Veysel Kiyak, Ozgur Demir, Fikret Gevrek, Osman Demir, Muzaffer Katar
{"title":"Syringic Acid Reduces Subarachnoid Hemorrhage?Induced Oxidative Damage in Rats.","authors":"Veysel Kiyak, Ozgur Demir, Fikret Gevrek, Osman Demir, Muzaffer Katar","doi":"10.5137/1019-5149.JTN.48257-24.3","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>To investigate the neuroprotective effects of various amounts of syringic acid (SA) on cerebral damage resulting from experimentally induced subarachnoid hemorrhage (SAH) in rats, utilizing both histological and biochemical analyses.</p><p><strong>Material and methods: </strong>In total, 40 male Wistar albino rats were randomly and equally assigned to four groups: Control, SAH, SAH + 50 mg/kg/day SA (po), and SAH + 250 mg/kg/day SA (po). The rats in the SAH, SAH + 50 mg/kg/day SA, and SAH + 250 mg/kg/day SA groups were induced with SAH by administering 0.15 mL of autologous blood, collected from each rat?s heart, into the subarachnoid space through the foramen magnum. On day 10th, the rats were sacrificed, and their blood and brain tissues were collected for biochemical, and histological analyses.</p><p><strong>Results: </strong>Glutathione peroxidase levels were considerably elevated in the SAH + 250 mg/kg/day SA group compared to both the control and SAH groups. Although not statistically significant, IL-6 levels were lower in the SAH + 250 mg/kg/day SA group compared with those in the control group. In the SAH + 250 mg/kg/day SA group, the histological and cellular damages in the cortical brain tissue reduced significantly.</p><p><strong>Conclusion: </strong>SA (250 mg/kg/day) ameliorated the oxidative and histopathological changes in blood profile and cerebral tissue of rats when exposed to experimentally induced SAH. Thus, SA can reduce secondary cerebral damage in an SAH-induced rat model.</p>","PeriodicalId":94381,"journal":{"name":"Turkish neurosurgery","volume":" ","pages":"570-576"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish neurosurgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5137/1019-5149.JTN.48257-24.3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Aim: To investigate the neuroprotective effects of various amounts of syringic acid (SA) on cerebral damage resulting from experimentally induced subarachnoid hemorrhage (SAH) in rats, utilizing both histological and biochemical analyses.
Material and methods: In total, 40 male Wistar albino rats were randomly and equally assigned to four groups: Control, SAH, SAH + 50 mg/kg/day SA (po), and SAH + 250 mg/kg/day SA (po). The rats in the SAH, SAH + 50 mg/kg/day SA, and SAH + 250 mg/kg/day SA groups were induced with SAH by administering 0.15 mL of autologous blood, collected from each rat?s heart, into the subarachnoid space through the foramen magnum. On day 10th, the rats were sacrificed, and their blood and brain tissues were collected for biochemical, and histological analyses.
Results: Glutathione peroxidase levels were considerably elevated in the SAH + 250 mg/kg/day SA group compared to both the control and SAH groups. Although not statistically significant, IL-6 levels were lower in the SAH + 250 mg/kg/day SA group compared with those in the control group. In the SAH + 250 mg/kg/day SA group, the histological and cellular damages in the cortical brain tissue reduced significantly.
Conclusion: SA (250 mg/kg/day) ameliorated the oxidative and histopathological changes in blood profile and cerebral tissue of rats when exposed to experimentally induced SAH. Thus, SA can reduce secondary cerebral damage in an SAH-induced rat model.