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British journal of pharmacology and chemotherapy最新文献

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A correlation between inhibition of the uptake of 3H from (+)-3H-noradrenaline and potentiation of the responses to (-)-noradrenaline in the guinea-pig isolated trachea. 豚鼠离体气管中(+)-3H-去甲肾上腺素对3H摄取的抑制与(-)-去甲肾上腺素反应增强的相关性
Pub Date : 1968-06-01 DOI: 10.1111/j.1476-5381.1968.tb00996.x
R W Foster
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引用次数: 27
Analysis of direct renal actions of alpha and beta adrenergic stimulation upon sodium excretion compared to acetylcholine. 与乙酰胆碱相比,肾上腺素能刺激对钠排泄的直接肾作用分析。
Pub Date : 1968-06-01 DOI: 10.1111/j.1476-5381.1968.tb00984.x
J E Pearson, R L Williams
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引用次数: 21
Aspects of the biogenic amine-depleting activity of ethyl 3-acetamido-4H-pyrrolo-[3,4-c]isoxazole-5(6H)-carboxylate in the rat. 3-乙酰氨基- 4h -吡咯-[3,4-c]异恶唑-5(6H)-羧酸酯在大鼠体内生物源性耗胺活性的研究
Pub Date : 1968-06-01 DOI: 10.1111/j.1476-5381.1968.tb00987.x
W Lippmann, M Wishnick
Agents have been found which cause marked lowering of the catecholamine and/or 5-hydroxytryptamine concentrations in tissues and some (for example, a-methyldihydroxyphenylalanine, guanethidine and reserpine) are useful in the treatment of hypertension (Hafkenschiel & Sellers, 1954; Richardson & Wyso, 1959; Hollander, 1961; Page, Hurley & Dustan, 1961; Gillespie, Oates, Crout & Sjoerdsma, 1962; Cannon, Whitlock, Morris, Angers & Laragh, 1962). Ethyl 3-acetamido-4H-pyrrolo[3,4-c]isoxazole-5(6H)-carboxylate (CL-62375) has been reported to decrease both the catecholamine and 5-hydroxytryptamine concentrations in tissues of the rat (Lippmann & Wishnick, 1967). After a single administration of CL-62375 there is an appreciable lowering of the catecholamine concentration in the heart and brain and a slight fall in brain 5-hydroxytryptamine. After repeated administration of CL-62375 the heart shows the largest decrease in the catecholamine concentration followed by the brain and the adrenals; the brain 5-hydroxytryptamine decreases appreciably. CL-62375 causes a lowering of blood pressure in the rat (Cummings & Welter, 1967, personal communication). Studies on the mechanism of the biogenic amine-depleting activity of CL-62375 were carried out and the results are presented in the present paper.
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引用次数: 1
The effects of drugs on the release of vasopressin. 药物对加压素释放的影响。
Pub Date : 1968-06-01 DOI: 10.1111/j.1476-5381.1968.tb00994.x
R E Dyball
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引用次数: 22
Influence of antimuscarinic substances on in vitro synthesis of acetylcholine by rat cerebral cortex. 抗蛇毒碱物质对大鼠大脑皮质体外合成乙酰胆碱的影响。
Pub Date : 1968-06-01 DOI: 10.1111/j.1476-5381.1968.tb00997.x
M M Bertels-Meeuws, R L Polak
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引用次数: 47
Pharmacological actions of pseudoscopine and some of its derivatives. 假莨菪碱及其衍生物的药理作用。
Pub Date : 1968-06-01 DOI: 10.1111/j.1476-5381.1968.tb00985.x
K Vidal-Beretervide
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引用次数: 0
Kinetic parameters of narcotic agonists and antagonists, with particular reference to N-allylnoroxymorphone (naloxone). 麻醉激动剂和拮抗剂的动力学参数,特别是n -烯丙基去氧吗啡酮(纳洛酮)。
Pub Date : 1968-06-01 DOI: 10.1111/j.1476-5381.1968.tb00988.x
H W Kosterlitz, A J Watt
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引用次数: 359
Anti-inflammatory and related properties of 4-(p-biphenylyl)-3-hydroxybutyric acid. 4-(对联苯基)-3-羟基丁酸的抗炎及相关特性。
Pub Date : 1968-06-01 DOI: 10.1111/j.1476-5381.1968.tb01000.x
D I Barron, A R Copley, D K Vallance
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引用次数: 13
A simple chemical procedure for distinguishing E from F prostaglandins, with application to tissue extracts. 区分前列腺素E和前列腺素F的简单化学程序,应用于组织提取物。
Pub Date : 1968-05-01 DOI: 10.1111/J.1476-5381.1968.TB00484.X
N. Ambache, Hilary C. Brummer
An easy and relatively rapid procedure for distinguishihg the ketonic prostaglandins E (PGEs) from the nonketonic prostaglandins F (PGFs) and other hydroxy-acid lipid spasmogens is presented. The method depends on the ability of certain hydrazine derivatives to combine specifically with keto groups. Girard's reagent T (trimethyl-ammonium-acetohydrazide chloride) was used for differentiation. PGFs were unaffected by the reagent, whereas the reagent affected E series prostaglandins by apparently inactivating them. In addition, apparent inactivation also occurred when the reagent was applied to a mixture of the PGEs and PGFs. After treatment of PGEs in aqueous solution with the reagent for 1 hour, at room temperature or 0 degrees centigrade, their extraction into ether on partition at pH 3-4 was reduced. Freezing to -15 degrees centigrade after the 1 hour treatment, and thawing before the ether partition, further reduced the recovery of PGEs. After reagent treatment in these different conditions, PGFs were recovered fully. The presence of a PGE-like ketonic component in the hydroxy-acid constituents of rabbit and cat irins was demonstrated, along with a lower proportion of the ketonic components in ether-purified rabbit cerebral hemisphere extract.
提出了一种简单而相对快速的方法来区分酮性前列腺素E (PGEs)与非酮性前列腺素F (PGFs)和其他羟基酸脂质痉挛原。该方法依赖于某些肼衍生物与酮基特异性结合的能力。用吉拉德试剂T(三甲基-氨-乙酰肼氯)进行鉴别。PGFs不受该试剂的影响,而该试剂通过明显灭活E系列前列腺素来影响它们。此外,当该试剂应用于PGEs和PGFs的混合物时,也发生了明显的失活。在室温或0℃条件下,PGEs在水溶液中处理1小时后,在pH为3-4的条件下,PGEs被萃取到乙醚中。处理1小时后冷冻至-15℃,乙醚分割前解冻,进一步降低了PGEs的恢复。在这些不同条件下经过试剂处理后,PGFs完全恢复。在兔和猫铁素的羟基酸成分中存在类似pge的酮类成分,同时在醚纯化的兔大脑半球提取物中酮类成分的比例较低。
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引用次数: 67
A simple chemical procedure for distinguishing E from F prostaglandins, with application to tissue extracts. 区分前列腺素E和前列腺素F的简单化学程序,应用于组织提取物。
N Ambache, H C Brummer
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引用次数: 0
期刊
British journal of pharmacology and chemotherapy
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