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
{"title":"美洲椴对Kainic酸致脑、肝、肾损伤的保护作用:行为和生化变化。","authors":"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","doi":"10.5812/ijpr-126914","DOIUrl":null,"url":null,"abstract":"<p><p><i>Tiliaamericana</i> var. <i>mexicana (Tilia)</i> 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 <i>Tilia</i> extract (100 mg/kg). The EAc and ME <i>Tilia</i> extracts significantly decreased the severity of phase 1 and phase 2 seizures, respectively. The ME <i>Tilia</i> extract increased the latency to seizure (27 ± 2 min) compared to the control (13 ± 2 min). The ME and EAc <i>Tilia</i> 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 <i>Tilia</i> 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.</p>","PeriodicalId":416671,"journal":{"name":"Iranian Journal of Pharmaceutical Research : IJPR","volume":" ","pages":"e126914"},"PeriodicalIF":0.0000,"publicationDate":"2022-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/32/fc/ijpr-21-1-126914.PMC9420231.pdf","citationCount":"0","resultStr":"{\"title\":\"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.\",\"authors\":\"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\",\"doi\":\"10.5812/ijpr-126914\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Tiliaamericana</i> var. <i>mexicana (Tilia)</i> 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 <i>Tilia</i> extract (100 mg/kg). The EAc and ME <i>Tilia</i> extracts significantly decreased the severity of phase 1 and phase 2 seizures, respectively. The ME <i>Tilia</i> extract increased the latency to seizure (27 ± 2 min) compared to the control (13 ± 2 min). The ME and EAc <i>Tilia</i> 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 <i>Tilia</i> 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.</p>\",\"PeriodicalId\":416671,\"journal\":{\"name\":\"Iranian Journal of Pharmaceutical Research : IJPR\",\"volume\":\" \",\"pages\":\"e126914\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-05-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/32/fc/ijpr-21-1-126914.PMC9420231.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Iranian Journal of Pharmaceutical Research : IJPR\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.5812/ijpr-126914\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2022/12/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Iranian Journal of Pharmaceutical Research : IJPR","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.5812/ijpr-126914","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/12/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
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.