首页> 美国卫生研究院文献>The Journal of Physiology >Modulation of cholinergic neurotransmission by the peptide VIP VIP antiserum and VIP antagonists in dog and cat trachea.
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Modulation of cholinergic neurotransmission by the peptide VIP VIP antiserum and VIP antagonists in dog and cat trachea.

机译:犬和​​猫气管中肽VIPVIP抗血清和VIP拮抗剂对胆碱能神经传递的调节。

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摘要

1. Comparative studies on the effects of vasoactive intestinal polypeptide (VIP), commercially available VIP antiserum or VIP antagonists [Ac-Tyr1, D-Phe2]-GRF(1-29)-NH2 and [4-Cl-D-Phe6, Leu17]-VIP on excitatory neuroeffector transmission in the dog and cat trachea were performed with microelectrode, double sucrose-gap, and tension recording methods. 2. VIP (10(-11)-10(-9) M) had no effect on the resting membrane potential or on the input resistance of the smooth muscle cells of dog and cat trachea. However, with increased concentrations (greater than 10(-8) M) VIP hyperpolarized the membrane and decreased the input resistance of the membrane in both tissues. 3. VIP (10(-10)-10(-7) M) dose-dependently reduced the amplitude of the contractions evoked through the nervous structure excited by field stimulation in the combined presence of indomethacin (10(-5) M) and guanethidine (10(-6) M) in the dog, and in the presence of guanethidine (10(-6) M) in cat trachea. In parallel with actions on twitch contractions, VIP (10(-11)-10(-7) M) reduced the amplitude of the excitatory junction potentials (EJPs) evoked through the nervous structure excited by single pulse field stimulation in both tissues. 4. VIP (10(-9) M) had no effect on the post-junctional response of smooth muscle cells to exogenous acetylcholine (ACh) (10(-9)-10(-5) M). 5. During repetitive field stimulation at the stimulus frequency of 0.033-0.1 Hz, the amplitude of the EJPs was gradually reduced, and VIP (10(-9) M) enhanced this depression phenomenon in the dog and cat trachea. 6. EJPs also showed summation when repetitive field stimulation was applied at high frequency (20 Hz) in the dog trachea. The slope of the relationship between the relative amplitude of the EJP and number of stimuli at 20 Hz was 2.2 +/- 0.4 mV/stimulation (n = 4) in the dog trachea. However, in the cat trachea, summation of EJPs was not prominent, giving a mean slope of 0.6 +/- 0.2 mV/stimulation (n = 6) measured by the microelectrode method. VIP (10(-9) M) shifted downward the relationship between the relative amplitude of the EJP and the number of stimuli at 20 Hz in both tissues. 7. Overnight incubation with VIP antiserum (10(-6) g/ml) had little effect on the depression of the EJP in the dog and cat trachea, or the summation of the EJP observed in the dog trachea.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.比较研究血管活性肠多肽(VIP),市售VIP抗血清或VIP拮抗剂[Ac-Tyr1,D-Phe2] -GRF(1-29)-NH2和[4-Cl-D-Phe6]的效果, Leu17] -VIP用微电极,双蔗糖间隙和张力记录方法进行了在狗和猫气管中兴奋性神经效应物传递的研究。 2. VIP(10(-11)-10(-9)M)对犬和猫气管的静息膜电位或平滑肌细胞的输入阻力没有影响。但是,随着浓度的增加(大于10(-8)M),VIP使膜超极化,并降低了两个组织中膜的输入阻力。 3. VIP(10(-10)-10(-7)M)剂量依赖性降低在吲哚美辛(10(-5)M)和吲哚美辛联合存在下通过场刺激激发的神经结构引起的收缩幅度犬中的胍乙啶(10(-6)M),猫气管中存在胍乙啶(10(-6)M)。与对抽搐收缩的作用同时,VIP(10(-11)-10(-7)M)减小了在两个组织中单脉冲场刺激所激发的神经结构引起的兴奋性连接电位(EJPs)的幅度。 4. VIP(10(-9)M)对平滑肌细胞对外源性乙酰胆碱(ACh)(10(-9)-10(-5)M)的结后反应没有影响。 5.在以0.033-0.1 Hz的刺激频率进行重复场刺激期间,EJPs的振幅逐渐降低,而VIP(10(-9)M)增强了狗和猫气管的这种抑郁现象。 6.当在犬气管中以高频(20 Hz)施加重复场刺激时,EJP也显示出总和。在犬气管中,EJP的相对振幅与20 Hz刺激次数之间的关系斜率为2.2 +/- 0.4 mV /刺激(n = 4)。但是,在猫的气管中,EJP的总和并不明显,通过微电极法测得的平均斜率为0.6 +/- 0.2 mV /刺激(n = 6)。 VIP(10(-9)M)向下移动了两个组织中EJP的相对振幅与20 Hz刺激次数之间的关系。 7.隔夜与VIP抗血清(10(-6)g / ml)孵育对狗和猫气管中EJP的抑制或在狗气管中观察到的EJP的累加几乎没有影响。(摘要摘录于400话)

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