De Beurme F A, Lefebvre R A
Br J Pharmacol. 1987 May;91(1):171-7. doi: 10.1111/j.1476-5381.1987.tb08996.x.
Relaxations of the rat gastric fundus were induced by electrical stimulation of the non-adrenergic non-cholinergic (NANC) neurones, by vasoactive intestinal polypeptide (VIP), by noradrenaline and by isopropylnoradrenaline. The influence of alpha-chymotrypsin and trypsin thereupon was studied. alpha-Chymotrypsin 2 u ml-1, present for 30 min, antagonized completely the VIP-induced relaxation, but not the stimulation-induced relaxation; alpha-chymotrypsin 10 u ml-1 also partially antagonized the stimulation-induced relaxation. When alpha-chymotrypsin 2 u ml-1 was added after the relaxation had occurred, it antagonized completely the VIP-induced relaxation, but it also partially antagonized the stimulation-induced relaxation. The partial antagonism of the stimulation-induced relaxation was more pronounced with alpha-chymotrypsin 10 u ml-1. Trypsin, 10(-6) M and 3 X 10(-6) M, had effects on VIP- and stimulation-induced relaxations similar to those of alpha-chymotrypsin. The relaxations induced by noradrenaline and isopropylnoradrenaline were not influenced by alpha-chymotrypsin or trypsin, respectively. The results suggest that a peptide, possibly VIP, is involved in the NANC relaxation of the rat gastric fundus.
通过电刺激非肾上腺素能非胆碱能(NANC)神经元、血管活性肠肽(VIP)、去甲肾上腺素和异丙肾上腺素可诱导大鼠胃底松弛。研究了α-糜蛋白酶和胰蛋白酶对其的影响。2 U/ml的α-糜蛋白酶作用30分钟,可完全拮抗VIP诱导的松弛,但不能拮抗电刺激诱导的松弛;10 U/ml的α-糜蛋白酶也可部分拮抗电刺激诱导的松弛。当在松弛发生后加入2 U/ml的α-糜蛋白酶时,它可完全拮抗VIP诱导的松弛,但也可部分拮抗电刺激诱导的松弛。10 U/ml的α-糜蛋白酶对电刺激诱导的松弛的部分拮抗作用更明显。10⁻⁶ M和3×10⁻⁶ M的胰蛋白酶对VIP和电刺激诱导的松弛的作用与α-糜蛋白酶相似。去甲肾上腺素和异丙肾上腺素诱导的松弛分别不受α-糜蛋白酶或胰蛋白酶的影响。结果表明,一种肽,可能是VIP,参与了大鼠胃底的NANC松弛。