Department of Pharmacology, Karadeniz Technical University, School of Medicine, Trabzon, Turkey.
Eur Rev Med Pharmacol Sci. 2012 Jun;16(6):789-96.
Simvastatin, pravastatin and atorvastatin have been evaluated whether to have analgesic effects in mice in hot plate test.
Simvastatin (5, 10, 30 mg/kg), pravastatin (5, 10, 30 mg/kg) and atorvastatin (5, 10, 30 mg/kg) were administered acute and chronically by oral gavage in mice. Control (pretreatment value) and posttreatment (after drugs application) values in 60th and 120th minutes were measured in hot-plate test.
All three drugs at 10, 30 mg/kg doses produced analgesic effects compared with their control values in 60th and 120th minutes on acute and chronic application in mice. The analgesic effects of drugs were evaluated after the application of L-nitro arginine methyl ester (L-NAME) (10 mg/kg) or naloxone (0.5 mg/kg). L-NAME (10 mg/kg) has no effect compared to the control value on both minutes. The analgesic effects of both atorvastatin (30 mg/kg) and simvastatin (30 mg/kg) in the presence of L-NAME (10 mg/kg) were not inhibited. However, the analgesic effect of pravastatin (30 mg/kg) in the presence of L-NAME (10 mg/kg) was inhibited significantly on both minutes (p < 0.05). Naloxone (0.5 mg/kg) has no effect compared to the control value on both minutes. The analgesic effect of atorvastatin (30 mg/kg) in the presence of naloxone (0.5 mg/kg) was partially (43%) but significantly inhibited only on 60th minute (p < 0.05). The analgesic effect of pravastatin (30 mg/kg) in the presence of naloxone (0.5 mg/kg) was partially (48-40%) but significantly inhibited on both minutes (p < 0.05). However, the analgesic effect of simvastatin (30 mg/kg) in the presence of naloxone (0.5 mg/kg) was inhibited significantly on both minutes (p < 0.05).
These finding indicated that the analgesic effect of pravastatin was related to nitrergic systems and partially opioidergic system; analgesic effect of simvastatin was related to opiodergic system in hot plate test. However, the analgesic effect of atorvastatin was not directly related to both system.
在热板试验中,评估辛伐他汀、普伐他汀和阿托伐他汀是否对小鼠具有镇痛作用。
辛伐他汀(5、10、30mg/kg)、普伐他汀(5、10、30mg/kg)和阿托伐他汀(5、10、30mg/kg)通过灌胃急性和慢性给药。在热板试验中,分别测量 60 分钟和 120 分钟时的对照(预处理值)和治疗后(药物应用后)值。
在急性和慢性应用中,所有三种药物在 10、30mg/kg 剂量下,与对照值相比,在 60 分钟和 120 分钟时均产生镇痛作用。在应用 L-硝基精氨酸甲酯(L-NAME)(10mg/kg)或纳洛酮(0.5mg/kg)后,评估药物的镇痛作用。L-NAME(10mg/kg)与两种药物的对照值相比在这两种情况下都没有影响。阿托伐他汀(30mg/kg)和辛伐他汀(30mg/kg)的镇痛作用在 L-NAME(10mg/kg)存在下均未被抑制。然而,普伐他汀(30mg/kg)的镇痛作用在 L-NAME(10mg/kg)存在下在两种情况下均显著抑制(p<0.05)。纳洛酮(0.5mg/kg)与对照值相比在两种情况下均无影响。阿托伐他汀(30mg/kg)的镇痛作用在纳洛酮(0.5mg/kg)存在下部分(43%)但在 60 分钟时显著抑制(p<0.05)。普伐他汀(30mg/kg)的镇痛作用在纳洛酮(0.5mg/kg)存在下部分(48-40%)但在两种情况下均显著抑制(p<0.05)。然而,辛伐他汀(30mg/kg)的镇痛作用在纳洛酮(0.5mg/kg)存在下在两种情况下均显著抑制(p<0.05)。
这些发现表明,普伐他汀的镇痛作用与氮能系统有关,部分与阿片能系统有关;辛伐他汀在热板试验中的镇痛作用与阿片能系统有关。然而,阿托伐他汀的镇痛作用与这两个系统无关。