Thaakur S R, Jyothi B
Department of Pharmacology, School of Pharmaceutical Sciences, Sri Padmavathi Mahila Viswa Vidyalayam, Andhra Pradesh, India.
J Neural Transm (Vienna). 2007 Sep;114(9):1217-25. doi: 10.1007/s00702-007-0744-2. Epub 2007 May 26.
Haloperidol is a widely used neuroleptic drug for the treatment of acute and chronic psychosis. The use of haloperidol is limited by extrapyramidal movement disorders such as Parkinsonism, akathesia, dystonia, and tardive dyskinesia (TD). Treatment with haloperidol increases oxyradicals which are implicated in TD. Spirulina is widely used as nutritional supplement rich in proteins and antioxidants. The present study is proposed to study the effect of spirulina on haloperidol induced TD and oxidative stress by studying TD, various enzymatic and nonenzymatic antioxidants and lipid peroxidation. Haloperidol 1 mg/kg/i.p was used to induce vacuous chewing movements in rats. Spirulina maxima suspended in 1% between 80 at a dose of 45, 90 and 180 mg/kg were administered by gavage along with haloperidol from 21st day to 49th day of treatment. Spirulina supplementation at a dose of 180 mg/kg significantly improved enzymatic and nonenzymatic antioxidants and decreased the tardive dyskinesia induced by haloperidol. In conclusion, the results of present investigation suggest that spirulina decreases haloperidol induced oxidative stress and TD by many mechanisms as it is cocktail of antioxidants. On chronic use it may inhibit haloperidol induced reduced expression of DNA thereby increases the expression of enzymatic and nonenzymatic antioxidants and protects against oxidative stress induced neurodegeneration and TD.
氟哌啶醇是一种广泛用于治疗急慢性精神病的抗精神病药物。氟哌啶醇的使用受到锥体外系运动障碍的限制,如帕金森症、静坐不能、肌张力障碍和迟发性运动障碍(TD)。氟哌啶醇治疗会增加与TD有关的氧自由基。螺旋藻作为富含蛋白质和抗氧化剂的营养补充剂被广泛使用。本研究旨在通过研究TD、各种酶促和非酶促抗氧化剂以及脂质过氧化作用,来探讨螺旋藻对氟哌啶醇诱导的TD和氧化应激的影响。用1mg/kg腹腔注射氟哌啶醇诱导大鼠出现空嚼运动。从治疗的第21天到第49天,将剂量为45、90和180mg/kg的极大螺旋藻悬浮于1%的溶液中,与氟哌啶醇一起通过灌胃给药。180mg/kg剂量的螺旋藻补充剂显著改善了酶促和非酶促抗氧化剂,并减少了氟哌啶醇诱导的迟发性运动障碍。总之,本研究结果表明,螺旋藻可通过多种机制降低氟哌啶醇诱导的氧化应激和TD,因为它是一种抗氧化剂混合物。长期使用时,它可能抑制氟哌啶醇诱导的DNA表达降低,从而增加酶促和非酶促抗氧化剂的表达,并预防氧化应激诱导的神经退行性变和TD。