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灭酸类药物对豚鼠和人体消化道肌肉中前列腺素作用的拮抗作用。

Antagonism by fenamates of prostaglandin action in guinea-pig and human alimentary muscle.

作者信息

Bennett A, Pratt D, Sanger G J

出版信息

Br J Pharmacol. 1980 Mar;68(3):357-62. doi: 10.1111/j.1476-5381.1980.tb14548.x.

Abstract

1 Low concentrations of meclofenamate, flufenamate or mefenamate had little effect on contractions in response to acetylcholine in any tissue studied. 2 Sodium meclofenamate potently antagonized contractions of guinea-pig ileum longitudinal muscle to prostaglandin E2 (PGE2), PGF2 alpha or PGD2. 3 In guinea-pig colonic longitudinal muscle, contractions to PGE2 were reduced by sodium meclofenamate, but contractions of the longitudinal or circular muscle to PGF2 alpha or PGD2 were less effectively inhibited. 4 In human gastrointestinal longitudinal muscle, sodium meclofenamate or flufenamate potently inhibited contractions to PGF2 alpha, but not to PGE2. 5 Sodium mefenamate or mefenamic acid, even in high concentrations, had little effect on contractions to PGF2 alpha, but tended to inhibit PGE2-induced contractions of human gastrointestinal longitudinal muscle. 6 The therapeutic advantages of prostaglandin synthesis inhibitors which also antagonize responses to certain prostaglandins are discussed.

摘要
  1. 在任何研究的组织中,低浓度的甲氯芬那酸、氟芬那酸或甲芬那酸对乙酰胆碱引起的收缩几乎没有影响。2. 甲氯芬那酸钠能有效拮抗豚鼠回肠纵肌对前列腺素E2(PGE2)、前列腺素F2α或前列腺素D2的收缩。3. 在豚鼠结肠纵肌中,甲氯芬那酸钠可减少对PGE2的收缩,但对纵肌或环肌对前列腺素F2α或前列腺素D2的收缩抑制效果较差。4. 在人胃肠道纵肌中,甲氯芬那酸钠或氟芬那酸能有效抑制对前列腺素F2α的收缩,但对PGE2无效。5. 甲芬那酸钠或甲芬那酸即使在高浓度下,对前列腺素F2α引起的收缩影响也很小,但倾向于抑制人胃肠道纵肌中PGE2诱导的收缩。6. 讨论了同时拮抗对某些前列腺素反应的前列腺素合成抑制剂的治疗优势。

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Multiple sites of interaction between prostaglandins and non-steroidal anti-inflammatory agents.
Prostaglandins. 1975 Mar;9(3):349-59. doi: 10.1016/0090-6980(75)90139-2.

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