Popowicz U, Paluszak J
Acta Physiol Pol. 1979 Sep-Dec;30(5-6):627-32.
It was demonstrated that Ledakrin, an antitumour drug, causes mobilization of free fatty acids and glycerol from the epididymal adipose tissue of rat in vitro. The disproportion observed in the release of glycerol and free fatty acids following Ledakrin administration suggested a biphasic effect of this drug, with initial stimulation and later inhibition of the processes of lipolysis and lipogenesis. Blockade of adrenergic membrane receptors (with propranolol or regitine) abolished the lipolytic effect of Ledakrin.
已证明,抗肿瘤药物莱达克林(Ledakrin)在体外可引起大鼠附睾脂肪组织中游离脂肪酸和甘油的动员。给予莱达克林后,甘油和游离脂肪酸释放中观察到的不均衡表明该药物具有双相效应,最初刺激脂解和脂肪生成过程,随后抑制这些过程。肾上腺素能膜受体阻断剂(普萘洛尔或酚妥拉明)可消除莱达克林的脂解作用。