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      Short term toxicity study in rats dosed with pulegone and menthol

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      Toxicology Letters
      Elsevier BV

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          Abstract

          Pulegone and menthol, components of peppermint oil, were investigated in rats. The substances were administered by gavage for 28 days at 0, 20, 80, 160 mg pulegone and 0, 200, 400, 800 mg menthol/kg body wt./day, respectively. At the two highest doses, pulegone induced atonia, decreased blood creatinine content, lowered terminal body weight and caused histopathological changes in the liver and in the white matter of cerebellum. For menthol at all dose levels a significant increase in absolute and relative liver weights and vacuolisation of hepatocytes was found. No sign of encephalopathy was observed in rats given menthol. The no effect level for pulegone was 20 mg/kg body wt./day and for menthol less than 200 mg/kg body wt./day.

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          Hepatotoxicity and pulmonary toxicity of pennyroyal oil and its constituent terpenes in the mouse.

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            Pennyroyal oil poisoning and hepatotoxicity.

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              Short term toxicity study in rats dosed with peppermint oil.

              Peppermint oil was given p.o. to groups of 10 male and 10 female rats at dosage levels of 0, 10, 40 and 100 mg/kg bw/day respectively for 28 days. Histopathological changes in the white matter of the cerebellum especially were seen at dose levels of 40 and 100 mg/kg bw/day and consisted of cyst-like spaces scattered in the white matter. There were no obvious signs of clinical symptoms due to the encephalopathy.
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                Author and article information

                Journal
                Toxicology Letters
                Toxicology Letters
                Elsevier BV
                03784274
                December 1983
                December 1983
                : 19
                : 3
                : 207-210
                Article
                10.1016/0378-4274(83)90120-0
                6658833
                ab21d9f8-84a6-4a5d-9988-0c99fe9706df
                © 1983

                https://www.elsevier.com/tdm/userlicense/1.0/

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