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戒酒期间注射氨基氰会增加酒精摄入量。

Cyanamide injections during alcohol deprivation increase alcohol drinking.

作者信息

Sinclair J D, Gribble P A

出版信息

Alcohol. 1985 Jul-Aug;2(4):627-30. doi: 10.1016/0741-8329(85)90091-6.

DOI:10.1016/0741-8329(85)90091-6
PMID:4026987
Abstract

Long-Evans male rats were given 7 weeks of choice between 10% ethanol and water and then were divided into 6 matched groups, 3 of which were then deprived of alcohol for 6 days. Subcutaneous cyanamide injections (10 mg/kg, 3 times daily, for 4 days) during alcohol deprivation produced a long lasting, significant increase in subsequent alcohol selection, over and above the increase produced by alcohol deprivation alone. The same injections given to a group not deprived of alcohol caused a significant suppression of alcohol drinking during the treatment and had disappeared 4 days after the last injection. Thereafter the drinking remained at the control level and did not rise to that of the group given the injections during deprivation. The groups did not differ in their subsequent selection of saline solutions.

摘要

将Long-Evans雄性大鼠置于10%乙醇和水之间进行7周的选择,然后分为6个匹配组,其中3组随后戒酒6天。在戒酒期间皮下注射氨甲酰(10毫克/千克,每日3次,共4天),与仅戒酒所产生的增加相比,随后的酒精选择有长期显著增加。对未戒酒的一组给予相同注射,在治疗期间导致酒精摄入量显著减少,且在最后一次注射后4天消失。此后,饮酒量保持在对照水平,未升至在戒酒期间接受注射组的水平。这些组在随后对盐溶液的选择上没有差异。

相似文献

1
Cyanamide injections during alcohol deprivation increase alcohol drinking.戒酒期间注射氨基氰会增加酒精摄入量。
Alcohol. 1985 Jul-Aug;2(4):627-30. doi: 10.1016/0741-8329(85)90091-6.
2
Cyanamide given ICV or systemically to the rat alters subsequent alcohol drinking.向大鼠脑室内或全身给予氨基氰会改变其随后的酒精摄入量。
Alcohol. 1987 Sep-Oct;4(5):347-53. doi: 10.1016/0741-8329(87)90066-8.
3
Inhibition of brain dopa-decarboxylase by RO 4-4602 infused ICV blocks alcohol drinking induced in rats by cyanamide.通过脑室内注入RO 4-4602抑制脑内多巴脱羧酶,可阻断氨甲酰诱导的大鼠饮酒行为。
Psychopharmacology (Berl). 1989;98(2):176-82. doi: 10.1007/BF00444688.
4
Central action of an inhibitor of brain dopa-decarboxylase, NSD-1015, on cyanamide-induced alcohol drinking in rats.脑多巴脱羧酶抑制剂NSD - 1015对氰胺诱导的大鼠酒精摄入的中枢作用
Pharmacol Biochem Behav. 1990 Feb;35(2):465-8. doi: 10.1016/0091-3057(90)90186-l.
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Effects of cyanamide and clofibrate on the enzymes of ethanol oxydation and on ethanol consumption in the rat.氨甲酰和氯贝丁酯对大鼠乙醇氧化酶及乙醇消耗的影响。
Arch Int Pharmacodyn Ther. 1980 Jan;243(1):17-26.
6
Drinking patterns in genetic low-alcohol-drinking (LAD) rats after systemic cyanamide and cerebral injections of THP or 6-OHDA.全身性给予氨基氰以及脑内注射四氢吡啶(THP)或6-羟基多巴胺(6-OHDA)后,遗传性低酒精摄入(LAD)大鼠的饮酒模式。
Alcohol. 1998 Apr;15(3):239-47. doi: 10.1016/s0741-8329(97)00126-2.
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Suppression of alcohol drinking with brain aldehyde dehydrogenase inhibition.通过抑制脑醛脱氢酶来抑制饮酒。
Pharmacol Biochem Behav. 1981 Mar;14(3):377-83. doi: 10.1016/0091-3057(81)90405-6.
8
The role of acetaldehyde-metabolizing enzymes in the mediation of ethanol consumption: an investigation using a simulated drinking bout.乙醛代谢酶在乙醇摄入调节中的作用:一项使用模拟饮酒发作的研究。
Alcohol Alcohol Suppl. 1987;1:361-5.
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Blood acetaldehyde levels in alcohol-dosed rats after treatment with ANIT, ANTU, dithiocarbamate derivatives, or cyanamide.给予ANIT、ANTU、二硫代氨基甲酸盐衍生物或氰胺后,用酒精处理的大鼠的血液乙醛水平。
Drug Chem Toxicol. 1983;6(4):317-28. doi: 10.3109/01480548309082713.
10
Age dependent development of ethanol drinking in rats after inhibition of aldehyde dehydrogenase.乙醛脱氢酶抑制后大鼠乙醇摄入的年龄依赖性发展
Alcohol. 1992 Nov-Dec;9(6):501-7. doi: 10.1016/0741-8329(92)90087-q.

引用本文的文献

1
Inhibition of brain dopa-decarboxylase by RO 4-4602 infused ICV blocks alcohol drinking induced in rats by cyanamide.通过脑室内注入RO 4-4602抑制脑内多巴脱羧酶,可阻断氨甲酰诱导的大鼠饮酒行为。
Psychopharmacology (Berl). 1989;98(2):176-82. doi: 10.1007/BF00444688.