Department of Biology, Medgar Evers College, 1150 Carroll Street, Brooklyn, NY 11225, USA.
Comp Biochem Physiol C Toxicol Pharmacol. 2010 Mar;151(2):264-70. doi: 10.1016/j.cbpc.2009.11.005.
The lateral cilia of the gill of Crassostrea virginica are controlled by a dopaminergic-serotonergic innervation. Dopamine is the neurotransmitter causing cilio-inhibition. High levels of manganese are neurotoxic to people, causing Manganism, a Parkinson-like disease. Clinical interventions for Manganism have not been very successful. Recently, p-Aminosalicylic acid (PAS) was reported as an effective treatment of severe Manganism in humans; however, its mechanism of action is unknown. Previously, we reported that manganese treatments caused disruption of the dopaminergic innervation of gill of C. virginica. Here we compared the effects of manganese on gill innervation in the presence of PAS, EDTA or Acetylsalicylic acid (ASA), and examined whether co-treating animals with PAS could block the deleterious effects of manganese on the oyster's dopaminergic innervation of the gill. Beating rates of the lateral cilia of the gill were measured by stroboscopic microscopy. Pre-treating gill preparations with PAS or EDTA blocked the neurotoxic effects of manganese, while ASA did not. In other experiments, animals exposed to three day treatments with manganese produced a dose dependent impairment of the dopaminergic, cilio-inhibitory system, which was decreased by co-treatment with PAS. The study shows that PAS protects the animal against neurotoxic effects of manganese and the mechanism of action of PAS in alleviating Manganism is more likely related to its chelating abilities than its anti-inflammatory actions.
美洲帘蛤的鳃侧纤毛受多巴胺-5-羟色胺能神经支配。多巴胺是引起纤毛抑制的神经递质。高水平的锰对人体具有神经毒性,导致锰中毒,类似于帕金森病。锰中毒的临床干预措施并不十分成功。最近,对氨基水杨酸(PAS)被报道为治疗人类严重锰中毒的有效方法;然而,其作用机制尚不清楚。以前,我们报道过锰处理会破坏美洲帘蛤鳃的多巴胺能神经支配。在这里,我们比较了 PAS、EDTA 或乙酰水杨酸(ASA)存在时锰对鳃神经支配的影响,并研究了同时用 PAS 处理动物是否可以阻断锰对牡蛎鳃多巴胺能神经支配的有害影响。用频闪显微镜测量鳃侧纤毛的拍打率。PAS 或 EDTA 预处理鳃制剂可阻断锰的神经毒性作用,而 ASA 则不能。在其他实验中,动物暴露于 3 天的锰处理后,多巴胺能、纤毛抑制系统受到剂量依赖性损害,同时用 PAS 处理可减轻损害。该研究表明,PAS 可保护动物免受锰的神经毒性作用,PAS 缓解锰中毒的作用机制可能与其螯合能力有关,而与其抗炎作用关系不大。