Chin Young-Won, Kinghorn A Douglas, Patil Popat N
Division of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, The Ohio State University, Columbus, OH 43210, USA.
Phytother Res. 2007 Oct;21(10):1002-5. doi: 10.1002/ptr.2155.
Pervilleine A is an aromatic ester tropane alkaloid from Erythroxylum pervillei that has shown promising activity as a multidrug resistance inhibitor. Due to its structural similarity with the well known (-)-hyoscyamine and (-)-cocaine, the cholinergic and adrenergic activities of pervilleine A were evaluated. At 30 microm (+/-)-pervilleine A hydrochloride exhibited non-competitive inhibition of the cholinergic response in the guinea-pig ileum and did not affect the carbachol-induced contraction of the rat anococcygeus smooth muscle. (+/-)-Pervilleine A hydrochloride blocked nonspecifically the vascular response of (-)-norepinephrine in the rat aorta ring, while the contractile response of rat vas deferens to (-)-norepinephrine was not affected significantly at a 100 microm concentration. An analogue of pervilleine A, (+/-)-pervilleine H, without a 6-O-trans-3,4,5-trimethoxycinnamoyl ester substituent required for anti-multidrug resistance activity, did not exhibit any effects in these experiments. The data suggest that (+/-)-pervilleine A hydrochloride has weak nonspecific anticholinergic and vascular antiadrenergic activities. The lack of significant cholinergic and adrenergic receptor-mediated activities may be considered advantageous for the further development of pervilleine A as a new adjuvant in cancer chemotherapy.
佩维林A是一种从佩氏古柯中提取的芳香酯类托烷生物碱,已显示出作为多药耐药抑制剂的潜在活性。由于其与著名的(-)-莨菪碱和(-)-可卡因在结构上相似,因此对佩维林A的胆碱能和肾上腺素能活性进行了评估。在30微摩尔浓度时,(±)-盐酸佩维林A对豚鼠回肠的胆碱能反应表现出非竞争性抑制,并且不影响卡巴胆碱诱导的大鼠肛尾肌平滑肌收缩。(±)-盐酸佩维林A非特异性地阻断了大鼠主动脉环中(-)-去甲肾上腺素的血管反应,而在100微摩尔浓度时,大鼠输精管对(-)-去甲肾上腺素的收缩反应未受到显著影响。佩维林A的一种类似物,(±)-佩维林H,没有抗多药耐药活性所需的6-O-反式-3,4,5-三甲氧基肉桂酰酯取代基,在这些实验中未表现出任何作用。数据表明,(±)-盐酸佩维林A具有较弱的非特异性抗胆碱能和血管抗肾上腺素能活性。缺乏显著的胆碱能和肾上腺素能受体介导的活性可能被认为有利于将佩维林A进一步开发为癌症化疗中的一种新佐剂。