Toxicological assessment of heavy straight run naphtha in a repeated dose/reproductive toxicity screening test

• Published in: International journal of toxicology Vol. 33; no. 1 Suppl; p. 52S
• Main Authors: McKee, Richard H, Steup, David, Schreiner, Ceinwen, Podhasky, Paula, Malley, Linda A, Roberts, Linda
• Format: Journal Article
• Language: English
• Published: United States 01.01.2014
• Subjects: Alkanes - toxicity; Animals; Body Weight - drug effects; Dose-Response Relationship, Drug; Female; Fertility - drug effects; Kidney - drug effects; Kidney - metabolism; Liver - drug effects; Liver - metabolism; Male; Organ Size - drug effects; Petroleum - toxicity; Rats; Rats, Sprague-Dawley; Reproduction - drug effects; Toxicity Tests - methods; naphtha reproductive toxicity; toxicity assessment; repeated dose toxicity; OECD 422; heavy straight run naphtha; gasoline; CAS number 64741-41-9
• ISSN: 1092-874X
• DOI: 10.1177/1091581813504224

Gasoline blending stocks (naphthas) are comprised of normal, iso- and cycloparaffins and aromatic hydrocarbons with carbon numbers ranging from C4 to C12. Heavy straight run naphtha (HSRN, CAS number 64741-41-9) was selected for toxicity screening because substances of this type contain relatively high levels (28%) of cycloparaffins by comparison to other naphtha streams and the data complement toxicity information on other gasoline blending streams. Rats were exposed by inhalation to wholly vaporized material at levels of approximately 100, 500, or 3000 parts per million (ppm) daily to screen the potential for systemic toxicity, neurotoxicity, reproductive toxicity, and developmental effects to postnatal day 4. All animals survived the treatment period. Principal effects of repeated exposure included increased liver weights in males and females, increased kidney weights in males, and histological changes in the thyroid, secondary to liver enzyme induction. These changes were not considered to be toxicologically meaningful and are not relevant to humans. There were no treatment-related effects in functional observation tests or motor activity; no significant reductions in fertility or changes in other reproductive parameters; and no evidence of developmental toxicity in offspring. The overall no observed adverse effect concentration was 3000 ppm (approximately 13, 600 mg/m(3)). In conclusion the HSRN effects on liver and kidney are consistent with the results of other studies of volatile fractions or other naphthas or formulated gasoline, and there were no HSRN effects on neurological developmental or reproductive parameters.