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黑升麻草药提取物和 B6C3F1/N 小鼠血液学改变。

Black Cohosh Herbal Extract and Hematologic Alterations in B6C3F1/N Mice.

机构信息

Antech Diagnostics, Cary, North Carolina, USA.

National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA.

出版信息

Toxicol Pathol. 2022 Oct;50(7):886-889. doi: 10.1177/01926233221133549. Epub 2022 Nov 14.

Abstract

Black cohosh is a readily available dietary supplement currently marketed as a remedy for dysmenorrhea and menopausal symptoms and is one of the top-selling herbal supplements in the United States. Black cohosh extract (BCE) was nominated to the National Toxicology Program (NTP) by the National Cancer Institute and the National Institute of Environmental Health Sciences due to its widespread use and lack of animal toxicity studies. Results of the NTP BCE subchronic mouse toxicity study revealed a dose-dependent, non-regenerative decrease in the erythron with an increase in the mean corpuscular volume (macrocytosis). Howell-Jolly bodies, or micronuclei, were significantly increased. These particular changes indicated an ineffective erythropoiesis consistent with a condition known as megaloblastic anemia. Megaloblastic anemia is due to disruptions in DNA synthesis during hematopoiesis and can be a result of an inherited or drug-induced disorder or a consequence of folate or cobalamin deficiency. Subsequent mouse studies revealed hematological and biochemical changes that were consistent with a functional cobalamin deficiency. This article will review basic mechanisms and laboratory features of megaloblastic anemia. The results of our studies including morphological abnormalities of the erythron and biomarkers of folate and cobalamin deficiencies, as well as hepatic microarray gene changes, are also discussed.

摘要

黑升麻是一种现成的膳食补充剂,目前作为治疗痛经和更年期症状的药物销售,是美国最畅销的草药补充剂之一。由于其广泛使用但缺乏动物毒性研究,美国国家癌症研究所和国家环境卫生科学研究所将黑升麻提取物(BCE)提名给国家毒理学计划(NTP)。NTP BCE 亚慢性小鼠毒性研究的结果显示,红细胞呈剂量依赖性、非再生性减少,平均红细胞体积(大细胞症)增加。Howell-Jolly 体或微核显着增加。这些特殊变化表明无效的红细胞生成与巨幼细胞性贫血的一种已知病症一致。巨幼细胞性贫血是由于造血过程中 DNA 合成的中断引起的,可能是遗传或药物诱导的疾病的结果,也可能是叶酸或钴胺素缺乏的结果。随后的小鼠研究显示出与功能性钴胺素缺乏一致的血液学和生化变化。本文将综述巨幼细胞性贫血的基本机制和实验室特征。还讨论了我们的研究结果,包括红细胞的形态异常以及叶酸和钴胺素缺乏的生物标志物,以及肝微阵列基因变化。

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