Literature DB >> 1759851

Toxicity of oleic acid anilide in rats.

M F Khan1, B S Kaphalia, A Palafox, T R Jerrells, G A Ansari.   

Abstract

In the present investigation, we have studied the toxic potential of oleic acid anilide (OAA) and heated oleic acid anilide (HOAA) in relation to the toxic oil syndrome (TOS). Male Sprague-Dawley rats were given 250 mg/kg of OAA or HOAA in mineral oil by gavage, on alternate days for 2 weeks (total 7 doses). The control rats received an equal volume of mineral oil only. The animals were sacrificed at days 1, 7, and 28 following the last dose. Ratio of organ-to-body weight showed increases in spleen and kidney of HOAA and OAA treated rats, respectively, at day 1 while this ratio for liver in HOAA treated group showed a decrease at day 1. Among blood parameters, white blood cells increased in HOAA treated group at day 1 and in both OAA and HOAA groups at day 28. Mean corpuscular hemoglobin (MCH) and mean cell volume (MCV) also showed increases in the HOAA treated rats at days 7 and 28. Serum lactate dehydrogenase (LDH) decreased in both OAA and HOAA treated rats at day 1, while at day 7 the decrease was confined only to the HOAA group. Serum glutamic oxalacetic transaminase (GOT) and glutamic pyruvic transaminase (GPT) activities also decreased at most of the time points. Liver mitochondrial ATPase activity decreased in the HOAA group at day 7 and in the OAA group at day 28. Among serum immunoglobulins, IgA levels increased throughout the study but the changes were more pronounced in HOAA treated rats.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1991        PMID: 1759851     DOI: 10.1007/bf01183880

Source DB:  PubMed          Journal:  Arch Environ Contam Toxicol        ISSN: 0090-4341            Impact factor:   2.804


  27 in total

1.  Serum transaminase activity; observations in a large group of patients.

Authors:  M CHINSKY; G L SHMAGRANOFF; S SHERRY
Journal:  J Lab Clin Med       Date:  1956-01

2.  Chemical correlates of pathogenicity of oils related to the toxic oil syndrome epidemic in Spain.

Authors:  E M Kilbourne; J T Bernert; M Posada de la Paz; R H Hill; I Abaitua Borda; B W Kilbourne; M M Zack
Journal:  Am J Epidemiol       Date:  1988-06       Impact factor: 4.897

3.  HLA-DR3, DR4 increase in chronic stage of Spanish oil disease.

Authors:  J L Vicario; M Serrano-Rios; F San Andrés; A Arnaiz-Villena
Journal:  Lancet       Date:  1982-01-30       Impact factor: 79.321

4.  Toxic-allergic syndrome caused by ingestion of rapeseed oil denatured with aniline.

Authors:  J M Tabuenca
Journal:  Lancet       Date:  1981-09-12       Impact factor: 79.321

5.  A single reagent method of phosphate estimation in phosphatase(s) assay.

Authors:  M K Sapru; H Geetha; K T Shetty
Journal:  Indian J Biochem Biophys       Date:  1987-12       Impact factor: 1.918

6.  Chronic toxicity, oncogenic potential, and reproductive toxicity of p-nitroaniline in rats.

Authors:  R S Nair; C S Auletta; R E Schroeder; F R Johannsen
Journal:  Fundam Appl Toxicol       Date:  1990-10

7.  The microviscosity of liver plasma membranes of rats fed with oleoylanilide.

Authors:  R Pagani; M T Portoles; F G Gavilanes; P Garcia-Barreno; A M Municio
Journal:  Biochem J       Date:  1984-02-15       Impact factor: 3.857

Review 8.  The neurotoxicological aspects of the toxic oil syndrome (TOS) in Spain.

Authors:  H Altenkirch; G Stoltenburg-Didinger; C Koeppel
Journal:  Toxicology       Date:  1988-04       Impact factor: 4.221

9.  NADPH-diaphorase used to estimate alterations in the toxic rapeseed oil syndrome.

Authors:  P Sanz; P Villar; M Repetto
Journal:  Vet Hum Toxicol       Date:  1983-12

10.  Immunogenicity of fatty acid anilides in rabbits and the pathogenesis of the Spanish toxic oil syndrome.

Authors:  A Marquet; V Larraga; J L Diez; C Amela; J Rodrigo; E Muñoz; A Pestaña
Journal:  Experientia       Date:  1984-09-15
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