Sato K, Sato F
Marshall Dermatology Research Laboratories, Department of Dermatology, University of Iowa College of Medicine, Iowa City 52242.
Am J Physiol. 1987 Dec;253(6 Pt 2):R935-41. doi: 10.1152/ajpregu.1987.253.6.R935.
Although vasoactive intestinal peptide (VIP)-immunoreactive nerves have been identified around the eccrine sweat glands, their functional significance is unknown. We found that VIP evokes eccrine sweat secretion in isolated monkey palm eccrine sweat glands in vitro as profusely as does isoproterenol (Iso), however, at concentrations two orders of magnitude lower than that of Iso. Like Iso sweating, the VIP sweating was relatively insensitive to removal of Ca2+ from the medium. The time course of adenosine 3',5'-cyclic monophosphate (cAMP) accumulation in the secretory coil paralleled that of sweat secretion. However, unlike Iso stimulations, both VIP-induced cAMP level and VIP sweat rate markedly declined with time. The attenuation of VIP sweat rate was reversed by forskolin and by theophylline, suggesting that the attenuation is caused partially by desensitization of the receptor-cyclase complex and/or by cAMP breakdown by phosphodiesterase. Forskolin stimulated the VIP-induced cAMP level more than can be expected from a simple additive effect. The sudorific effects of a submaximal concentration of VIP (6 X 10(-9) M) and that of methacholine (MCh) (10(-8) M) were only additive. The VIP-induced cAMP level was markedly augmented by MCh and further enhanced by Iso with or without theophylline. Thus the most salient biochemical consequence of the VIP-ergic component of sweat gland innervation is to induce synergistic amplification of tissue cAMP accumulation. The functional significance of synergistically accumulated cAMP in physiological eccrine sweating remains to be studied.
尽管在小汗腺周围已鉴定出血管活性肠肽(VIP)免疫反应性神经,但其功能意义尚不清楚。我们发现,VIP在体外可引起分离的猴掌小汗腺大量分泌汗液,其程度与异丙肾上腺素(Iso)相当,但浓度比Iso低两个数量级。与Iso引起的出汗一样,VIP引起的出汗对从培养基中去除Ca2+相对不敏感。分泌盘内3',5'-环磷酸腺苷(cAMP)积累的时间进程与汗液分泌的时间进程平行。然而,与Iso刺激不同,VIP诱导的cAMP水平和VIP出汗率均随时间显著下降。福斯可林和茶碱可逆转VIP出汗率的衰减,这表明衰减部分是由受体-环化酶复合物脱敏和/或磷酸二酯酶对cAMP的分解所致。福斯可林对VIP诱导的cAMP水平的刺激作用超过了简单相加效应的预期。亚最大浓度的VIP(6×10−9 M)和乙酰甲胆碱(MCh)(10−8 M)的发汗作用仅为相加。MCh可显著提高VIP诱导的cAMP水平,Iso在有或没有茶碱的情况下可进一步增强该水平。因此,汗腺神经支配的VIP能成分最显著的生化后果是诱导组织cAMP积累的协同放大。协同积累的cAMP在生理性小汗腺出汗中的功能意义仍有待研究。