Currò Diego, De Marco Teresina, Preziosi Paolo
Institute of Pharmacology, School of Medicine, Catholic University of the Sacred Heart, L.go F. Vito, 1, 00168 Rome, Italy.
Naunyn Schmiedebergs Arch Pharmacol. 2002 Dec;366(6):578-86. doi: 10.1007/s00210-002-0633-z. Epub 2002 Sep 27.
The role of peptide histidine isoleucine (PHI) as a neurotransmitter of the inhibitory motor neurones, the physiological role of PHI and vasoactive intestinal polypeptide (VIP) in the non-adrenergic non-cholinergic (NANC) relaxation and the relative amounts of VIP- and PHI-like immunoreactivity (LI) co-released by neuronal activation were investigated in the rat gastric fundus. Longitudinal muscle strips from the rat gastric fundus precontracted by the thromboxane receptor agonist U46619 (0.1 micro M) were studied in organ baths under conditions of muscarinic receptor blockade by atropine (1 micro M) and adrenergic neurone blockade by guanethidine (5 micro M) ("NANC conditions"). Concentration-response curves were plotted for both amplitude and area under the curve (AUC) of the relaxant responses induced by VIP (0.3 nM-0.3 micro M), PHI (0.3 nM-1 micro M) and peptide histidine valine [PHV(1-42); 0.3 nM-1 micro M]. All three peptides were more potent in the curve based on amplitude than in that based on the AUC of relaxation. In addition, VIP was 5.3 and 7 times more potent than PHI and PHV(1-42), respectively, in producing relaxation expressed as amplitude, and 2.7 and 2.8 times, respectively, in producing relaxation expressed as AUC. PHI and PHV(1-42) behaved as partial agonists with respect to VIP in producing relaxation expressed as AUC. Electrical field stimulation (EFS; 120 mA, 1 ms, 4-32 Hz, pulse trains of 2 min) evoked frequency-dependent relaxant responses. Alpha-chymotrypsin (1 u/ml or 3 u/ml), an anti-VIP serum (1:100 or 1:50) and an anti-PHI serum (1:25), slightly reduced the amplitude, but greatly inhibited the AUC of the NANC relaxation induced by EFS (13 Hz) [approximately 72%, 47% and 28% less than that seen in time controls or with normal rabbit serum (1:100 or 1:25), respectively]. EFS (8-32 Hz) caused significant, frequency-dependent increases in the outflow of VIP- and PHI-LI from the strips. The EFS-induced release of VIP-LI was approximately 20% of the PHI-LI release. These findings indicate that PHI is involved in EFS-induced NANC relaxation of the rat gastric fundus, the major physiological role of VIP and PHI is the maintenance of smooth muscle relaxation and VIP is co-released in equimolar amounts mainly with PHI.
在大鼠胃底中,研究了肽组氨酸异亮氨酸(PHI)作为抑制性运动神经元神经递质的作用、PHI和血管活性肠肽(VIP)在非肾上腺素能非胆碱能(NANC)舒张中的生理作用,以及神经元激活共同释放的VIP样和PHI样免疫反应性(LI)的相对量。在器官浴中研究了由血栓素受体激动剂U46619(0.1微摩尔)预收缩的大鼠胃底纵行肌条,实验条件为用阿托品(1微摩尔)阻断毒蕈碱受体和用胍乙啶(5微摩尔)阻断肾上腺素能神经元(“NANC条件”)。绘制了由VIP(0.3纳摩尔至0.3微摩尔)、PHI(0.3纳摩尔至1微摩尔)和肽组氨酸缬氨酸[PHV(1 - 42);0.3纳摩尔至1微摩尔]诱导的舒张反应的幅度和曲线下面积(AUC)的浓度 - 反应曲线。基于幅度的曲线中,所有三种肽都比基于舒张AUC的曲线更有效。此外,以幅度表示的舒张作用中,VIP分别比PHI和PHV(1 - 42)强5.3倍和7倍,以AUC表示的舒张作用中,VIP分别比它们强2.7倍和2.8倍。在以AUC表示的舒张作用中,相对于VIP,PHI和PHV(1 - 42)表现为部分激动剂。电场刺激(EFS;120毫安,1毫秒,4 - 32赫兹,2分钟的脉冲串)诱发频率依赖性舒张反应。α - 糜蛋白酶(1单位/毫升或3单位/毫升)、抗VIP血清(1:100或1:50)和抗PHI血清(1:25)略微降低了幅度,但极大地抑制了EFS(13赫兹)诱导的NANC舒张的AUC[分别比时间对照或正常兔血清(1:100或1:25)时减少约72%、47%和28%]。EFS(8 - 32赫兹)导致条带中VIP - LI和PHI - LI流出量显著的频率依赖性增加。EFS诱导的VIP - LI释放约为PHI - LI释放的20%。这些发现表明,PHI参与EFS诱导的大鼠胃底NANC舒张,VIP和PHI的主要生理作用是维持平滑肌舒张,并且VIP主要与PHI等摩尔共同释放。