ABSTRACT
The present study was undertaken to provide date on acute toxicity of ß-myrcene, a peripheral analgesic substance found in the essential oils of several plants. Although myrcene has long been used in perfumes and as a food additive, there is almost no information on its toxicological hazards. The acute oral toxicity of myrcene was low in rodents, with with approximate lethal doses (ALD) of 5.06g/Kg body weight for mice and greater than 11.39 g/Kg body weight for rats. Necropsy data did not reveal any relevant alteration in rats but histophatology findings in mice suggested that the liver and stomach may be target organs for myrcene toxicity after oral administration. Myrcene is highly irritant to the peritoneum, and deaths after intraperitoneal injection of this monoterpene in rats (ALD 5.06 g/Kg body weight) and in mice (ALD 2.25 g/Kg body weight) were probably due to drug-induced chemical peritonitis
Subject(s)
Animals , Mice , Rats , Male , Female , Analgesics , Acute Disease , Kidney/drug effects , Liver/drug effects , Peritonitis/chemically induced , Rats, WistarABSTRACT
The new field of immunotoxicology may be expected to gain considerable importance in the assessment of possible toxic risks of chemicals. It is an applied science based on the considerable experience gained in basic immunological research within the last decades. Some possibilities are discussed and procedures suggested for evaluating toxic effects induced by chemicals (including drugs) in experimental animals and man. Original data are presented on thymus atrophy induced in the offspring of rats treated on day 10 of pregnancy with the virostatic drug acyclovir. Experimental data are presented on the effect of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on the distribution of lymphocyte populations (peripheral blood) in primates in vivo and in vitro, as determined with monoclonal antibodies as probes