{"title":"玉米叶提取物Maizinol (UP165)的口服亚慢性毒性评价","authors":"J Kyle Weston, Barry S Lynch, James A Akingbasote","doi":"10.1002/jat.4882","DOIUrl":null,"url":null,"abstract":"<p><p>Maize (Zea mays) has been consumed by humans for millennia and represents the third most abundant crop grown globally. Maize and maize-derived products have a long history of safe consumption from bread and other cereal products in human diets worldwide. Aside from key dietary components like carbohydrates and proteins, the corn plant contains endogenous biomolecules like benzoxazinoids. Benzoxazinoids are a group of secondary metabolites produced in monocotyledons and some species of dicotyledons from the Acanthaceae, Ranunculaceae, Scrophulariaceae, Plantaginaceae, and Lamiaceae families, and benzoxazinoids play a vital role in plant physiology. The current research aims to evaluate the safety of Maizinol (UP165), an ethanolic corn leaf extract containing 0.2%-0.3% of the benzoxazinoid, benzoxazolinone 6-methoxy-2-benzoxazolinone (6-MBOA) in Sprague Dawley rats. Animals were orally dosed with 0-, 750-, 1500-, or 3000-mg Maizinol/kg body weight/day for 90 days and observed for mortality and morbidity. Results revealed that Maizinol was well tolerated at all tested doses, as no significant effects were observed in hematological, biochemical, and histological endpoints at all doses. A subchronic 90-day toxicity no-observed-adverse-effect level for UP165 in Sprague Dawley rats was determined to be 3000 mg/kg body weight/day.</p>","PeriodicalId":15242,"journal":{"name":"Journal of Applied Toxicology","volume":" ","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"An Evaluation of Oral Subchronic Toxicity of Maizinol (UP165), a Zea mays Leaf Extract.\",\"authors\":\"J Kyle Weston, Barry S Lynch, James A Akingbasote\",\"doi\":\"10.1002/jat.4882\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Maize (Zea mays) has been consumed by humans for millennia and represents the third most abundant crop grown globally. Maize and maize-derived products have a long history of safe consumption from bread and other cereal products in human diets worldwide. Aside from key dietary components like carbohydrates and proteins, the corn plant contains endogenous biomolecules like benzoxazinoids. Benzoxazinoids are a group of secondary metabolites produced in monocotyledons and some species of dicotyledons from the Acanthaceae, Ranunculaceae, Scrophulariaceae, Plantaginaceae, and Lamiaceae families, and benzoxazinoids play a vital role in plant physiology. The current research aims to evaluate the safety of Maizinol (UP165), an ethanolic corn leaf extract containing 0.2%-0.3% of the benzoxazinoid, benzoxazolinone 6-methoxy-2-benzoxazolinone (6-MBOA) in Sprague Dawley rats. Animals were orally dosed with 0-, 750-, 1500-, or 3000-mg Maizinol/kg body weight/day for 90 days and observed for mortality and morbidity. Results revealed that Maizinol was well tolerated at all tested doses, as no significant effects were observed in hematological, biochemical, and histological endpoints at all doses. A subchronic 90-day toxicity no-observed-adverse-effect level for UP165 in Sprague Dawley rats was determined to be 3000 mg/kg body weight/day.</p>\",\"PeriodicalId\":15242,\"journal\":{\"name\":\"Journal of Applied Toxicology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Applied Toxicology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1002/jat.4882\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"TOXICOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Toxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/jat.4882","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"TOXICOLOGY","Score":null,"Total":0}
An Evaluation of Oral Subchronic Toxicity of Maizinol (UP165), a Zea mays Leaf Extract.
Maize (Zea mays) has been consumed by humans for millennia and represents the third most abundant crop grown globally. Maize and maize-derived products have a long history of safe consumption from bread and other cereal products in human diets worldwide. Aside from key dietary components like carbohydrates and proteins, the corn plant contains endogenous biomolecules like benzoxazinoids. Benzoxazinoids are a group of secondary metabolites produced in monocotyledons and some species of dicotyledons from the Acanthaceae, Ranunculaceae, Scrophulariaceae, Plantaginaceae, and Lamiaceae families, and benzoxazinoids play a vital role in plant physiology. The current research aims to evaluate the safety of Maizinol (UP165), an ethanolic corn leaf extract containing 0.2%-0.3% of the benzoxazinoid, benzoxazolinone 6-methoxy-2-benzoxazolinone (6-MBOA) in Sprague Dawley rats. Animals were orally dosed with 0-, 750-, 1500-, or 3000-mg Maizinol/kg body weight/day for 90 days and observed for mortality and morbidity. Results revealed that Maizinol was well tolerated at all tested doses, as no significant effects were observed in hematological, biochemical, and histological endpoints at all doses. A subchronic 90-day toxicity no-observed-adverse-effect level for UP165 in Sprague Dawley rats was determined to be 3000 mg/kg body weight/day.
期刊介绍:
Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.