ABDOMINAL CONSTRICTION RESPONSE AND ITS SUPPRESSION BY ANALGESIC DRUGS IN MOUSE
ABDOMINAL CONSTRICTION RESPONSE AND ITS SUPPRESSION BY ANALGESIC DRUGS IN MOUSE
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DOI:
10.1111/j.1476-5381.1968.tb00973.x
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发表时间:
1968-01-01
影响因子:
7.3
通讯作者:
SCHNEIDER, C
中科院分区:
文献类型:
--
作者:
COLLIER, HOJ;DINNEEN, LC;SCHNEIDER, C
Of 31 substances tested for ability to elicit abdominal constriction (writhing) responses when injected intraperitoneally into T.O. strain mice, 26 were effective within 10 sec. to 30 min. There was a significant incidence of responses within 30 sec. of injecting each of 12 substances, including acetylcholine, adenosine triphosphate, bradykinin, histamine, 5-hydroxytryptamine, 2.5% KC1 solution, 4% NaCl solution or tryptamine. There was a longer delay before the onset of responses to acetic acid, 1.8% CaCl2 solution, chlorbutol, 5-hydroxytryptophan, 2% magnesium sulphate solution, phenylbenzoquinone or tryptophan. To maximally effective intraperitoneal doses of acetylcholine, ATP, bradykinin, KC1 or tryptamine, 70% or more mice responded within 2 min. After 2-4 min., the incidence of responses declined. Ten analgesic drugs were tested for ability to lessen the incidence of abdominal constriction responses within 2 min. of intraperitoneal injection of at least 4 of the 5 challenge substances. Codeine, morphine, cyclazocine, nalorphine, pentazocine, aspirin, flufenamate, meclofenamate and mefenamate were effective to different extents against these challenge substances. Paracetamol was effective only against acetylcholine. All the antipyretic, but none of the narcotic or narcotic antagonist drugs, were more effective against acetylcholine than against tryptamine challenge. Eighty-one drugs were tested as antagonists of abdominal constrictions induced by acetylcholine. All those having analgesic activity in man were effective in the mouse. For 27 analgesic drugs there was a very significant (P