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向绵羊脑室内注入促肾上腺皮质激素释放因子(CRF)和促肾上腺皮质激素(ACTH)会使血压升高。

Intracerebroventricular infusions of corticotrophin releasing factor (CRF) and ACTH raise blood pressure in sheep.

作者信息

Scoggins B A, Coghlan J P, Denton D A, Fei D W, Nelson M A, Tregear G W, Tresham J, Wang X M

出版信息

Clin Exp Pharmacol Physiol. 1984 Jul-Aug;11(4):365-7. doi: 10.1111/j.1440-1681.1984.tb00280.x.

DOI:10.1111/j.1440-1681.1984.tb00280.x
PMID:6097379
Abstract

Infusion of synthetic ovine CRF (10 or 100 micrograms/h) into the lateral lateral cerebral ventricle for 24 h increased mean arterial blood pressure of conscious sheep. CRF infusion also increased urine output and sodium excretion. Intravenous infusion of CRF (100 micrograms/h) or intraventricular infusion of artificial CSF had no effect on blood pressure. Intraventricular infusion of ACTH (1-24) at 0.5 micrograms/kg per day, a rate of infusion which has no systemic effect on blood pressure, also raised mean arterial pressure. These studies suggest that two peptides involved in the physiological response to 'stress' may influence blood pressure by mechanisms which do not involve stimulation of adrenocortical steroid production.

摘要

向清醒绵羊的侧脑室输注合成羊促肾上腺皮质激素释放因子(CRF)(10或100微克/小时)24小时可升高其平均动脉血压。输注CRF还可增加尿量和钠排泄。静脉输注CRF(100微克/小时)或脑室内输注人工脑脊液对血压无影响。以每天0.5微克/千克的速率脑室内输注促肾上腺皮质激素(ACTH)(1-24),该输注速率对血压无全身影响,但也可升高平均动脉压。这些研究表明,参与对“应激”生理反应的两种肽可能通过不涉及刺激肾上腺皮质类固醇生成的机制影响血压。

相似文献

1
Intracerebroventricular infusions of corticotrophin releasing factor (CRF) and ACTH raise blood pressure in sheep.向绵羊脑室内注入促肾上腺皮质激素释放因子(CRF)和促肾上腺皮质激素(ACTH)会使血压升高。
Clin Exp Pharmacol Physiol. 1984 Jul-Aug;11(4):365-7. doi: 10.1111/j.1440-1681.1984.tb00280.x.
2
The effect of intracerebroventricular infusions of CRF, sauvagine, ACTH (1-24) and ACTH (4-10) on blood pressure in sheep.
J Hypertens Suppl. 1984 Dec;2(3):S67-8.
3
Cardiovascular effects of long-term central and peripheral administration of urocortin, corticotropin-releasing factor, and adrenocorticotropin in sheep.长期向绵羊中枢和外周给予尿皮质素、促肾上腺皮质激素释放因子和促肾上腺皮质激素的心血管效应。
Endocrinology. 2004 Dec;145(12):5598-604. doi: 10.1210/en.2004-0432. Epub 2004 Aug 19.
4
Pressor, tachycardic and behavioral excitatory responses in conscious rats following ICV administration of ACTH and CRF are blocked by naloxone pretreatment.在清醒大鼠中,经脑室内注射促肾上腺皮质激素(ACTH)和促肾上腺皮质激素释放因子(CRF)后出现的升压、心动过速及行为兴奋反应,可被纳洛酮预处理所阻断。
Peptides. 1986 Jul-Aug;7(4):597-601. doi: 10.1016/0196-9781(86)90033-1.
5
Effects of synthetic ovine CRF on ACTH, cortisol and blood pressure in sheep.合成羊促肾上腺皮质激素释放因子对绵羊促肾上腺皮质激素、皮质醇和血压的影响。
Peptides. 1983 Mar-Apr;4(2):221-3. doi: 10.1016/0196-9781(83)90118-3.
6
Plasma cortisol and catecholamine responses to intracerebroventricular administration of CRF to rhesus monkeys.恒河猴脑室内注射促肾上腺皮质激素释放因子后血浆皮质醇和儿茶酚胺的反应
Life Sci. 1984 May 7;34(19):1873-8. doi: 10.1016/0024-3205(84)90682-9.
7
Effect of synthetic ovine corticotropin-releasing factor. Dose response of plasma adrenocorticotropin and cortisol.合成羊促肾上腺皮质激素释放因子的作用。血浆促肾上腺皮质激素和皮质醇的剂量反应。
J Clin Invest. 1983 Mar;71(3):587-95. doi: 10.1172/jci110804.
8
Evidence against a central pressor mechanism for adrenocortical steroid hypertension in sheep.反对绵羊肾上腺皮质类固醇性高血压存在中枢加压机制的证据。
Clin Exp Hypertens. 1996 Aug;18(6):831-49. doi: 10.3109/10641969609081783.
9
Corticotropin-releasing factor alone, but not arginine vasopressin alone, stimulates the release of adrenocorticotropin in the conscious intact sheep.单独使用促肾上腺皮质激素释放因子可刺激清醒完整绵羊释放促肾上腺皮质激素,而单独使用精氨酸加压素则无此作用。
Endocrinology. 1995 May;136(5):1821-7. doi: 10.1210/endo.136.5.7720626.
10
Effect of ICV infusion of CRF on blood pressure and adrenal steroids in rabbits.脑室内注射促肾上腺皮质激素释放因子对家兔血压和肾上腺类固醇的影响。
Neuropeptides. 1995 Jun;28(6):325-31. doi: 10.1016/0143-4179(95)90097-7.

引用本文的文献

1
CRHR2 (Corticotropin-Releasing Hormone Receptor 2) in the Nucleus of the Solitary Tract Contributes to Intermittent Hypoxia-Induced Hypertension.孤束核中的 CRHR2(促肾上腺皮质激素释放激素受体 2)有助于间歇性低氧诱导的高血压。
Hypertension. 2018 Oct;72(4):994-1001. doi: 10.1161/HYPERTENSIONAHA.118.11497.
2
Hypotensive effects of ovine and human corticotrophin-releasing factors in man.
Eur J Clin Pharmacol. 1987;31(5):531-4. doi: 10.1007/BF00606625.