Okuda H, Saito Y, Matsuoka N, Takeda E, Kumagai A
J Biochem. 1978 Mar;83(3):887-92. doi: 10.1093/oxfordjournals.jbchem.a131986.
Lipid micelles consisting of a glyceride mixture (triolein, diolein, and monoolein) and lecithin bound adrenaline-14C more strongly than did micelles consisting of the glyceride mixture only. Lipid micelles consisting of the glyceride mixture and phosphatidic acid also bound adrenaline-14C effectivily, whereas lipid micelles consisting of the glyceride mixture and diglyceride, obtained from lecithin, did not bind the hormone strongly. Both phenoxybenzamine (an alpha- blocker) and propranolol (a beta-blocker) strongly inhibited the association between adrenaline-14C and lipid micelles consisting of the glyceride mixture and lecithin. Propranolol, inhibited adrenaline-induced lipolysis in both fat cells and fat globules, whereas, phenoxybenzamine, did not affect adrenaline-induced lipolysis. Both agents reduced adrenaline-induced adenyl-cyclase activation in fat cell ghosts. Phospholipid was also found to be related with adrenaline-mediated adenylcyclase activation.
由甘油酯混合物(三油精、二油精和单油精)和卵磷脂组成的脂质微团比仅由甘油酯混合物组成的微团更牢固地结合肾上腺素 - 14C。由甘油酯混合物和磷脂酸组成的脂质微团也能有效结合肾上腺素 - 14C,而由甘油酯混合物和从卵磷脂获得的甘油二酯组成的脂质微团则不能牢固结合该激素。酚苄明(一种α受体阻滞剂)和普萘洛尔(一种β受体阻滞剂)都强烈抑制肾上腺素 - 14C与由甘油酯混合物和卵磷脂组成的脂质微团之间的结合。普萘洛尔抑制脂肪细胞和脂肪球中肾上腺素诱导的脂解作用,而酚苄明不影响肾上腺素诱导的脂解作用。两种药物都降低了脂肪细胞膜微粒中肾上腺素诱导的腺苷酸环化酶激活。还发现磷脂与肾上腺素介导的腺苷酸环化酶激活有关。