期刊论文详细信息
NEUROSCIENCE LETTERS 卷:683
Effects of nerve growth factor neutralization on TRP channel expression in laser-captured bladder afferent neurons in mice with spinal cord injury
Article
Shimizu, Nobutaka1,5  Wada, Naoki1  Shimizu, Takahiro1  Suzuki, Takahisa1  Takaoka, Ei-ichiro1  Kanai, Anthony J.2  de Groat, William C.3  Hirayama, Akihide4  Hashimoto, Mamoru5  Uemura, Hirotsugu5  Yoshimura, Naoki1,3 
[1] Univ Pittsburgh, Dept Urol, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Med, 930 Scaife Hall, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Dept Pharmacol & Chem Biol, Pittsburgh, PA 15213 USA
[4] Kindai Univ, Nara Hosp, Fac Med, Dept Urol, Nara, Japan
[5] Kindai Univ, Fac Med, Dept Urol, 377-2 Ohno Higashi, Osaka, Osaka 5898511, Japan
关键词: Spinal cord injury;    Mouse;    Dorsal root ganglia;    Laser-capture microdissection;    TRP channel;    Nerve growth factor;    TRPC channels;   
DOI  :  10.1016/j.neulet.2018.06.049
来源: Elsevier
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【 摘 要 】

Nerve growth factor (NGF) is reportedly involved in the changes in C-fiber bladder afferent pathways that induce detrusor overactivity (DO) following spinal cord injury (SCI). This study examined the roles of NGF in TRP channel expression in bladder afferent neurons in mice with SCI using laser-capture microdissection (LCM) methods. Spinal intact (SI) and SCI mice were divided into 3 groups: (1) SI with vehicle treatment; (2) SCI with vehicle treatment; and (3) SCI with anti-NGF antibody. Two weeks after SCI, an osmotic pump was placed subcutaneously into the back of the mice and vehicle or anti-NGF antibody was administered at a rate of 10 mu g/kg per hour for two weeks. Four weeks after SCI, the L6 dorsal root ganglia (DRG) were removed. Expression of the TRPV1, TRPC1, TRPC3, and TRPC6 genes was analyzed using real-time polymerase chain reaction (PCR) following LCM of the bladder afferent neurons, which were labeled by Fast Blue injected into the bladder wall 1 week prior to tissue removal. The mRNA expression of TRPV1 was found to be higher in vehicle-treated SCI mice than in SI mice. The expression level of TRPC3 and TRPC6 in vehicle-treated SCI mice was lower than in SI mice. However, in SCI mice treated with anti-NGF antibody, the mRNA expression of TRPV1 was lower, and the mRNA levels of TRPC3 and TRPC6 were higher than in vehicle-SCI mice. These results suggest that the NGF-dependent changes in specific TRP channel genes, such as TRPV1, TRPC3, and TRPC6, could be involved in SCI-induced afferent hyperexcitability and DO.

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