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在兔体内,选择性内皮素-A受体拮抗剂BQ 610不能减轻全身性聚集性过敏反应相关的低血压。

Hypotension associated with systemic aggregated anaphylaxis is not attenuated by a selective endothelin-A receptor antagonist, BQ 610, in rabbits in vivo.

作者信息

Kawakami Takayuki, Mitsuhata Hiromasa, Saitoh Jin, Takeuchi Haruhiko, Hasome Naoki, Hiruta Masahiro, Horikawa Yukari, Seo Norimasa

机构信息

Department of Anesthesiology and Critical Care Medicine, Jichi Medical School, 3311-1 Yakushiji, Minamikawachi, Tochigi 329-0498, Japan.

出版信息

J Anesth. 2003;17(1):22-9. doi: 10.1007/s005400300004.

Abstract

PURPOSE

The present study was done to investigate the role of endothelin-1 (ET-1) in hypotension and bronchospasm provoked by anaphylaxis in rabbits in vivo.

METHODS

Forty-five rabbits sensitized to horse serum were randomly allocated to five groups: Group 1 (n = 10) received 0.5 nmol x kg(-1) of ET-1; Group 2 (n = 10) received 0.5 nmol x kg(-1) of ET-1 and 200 nmol x kg(-1) of a selective ETA receptor antagonist, BQ 610, without anaphylaxis; Group 3 (n = 5) received 200nmol x kg(-1) of BQ 610 alone without anaphylaxis, Group 4 (n = 10) received normal saline alone before being antigen challenged to induce anaphylaxis; Group 5 (n = 10) received 200 nmol x kg(-1) of BQ 610 before antigen challenge.

RESULTS

Mean arterial pressure (MAP) values were significantly different between Groups 1 and 2. Heart rate (HR), central venous pressure (CVP), dynamic pulmonary compliance (C(dyn)), and pulmonary airway resistance (R(L)) did not differ significantly between Groups 1 and 2. MAP values were significantly decreased compared with baseline in both Groups 4 and 5; however, the values were not significantly different between two groups. CVP values were significantly different between Groups 4 and 5 only at the 15-min time point following antigen challenge. HR, R(L), and C(dyn) values were not significantly different between Groups 4 and 5, nor were the survival rates.

CONCLUSION

BQ 610 does not improve hypotension or survival rates in systemic aggregated anaphylactic rabbits in vivo, implying that circulating ET-1 may not play an important role in anaphylaxis, although direct proof of production of circulating ET-1 or activation of ETA receptors is lacking in this study.

摘要

目的

本研究旨在探讨内皮素 -1(ET-1)在兔体内过敏性反应诱发的低血压和支气管痉挛中的作用。

方法

将45只对马血清致敏的兔子随机分为五组:第1组(n = 10)给予0.5 nmol·kg⁻¹的ET-1;第2组(n = 10)给予0.5 nmol·kg⁻¹的ET-1和200 nmol·kg⁻¹的选择性ETA受体拮抗剂BQ 610,未发生过敏反应;第3组(n = 5)仅给予200 nmol·kg⁻¹的BQ 610,未发生过敏反应;第4组(n = 10)在抗原激发诱导过敏反应前仅给予生理盐水;第5组(n = 10)在抗原激发前给予200 nmol·kg⁻¹的BQ 610。

结果

第1组和第2组之间平均动脉压(MAP)值有显著差异。第1组和第2组之间心率(HR)、中心静脉压(CVP)、动态肺顺应性(C(dyn))和肺气道阻力(R(L))无显著差异。第4组和第5组的MAP值与基线相比均显著降低;然而,两组之间的值无显著差异。仅在抗原激发后15分钟时间点,第4组和第5组的CVP值有显著差异。第4组和第5组之间的HR、R(L)和C(dyn)值无显著差异,生存率也无显著差异。

结论

BQ 610不能改善兔体内全身性聚集性过敏反应的低血压或生存率,这意味着循环中的ET-1在过敏反应中可能不起重要作用,尽管本研究缺乏循环ET-1产生或ETA受体激活的直接证据。

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