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抗胆碱能药物:对氧消耗和能量消耗的影响。

Anticholinergic drugs: effects on oxygen consumption and energy expenditure.

作者信息

Kirvelä O A, Kanto J H, Räty H M, Iisalo E

机构信息

Department of Anesthesiology, Turku University Hospital, Finland.

出版信息

Anesth Analg. 1994 May;78(5):995-9.

PMID:8161002
Abstract

Premedication has been shown to affect both oxygen consumption (VO2) and energy expenditure (EE). The metabolic responses to anticholinergic drugs have not been studied. In this study the effects of anticholinergic drugs on VO2 and EE (calculated from the measured rates of VO2 and carbon dioxide production [VCO2]: EE [kcal/d] = 3.581 x VO2 [L/d] + 1.448 x VCO2 [L/d] - 32.4) were measured in six healthy female volunteers. They were given intramuscular atropine (15 micrograms/kg), glycopyrrolate (8 micrograms/kg), scopolamine (8 micrograms/kg), and placebo in a random double-blind cross-over design. The consecutive sessions were at least 1 wk apart for each subject. VO2 and EE were measured using an indirect calorimetry (Deltatrac). Cardiovascular responses were assessed using standard noninvasive monitoring. Plasma drug concentrations were analyzed using a sensitive modification of radioreceptor assay. Subjective responses were measured with visual analog scale (VAS). Atropine and glycopyrrolate induced a significant increase in heart rate with a simultaneous decrease in pressure rate quotient (PRQ), while scopolamine caused a significant decrease in heart rate with a simultaneous increase in PRQ. Scopolamine significantly decreased both VO2 and EE, whereas glycopyrrolate increased VO2. Atropine had no significant effect on metabolic variables. Only scopolamine induced sedation in this study. In conclusion, atropine, glycopyrrolate, and scopolamine differ not only in their cardiovascular and central nervous system effects, but also in their effects on metabolism.

摘要

术前用药已被证明会影响耗氧量(VO2)和能量消耗(EE)。抗胆碱能药物的代谢反应尚未得到研究。在本研究中,对6名健康女性志愿者测量了抗胆碱能药物对VO2和EE的影响(根据测得的VO2和二氧化碳产生率[VCO2]计算:EE[千卡/天]=3.581×VO2[升/天]+1.448×VCO2[升/天]-32.4)。采用随机双盲交叉设计,给她们肌肉注射阿托品(15微克/千克)、格隆溴铵(8微克/千克)、东莨菪碱(8微克/千克)和安慰剂。每个受试者连续的实验至少间隔1周。使用间接测热法(Deltatrac)测量VO2和EE。使用标准的非侵入性监测评估心血管反应。使用放射性受体测定法的灵敏改进方法分析血浆药物浓度。用视觉模拟量表(VAS)测量主观反应。阿托品和格隆溴铵引起心率显著增加,同时压力心率商(PRQ)降低,而东莨菪碱导致心率显著降低,同时PRQ增加。东莨菪碱显著降低VO2和EE,而格隆溴铵增加VO2。阿托品对代谢变量无显著影响。在本研究中只有东莨菪碱引起镇静作用。总之,阿托品、格隆溴铵和东莨菪碱不仅在心血管和中枢神经系统作用方面存在差异,而且在对代谢的影响方面也存在差异。

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