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牛气管体外反应性:上皮和一氧化氮的作用

Bovine tracheal responsiveness in vitro: role of the epithelium and nitric oxide.

作者信息

Sadeghi-Hashjin G, Henricks P A, Folkerts G, Verheyen A K, van der Linde H J, Nijkamp F P

机构信息

Dept of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, The Netherlands.

出版信息

Eur Respir J. 1996 Nov;9(11):2286-93. doi: 10.1183/09031936.96.09112286.

Abstract

Airway epithelium releases inhibitory factors, such as nitric oxide (NO) and prostaglandin E2 (PGE2), which may counteract bronchoconstriction. We investigated whether epithelium-derived inhibitory substances exert a crucial influence on bovine tracheal responsiveness in vitro. Isotonic and isometric contractions in response to histamine of intact and epithelium-denuded tracheal smooth muscle strips were compared. In addition, the effects of L-arginine (L-arg), N(G)-nitro-L-arginine methyl esther (L-NAME), and N(G)-monomethyl L-arginine (L-NMMA) on histamine responsiveness were investigated. The release of NO and PGE2 from tracheal epithelium was measured. Removal of the epithelium from tracheal smooth muscle strips did not change the negative log of the concentration of histamine producing half the maximal effect (pD2) or the maximal effect (Emax). Incubation of the tissues for 25 min with L-arg or L-NAME did not influence basal tone or the contractions induced by histamine. However, incubation with L-NMMA increased the basal tone and caused a slight hyporesponsiveness to histamine. S-nitroso-N-acetyl-penicillamine (SNAP, a direct NO donor) reversed the contraction induced by histamine in a concentration-dependent manner. Stimulation of the epithelial layer by 0.1 microM histamine increased the release of NO 3-4 fold compared to basal levels; this effect was completely inhibited in the presence of L-NMMA. In addition, 1 mM histamine caused a significant increase in the release of PGE2 from the epithelial tissue. In conclusion, no functional inhibitory influence of the epithelium can be identified in bovine airways. The S-nitroso-N-acetyl-penicillamine-induced relaxation demonstrates the presence of a nitric oxide sensitive pathway in bovine airways. However, the amounts of nitric oxide and prostaglandin E2 released from bovine tracheal epithelium are probably too low to exert a significant effect on the histamine-induced contractions.

摘要

气道上皮会释放抑制因子,如一氧化氮(NO)和前列腺素E2(PGE2),它们可能会对抗支气管收缩。我们研究了上皮来源的抑制物质在体外是否对牛气管反应性产生关键影响。比较了完整和去上皮的气管平滑肌条对组胺的等渗和等长收缩。此外,研究了L-精氨酸(L-arg)、N(G)-硝基-L-精氨酸甲酯(L-NAME)和N(G)-单甲基-L-精氨酸(L-NMMA)对组胺反应性的影响。测定了气管上皮中NO和PGE2的释放。去除气管平滑肌条的上皮并没有改变产生最大效应一半时组胺浓度的负对数(pD2)或最大效应(Emax)。用L-arg或L-NAME孵育组织25分钟对基础张力或组胺诱导的收缩没有影响。然而,用L-NMMA孵育会增加基础张力并导致对组胺的轻微反应性降低。S-亚硝基-N-乙酰青霉胺(SNAP,一种直接的NO供体)以浓度依赖的方式逆转组胺诱导的收缩。与基础水平相比,0.1微摩尔组胺刺激上皮层使NO释放增加3-4倍;在L-NMMA存在下这种效应被完全抑制。此外,1毫摩尔组胺导致上皮组织中PGE2的释放显著增加。总之,在牛气道中未发现上皮的功能性抑制作用。S-亚硝基-N-乙酰青霉胺诱导的舒张表明牛气道中存在一氧化氮敏感途径。然而,从牛气管上皮释放的一氧化氮和前列腺素E2的量可能太低,无法对组胺诱导的收缩产生显著影响。

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