Cenac Nicolas, Altier Christophe, Chapman Kevin, Liedtke Wolfgang, Zamponi Gerald, Vergnolle Nathalie
Department of Pharmacology and Therapeutics, University of Calgary, Calgary, Alberta, Canada.
Gastroenterology. 2008 Sep;135(3):937-46, 946.e1-2. doi: 10.1053/j.gastro.2008.05.024. Epub 2008 May 10.
BACKGROUND & AIMS: The transient receptor potential vanilloid-4 (TRPV4) is an osmosensitive channel that responds to mechanical stimulation. We hypothesized that TRPV4 could be important in visceral nociception and in the development of hypersensitivity.
TRPV4 expression was investigated by immunohistochemistry and reverse transcription-polymerase chain reaction. Calcium signaling and patch-clamp studies were performed in dorsal root ganglia (DRG) neurons validating the use of 4alphaPDD as a selective TRPV4 agonist. The effects of TRPV4 activation on visceral nociception were evaluated in mice that received intracolonically TRPV4 agonist (4 alpha-phorbol 12,13-didecanoate [4alphaPDD]) and in TRPV4-deficient mice in which abdominal muscle contractions in response to colorectal distention (CRD) were recorded. Intervertebral injections of TRPV4 or mismatch small interfering RNA (siRNA) were used to specifically down-regulate TRPV4 expression in sensory neurons and to investigate the role of TRPV4 in basal visceral nociception or in protease-activated receptor 2 (PAR(2)) activation-induced visceral hypersensitivity.
TRPV4 agonist 4alphaPDD specifically activated a cationic current and calcium influx in colonic projections of DRG neurons and caused dose-dependent visceral hypersensitivity. TRPV4-targeted but not mismatched siRNA intervertebral treatments were effective at reducing basal visceral nociception, as well as 4alphaPDD or PAR(2) agonist-induced hypersensitivity. Effects of the TRPV4 ligand were lost in TRPV4-deficient mice.
4alphaPDD selectively activates TRPV4 in sensory neurons projecting from the colon, and TRPV4 activation causes visceral hypersensitivity. TRPV4 activation is implicated in the nociceptive response to CRD in basal conditions and in PAR(2) agonist-induced hypersensitivity. These results suggest a pivotal role for TRPV4 in visceral nociception and hypersensitivity.
瞬时受体电位香草酸受体4(TRPV4)是一种对渗透压敏感的通道,可对机械刺激产生反应。我们推测TRPV4在内脏痛觉感受及超敏反应的发生中可能起重要作用。
采用免疫组织化学和逆转录-聚合酶链反应研究TRPV4的表达。在背根神经节(DRG)神经元中进行钙信号和膜片钳研究,验证4αPDD作为选择性TRPV4激动剂的作用。通过给小鼠结肠内注射TRPV4激动剂(4α-佛波醇12,13-二癸酸酯[4αPDD]),以及记录TRPV4基因敲除小鼠对结直肠扩张(CRD)的腹肌收缩反应,评估TRPV4激活对内脏痛觉感受的影响。通过椎间注射TRPV4或错配小干扰RNA(siRNA)特异性下调感觉神经元中TRPV4的表达,研究TRPV4在基础内脏痛觉感受或蛋白酶激活受体2(PAR(2))激活诱导的内脏超敏反应中的作用。
TRPV4激动剂4αPDD特异性激活DRG神经元结肠投射中的阳离子电流和钙内流,并引起剂量依赖性内脏超敏反应。靶向TRPV4而非错配的siRNA椎间治疗可有效降低基础内脏痛觉感受以及4αPDD或PAR(2)激动剂诱导的超敏反应。TRPV4配体的作用在TRPV4基因敲除小鼠中消失。
4αPDD选择性激活结肠投射感觉神经元中的TRPV4,TRPV4激活导致内脏超敏反应。TRPV4激活与基础状态下对CRD的伤害性反应以及PAR(2)激动剂诱导的超敏反应有关。这些结果表明TRPV4在内脏痛觉感受和超敏反应中起关键作用。