Unidade de Biotecnologia, Universidade de Ribeirão Preto, UNAERP, Ribeirão Preto-SP, Brazil.
Pharm Biol. 2012 Mar;50(3):366-75. doi: 10.3109/13880209.2011.608072. Epub 2011 Dec 1.
Sapindus saponaria L. (Sapindaceae) bark, root, and fruits are used as sedatives and to treat gastric ulcer and also demonstrate diuretic and expectorant effects.
The anti-snake venom properties of callus of S. saponaria are investigated here for the first time.
In vitro cultivated callus of Sapindus saponaria were lyophilized, and the extracts were prepared with different solvents, before submitting to phytochemical studies and evaluation of the anti-ophidian activity. Crude extracts were fractionated by liquid-liquid partition and the fractions were monitored by thin layer chromatography (TLC). Subsequently, anti-ophidian activities were analyzed toward Bothrops jararacussu Lacerda (Viperidae), B. moojeni Hoge (Viperidae), B. alternates Duméril (Viperidea) and Crotalus durissus terrificus Lineu (Viperidae) venoms and isolated myotoxins and phospholipase A(2) (PLA(2)).
Fractions A1, A2 and the extract in MeOH:H(2)O (9:1) significantly inhibited the toxic and pharmacological activities induced by snake venoms and toxins, when compared to other extracts and fractions. The lethal, clotting, phospholipase, edema-inducing, hemorrhagic and myotoxic activities were partially inhibited by the different extracts and fractions. TLC profiles of the crude extracts (B and C) and fractions (A1 and A2) showed β-sitosterol and stigmasterol as their main compounds. Stigmasterol exhibited inhibitory effects on enzymatic and myotoxic activities of PLA(2).
Sapindus saponaria extracts and fractions presented anti-ophidian activity and could be used as an adjuvant to serum therapy or for its supplementation, and in addition, as a rich source of potential inhibitors of enzymes involved in several pathophysiological human and animal diseases.
无患子(无患子科)的树皮、根和果实被用作镇静剂,用于治疗胃溃疡,还具有利尿和祛痰作用。
首次研究无患子愈伤组织的抗蛇毒特性。
体外培养的无患子愈伤组织经冷冻干燥后,用不同溶剂提取,进行植物化学研究和抗蛇毒活性评价。粗提物经液-液分配进行分离,各馏分经薄层色谱(TLC)监测。随后,分析粗提物对矛头蝮属(矛头蝮科)、矛头蝮属(矛头蝮科)、矛头蝮属(矛头蝮科)和矛头蝮属(矛头蝮科)毒液以及分离的肌肉毒素和磷脂酶 A₂(PLA₂)的抗蛇毒活性。
与其他提取物和馏分相比,馏分 A1、A2 和甲醇:水(9:1)提取物显著抑制了蛇毒和毒素诱导的毒性和药理活性。不同的提取物和馏分部分抑制了致死、凝血、磷脂酶、水肿诱导、出血和肌肉毒性活性。粗提物(B 和 C)和馏分(A1 和 A2)的 TLC 图谱显示β-谷甾醇和豆甾醇是其主要成分。豆甾醇对 PLA₂的酶和肌肉毒性活性具有抑制作用。
无患子提取物和馏分具有抗蛇毒活性,可作为血清疗法的辅助剂或补充剂,此外,还可作为涉及人类和动物多种病理生理疾病的潜在酶抑制剂的丰富来源。