Feeding Studies in Rats with Mineral Hydrocarbon Food Grade White Oils

Author:

Baldwin Michael K.1,Berry Peter H.1,Esdaile David J.1,Linnett Suzanne L.2,Martin John G.1,Peristianis George C.1,Priston Robert A.J.3,Simpson Barry J.E.4,Smith John D.5

Affiliation:

1. Shell Research Ltd., Sittingbourne Research Centre, Sittingbourne, Kent ME9 8AG, United Kingdom

2. Shell International Chemical Company, London, SE1 7NA, United Kingdom

3. Shell International Petroleum Maatschappij BV, 2501 AN, The Hague, The Netherlands

4. CONCAWE, B-1030, Brussels, Belgium

5. Shell International Petroleum Company Ltd., London, Sel 7NA, United Kingdom

Abstract

This investigation compared the effects of feeding rats diets containing food grade white oil processed by either conventional oleum treatment or the more modem method of catalytic hydrogenation. In two separate experiments, male or female Fischer-344 rats were given free access for 90 days to diets containing 0, 10, 100, 500, 5,000, 10,000, or 20,000 ppm of either oleum-treated white oil (OTWO) or hydrotreated white oil (HTWO). There were no mortalities and no adverse clinical signs associated with feeding either white oil. Treatment-related effects evidenced by hematological, clinical chemical, and pathological changes were generally dose-related and more marked in female than in male rats, and the OTWO caused a greater pathological response than the HTWO. Tissue residues of saturated hydrocarbons were up to 5.2 times higher in female rats than in males. Rats fed 5,000 ppm or more of either white oil showed dose-related alterations in several hematological and clinical chemistry variates associated mainly with hepatic damage or functional alteration. At necropsy, mesenteric lymph nodes were enlarged, and increases in weight of liver, kidney, and spleen were significant. Microscopic changes were characterized by multifocal lipogranulomata in mesenteric lymph node and liver. No changes were observed in rats fed OTWO or HTWO for 90 days at dietary concentrations of 10 or 100 ppm, equivalent to a minimum intake of 0.65 and 6.4 mg/kg/day, respectively. Differences in degree of pathological response associated with each oil may have been due to their differences in specification rather than processing method.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

Reference41 articles.

1. Absorption of aliphatic hydrocarbons by rats

2. Hepatic damage associated with mineral oil deposits.

3. British Pharmacopoeia ( 1988 ). Monographs. Medicinal and Pharmaceutical Substances . Her Majesty's Stationery Office, London , pp. 415-416.

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