{"title":"氯化铝对成年Wistar大鼠脑皮质损伤的影响","authors":"A. Ajibade, P. Fakunle, O. O. Omoola","doi":"10.9734/AJRIMPS/2019/V7I330121","DOIUrl":null,"url":null,"abstract":"This study investigated some effects of aluminium chloride on the cerebral cortex of adult Wistar rats. Aluminium chloride as one of the toxic metals has been known to be one of the major environmental pollutants across the world which has been reported in relation to Neurodegenerative diseases (ND) associated with metallic intoxication. It is present in many pharmaceutical drugs, food products and also used in the treatment of domestic water being involved in skeletal, haematological and neurological diseases. \nThirty-two adult Wistar of both sexes weighing between 143 g-189 g were randomly grouped into four groups, group A, B, C and D each group containing 8 rats. Group A rats which were the controls, were maintained on standard feed (grower mash) and water for 21 days. Rats in group B, C and D were treated with 0.2 g/kg, 0.4 g/kg and 0.6 g/kg of aluminium chloride respectively for 21days. The aluminium chloride solution was administered orally on a daily basis for that period. \nThe weight of the Wistar rats was recorded on a weekly basis (before and at the end of each week of administration). On the 22nd day the Wistar rats in group A, B, C and D were sacrificed by cervical dislocation, blood was collected through cardiac puncture, the brain was removed and weighed immediately using sensitive balance, part of the brain of all Wistar rats in each group was collected and homogenized for biochemical analysis, the remaining part was then fixed in 10% formol saline, the tissue was processed and sectioned at 5µm and stained with hematoxylin and eosin for histological study. \nResults showed that the mean body weights of the Wistar rats significantly increased in the treated groups when compared with the control group. The mean brain weights of the aluminium- treated groups showed insignificant decreased (P>0.05) when compared to the control group. In the biochemical analysis, there was a statistically significant increase (P<0.05) in the level of Malondialdehyde (MDA) in the aluminium-treated groups, and a significant decrease (P<0.05) in the level of Superoxide dismutase (SOD), and Succinate Dehydrogenase (SDH) in the aluminium treated group. Histological study of the brain (cerebral cortex) revealed that the cerebral cortical layers of the aluminium treated groups appeared distorted and degenerated, in a dose-dependent manner. The study concluded that aluminium chloride has a neurotoxic effect on the cerebral cortex of adult Wistar rats which invariably may alter some cerebral functions.","PeriodicalId":8536,"journal":{"name":"Asian Journal of Research in Medical and Pharmaceutical Sciences","volume":"83 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cerebral Cortical Damage in Adult Wistar Rats Following Aluminium Chloride Administration\",\"authors\":\"A. Ajibade, P. Fakunle, O. O. Omoola\",\"doi\":\"10.9734/AJRIMPS/2019/V7I330121\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This study investigated some effects of aluminium chloride on the cerebral cortex of adult Wistar rats. Aluminium chloride as one of the toxic metals has been known to be one of the major environmental pollutants across the world which has been reported in relation to Neurodegenerative diseases (ND) associated with metallic intoxication. It is present in many pharmaceutical drugs, food products and also used in the treatment of domestic water being involved in skeletal, haematological and neurological diseases. \\nThirty-two adult Wistar of both sexes weighing between 143 g-189 g were randomly grouped into four groups, group A, B, C and D each group containing 8 rats. Group A rats which were the controls, were maintained on standard feed (grower mash) and water for 21 days. Rats in group B, C and D were treated with 0.2 g/kg, 0.4 g/kg and 0.6 g/kg of aluminium chloride respectively for 21days. The aluminium chloride solution was administered orally on a daily basis for that period. \\nThe weight of the Wistar rats was recorded on a weekly basis (before and at the end of each week of administration). On the 22nd day the Wistar rats in group A, B, C and D were sacrificed by cervical dislocation, blood was collected through cardiac puncture, the brain was removed and weighed immediately using sensitive balance, part of the brain of all Wistar rats in each group was collected and homogenized for biochemical analysis, the remaining part was then fixed in 10% formol saline, the tissue was processed and sectioned at 5µm and stained with hematoxylin and eosin for histological study. \\nResults showed that the mean body weights of the Wistar rats significantly increased in the treated groups when compared with the control group. The mean brain weights of the aluminium- treated groups showed insignificant decreased (P>0.05) when compared to the control group. In the biochemical analysis, there was a statistically significant increase (P<0.05) in the level of Malondialdehyde (MDA) in the aluminium-treated groups, and a significant decrease (P<0.05) in the level of Superoxide dismutase (SOD), and Succinate Dehydrogenase (SDH) in the aluminium treated group. Histological study of the brain (cerebral cortex) revealed that the cerebral cortical layers of the aluminium treated groups appeared distorted and degenerated, in a dose-dependent manner. The study concluded that aluminium chloride has a neurotoxic effect on the cerebral cortex of adult Wistar rats which invariably may alter some cerebral functions.\",\"PeriodicalId\":8536,\"journal\":{\"name\":\"Asian Journal of Research in Medical and Pharmaceutical Sciences\",\"volume\":\"83 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-07-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Research in Medical and Pharmaceutical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.9734/AJRIMPS/2019/V7I330121\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Research in Medical and Pharmaceutical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/AJRIMPS/2019/V7I330121","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
本研究探讨了氯化铝对成年Wistar大鼠大脑皮层的影响。氯化铝作为一种有毒金属,是世界范围内主要的环境污染物之一,已被报道与金属中毒相关的神经退行性疾病(ND)有关。它存在于许多药品、食品中,也用于处理与骨骼、血液病和神经疾病有关的生活用水。选取体重143 g ~ 189 g的雄性成年Wistar大鼠32只,随机分为A、B、C、D组,每组8只。A组大鼠为对照组,饲喂标准饲料(种植者醪)和水21 d。B、C、D组大鼠分别给予0.2 g/kg、0.4 g/kg、0.6 g/kg氯化铝处理21 D。在此期间,每天口服氯化铝溶液。每周(给药前和给药周结束时)记录Wistar大鼠体重。第22天,A、B、C、D组Wistar大鼠颈椎脱臼处死,经心脏穿刺采血,立即取脑组织,用灵敏平衡法称重,每组Wistar大鼠取部分脑组织,均质化进行生化分析,剩余部分固定于10%福尔mol生理盐水中,在5µm处处理切片,苏木精和伊红染色进行组织学研究。结果显示,与对照组相比,各给药组Wistar大鼠的平均体重明显增加。与对照组相比,铝处理组的平均脑质量下降不显著(P>0.05)。生化分析中,铝处理组丙二醛(MDA)水平显著升高(P<0.05),超氧化物歧化酶(SOD)、琥珀酸脱氢酶(SDH)水平显著降低(P<0.05)。脑(大脑皮层)的组织学研究显示,铝处理组的大脑皮层出现扭曲和退化,并呈剂量依赖性。该研究得出结论,氯化铝对成年Wistar大鼠的大脑皮层有神经毒性作用,这必然会改变一些大脑功能。
Cerebral Cortical Damage in Adult Wistar Rats Following Aluminium Chloride Administration
This study investigated some effects of aluminium chloride on the cerebral cortex of adult Wistar rats. Aluminium chloride as one of the toxic metals has been known to be one of the major environmental pollutants across the world which has been reported in relation to Neurodegenerative diseases (ND) associated with metallic intoxication. It is present in many pharmaceutical drugs, food products and also used in the treatment of domestic water being involved in skeletal, haematological and neurological diseases.
Thirty-two adult Wistar of both sexes weighing between 143 g-189 g were randomly grouped into four groups, group A, B, C and D each group containing 8 rats. Group A rats which were the controls, were maintained on standard feed (grower mash) and water for 21 days. Rats in group B, C and D were treated with 0.2 g/kg, 0.4 g/kg and 0.6 g/kg of aluminium chloride respectively for 21days. The aluminium chloride solution was administered orally on a daily basis for that period.
The weight of the Wistar rats was recorded on a weekly basis (before and at the end of each week of administration). On the 22nd day the Wistar rats in group A, B, C and D were sacrificed by cervical dislocation, blood was collected through cardiac puncture, the brain was removed and weighed immediately using sensitive balance, part of the brain of all Wistar rats in each group was collected and homogenized for biochemical analysis, the remaining part was then fixed in 10% formol saline, the tissue was processed and sectioned at 5µm and stained with hematoxylin and eosin for histological study.
Results showed that the mean body weights of the Wistar rats significantly increased in the treated groups when compared with the control group. The mean brain weights of the aluminium- treated groups showed insignificant decreased (P>0.05) when compared to the control group. In the biochemical analysis, there was a statistically significant increase (P<0.05) in the level of Malondialdehyde (MDA) in the aluminium-treated groups, and a significant decrease (P<0.05) in the level of Superoxide dismutase (SOD), and Succinate Dehydrogenase (SDH) in the aluminium treated group. Histological study of the brain (cerebral cortex) revealed that the cerebral cortical layers of the aluminium treated groups appeared distorted and degenerated, in a dose-dependent manner. The study concluded that aluminium chloride has a neurotoxic effect on the cerebral cortex of adult Wistar rats which invariably may alter some cerebral functions.