Literature DB >> 28025058

Moderate doses of commercial preparations of Ginkgo biloba do not alter markers of liver function but moderate alcohol intake does: A new approach to identify and quantify biomarkers of 'adverse effects' of dietary supplements.

Harris R Lieberman1, Mark D Kellogg2, Victor L Fulgoni3, Sanjiv Agarwal4.   

Abstract

It is difficult to determine if certain dietary supplements are safe for human consumption. Extracts of leaves of Ginkgo biloba trees are dietary supplements used for various purported therapeutic benefits. However, recent studies reported they increased risk of liver cancer in rodents. Therefore, this study assessed the association between ginkgo consumption and liver function using NHANES 2001-2012 data (N = 29,684). Since alcohol is known to adversely affect liver function, association of its consumption with liver function was also assessed. Alcohol and ginkgo extract intake of adult consumers and clinical markers of liver function (alkaline phosphatase, alanine aminotransferase, aspartate aminotransferase, gamma glutamyl transferase, lactate dehydrogenase, bilirubin) were examined. Moderate consumers of alcohol (0.80 ± 0.02 drinks/day) had higher levels of aspartate aminotransferase and gamma glutamyl transferase than non-consumers (P < 0.001). There was no difference (P > 0.01) in levels of markers of liver function in 616 ginkgo consumers (65.1 ± 4.4 mg/day intake) compared to non-consumers. While moderate alcohol consumption was associated with changes in markers of liver function, ginkgo intake as typically consumed by U.S. adults was not associated with these markers. Biomarkers measured by NHANES may be useful to examine potential adverse effects of dietary supplements for which insufficient human adverse event and toxicity data are available. TRIAL REGISTRATION NUMBER: Not applicable, as this is secondary analysis of publicly released observational data (NHANES 2001-2012). Published by Elsevier Inc.

Entities:  

Keywords:  Alanine aminotransferase; Aspartate aminotransferase; Bilirubin; Gamma glutamyl transferase; Lactate dehydrogenase; NHANES

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Year:  2016        PMID: 28025058     DOI: 10.1016/j.yrtph.2016.12.010

Source DB:  PubMed          Journal:  Regul Toxicol Pharmacol        ISSN: 0273-2300            Impact factor:   3.271


  6 in total

1.  Systemic exposure to Ginkgo biloba extract in male F344/NCrl rats: Relevance to humans.

Authors:  Suramya Waidyanatha; Esra Mutlu; Seth Gibbs; Billie Stiffler; Jon Andre; Brian Burback; Cynthia V Rider
Journal:  Food Chem Toxicol       Date:  2019-06-14       Impact factor: 6.023

2.  Alleviation of chemotherapy-induced acute lung injury via NLRP3/ ASC/ Caspase-1 signaling pathway.

Authors:  Iman O Sherif; Nora H Al-Shaalan
Journal:  Toxicol Res (Camb)       Date:  2022-04-27       Impact factor: 2.680

3.  Self-reported dietary supplement use in deployed United States service members pre-deployment vs. during deployment, Afghanistan, 2013-2014.

Authors:  Shawn M Varney; Patrick C Ng; Crystal A Perez; Allyson A Araña; Edwin R Austin; Rosemarie G Ramos; Vikhyat S Bebarta
Journal:  Mil Med Res       Date:  2017-10-26

4.  Combination of curcumin and ginkgolide B inhibits cystogenesis by regulating multiple signaling pathways.

Authors:  Yousong Li; Jinsheng Gao; Xi Yang; Tao Li; Baoxue Yang; Aixingzi Aili
Journal:  Mol Med Rep       Date:  2021-01-26       Impact factor: 2.952

Review 5.  Ginkgo biloba: A Treasure of Functional Phytochemicals with Multimedicinal Applications.

Authors:  Rajib Das; Mashia Subha Lami; Arka Jyoti Chakraborty; Saikat Mitra; Trina Ekawati Tallei; Rinaldi Idroes; Amany Abdel-Rahman Mohamed; Md Jamal Hossain; Kuldeep Dhama; Gomaa Mostafa-Hedeab; Talha Bin Emran
Journal:  Evid Based Complement Alternat Med       Date:  2022-02-28       Impact factor: 2.629

6.  Ginkgo biloba extract (EGb761) did not express estrogenic activity in an immature rat uterotrophic assay.

Authors:  Byeonghak Moon; Wonchan Kim; Cho Hee Park; Seung Min Oh
Journal:  Environ Health Toxicol       Date:  2018-09-28
  6 in total

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