Delgado I F, Carvalho R R, Nogueira A C, Mattos A P, Figueiredo L H, Oliveira S H, Chahoud I, Paumgartten F J
Department of Pharmacology and Toxicology, National Institute of Health Quality Control, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Food Chem Toxicol. 1993 Jan;31(1):31-5. doi: 10.1016/0278-6915(93)90175-x.
beta-Myrcene is a constituent of many essential oils that have been used extensively in cosmetic fragrances and as flavouring additives in the food industry. Recently, this monoterpene was reported to be an analgesic substance. Notwithstanding the widespread use of myrcene and essential oils containing myrcene in perfume and in food additives, experimental studies on the toxicity of this substance are still scarce. This study aimed to provide data on the embryo-foetotoxic potential of beta-myrcene in the rat. beta-Myrcene (0.25, 0.5 and 1.2 g/kg) in corn oil was given orally to Wistar rats from day 6 to 15 of pregnancy. Caesarean sections were performed on day 20 of pregnancy, and the number of resorptions and implantation sites were recorded. Foetuses were weighed, examined for external malformations, and fixed for visceral examination, or cleared and stained with Alizarin Red S for skeleton evaluation. No adverse effects were seen with the two lowest doses tested. Decreased weight gain during the first days of treatment and the death of one of 29 treated dams indicated that the highest dose tested (1.2 g/kg) induced maternal toxicity. A higher incidence of signs of retardation and of anomalies in the foetal skeleton indicated that 1.2 g/kg was also toxic to the rat embryo. From the data presented in this paper the no-observed-adverse-effect level for embryo-foetotoxicity could be set at 0.5 g beta-myrcene/kg body weight.
β-月桂烯是许多香精油的成分,这些香精油已广泛用于化妆品香料以及作为食品工业中的调味添加剂。最近,据报道这种单萜是一种镇痛物质。尽管月桂烯和含月桂烯的香精油在香水和食品添加剂中广泛使用,但关于该物质毒性的实验研究仍然很少。本研究旨在提供β-月桂烯对大鼠胚胎-胎儿毒性潜力的数据。在妊娠第6天至15天,将玉米油中的β-月桂烯(0.25、0.5和1.2 g/kg)口服给予Wistar大鼠。在妊娠第20天进行剖腹产,记录吸收和着床部位的数量。对胎儿称重,检查外部畸形,并固定进行内脏检查,或进行透明处理并用茜素红S染色以评估骨骼。在所测试的两个最低剂量下未观察到不良反应。治疗开始几天体重增加减少以及29只受试母鼠中有1只死亡表明所测试的最高剂量(1.2 g/kg)引起了母体毒性。胎儿骨骼发育迟缓迹象和异常的发生率较高表明1.2 g/kg对大鼠胚胎也有毒性。根据本文提供的数据,胚胎-胎儿毒性的未观察到不良反应水平可设定为0.5 gβ-月桂烯/千克体重。