长叶薄荷的解热和抗伤性。大鼠和小鼠的叶水提物。

G J Amabeoku, S J Erasmus, J A O Ojewole, J T Mukinda
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引用次数: 16

摘要

长叶薄荷的解热和抗伤性。采用脂多糖(LPS)诱导大鼠发热和小鼠醋酸和热板镇痛实验,研究了兰科(Lamiaceae)叶水提物的作用。以己酮茶碱、扑热息痛和吗啡为对照药。长叶水提物和己酮茶碱(37.5 ~ 150 mg/kg i.p)显著(P < 0.05 ~ 0.02)降低了LPS (50 g/kg i.m)引起的发热。己酮茶碱(50 mg/kg i.p.)也显著(P < 0.01)降低LPS (50 g/kg i.m.)引起的发热。长叶水提物(6.25 ~ 100 mg/kg .p)和对乙酰氨基酚(500 mg/kg .p)对3%乙酸产生的扭曲有较强的抑制作用。此外,植物提取物(25 ~ 400 mg/kg i.p)和吗啡(10 mg/kg i.p)显著(P < 0.001)延迟小鼠热板反应时间。口服和腹腔给药的LD(50)值分别> 3200mg /kg和1730mg /kg。植物化学分析表明,长叶参叶中含有黄酮、皂苷、单宁、还原糖、心糖苷和三萜甾体。这些数据表明,龙叶水提物具有解热和抗伤性。此外,口服和腹腔注射该植物提取物获得的相对较高的LD(50)值表明该植物提取物对小鼠无毒。
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Antipyretic and antinociceptive properties of Mentha longifolia Huds. (Lamiaceae) leaf aqueous extract in rats and mice.

The antipyretic and antinociceptive properties of Mentha longifolia Huds. (Lamiaceae) leaf aqueous extract were investigated using lipopolysaccharide (LPS)-induced pyrexia in rats, and acetic acid and hot plate analgesia tests in mice. Pentoxifylline, paracetamol and morphine were used as standard drugs for comparison. M. longifolia leaf aqueous extract and pentoxifylline (37.5-150 mg/kg i.p.) significantly (P < 0.05-0.02) reduced the LPS (50 g/kg i.m.)-elicited pyrexia. Pentoxifylline (50 mg/kg i.p.) also significantly (P < 0.01) reduced LPS (50 g/kg i.m.)-induced pyrexia. M. longifolia leaf aqueous extract (6.25-100 mg/kg i.p.) and paracetamol (500 mg/kg i.p.) profoundly inhibited the writhes produced by 3% acetic acid. Furthermore, the plant extract (25-400 mg/kg i.p.) and morphine (10 mg/kg i.p.) significantly (P < 0.001) delayed the hot plate reaction time in mice. The LD(50) values for oral and intraperitoneal administration of the plant extract were > 3200 mg/kg and 1730 mg/kg, respectively. Phytochemical analysis revealed the presence of flavonoids, saponins, tannins, reducing sugars, cardiac glycosides and triterpene steroids in the leaves of M. longifolia. These data indicate that M. longifolia leaf aqueous extract has antipyretic and antinociceptive properties. Furthermore, the relatively high LD(50) values obtained for oral and intraperitoneal administration of the plant extract demonstrate that the plant extract is non-toxic to mice.

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