Santos M E P, Moura L H P, Mendes M B, Arcanjo D D R, Monção N B N, Araújo B Q, Lopes J A D, Silva-Filho J C, Fernandes R M, Oliveira R C M, Citó A M G L, Oliveira A P
Medicinal Plants Research Center, Federal University of Piauí, 64049-550 Terezina, PI, Brazil.
Department of Chemistry, Federal University of Piauí, 64049-550 Terezina, PI, Brazil.
J Ethnopharmacol. 2015 Apr 22;164:120-8. doi: 10.1016/j.jep.2015.02.008. Epub 2015 Feb 12.
Caatinga is highly influenced by its seasonality. This species is endemic in the northeastern region, which is rich in plants with pharmacological potential. Many of these plants are used by the population and some of them have confirmed pharmacological properties. Mimosa caesalpiniifolia Benth. (Mimosaceae) is a native plant from northeastern Brazil׳s caatinga, popularly known as sabiá and cascudo. The tea from the inflorescence of this species is used by the population of the semi-arid for the treatment of hypertension, and the utilization of the plant bark for the staunching of bleedings and wound washing in order to prevent inflammation; also, the ingestion of the bark infusion is used in the treatment of bronchitis. However, its pharmacological effects and mechanisms of action have not yet been studied. The aim of the present study was to determine the effect of the ethanolic extract of M. caesalpiniifolia on the cardiovascular system in rats.
In a study for the assessment of the hypotensive effect of the extract, the polyethylene catheters were inserted in the aorta artery and inferior vena cava for the measurement of the arterial pressure and heart rate. When intragastric administration was performed, only one catheter was implanted in the abdominal aorta. In studies for the vasorelaxant activity, mesenteric arterial rings (1-2mm) were used: they were kept in Tyrode׳s solution (95% O2 and 5% CO2) and submitted to tension of 0.75 g/f for 1h. The results were expressed as mean ± S.E.M., significant to the values of p<0.05.
The administration of the doses through venous pathway (6.25; 12.5 and 25mg/kg, i.v.) promoted hypotension followed by bradycardia in the higher doses. The pre-treatment with atropine (2mg/kg, i.v.) interrupted both the hypotension and the bradycardia; with hexamethonium, hypotension was reverted and bradycardia was attenuated. While the administration of tea/flowers (25mg/kg i.v.) also promoted a following section of hypotension, a slight increase in heart rate was observed. When administered orally, MC-EtOH/flowers (100mg/kg, v.o.) promoted a decrease in the arterial pressure from 90 min on, without a significant alteration in the heart rate in relation to the control. In the in vitro study, a pharmacological trial was performed with the extracts obtained from parts of the species M. caesalpiifolia (leaves, bark, fruit and inflorescences). Among all extracts tested, the ethanolic extract from the inflorescences (MC-EtOH/flowers) presented higher vasorelaxant potency in relation to the other parts of the plant. Henceforth, MC-EtOH/flowers was used in the sequence. In mesenteric preparations pre-contracted with phenylephrine (10(-5)M), the MC-EtOH/flowers (0.1-750 µg/ml) promoted vasorelaxant effect regardless of the vascular endothelium. MC-EtOH/flowers inhibited the contractions induced by the cumulative addition of phenylephrine (10(-9)-10(-5)mol/l) or CaCl2 (10(-6)-3 × 10(-2)M), in a concentration-dependent way. In contractions induced by S(-)Bay K 8644, a Cav-L activator, the MC-EtOH/flowers promoted concentration-dependent relaxation, corroborating previous results.
The tea of flowers of M. caesalpiniifolia promotes hypotension and tachycardia, whereas ethanolic extract (MC-EtOH) promotes hypotension and bradycardia involving the participation of the muscarinic and ganglionic pathways, as well as vasorelaxant action involving the Ca(2+) influx inhibition blockade.
卡廷加地区受季节性影响很大。该物种是巴西东北部的特有物种,该地区富含具有药理潜力的植物。其中许多植物被当地居民使用,并且其中一些已被证实具有药理特性。含羞草(含羞草科)是一种原产于巴西东北部卡廷加地区的植物,俗称萨比亚和卡斯库多。该物种花序制成的茶被半干旱地区的居民用于治疗高血压,其树皮用于止血和清洗伤口以预防炎症;此外,树皮浸液的摄入还用于治疗支气管炎。然而,其药理作用和作用机制尚未得到研究。本研究的目的是确定含羞草乙醇提取物对大鼠心血管系统的影响。
在评估提取物降压作用的研究中,将聚乙烯导管插入主动脉和下腔静脉以测量动脉血压和心率。进行胃内给药时,仅在腹主动脉植入一根导管。在血管舒张活性研究中,使用肠系膜动脉环(1 - 2毫米):将其置于台氏液(95% O₂和5% CO₂)中,并施加0.75 g/f的张力1小时。结果以平均值±标准误表示,p < 0.05时具有显著性。
通过静脉途径给药(6.25;12.5和25毫克/千克,静脉注射),高剂量时会导致低血压并伴有心动过缓。用阿托品(2毫克/千克,静脉注射)预处理可阻断低血压和心动过缓;用六甲铵处理后,低血压得到逆转,心动过缓得到缓解。而给予茶/花(25毫克/千克,静脉注射)也会导致随后的低血压,同时观察到心率略有增加。口服含羞草乙醇提取物/花(100毫克/千克,口服)从90分钟起可使动脉血压降低,与对照组相比心率无显著变化。在体外研究中,对从含羞草的不同部位(叶、树皮、果实和花序)获得的提取物进行了药理试验。在所有测试的提取物中,花序的乙醇提取物(含羞草乙醇提取物/花)相对于植物的其他部位具有更高的血管舒张效力。此后,依次使用含羞草乙醇提取物/花。在预先用去氧肾上腺素(10⁻⁵摩尔/升)收缩的肠系膜制剂中,含羞草乙醇提取物/花(0.1 - 750微克/毫升)无论血管内皮情况如何均能促进血管舒张作用。含羞草乙醇提取物/花以浓度依赖的方式抑制去氧肾上腺素(10⁻⁹ - 10⁻⁵摩尔/升)或氯化钙(10⁻⁶ - 3×10⁻²摩尔/升)累积添加所诱导的收缩。在由Cav-L激活剂S(-)Bay K 8644诱导的收缩中,含羞草乙醇提取物/花促进浓度依赖性舒张,证实了先前的结果。
含羞草花制成的茶可促进低血压和心动过速,而乙醇提取物(含羞草乙醇提取物)可促进低血压和心动过缓,涉及毒蕈碱和神经节途径的参与,以及涉及抑制钙(2+)内流的血管舒张作用。