Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal de Sergipe, Cidade Universitária Prof. José Aloísio de Campos, Av. Marechal Rondon, s/n, São Cristóvão, SE, 49100-000, Brazil.
Programa de Pós-Graduação em Ciências Biológicas: Bioquímica Toxicológica, Universidade Federal de Santa Maria, Santa Maria, Brazil.
Naunyn Schmiedebergs Arch Pharmacol. 2017 Nov;390(11):1163-1172. doi: 10.1007/s00210-017-1416-x. Epub 2017 Aug 18.
Stigmasterol is a common sterol found in plants, but the anti-nociceptive effect of this compound and its mechanism of action are not fully explored. Thus, in the present study, the anti-nociceptive effect of stigmasterol was investigated in acute and chronic models of pain and its mechanism of action. We used adult male albino Swiss mice (25-35 g) to observe the anti-nociceptive effect of stigmasterol in acetic-acid writhing test or in complete Freund's adjuvant injection, surgical incision in hind paw, or partial sciatic nerve ligation. Moreover, we investigate the involvement of opioid receptors (naloxone, 2 mg/kg, intraperitoneally) in stigmasterol anti-nociceptive effect and stigmasterol action on acetylcholinesterase activity. Some possible adverse effects caused by stigmasterol were also investigated. Stigmasterol (0.3-3 mg/kg, orally) exhibited an anti-nociceptive effect on acetic-acid-induced writhing test. Furthermore, it markedly attenuated the mechanical allodynia caused by surgical incision (after acute treatment with stigmasterol, preventive and curative effects were observed) and partial sciatic nerve ligation (after acute treatment with stigmasterol) and complete Freund's adjuvant (after acute or repeated treatment with stigmasterol). The anti-nociceptive effect of stigmasterol was not reversed by naloxone. Moreover, stigmasterol did not alter in vitro acetylcholinesterase activity in spinal cord or brain samples. Also, stigmasterol did not cause gastric ulcers or alter the gastrointestinal transit of mice. Taken together, these results support the potential anti-nociceptive effect of stigmasterol in different models of pain.
豆甾醇是植物中常见的固醇,但这种化合物的镇痛作用及其作用机制尚未完全探索。因此,本研究旨在探讨豆甾醇在急性和慢性疼痛模型中的镇痛作用及其作用机制。我们使用成年雄性白化瑞士小鼠(25-35g)观察豆甾醇在醋酸扭体试验或完全弗氏佐剂注射、后爪手术切口或部分坐骨神经结扎中的镇痛作用。此外,我们还研究了阿片受体(纳洛酮,2mg/kg,腹腔内注射)在豆甾醇镇痛作用中的参与情况以及豆甾醇对乙酰胆碱酯酶活性的作用。还研究了豆甾醇可能引起的一些不良反应。豆甾醇(0.3-3mg/kg,口服)对醋酸诱导的扭体试验表现出镇痛作用。此外,它显著减轻了手术切口引起的机械性痛觉过敏(急性治疗后观察到预防和治疗作用)和部分坐骨神经结扎(急性治疗后)和完全弗氏佐剂(急性或重复治疗后)。纳洛酮不能逆转豆甾醇的镇痛作用。此外,豆甾醇对脊髓或脑组织样本中的体外乙酰胆碱酯酶活性没有影响。而且,豆甾醇不会引起胃溃疡或改变小鼠的胃肠道转运。综上所述,这些结果支持豆甾醇在不同疼痛模型中具有潜在的镇痛作用。