Assessing systemic, developmental, and reproductive toxicity and estrogenicity of Korean red ginseng extract G1899 in juvenile Sprague-Dawley Rats

IF 6.8 2区 医学 Q1 CHEMISTRY, MEDICINAL Journal of Ginseng Research Pub Date : 2024-01-21 DOI:10.1016/j.jgr.2024.01.002
Sangyun Kim , Ji-Seong Jeong , Woojin Kim , Onju Ham , Yixian Quah , Soontag Jung , Dong-Ju Park , Min Jae Kim , Byung-Cheol Han , Eunji Kim , Seung-Jin Lee , Wook-Joon Yu
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Abstract

Background

Korean red ginseng (KRG) is a product from ginseng roots, which is enriched with ginsenosides and has been utilized for a long time as an adaptogen to alleviate various physiological or disease conditions. While KRG is generally considered safe, conducting a thorough toxicological assessment of the spray-dried powder G1899 during the juvenile period is essential to establish its safety profile. This study aimed to assess the safety of G1899 during the juvenile period using Sprague-Dawley rats.

Methods

Two studies were conducted separately: a juvenile toxicity study and a uterotrophic bioassay. To assess the potential toxicity at systemic, postnatal developmental, and reproductive levels, G1899 was orally gavaged once a day in post-weaning juvenile Sprague-Dawley (SD) rats at 0, 1250, 2500, or 5000 mg/kg/day. Estrogenicity was assessed by orally gavaging G1899 in immature female SD rats at 0, 2500, or 5000 mg/kg/day on postnatal days (PND) 19–21, followed by a uterotrophic bioassay. These studies were conducted in accordance with the Good Laboratory Practice (GLP) regulations and regulatory test guidelines.

Results

Regarding juvenile toxicity, no abnormalities related to the G1899 treatment were observed in any group during the experiment. Moreover, no uterotrophic responses were observed in the dosed female group. Based on these results, the no observed adverse effect level (NOAEL) of G1899 was determined to be at least 5000 mg/kg/day for general systemic function, developmental/reproductive function, and estrogenic activity.

Conclusion

Our results suggest that G1899 is not toxic to juveniles at doses of up to 5000 mg/kg/day.

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评估高丽红参提取物 G1899 对幼年 Sprague-Dawley 大鼠全身、发育和生殖毒性及雌激素毒性
背景韩国红参(KRG)是一种从人参根部提取的产品,富含人参皂苷,长期以来一直作为一种适应原被用于缓解各种生理或疾病状况。虽然 KRG 一般被认为是安全的,但要确定其安全性,必须对 G1899 喷雾干燥粉在幼年期进行全面的毒理学评估。本研究旨在使用 Sprague-Dawley 大鼠评估 G1899 在幼鼠期的安全性。方法分别进行了两项研究:幼鼠毒性研究和子宫营养生物测定。为了评估 G1899 在全身、产后发育和生殖水平上的潜在毒性,断奶后的幼年 Sprague-Dawley (SD) 大鼠每天口服一次 G1899,剂量为 0、1250、2500 或 5000 毫克/千克/天。在出生后第 19-21 天(PND),对未成熟雌性 SD 大鼠口服 G1899,剂量为 0、2500 或 5000 毫克/千克/天,然后进行子宫营养生物测定,以评估雌激素毒性。这些研究是按照良好实验室规范(GLP)条例和监管测试指南进行的。结果在幼鼠毒性方面,实验期间未在任何组别中观察到与 G1899 处理有关的异常情况。此外,在施药的雌性组中也没有观察到子宫营养不良的反应。基于这些结果,G1899 的无观测不良效应水平(NOAEL)被确定为至少 5000 毫克/千克/天,包括一般系统功能、发育/生殖功能和雌激素活性。
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来源期刊
Journal of Ginseng Research
Journal of Ginseng Research CHEMISTRY, MEDICINAL-INTEGRATIVE & COMPLEMENTARY MEDICINE
CiteScore
11.40
自引率
9.50%
发文量
111
审稿时长
6-12 weeks
期刊介绍: Journal of Ginseng Research (JGR) is an official, open access journal of the Korean Society of Ginseng and is the only international journal publishing scholarly reports on ginseng research in the world. The journal is a bimonthly peer-reviewed publication featuring high-quality studies related to basic, pre-clinical, and clinical researches on ginseng to reflect recent progresses in ginseng research. JGR publishes papers, either experimental or theoretical, that advance our understanding of ginseng science, including plant sciences, biology, chemistry, pharmacology, toxicology, pharmacokinetics, veterinary medicine, biochemistry, manufacture, and clinical study of ginseng since 1976. It also includes the new paradigm of integrative research, covering alternative medicinal approaches. Article types considered for publication include review articles, original research articles, and brief reports. JGR helps researchers to understand mechanisms for traditional efficacy of ginseng and to put their clinical evidence together. It provides balanced information on basic science and clinical applications to researchers, manufacturers, practitioners, teachers, scholars, and medical doctors.
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