美洲椴对Kainic酸致脑、肝、肾损伤的保护作用:行为和生化变化。

Iranian Journal of Pharmaceutical Research : IJPR Pub Date : 2022-05-03 eCollection Date: 2022-12-01 DOI:10.5812/ijpr-126914
Elvia Coballase-Urrutia, Noemí Cárdenas-Rodríguez, Liliana Carmona-Aparicio, Vicente Sánchez-Valle, Liliana Rivera-Espinosa, José Pedraza-Chaverri, Hortencia Montesinos-Correa, Edith Bello-Robles, Aristides Iii Sampieri, David Martínez-Vargas, Leticia Granados-Rojas, María Eva González-Trujano
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引用次数: 0

摘要

Tiliaamericana变种墨西哥(Tilia)具有抗惊厥,抗氧化,神经保护和肝保护活性。癫痫持续状态模型的抗惊厥活性谱尚未得到充分的探讨。我们通过测量大鼠的行为(严重程度和潜伏期)和不同脑区(小脑、大脑半球、皮层和髓质)、肾脏和肝脏的脂质过氧化,评估乙酸乙酯(EAc)和甲醇(ME)提取物对kainic酸(KA)诱导的癫痫发作的影响。雄性Wistar大鼠在天麻提取物(100 mg/kg)预处理3天后给予KA (10 mg/kg, ig)。EAc和ME Tilia提取物分别显著降低了1期和2期癫痫发作的严重程度。与对照组(13±2分钟)相比,ME Tilia提取物增加了癫痫发作潜伏期(27±2分钟)。ME和EAc天青提取物显著阻止ka诱导的小脑、大脑半球、皮质、髓质、肝脏和肾脏的癫痫发作引起的脂质过氧化增加。橄榄油(OO)也显示出抗惊厥作用,将癫痫发作的严重程度降低到3期,并将小脑、大脑半球、皮层、髓质、肝脏和肾脏中的脂质过氧化水平降低。天莲的抗惊厥活性是通过中枢和全身区域的抗氧化作用介导的,这涉及到这些提取物的化学成分(槲皮素和山奈酚的糖苷)之间的协同相互作用,而植物OO也表现出同样的作用,可能是由于其成分橄榄苦苷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Protective Effect of <i>Tilia americana</i> var. <i>mexicana</i> Against Kainic Acid-induced Damage in Brain, Liver, and Kidney: Behavioral and Biochemical Changes.

Protective Effect of <i>Tilia americana</i> var. <i>mexicana</i> Against Kainic Acid-induced Damage in Brain, Liver, and Kidney: Behavioral and Biochemical Changes.

Protective Effect of <i>Tilia americana</i> var. <i>mexicana</i> Against Kainic Acid-induced Damage in Brain, Liver, and Kidney: Behavioral and Biochemical Changes.

Protective Effect of Tilia americana var. mexicana Against Kainic Acid-induced Damage in Brain, Liver, and Kidney: Behavioral and Biochemical Changes.

Tiliaamericana var. mexicana (Tilia) possesses anticonvulsant, antioxidant, neuroprotective, and hepatoprotective activities. The spectrum of anticonvulsant activity in status epilepticus models has not been sufficiently explored. We evaluated the effects of ethyl acetate (EAc), and methanol (ME) extracts on kainic acid (KA)-induced seizures by measuring rats'behavior (severity and latency) and lipoperoxidation in different brain areas (cerebellum, brain hemispheres, cortex, and medulla), kidneys, and liver. Male Wistar rats were administered KA (10 mg/kg, i.p.) after three days of pretreatment with Tilia extract (100 mg/kg). The EAc and ME Tilia extracts significantly decreased the severity of phase 1 and phase 2 seizures, respectively. The ME Tilia extract increased the latency to seizure (27 ± 2 min) compared to the control (13 ± 2 min). The ME and EAc Tilia extracts significantly prevented the increased lipid peroxidation caused by KA-induced seizures in the cerebellum, brain hemispheres, cortex, medulla, liver, and kidneys. The vehicle olive oil (OO) also showed anticonvulsant effects, decreasing the severity of seizures to phase 3 and lipoperoxidation levels in the cerebellum, brain hemispheres, cortex, medulla, liver, and kidneys. The anticonvulsant activity of Tilia is mediated by antioxidant effects in central and systemic areas that involve synergistic interactions among the chemical constituents of these extracts (glucosides of quercetin and kaempferol), while vehicle OO showed the same effects, probably due to its constituent oleuropein.

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