{"title":"胸腺醌通过NF-κB依赖性NeuN/GFAP/Ki-67抑制暴露于双酚A类似物混合物的高血压母鼠和F1雄性幼鼠的神经炎症介质和血管收缩损伤。","authors":"O S Okoh, J K Akintunde, A J Akamo, Ubong Akpan","doi":"10.1016/j.taap.2024.117162","DOIUrl":null,"url":null,"abstract":"<p><p>Bisphenol-A (BPA) analogues seem inevitable components of numerous domestic products, but these have been identified as agents of teratogenic disorders. This study, therefore, investigated the effect of thymoquinone (TMQ) on the striatum of hypertensive female rats and their F1 male offsprings, on exposure to a mixture of Bisphenol-B, Bisphenol-F and Bisphenol-S (MBFS). Female rats were divided into normotensive and hypertensive groups; and both were treated with MBFS only, MBFS + TMQ, and TMQ only. Exposure to MBFS and co-treatment with TMQ lasted at least 63 days. Neurobehavioural assessments were conducted using Open Field (OF). A spectrophotometer was used for cholinergic, dopaminergic and adenosinergic enzyme assays; Real-Time PCR for gene expression; and immunohistochemistry for protein quantification; while H&E, cresyl fast violent, and congo red stains were used for histological assessments. From the results, maternal exposure to MBFS mediated striatal dysfunction via p53 and NF-kB upregulation; decreased BCl-2, Ki-67 and NeuN; increased GFAP, nissl bodies and β-amyloid. Dysregulation of cholinergic, dopaminergic and adenosinergic enzymes in addition to decreased nitric oxide levels were also associated with MBFS toxicity. Hypertension was found to exacerbate MBFS toxicity. From OF test; increased anxiety and decreased psychomotor activity were associated with maternal exposure to MBFS. However, co-treatment with thymoquinone prevented striatal dysfunction in hypertensive dams and their F1 male offspring. In conclusion, disruption of the delicate balance between apoptosis and cell proliferation culminating in the reduction of mature neurons is responsible for neurodegeneration and neuropathy associated with MBFS exposure. However, these can be prevented through regular consumption of natural products and supplements rich in thymoquinone.</p>","PeriodicalId":23174,"journal":{"name":"Toxicology and applied pharmacology","volume":" ","pages":"117162"},"PeriodicalIF":3.3000,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Thymoquinone inhibits Neuroinflammatory mediators and vasoconstriction injury via NF-κB dependent NeuN/GFAP/Ki-67 in hypertensive Dams and F1 male pups on exposure to a mixture of Bisphenol-A analogues.\",\"authors\":\"O S Okoh, J K Akintunde, A J Akamo, Ubong Akpan\",\"doi\":\"10.1016/j.taap.2024.117162\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Bisphenol-A (BPA) analogues seem inevitable components of numerous domestic products, but these have been identified as agents of teratogenic disorders. This study, therefore, investigated the effect of thymoquinone (TMQ) on the striatum of hypertensive female rats and their F1 male offsprings, on exposure to a mixture of Bisphenol-B, Bisphenol-F and Bisphenol-S (MBFS). Female rats were divided into normotensive and hypertensive groups; and both were treated with MBFS only, MBFS + TMQ, and TMQ only. Exposure to MBFS and co-treatment with TMQ lasted at least 63 days. Neurobehavioural assessments were conducted using Open Field (OF). A spectrophotometer was used for cholinergic, dopaminergic and adenosinergic enzyme assays; Real-Time PCR for gene expression; and immunohistochemistry for protein quantification; while H&E, cresyl fast violent, and congo red stains were used for histological assessments. From the results, maternal exposure to MBFS mediated striatal dysfunction via p53 and NF-kB upregulation; decreased BCl-2, Ki-67 and NeuN; increased GFAP, nissl bodies and β-amyloid. Dysregulation of cholinergic, dopaminergic and adenosinergic enzymes in addition to decreased nitric oxide levels were also associated with MBFS toxicity. Hypertension was found to exacerbate MBFS toxicity. From OF test; increased anxiety and decreased psychomotor activity were associated with maternal exposure to MBFS. However, co-treatment with thymoquinone prevented striatal dysfunction in hypertensive dams and their F1 male offspring. In conclusion, disruption of the delicate balance between apoptosis and cell proliferation culminating in the reduction of mature neurons is responsible for neurodegeneration and neuropathy associated with MBFS exposure. However, these can be prevented through regular consumption of natural products and supplements rich in thymoquinone.</p>\",\"PeriodicalId\":23174,\"journal\":{\"name\":\"Toxicology and applied pharmacology\",\"volume\":\" \",\"pages\":\"117162\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2024-11-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Toxicology and applied pharmacology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.taap.2024.117162\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Toxicology and applied pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.taap.2024.117162","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
Thymoquinone inhibits Neuroinflammatory mediators and vasoconstriction injury via NF-κB dependent NeuN/GFAP/Ki-67 in hypertensive Dams and F1 male pups on exposure to a mixture of Bisphenol-A analogues.
Bisphenol-A (BPA) analogues seem inevitable components of numerous domestic products, but these have been identified as agents of teratogenic disorders. This study, therefore, investigated the effect of thymoquinone (TMQ) on the striatum of hypertensive female rats and their F1 male offsprings, on exposure to a mixture of Bisphenol-B, Bisphenol-F and Bisphenol-S (MBFS). Female rats were divided into normotensive and hypertensive groups; and both were treated with MBFS only, MBFS + TMQ, and TMQ only. Exposure to MBFS and co-treatment with TMQ lasted at least 63 days. Neurobehavioural assessments were conducted using Open Field (OF). A spectrophotometer was used for cholinergic, dopaminergic and adenosinergic enzyme assays; Real-Time PCR for gene expression; and immunohistochemistry for protein quantification; while H&E, cresyl fast violent, and congo red stains were used for histological assessments. From the results, maternal exposure to MBFS mediated striatal dysfunction via p53 and NF-kB upregulation; decreased BCl-2, Ki-67 and NeuN; increased GFAP, nissl bodies and β-amyloid. Dysregulation of cholinergic, dopaminergic and adenosinergic enzymes in addition to decreased nitric oxide levels were also associated with MBFS toxicity. Hypertension was found to exacerbate MBFS toxicity. From OF test; increased anxiety and decreased psychomotor activity were associated with maternal exposure to MBFS. However, co-treatment with thymoquinone prevented striatal dysfunction in hypertensive dams and their F1 male offspring. In conclusion, disruption of the delicate balance between apoptosis and cell proliferation culminating in the reduction of mature neurons is responsible for neurodegeneration and neuropathy associated with MBFS exposure. However, these can be prevented through regular consumption of natural products and supplements rich in thymoquinone.
期刊介绍:
Toxicology and Applied Pharmacology publishes original scientific research of relevance to animals or humans pertaining to the action of chemicals, drugs, or chemically-defined natural products.
Regular articles address mechanistic approaches to physiological, pharmacologic, biochemical, cellular, or molecular understanding of toxicologic/pathologic lesions and to methods used to describe these responses. Safety Science articles address outstanding state-of-the-art preclinical and human translational characterization of drug and chemical safety employing cutting-edge science. Highly significant Regulatory Safety Science articles will also be considered in this category. Papers concerned with alternatives to the use of experimental animals are encouraged.
Short articles report on high impact studies of broad interest to readers of TAAP that would benefit from rapid publication. These articles should contain no more than a combined total of four figures and tables. Authors should include in their cover letter the justification for consideration of their manuscript as a short article.