Literature DB >> 25711879

Germanium in ginseng is low and causes no sodium and water retention or renal toxicity in the diuretic-resistant rats.

Chunjiang Tan1, Lu Xiao1, Wenlie Chen1, Songming Chen2.   

Abstract

Ginseng preparations contain high concentrations of germanium (Ge), which was reported to contribute to diuretic resistance or renal failure. However, Ge content in ginseng and the influence on renal functions remain unclear. Forty rats were randomly divided into control group, low, moderate, and high Ge ginseng-treated group and observed for 25 days. Daily urine, renal functions, and serum and urine electrolytics were measured. Ge retention in the organs and renal histological changes were also evaluated. Ge content ranged from 0.007 to 0.450 µg/g in various ginseng samples. Four groups showed no difference in the daily urine output, glomerular filtration rate, urinary electrolytes excretions, 24 h-urine protein, as well as plasma and urine urea nitrogen, creatinine, osmotic pressure, and pH values. Ge did not cause any renal pathological effects in this study. No Na and water retention was detected in the ginseng-treated groups. Ge retention in various organs was found highest in spleen, followed by the kidney, liver, lung, stomach, heart, and pancreas. The total Ge contents in various ginsengs were low, and ginseng treatment did not affect renal functions or cause renal histological changes.
© 2015 by the Society for Experimental Biology and Medicine.

Entities:  

Keywords:  Germanium in ginseng; diuretic-resistant rats; renal toxicity; sodium and water retention

Mesh:

Substances:

Year:  2015        PMID: 25711879      PMCID: PMC4935308          DOI: 10.1177/1535370215571874

Source DB:  PubMed          Journal:  Exp Biol Med (Maywood)        ISSN: 1535-3699


  13 in total

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Journal:  Toxicol Ind Health       Date:  1987-03       Impact factor: 2.273

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Journal:  Nephron       Date:  1990       Impact factor: 2.847

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Journal:  Jpn J Med       Date:  1991 Jan-Feb

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Journal:  J Toxicol Sci       Date:  1985-11       Impact factor: 2.196

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Authors:  R Krapf; T Schaffner; P X Iten
Journal:  Nephron       Date:  1992       Impact factor: 2.847

9.  Dose translation from animal to human studies revisited.

Authors:  Shannon Reagan-Shaw; Minakshi Nihal; Nihal Ahmad
Journal:  FASEB J       Date:  2007-10-17       Impact factor: 5.191

10.  Response to repeated frusemide administration on low chloride and low sodium intake in the rat.

Authors:  T Kahn; A M Kaufman; F L Mac-Moune
Journal:  Clin Sci (Lond)       Date:  1983-06       Impact factor: 6.124

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