Grider J R, Makhlouf G M
Am J Physiol. 1986 Jul;251(1 Pt 1):G40-5. doi: 10.1152/ajpgi.1986.251.1.G40.
Isolated segments of rat and guinea pig midcolon were used to examine the neurotransmitters responsible for ascending contraction and descending relaxation components of the peristaltic reflex. Graded radial stretch of the extreme orad end caused only descending relaxation accompanied by significant release of vasoactive intestinal peptide (VIP) in rat (82%, P less than 0.005) and guinea pig (47%, P less than 0.05). Radial stretch of the caudad end caused only ascending contraction without VIP release. VIP antiserum (1:480 to 1:60) inhibited descending relaxation in a concentration-dependent manner at all grades of stretch (40 +/- 12% to 74 +/- 15%) but augmented ascending contraction (25 +/- 7% to 108 +/- 21%). Axonal blockade with tetrodotoxin and ganglionic blockade with hexamethonium abolished both components, indicating the participation of cholinergic neurons. Atropine and the tachykinin antagonist [D-Pro2,D-Trp7,9]substance P inhibited ascending contraction but not descending relaxation; their combination abolished ascending contraction at all grades of stretch. We conclude that cholinergic neurons coupled to VIP motor neurons regulate descending relaxation and that cholinergic neurons coupled to tachykinin and cholinergic motor neurons regulate ascending contraction.
采用大鼠和豚鼠结肠中段的离体节段,研究负责蠕动反射的升支收缩和降支舒张成分的神经递质。对最靠近口腔端进行分级径向拉伸,仅引起降支舒张,并伴有大鼠(82%,P<0.005)和豚鼠(47%,P<0.05)血管活性肠肽(VIP)的显著释放。对尾端进行径向拉伸,仅引起升支收缩,无VIP释放。VIP抗血清(1:480至1:60)在所有拉伸等级下均以浓度依赖性方式抑制降支舒张(40±12%至74±15%),但增强升支收缩(25±7%至108±21%)。河豚毒素引起的轴突阻断和六甲铵引起的神经节阻断使两个成分均消失,表明胆碱能神经元的参与。阿托品和速激肽拮抗剂[D-脯氨酸2,D-色氨酸7,9]P物质抑制升支收缩,但不抑制降支舒张;它们联合使用在所有拉伸等级下均消除升支收缩。我们得出结论,与VIP运动神经元耦联的胆碱能神经元调节降支舒张,与速激肽和胆碱能运动神经元耦联的胆碱能神经元调节升支收缩。