Masese Johnson, Kipkoech Gilbert, M. Peter, Nguka Gordon, M. Charles
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Group V mice received S. platensis extract 200 mg/kg/day and 200 µg/kg/day of AFB1 for 28 days. Levels of alanine aminotransferase (ALT), alkaline phosphatase (ALP), aspartate aminotransferase (AST), globulin, albumin and total plasma protein were analyzed in blood samples using an automated biochemistry analyser. Data analysis was done using one way ANOVA with Tukey’s Honestly Significantly Differenced (HSD) post-hoc analysis. Statistical significance level was set at P<0.05. Results showed that compared to group 1 (control), group 3 (200 µg/Kg/day AFB1) had increased levels of ALT; (44.0±6.83 IU/L vs. 61.0±8.19 IU/L; p=0.054), AST (176.75±44.34 IU/L vs. 256±115.99 IU/L; p=0.0195) and ALP (51.75±11.89 IU/L vs. 59.40±6.91 IU/L; p =0.049). Mice that were co-treated with 200 µg/Kg/day of AFB1 and 200 mg/Kg/day of S. platensis extract exhibited lower levels compared to mice treated with only 200 mg/Kg/day of AFB1; ALT (49.8±7.9 IU/L vs. 61.5±8.19 IU/L; p=0.039), AST (229.8±95 IU/L vs. 256±11.15 IU/L; p=0.04819) and ALP (26.5±13.48 IU/L vs. 49.75±4.1 IU/L; p=0.0444). In conclusion, our study findings suggest that supplementation of S. platensis extract at a level of 100 mg/Kg/day and 200 mg/Kg/day can reverse elevation of ALT, AST and ALP serum levels caused by 200 µg/Kg/day of AFB1 in male Swiss albino mice.","PeriodicalId":22851,"journal":{"name":"The Journal of Phytopharmacology","volume":"9 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Spirulina platensis Inhibits Aflatoxin B1 Induced Biochemical Changes in Male Swiss Albino Mice\",\"authors\":\"Masese Johnson, Kipkoech Gilbert, M. Peter, Nguka Gordon, M. Charles\",\"doi\":\"10.31254/phyto.2022.11505\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Aflatoxins (AF) are harmful metabolites produced by Aspergillums species principally by Aspergillus. flavus and Aspergillus parasiticus. Aflatoxins are hepatotoxic, teratogenic, mutagenic and carcinogenic. The main objective of the current study was to evaluate protective effects of Spirulina platensis extract against aflatoxin B1 (AFB1) induced biochemical changes in male Swiss albino mice. Randomly 25 healthy inbred mice were allocated into five groups, each having 5 mice. Group I (Control group), mice received normal diet. Group II mice received 100 mg/kg/day of S. platensis extract. Group III mice received 200 µg/kg/day of AFB1. Group IV mice received S. platensis extract 100 mg/kg/day and 200 µg/kg/day of AFB1. Group V mice received S. platensis extract 200 mg/kg/day and 200 µg/kg/day of AFB1 for 28 days. Levels of alanine aminotransferase (ALT), alkaline phosphatase (ALP), aspartate aminotransferase (AST), globulin, albumin and total plasma protein were analyzed in blood samples using an automated biochemistry analyser. Data analysis was done using one way ANOVA with Tukey’s Honestly Significantly Differenced (HSD) post-hoc analysis. Statistical significance level was set at P<0.05. Results showed that compared to group 1 (control), group 3 (200 µg/Kg/day AFB1) had increased levels of ALT; (44.0±6.83 IU/L vs. 61.0±8.19 IU/L; p=0.054), AST (176.75±44.34 IU/L vs. 256±115.99 IU/L; p=0.0195) and ALP (51.75±11.89 IU/L vs. 59.40±6.91 IU/L; p =0.049). Mice that were co-treated with 200 µg/Kg/day of AFB1 and 200 mg/Kg/day of S. platensis extract exhibited lower levels compared to mice treated with only 200 mg/Kg/day of AFB1; ALT (49.8±7.9 IU/L vs. 61.5±8.19 IU/L; p=0.039), AST (229.8±95 IU/L vs. 256±11.15 IU/L; p=0.04819) and ALP (26.5±13.48 IU/L vs. 49.75±4.1 IU/L; p=0.0444). In conclusion, our study findings suggest that supplementation of S. platensis extract at a level of 100 mg/Kg/day and 200 mg/Kg/day can reverse elevation of ALT, AST and ALP serum levels caused by 200 µg/Kg/day of AFB1 in male Swiss albino mice.\",\"PeriodicalId\":22851,\"journal\":{\"name\":\"The Journal of Phytopharmacology\",\"volume\":\"9 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-10-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Phytopharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31254/phyto.2022.11505\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Phytopharmacology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31254/phyto.2022.11505","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
摘要
黄曲霉毒素(Aflatoxins, AF)是由曲霉产生的有害代谢物。黄曲霉和寄生曲霉。黄曲霉毒素具有肝毒性、致畸性、诱变性和致癌性。本研究的主要目的是评价螺旋藻提取物对黄曲霉毒素B1 (AFB1)诱导的雄性瑞士白化小鼠生化变化的保护作用。选取健康近交系小鼠25只,随机分为5组,每组5只。第一组(对照组),小鼠给予正常饮食。II组小鼠给予白荆提取物100 mg/kg/d。第三组小鼠给予AFB1 200µg/kg/天。IV组小鼠分别给予白棘提取物100 mg/kg/d和AFB1 200µg/kg/d。V组小鼠分别给予白棘提取物200 mg/kg/d和AFB1 200µg/kg/d,连续28 d。采用全自动生化分析仪分析血液样品中丙氨酸转氨酶(ALT)、碱性磷酸酶(ALP)、天冬氨酸转氨酶(AST)、球蛋白、白蛋白和血浆总蛋白的水平。数据分析采用单因素方差分析和Tukey的诚实显著差异(HSD)事后分析。差异有统计学意义,P<0.05。结果显示,与1组(对照组)相比,3组(AFB1含量为200µg/Kg/day) ALT水平升高;(44.0±6.83 IU/L vs. 61.0±8.19 IU/L;p=0.054), AST(176.75±44.34 IU/L vs. 256±115.99 IU/L;p=0.0195)和ALP(51.75±11.89 IU/L vs. 59.40±6.91 IU/L;p = 0.049)。同时给予200µg/Kg/天AFB1和200 mg/Kg/天天山参提取物的小鼠比只给予200 mg/Kg/天AFB1的小鼠表现出更低的水平;ALT(49.8±7.9 IU/L vs. 61.5±8.19 IU/L;p=0.039), AST(229.8±95 IU/L vs. 256±11.15 IU/L;p=0.04819)和ALP(26.5±13.48 IU/L vs. 49.75±4.1 IU/L;p = 0.0444)。综上所述,我们的研究结果表明,添加100 mg/Kg/d和200 mg/Kg/d水平的白山参提取物可以逆转200µg/Kg/d AFB1引起的雄性瑞士白化小鼠血清ALT、AST和ALP水平升高。
Spirulina platensis Inhibits Aflatoxin B1 Induced Biochemical Changes in Male Swiss Albino Mice
Aflatoxins (AF) are harmful metabolites produced by Aspergillums species principally by Aspergillus. flavus and Aspergillus parasiticus. Aflatoxins are hepatotoxic, teratogenic, mutagenic and carcinogenic. The main objective of the current study was to evaluate protective effects of Spirulina platensis extract against aflatoxin B1 (AFB1) induced biochemical changes in male Swiss albino mice. Randomly 25 healthy inbred mice were allocated into five groups, each having 5 mice. Group I (Control group), mice received normal diet. Group II mice received 100 mg/kg/day of S. platensis extract. Group III mice received 200 µg/kg/day of AFB1. Group IV mice received S. platensis extract 100 mg/kg/day and 200 µg/kg/day of AFB1. Group V mice received S. platensis extract 200 mg/kg/day and 200 µg/kg/day of AFB1 for 28 days. Levels of alanine aminotransferase (ALT), alkaline phosphatase (ALP), aspartate aminotransferase (AST), globulin, albumin and total plasma protein were analyzed in blood samples using an automated biochemistry analyser. Data analysis was done using one way ANOVA with Tukey’s Honestly Significantly Differenced (HSD) post-hoc analysis. Statistical significance level was set at P<0.05. Results showed that compared to group 1 (control), group 3 (200 µg/Kg/day AFB1) had increased levels of ALT; (44.0±6.83 IU/L vs. 61.0±8.19 IU/L; p=0.054), AST (176.75±44.34 IU/L vs. 256±115.99 IU/L; p=0.0195) and ALP (51.75±11.89 IU/L vs. 59.40±6.91 IU/L; p =0.049). Mice that were co-treated with 200 µg/Kg/day of AFB1 and 200 mg/Kg/day of S. platensis extract exhibited lower levels compared to mice treated with only 200 mg/Kg/day of AFB1; ALT (49.8±7.9 IU/L vs. 61.5±8.19 IU/L; p=0.039), AST (229.8±95 IU/L vs. 256±11.15 IU/L; p=0.04819) and ALP (26.5±13.48 IU/L vs. 49.75±4.1 IU/L; p=0.0444). In conclusion, our study findings suggest that supplementation of S. platensis extract at a level of 100 mg/Kg/day and 200 mg/Kg/day can reverse elevation of ALT, AST and ALP serum levels caused by 200 µg/Kg/day of AFB1 in male Swiss albino mice.