Viana Alice, do Rego Jean-Claude, von Poser Gilsane, Ferraz Alexandre, Heckler Ana Paula, Costentin Jean, Kuze Rates Stela Maris
Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul. Av. Ipiranga, 2752 Porto Alegre, RS, Brazil.
Neuropharmacology. 2005 Dec;49(7):1042-52. doi: 10.1016/j.neuropharm.2005.06.002. Epub 2005 Jul 22.
A crude (ECH) and a purified cyclohexane extract (HCP) of Hypericum caprifoliatum and their main phloroglucinol derivative (HC1) were evaluated regarding their action on monoaminergic systems, more precisely on dopamine. In rats and mice forced swimming test, ECH and HCP dose-dependently reduced the immobility time. The effect of the highest dose was prevented by a prior administration of either sulpiride or SCH 23390 (D(2) and D(1) dopamine receptor antagonist, respectively). HCP (360 mg/kg) decreased the locomotor activity of mice. ECH (90 mg/kg) caused hypothermia and potentiated apomorphine-induced (16 mg/kg) hypothermia in mice. HCP and HC1 inhibited, in a concentration-dependent and monophasic manner, the [(3)H]-DA, [(3)H]-NA and [(3)H]-5HT synaptosomal uptakes, but did not prevent the binding of specific ligands to the monoamine transporters. Moreover, when tested at the concentrations corresponding to its IC(50) on [(3)H]-DA uptake, HC1 did not induce a significant [(3)H]-DA release, while at a higher concentration (200 ng/ml) it enhanced significantly (by 12%) the synaptosomal DA release. These data suggest that the antidepressant-like effect of H. caprifoliatum on the forced swimming test is due to an increase in monoaminergic transmission, resulting from monoamine uptake inhibition, more potently of dopamine, which may be related to their phloroglucinol contents.
对金丝桃(Hypericum caprifoliatum)的粗提物(ECH)、纯化的环己烷提取物(HCP)及其主要间苯三酚衍生物(HC1)对单胺能系统,更确切地说是对多巴胺的作用进行了评估。在大鼠和小鼠强迫游泳试验中,ECH和HCP剂量依赖性地减少了不动时间。预先给予舒必利或SCH 23390(分别为D₂和D₁多巴胺受体拮抗剂)可阻断最高剂量的作用。HCP(360mg/kg)降低了小鼠的运动活性。ECH(90mg/kg)导致小鼠体温过低,并增强了阿扑吗啡(16mg/kg)诱导的小鼠体温过低。HCP和HC1以浓度依赖性和单相方式抑制[³H]-多巴胺、[³H]-去甲肾上腺素和[³H]-5-羟色胺的突触体摄取,但不阻止特异性配体与单胺转运体的结合。此外,当以其对[³H]-多巴胺摄取的IC₅₀浓度进行测试时,HC1不会诱导显著的[³H]-多巴胺释放,而在较高浓度(200ng/ml)时,它会显著增强(12%)突触体多巴胺释放。这些数据表明,金丝桃在强迫游泳试验中的抗抑郁样作用是由于单胺能传递增加,这是由单胺摄取抑制引起的,对多巴胺的抑制作用更强,这可能与其间苯三酚含量有关。