SAGE Journals Online
Advertisement
Sign In to gain access to subscriptions and/or personal tools.

 

Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Advertisement

Sign In to gain access to subscriptions and/or personal tools.
Human & Experimental Toxicology
This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Roomi, M.
Right arrow Articles by Niedzwiecki, A
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Roomi, M.
Right arrow Articles by Niedzwiecki, A
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

research-article

A nutrient mixture prevents acetaminophen hepatic and renal toxicity in ICR mice

MW Roomi

Dr Rath Research Institute, Santa Clara, California, USA

T Kalinovsky

Dr Rath Research Institute, Santa Clara, California, USA

V Ivanov

Dr Rath Research Institute, Santa Clara, California, USA

M Rath

Dr Rath Research Institute, Santa Clara, California, USA

A Niedzwiecki

Dr Rath Research Institute, Santa Clara, California, USA author{at}drrath.com

Acetaminophen (APAP) overdose is often fatal, leading to fulminant hepatic and renal tubular necrosis in humans and animals. We studied the effect of a nutrient mixture (NM) containing, among other nutrients, lysine, proline, ascorbic acid, N-acetyl cysteine, and green tea extract, which has previously been demonstrated to exhibit a broad spectrum of therapeutic properties on APAP-induced hepatic and renal damage in ICR (Imprinting Control Region) mice. Seven-week-old male ICR mice were divided into four groups (A–D) of five animals each. Groups A and C mice were fed a regular diet for 2 weeks, while groups B and D mice were supplemented with 0.5% NM (w/w) during that period. Groups A and B received saline i.p., while groups C and D received APAP (600 mg/kg) i.p. All animals were killed 24 h after APAP administration, serum was collected to assess the liver and kidney functions, and the livers and kidneys were excised for histology. Mean serum aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, BUN (Blood Urea Nitrogen), creatinine, and BUN/creatinine ratios were comparable in groups A and B, increased markedly in group C and significantly lower in group D compared with group C. APAP caused significant centrilobular necrosis and glomerular damage in unsupplemented animals, while NM prevented these alterations. The results indicate that NM has potential to protect against APAP-induced liver and kidney damage.

Key Words: acetaminophen • APAP • hepatic • nutrients • renal • toxicity

Human & Experimental Toxicology, Vol. 27, No. 3, 223-230 (2008)
DOI: 10.1177/0960327108090276


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Hum Exp ToxicolHome page
M. Roomi, T Kalinovsky, N. Roomi, V Ivanov, M Rath, and A Niedzwiecki
A nutrient mixture suppresses carbon tetrachloride-induced acute hepatic toxicity in ICR mice
Human and Experimental Toxicology, July 1, 2008; 27(7): 559 - 566.
[Abstract] [PDF]



Advertisement