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BRL 13776:一种具有独特单胺消耗特性的新型抗高血压药物。

BRL 13776: a novel antihypertensive agent with interesting monoamine depleting properties.

作者信息

Melrose J, Palfreyman M G, Poyser R H, Whiting R L

出版信息

Br J Pharmacol. 1977 Nov;61(3):357-69. doi: 10.1111/j.1476-5381.1977.tb08428.x.

Abstract
  1. Oral doses of 10-100 mg/kg of BRL 13776 lowered the blood pressure of both deoxycorticosterone acetate (DOCA)/NaCl-treated hypertensive rats and untreated normotensive rats. 2. BRL 13776 (100 mg/kg, orally) also reduced the blood pressure of renal hypertensive cats (cellophane perinephritis model). 3. No tolerance developed to the blood-pressure lowering action of BRL 13776 when an oral daily dose of 100 mg/kg was administered repeatedly for up to 15 days to hypertensive rats and cats. 4. The fall in blood pressure to BRL 13776 in rats was associated with a reduction of tissue catecholamines. 5. The catecholamine depletion occurred in all the peripheral tissues examined but in the brain was restricted to certain regions, these being the hind-brain on single dosing and the hind-brain, hypothalamus and mid-brain on repeated dosing. Catecholamine levels in the cerebral hemispheres were not affected by either single or repeated doses of BRL 13776. 6. BRL 13776 caused some reduction of the 5-hydroxytryptamine content of the heart but not of whole brain or any brain region. 7. Neither single doses (up to 900 mg/kg orally) nor repeated doses (100-300 mg/kg orally) of BRL 13776 produced any significant behavioural effects in animals. 8. BRL 13776 is a new type of agent to display both antihypertensive and monoamine-depleting properties. The reduction of noradrenaline in certain brain regions may be a cause of the antihypertensive response but depletion in the periphery could contribute in a major or minor way. The differential action on noradrenaline in the brain together with the lack of effect on 5-hydroxytryptamine might also explain the apparent absence of behavioural effects.
摘要
  1. 口服剂量为10 - 100毫克/千克的BRL 13776可降低醋酸去氧皮质酮(DOCA)/氯化钠处理的高血压大鼠和未处理的正常血压大鼠的血压。2. BRL 13776(100毫克/千克,口服)也可降低肾性高血压猫(玻璃纸肾周炎模型)的血压。3. 当对高血压大鼠和猫每日口服100毫克/千克的剂量,重复给药长达15天时,对BRL 13776的降压作用未产生耐受性。4. 大鼠血压下降与组织儿茶酚胺减少有关。5. 在所检查的所有外周组织中均发生了儿茶酚胺耗竭,但在脑中仅限于某些区域,单次给药时为后脑,重复给药时为后脑、下丘脑和中脑。BRL 13776的单次或重复剂量均未影响大脑半球中的儿茶酚胺水平。6. BRL 13776可使心脏的5 - 羟色胺含量有所降低,但对全脑或任何脑区均无此作用。7. BRL 13776的单次剂量(高达900毫克/千克,口服)或重复剂量(100 - 300毫克/千克,口服)均未在动物中产生任何显著的行为影响。8. BRL 13776是一种新型药物,兼具降压和单胺耗竭特性。某些脑区去甲肾上腺素的减少可能是降压反应的原因,但外周去甲肾上腺素的耗竭可能或多或少也有作用。脑中去甲肾上腺素的差异作用以及对5 - 羟色胺缺乏作用也可能解释了明显缺乏行为影响的原因。

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