Carpene C, De Pablos I, Viguera L, Moratinos J
Eur J Pharmacol. 1984 Mar 16;99(1):111-4. doi: 10.1016/0014-2999(84)90440-0.
Both alpha- and beta-agonists were infused i.v. in unanesthetized rabbits. The alpha-adrenergic effect on lipid mobilization was investigated by comparing the modifications of blood glycerol levels induced by clonidine (alpha 2-agonist) and amidephrine (alpha 1-agonist) alone or in combination with isoprenaline (beta-agonist). Clonidine (2 micrograms X kg-1 X min-1) was found to significantly reduce the basal or isoprenaline-stimulated glycerol levels whereas amidephrine (10 micrograms X kg-1 X min-1) was without any effect. Plasma IRI levels were also reduced by clonidine. The results suggest that the reduction of lipid mobilization produced by clonidine could have been the consequence of the stimulation of the alpha 2-adrenergic antilipolytic receptors previously shown to be present in isolated fat cell membranes.
在未麻醉的兔子身上静脉注射α-和β-激动剂。通过比较可乐定(α2-激动剂)和去氧肾上腺素(α1-激动剂)单独使用或与异丙肾上腺素(β-激动剂)联合使用时引起的血液甘油水平变化,研究了α-肾上腺素能对脂质动员的影响。发现可乐定(2微克·千克-1·分钟-1)能显著降低基础或异丙肾上腺素刺激后的甘油水平,而去氧肾上腺素(10微克·千克-1·分钟-1)则无任何作用。可乐定还能降低血浆IRI水平。结果表明,可乐定引起的脂质动员减少可能是先前在分离的脂肪细胞膜中发现的α2-肾上腺素能抗脂解受体受到刺激的结果。