Ahmad Salimi, Mahshad Pourgholi, Saleh Khezri, Shadi Haddadi, Bahare Asgari
{"title":"辛酸对n -乙基- n -亚硝基脲致小鼠死亡和毒性的保护作用。","authors":"Ahmad Salimi, Mahshad Pourgholi, Saleh Khezri, Shadi Haddadi, Bahare Asgari","doi":"10.1055/a-2687-0870","DOIUrl":null,"url":null,"abstract":"<p><p>We investigated, in vivo, the chemopreventive efficacy of sinapic acid, as a known radical scavenger and antioxidant on mortality and toxicity in a N-ethyl-N-nitrosourea (ENU)-induced chronic lymphocytic leukemia (CLL) model in mice.Mice were divided into three groups: control (normal saline), ENU (80 mg/kg, i.p., single dose on day 31), and sinapic acid+ENU (pretreated with 30 mg/kg of sinapic acid, i.p., daily for 30 days, followed by 80 mg/kg of ENU). Body weight changes and mortality were monitored over 120 days. After this period, the animals were sacrificed, and lymphocytes, the target cells in CLL, were isolated and evaluated for various cellular parameters.Sinapic acid significantly (P<0.001) increased mouse survival up to 71%, delayed time of death, and prevented weight loss following ENU exposure. Additionally, sinapic acid inhibited the formation of reactive oxygen species (ROS) (P<0.001), lysosomal and mitochondrial dysfunction (P<0.001), and lipid peroxidation (P<0.05) in the isolated lymphocytes. These findings indicate a protective effect of sinapic acid against ENU-induced lethal toxicity.This study confirms that sinapic acid may serve as a promising chemopreventive agent against carcinogenicity induced by alkylating agents, primarily through the inhibition of oxidative stress and lysosomal/mitochondrial dysfunction.</p>","PeriodicalId":11451,"journal":{"name":"Drug Research","volume":" ","pages":"334-342"},"PeriodicalIF":2.1000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sinapic Acid Protects Mortality and Toxicity Induced by N-Ethyl-N-Nitrosourea, a Full Carcinogen Agent, in Mice.\",\"authors\":\"Ahmad Salimi, Mahshad Pourgholi, Saleh Khezri, Shadi Haddadi, Bahare Asgari\",\"doi\":\"10.1055/a-2687-0870\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>We investigated, in vivo, the chemopreventive efficacy of sinapic acid, as a known radical scavenger and antioxidant on mortality and toxicity in a N-ethyl-N-nitrosourea (ENU)-induced chronic lymphocytic leukemia (CLL) model in mice.Mice were divided into three groups: control (normal saline), ENU (80 mg/kg, i.p., single dose on day 31), and sinapic acid+ENU (pretreated with 30 mg/kg of sinapic acid, i.p., daily for 30 days, followed by 80 mg/kg of ENU). Body weight changes and mortality were monitored over 120 days. After this period, the animals were sacrificed, and lymphocytes, the target cells in CLL, were isolated and evaluated for various cellular parameters.Sinapic acid significantly (P<0.001) increased mouse survival up to 71%, delayed time of death, and prevented weight loss following ENU exposure. Additionally, sinapic acid inhibited the formation of reactive oxygen species (ROS) (P<0.001), lysosomal and mitochondrial dysfunction (P<0.001), and lipid peroxidation (P<0.05) in the isolated lymphocytes. These findings indicate a protective effect of sinapic acid against ENU-induced lethal toxicity.This study confirms that sinapic acid may serve as a promising chemopreventive agent against carcinogenicity induced by alkylating agents, primarily through the inhibition of oxidative stress and lysosomal/mitochondrial dysfunction.</p>\",\"PeriodicalId\":11451,\"journal\":{\"name\":\"Drug Research\",\"volume\":\" \",\"pages\":\"334-342\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Drug Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1055/a-2687-0870\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/9/8 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/a-2687-0870","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/9/8 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
Sinapic Acid Protects Mortality and Toxicity Induced by N-Ethyl-N-Nitrosourea, a Full Carcinogen Agent, in Mice.
We investigated, in vivo, the chemopreventive efficacy of sinapic acid, as a known radical scavenger and antioxidant on mortality and toxicity in a N-ethyl-N-nitrosourea (ENU)-induced chronic lymphocytic leukemia (CLL) model in mice.Mice were divided into three groups: control (normal saline), ENU (80 mg/kg, i.p., single dose on day 31), and sinapic acid+ENU (pretreated with 30 mg/kg of sinapic acid, i.p., daily for 30 days, followed by 80 mg/kg of ENU). Body weight changes and mortality were monitored over 120 days. After this period, the animals were sacrificed, and lymphocytes, the target cells in CLL, were isolated and evaluated for various cellular parameters.Sinapic acid significantly (P<0.001) increased mouse survival up to 71%, delayed time of death, and prevented weight loss following ENU exposure. Additionally, sinapic acid inhibited the formation of reactive oxygen species (ROS) (P<0.001), lysosomal and mitochondrial dysfunction (P<0.001), and lipid peroxidation (P<0.05) in the isolated lymphocytes. These findings indicate a protective effect of sinapic acid against ENU-induced lethal toxicity.This study confirms that sinapic acid may serve as a promising chemopreventive agent against carcinogenicity induced by alkylating agents, primarily through the inhibition of oxidative stress and lysosomal/mitochondrial dysfunction.
期刊介绍:
Drug Research (formerly Arzneimittelforschung) is an international peer-reviewed journal with expedited processing times presenting the very latest research results related to novel and established drug molecules and the evaluation of new drug development. A key focus of the publication is translational medicine and the application of biological discoveries in the development of drugs for use in the clinical environment. Articles and experimental data from across the field of drug research address not only the issue of drug discovery, but also the mathematical and statistical methods for evaluating results from industrial investigations and clinical trials. Publishing twelve times a year, Drug Research includes original research articles as well as reviews, commentaries and short communications in the following areas: analytics applied to clinical trials chemistry and biochemistry clinical and experimental pharmacology drug interactions efficacy testing pharmacodynamics pharmacokinetics teratology toxicology.