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Mediators of non‐adrenergic non‐cholinergic inhibitory neurotransmission in porcine jejunum
Author(s) -
Matsuda N. M.,
Miller S. M.,
Sha L.,
Farrugia G.,
Szurszewski J. H.
Publication year - 2004
Publication title -
neurogastroenterology and motility
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.489
H-Index - 105
eISSN - 1365-2982
pISSN - 1350-1925
DOI - 10.1111/j.1365-2982.2004.00574.x
Subject(s) - apamin , medicine , endocrinology , vasoactive intestinal peptide , inhibitory postsynaptic potential , membrane potential , biology , chemistry , biochemistry , potassium channel , receptor , neuropeptide
The purpose of this study was to determine the non‐adrenergic non‐cholinergic inhibitory neurotransmitter in pig jejunum. Intracellular electrical activity was recorded from circular smooth muscle cells. Inhibitory junction potentials (IJPs) evoked by electrical field stimulation were inhibited by tetrodotoxin (1 μmol L −1 ), ω‐conotoxin GVIA (0.1 μmol L −1 ) tetrodotoxin, apamin (1 μ mol L −1 ), 1‐[6‐((17β‐3‐methoxyestra‐1,3,5(10)‐trien‐17‐yl)amino)hexyl]‐1H‐pyrrole‐2,5‐dione (U‐73122; 10 μmol L −1 ) but not by N ω‐nitro‐ l ‐arginine ( l ‐NNA; 100 μ mol L −1 ), haemoglobin (10 μ mol L −1 ), 1H‐[1,2,4]oxadiazolo[4,3‐a]quinoxalin‐1‐one (ODQ; 10 μ mol L −1 ) or 9‐(tetrahydro‐2‐furyl)adenine (SQ‐22536; 10 μmol L −1 ). S‐nitroso‐N‐acetylpenicillamine (SNAP) hyperpolarized the membrane potential. This was inhibited by ODQ (3 μmol L −1 ) and charybdotoxin (0.1 μ mol L −1 ). Adenosine‐5‐triphosphate (ATP; 100 μ mol L −1 ) and 2‐methylthio ATP (2‐MeS‐ATP; 100 μmol L −1 ) did not hyperpolarize the membrane potential and 6‐N‐N‐diethyl‐β‐ γ ‐dibromomethylene‐ d ‐adenosine‐5′‐triphosphate (ARL67156; 100 μ mol L −1 ) did not modify IJPs. Carbon monoxide (CO; 10%) and tricarbonyl dichlororuthenium dimer ([Ru(CO 3 Cl 2 )] 2 ; 100 μ mol L −1 ) hyperpolarized the membrane potential however zinc, copper and tin protoporphyrin IX (100 μmol L −1 ) did not alter IJPs. Vasoactive intestinal peptide (VIP) hyperpolarized the membrane potential but 4‐Cl‐ d ‐Phe 6 ‐Leu 17 ‐VIP (1 μmol L −1 ) did not modify IJPs. Pituitary adenylate cyclase activating peptide (PACAP)38 (0.5 μ mol L −1 ) hyperpolarized the membrane potential. This was inhibited by apamin (1 μmol L −1 ) but not by tetrodotoxin (1 μ mol L −1 ). Pituitary adenylate cyclase activating peptide6‐38 (1 μ mol L −1 ) inhibited IJPs. These data suggest that inhibitory neurotransmission in pig jejunum is mediated partly by PACAP.