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胍乙啶和氢氯噻嗪对自发性高血压大鼠血压及血管酪氨酸羟化酶活性的影响

The effect of guanethidine and hydrochlorothiazide on blood pressure and vascular tyrosine hydroxylase activity in the spontaneously hypertensive rat.

作者信息

Kohler C, Berkowitz B, Spector S

出版信息

Eur J Pharmacol. 1977 Mar 21;42(2):161-9. doi: 10.1016/0014-2999(77)90356-9.

Abstract

The present study examined the effects of antihypertensive drugs (hydrochlorothiazide and guanethidine) on blood pressure and tyrosine hydroxylase (TH) activity in the spontaneously hypertensive rat (SHR). Hydrochlorothiazide (50 mg/kg X 4 days) lowered blood pressure in the SHR to a degree equivalent to that produced by reserpine (0.3 mg/kg X 3 days). However, while reserpine increased vascular and adrenal TH activity, hydrochlorothiazide had no effect. Guanethidine (30 mg/kg X 2 days) reduced blood pressure in the SHR and also depleted cardiac, vascular and adrenal gland catecholamines; However, guanethidine administration did not increase TH activity in the mesenteric vasculature or adrenal glands. These studies indicate that at equieffective blood pressure lowering doses, different antihypertensive drugs have different effects on TH activity in the SHR. Neither blood pressure reduction nor catecholamine depletion in peripheral tissues are sufficient prerequisties for increasing TH activity. The data support the suggestion, however, that amine depletion in the central nervous system or ganglia may be an important factor in the regulation of TH.

摘要

本研究考察了抗高血压药物(氢氯噻嗪和胍乙啶)对自发性高血压大鼠(SHR)血压及酪氨酸羟化酶(TH)活性的影响。氢氯噻嗪(50mg/kg×4天)可使SHR血压降低至与利血平(0.3mg/kg×3天)相当的程度。然而,利血平可增加血管和肾上腺的TH活性,而氢氯噻嗪却无此作用。胍乙啶(30mg/kg×2天)可降低SHR血压,并使心脏、血管和肾上腺的儿茶酚胺耗竭;然而,给予胍乙啶并未增加肠系膜血管或肾上腺的TH活性。这些研究表明,在等效的降压剂量下,不同的抗高血压药物对SHR的TH活性有不同影响。外周组织中血压降低和儿茶酚胺耗竭均不是增加TH活性的充分前提条件。不过,这些数据支持如下观点,即中枢神经系统或神经节中的胺类耗竭可能是TH调节中的一个重要因素。

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