Eroğlu L, Cağlayan B
Istanbul University, Istanbul Medical Faculty, Department of Pharmacology and Clinical Pharmacology, Capa, Turkey.
Pharmacol Res. 1997 Nov;36(5):381-5. doi: 10.1006/phrs.1997.0245.
Methylene blue (MB) has been intermittently used in manic depressive illness over the past century. However, to our knowledge, it has not been studied in the behavioural animal models. The present study was designed to evaluate whether the intravenous (i.v.) administration of MB in a dose range of 1.87-60 mg kg-1 would affect the performance of rats in the elevated plus-maze and the forced swimming (FST) tests. In the plus-maze, MB in doses ranging from 3.25 to 30 mg kg-1 significantly increased the percentage of open arm entries and exhibited an inverted U-shaped dose-response curve. Over a dose range, 7.5-30 mg kg-1, MB also increased time spent in open arms. These data suggest that MB has anxiolytic properties. On the other hand, MB, at doses of 15 and 30 mg kg-1 significantly decreased the immobility time in the FST and behaved as an antidepressant compound in these doses. As known, MB has prominent effects on the nitrergic system; Nitric oxide (NO) produced from L-arginine by the enzyme NO-synthase (NOS) activates soluble guanylyl cyclase (sGC) and exerts its effects on tissues through cGMP. MB acts as a direct inhibitor of NOS as well as of sGC. It also inactivates NO extracellularly through generation of superoxide anions. Thus, it can be speculated that NOS-NO-cGMP pathway may be involved in the antidepressant and anxiolytic actions of MB, and this may lead to search for new antidepressant and anxiolytic compounds.
在过去的一个世纪里,亚甲蓝(MB)一直被间歇性地用于治疗躁郁症。然而,据我们所知,它尚未在行为动物模型中进行研究。本研究旨在评估静脉注射(i.v.)剂量范围为1.87 - 60 mg kg-1的MB是否会影响大鼠在高架十字迷宫和强迫游泳(FST)试验中的表现。在十字迷宫中,剂量范围为3.25至30 mg kg-1的MB显著增加了进入开放臂的百分比,并呈现出倒U形剂量反应曲线。在7.5 - 30 mg kg-1的剂量范围内,MB还增加了在开放臂中停留的时间。这些数据表明MB具有抗焦虑特性。另一方面,剂量为15和30 mg kg-1的MB显著减少了FST中的不动时间,在这些剂量下表现为一种抗抑郁化合物。众所周知,MB对硝化能系统有显著影响;由一氧化氮合酶(NOS)从L-精氨酸产生的一氧化氮(NO)激活可溶性鸟苷酸环化酶(sGC),并通过cGMP对组织发挥作用。MB既是NOS的直接抑制剂,也是sGC的直接抑制剂。它还通过产生超氧阴离子在细胞外使NO失活。因此,可以推测NOS-NO-cGMP途径可能参与了MB的抗抑郁和抗焦虑作用,这可能会促使人们寻找新的抗抑郁和抗焦虑化合物。