
500 |a 10.3389/fnana.2019.00029 
520 |a 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. 
546 |a EN 
690 |a perirenal adipose tissue 
690 |a neural tracing 
690 |a dorsal root ganglia 
690 |a TRPV1 
690 |a resiniferatoxin 
690 |a Neurosciences. Biological psychiatry. Neuropsychiatry 
690 |a RC321-571 
690 |a Human anatomy 
690 |a QM1-695 
655 7 |a article  |2 local 
786 0 |n Frontiers in Neuroanatomy, Vol 13 (2019) 
787 0 |n https://www.frontiersin.org/article/10.3389/fnana.2019.00029/full 
787 0 |n https://doaj.org/toc/1662-5129 
856 4 1 |u https://doaj.org/article/f13f4b1161ef4786b4cee5a89aec87d5  |z Connect to this object online.