Ishizawa M
Laboratory of Physiology, School of Allied Health Professions, Sapporo Medical College.
Nihon Heikatsukin Gakkai Zasshi. 1988 Jun;24(3):185-92. doi: 10.1540/jsmr1965.24.185.
The effects of vasoactive intestinal peptide (VIP) on longitudinal and circular muscle strips of guinea-pig proximal and distal colons, and on propulsive activity of guinea-pig distal colon were investigated in vitro. VIP (10(-9)-10(-6) M) produced relaxations of longitudinal and circular muscle strips in proximal colon and of circular muscle strip in distal colon, but produced a contraction of longitudinal muscle strip in distal colon. VIP-induced responses of the muscle strips were not influenced by indomethacin (10(-6) M). Tetrodotoxin (10(-6) M) and atropine (10(-6) M) converted VIP-induced contraction into relaxation in longitudinal muscle strip of distal colon, although these nerve blockers did not influence VIP-induced relaxations of longitudinal and circular muscle strips in proximal colon and of circular muscle strip in distal colon. VIP (10(-6) M) inhibited spontaneous and carbachol (10(-8) M)-stimulated propulsive activities of the isolated segment in distal colon. These results suggest that VIP may directly relax colonic smooth muscle cells and may indirectly contract longitudinal muscle strip of distal colon, mainly via stimulation of cholinergic neurones in the myenteric plexus of the muscle strip. It is also suggested that VIP-induced watery diarrhea in WDHA syndrome may not due to a direct stimulation of colonic motility.
研究了血管活性肠肽(VIP)对豚鼠近端和远端结肠纵行肌条和环行肌条的影响,以及对豚鼠远端结肠推进性活动的影响。VIP(10⁻⁹ - 10⁻⁶ M)可使近端结肠的纵行肌条和环行肌条以及远端结肠的环行肌条舒张,但可使远端结肠的纵行肌条收缩。VIP诱导的肌条反应不受吲哚美辛(10⁻⁶ M)影响。河豚毒素(10⁻⁶ M)和阿托品(10⁻⁶ M)可使VIP诱导的远端结肠纵行肌条收缩转变为舒张,尽管这些神经阻滞剂不影响VIP诱导的近端结肠纵行肌条和环行肌条以及远端结肠环行肌条的舒张。VIP(10⁻⁶ M)可抑制远端结肠离体节段的自发推进性活动和卡巴胆碱(10⁻⁸ M)刺激的推进性活动。这些结果表明,VIP可能直接舒张结肠平滑肌细胞,并可能主要通过刺激肌条肌间神经丛中的胆碱能神经元间接使远端结肠纵行肌条收缩。还表明,VIP在WDHA综合征中诱导的水样腹泻可能不是由于直接刺激结肠运动。