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致热原多聚肌苷酸:多聚胞苷酸激活清醒家兔的下丘脑-垂体-肾上腺皮质轴依赖于促肾上腺皮质激素释放因子-41。

Activation of the hypothalamo-pituitary-adrenocortical axis in the conscious rabbit by the pyrogen polyinosinic:polycytidylic acid is dependent on corticotrophin-releasing factor-41.

作者信息

Milton N G, Hillhouse E W, Milton A S

机构信息

Department of Clinical Biochemistry, University of Newcastle upon Tyne, U.K.

出版信息

J Endocrinol. 1992 Oct;135(1):69-75. doi: 10.1677/joe.0.1350069.

DOI:10.1677/joe.0.1350069
PMID:1431685
Abstract

The pyrogenic interferon inducer polyinosinic:polycytidylic acid (Poly I:C) was shown to activate the rabbit hypothalamo-pituitary-adrenocortical (HPA) axis in vivo. The immunoreactive cortisol response to Poly I:C (2.5 micrograms/kg) was shown to have a corticotrophin-releasing factor-41 (CRF-41)-dependent component which was abolished by peripheral immunoneutralization using an anti-CRF-41 monoclonal antibody (KCHMB001; 2.5 mg/kg i.v.). Peripheral administration of the arginine vasopressin (AVP) V1 receptor antagonist ([deamino-Pen1, O-Me-Tyr2, Arg8]-vasopressin; 225 nmol/kg i.v.) had no effect on the response of immunoreactive cortisol to Poly I:C, suggesting that AVP was not involved in activation of the HPA axis. Poly I:C increased both body temperature and circulating immunoreactive prostaglandin E2; these responses were abolished by the cyclo-oxygenase inhibitor ketoprofen (3 mg/kg s.c.). The immunoreactive cortisol response to Poly I:C, however, remained after the administration of ketoprofen, indicating a prostaglandin (PG)-independent component. The immunoreactive cortisol levels in control, saline vehicle-treated, animals were reduced by both the CRF-41 receptor antagonist (alpha-helical CRF (9-41); 6.25 nmol/kg i.v.) and ketoprofen (3 mg/kg s.c.) indicating that this basal state is dependent on both CRF-41 and PGs.

摘要

已证明,热原性干扰素诱导剂聚肌苷酸:聚胞苷酸(Poly I:C)在体内可激活兔下丘脑-垂体-肾上腺皮质(HPA)轴。已证明,对Poly I:C(2.5微克/千克)的免疫反应性皮质醇反应具有促肾上腺皮质激素释放因子41(CRF-41)依赖性成分,使用抗CRF-41单克隆抗体(KCHMB001;2.5毫克/千克静脉注射)进行外周免疫中和可消除该成分。外周给予精氨酸加压素(AVP)V1受体拮抗剂([脱氨基-Pen1,O-甲基-Tyr2,Arg8]-加压素;225纳摩尔/千克静脉注射)对免疫反应性皮质醇对Poly I:C的反应无影响,这表明AVP不参与HPA轴的激活。Poly I:C可提高体温和循环免疫反应性前列腺素E2;这些反应可被环氧化酶抑制剂酮洛芬(3毫克/千克皮下注射)消除。然而,给予酮洛芬后,对Poly I:C的免疫反应性皮质醇反应仍然存在,表明存在前列腺素(PG)非依赖性成分。对照动物(经生理盐水处理)的免疫反应性皮质醇水平因CRF-41受体拮抗剂(α-螺旋CRF(9-41);6.25纳摩尔/千克静脉注射)和酮洛芬(3毫克/千克皮下注射)而降低,这表明这种基础状态依赖于CRF-41和PGs。

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