Pagán Oné R, Baker Debra, Deats Sean, Montgomery Erica, Tenaglia Matthew, Randolph Clinita, Kotturu Dharini, Tallarida Christopher, Bach Daniel, Wilk Galia, Rawls Scott, Raffa Robert B
Department of Biology, West Chester University, West Chester, PA 19383, USA.
Int J Dev Biol. 2012;56(1-3):193-6. doi: 10.1387/ijdb.113486op.
Planarians are traditional animal models in developmental and regeneration biology. Recently, these organisms are arising as vertebrate-relevant animal models in neuropharmacology. Using an adaptation of published behavioral protocols, we have described the alleviation of cocaine-induced planarian seizure-like movements (pSLM) by a naturally-occurring sesquiterpene lactone, parthenolide. Interestingly, parthenolide does not prevent the expression of pSLM induced by amphetamines; in vertebrates, amphetamines interact with the same protein target as cocaine. Parthenolide is also unable to prevent pSLM elicited by the cholinergic com-pounds nicotine and cytisine or by the glutamatergic agents L- or D- glutamic acid or NMDA. Thus, we conclude that parthenolide is a specific anti-cocaine agent in this experimental organism.
涡虫是发育生物学和再生生物学中的传统动物模型。最近,这些生物体在神经药理学中作为与脊椎动物相关的动物模型而兴起。通过改编已发表的行为学实验方案,我们描述了一种天然存在的倍半萜内酯——小白菊内酯可减轻可卡因诱导的涡虫癫痫样运动(pSLM)。有趣的是,小白菊内酯并不能阻止苯丙胺诱导的pSLM的表达;在脊椎动物中,苯丙胺与可卡因作用于相同的蛋白质靶点。小白菊内酯也无法阻止由胆碱能化合物尼古丁和金雀花碱或谷氨酸能药物L-或D-谷氨酸或N-甲基-D-天冬氨酸引起的pSLM。因此,我们得出结论,在这种实验生物体中,小白菊内酯是一种特异性抗可卡因药物。