Literature DB >> 19445996

A different kinetic profile of ochratoxin A in mature male rats.

A Vettorazzi1, E Gonzalez-Peñas, I F Trocóniz, L Arbillaga, L A Corcuera, A G Gil, A López de Cerain.   

Abstract

Ochratoxin A (OTA) is a mycotoxin that causes renal tumors in rodents, particularly in male rats. The present work explored the impact of gender and age on OTA toxicokinetics in F344 rats after a single oral dose (0.5mg/kg b.w.). OTA plasma concentrations were analysed with a validated HPLC-FLD method and a population approach (NONMEM VI) was used to perform the kinetic analysis and the one year exposure simulation (0.21 mg/kg daily). Maximum observed OTA concentration (CMAX(obs)) was at 2h in all groups except in mature females (6h). Mature females reached higher CMAX(obs) than males of the same age. Apparent volume of distribution, but not apparent total plasma clearance, increased significantly with body weight (P<0.01) resulting in the following values for the terminal plasma half life (h) in males: 219 (young), 264 (matures) and females: 191 (young), 205 (matures). In addition mature males showed a significant lower relative bioavailability. The simulation showed similar plasma concentrations in males and females after two-months. Thus, toxicokinetic does not seem to explain sex-differences in toxicity in long-term studies. However, the age and weight should be taken into account in short-term toxicological studies if sex-differences are studied.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19445996     DOI: 10.1016/j.fct.2009.05.003

Source DB:  PubMed          Journal:  Food Chem Toxicol        ISSN: 0278-6915            Impact factor:   6.023


  7 in total

1.  Mycobiota and Ochratoxin A in laboratory mice feed: preliminary study.

Authors:  Inês Almeida; H Marina Martins; Marta F Marques; Salomé Magalhães; Fernando Bernardo
Journal:  Vet Res Commun       Date:  2010-04-27       Impact factor: 2.459

Review 2.  Ochratoxins in feed, a risk for animal and human health: control strategies.

Authors:  Muzaffer Denli; Jose F Perez
Journal:  Toxins (Basel)       Date:  2010-05-13       Impact factor: 4.546

3.  Oncological outcomes in rats given nephrocarcinogenic exposure to dietary ochratoxin a, followed by the tumour promoter sodium barbital for life: a pilot study.

Authors:  Peter G Mantle; Miloslav Dobrota; Cheryl E Gillett; Edward W Odell; Sarah E Pinder
Journal:  Toxins (Basel)       Date:  2010-03-31       Impact factor: 4.546

4.  Pathological outcomes in kidney and brain in male Fischer rats given dietary ochratoxin A, commencing at one year of age.

Authors:  Peter G Mantle; Christopher C Nolan
Journal:  Toxins (Basel)       Date:  2010-05-13       Impact factor: 4.546

5.  H NMR spectroscopy-based metabolomic assessment of uremic toxicity, with toxicological outcomes, in male rats following an acute, mid-life insult from ochratoxin a.

Authors:  Peter G Mantle; Andrew W Nicholls; John P Shockcor
Journal:  Toxins (Basel)       Date:  2011-05-26       Impact factor: 4.546

6.  First evidence of placental transfer of ochratoxin A in horses.

Authors:  Fiorenza Minervini; Alessandra Giannoccaro; Michele Nicassio; Giuseppe Panzarini; Giovanni Michele Lacalandra
Journal:  Toxins (Basel)       Date:  2013-01-11       Impact factor: 4.546

7.  Changes in male rat urinary protein profile during puberty: a pilot study.

Authors:  Ariane Vettorazzi; Robin Wait; Judit Nagy; Jose Ignacio Monreal; Peter Mantle
Journal:  BMC Res Notes       Date:  2013-06-15
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.