CREMER J E, CALLAWAY S
Br J Ind Med. 1961 Oct;18(4):277-82. doi: 10.1136/oem.18.4.277.
The toxicity of tetra and trimethyl and propyl lead compounds has been studied after their administration to rats and rabbits. The toxicity to rats of tetramethyl lead has been compared with tetraethyl lead when given by inhalation. Both tetramethyl and tetrapropyl lead were found to be considerably less toxic than trimethyl and tripropyl lead. There was evidence of a slow rate of conversion of the tetra to the trialkyl lead forms in rats Although there was a distinct difference between the signs of poisoning seen after giving the methyl or the propyl lead compounds the primary site of action for both groups appeared to be the central nervous system. Some biochemical studies using slices of rat brain cortex showed that trimethyl and tripropyl lead inhibited the oxidation of glucose whereas tetramethyl and tetrapropyl lead were a hundred times less active in this respect.
已对四甲基、三甲基和丙基铅化合物给大鼠和兔子用药后的毒性进行了研究。通过吸入给药时,已将四甲基铅对大鼠的毒性与四乙基铅进行了比较。发现四甲基铅和四丙基铅的毒性均远低于三甲基铅和三丙基铅。有证据表明大鼠体内四烷基铅向三烷基铅形式的转化速度较慢。尽管给予甲基或丙基铅化合物后出现的中毒症状存在明显差异,但两组的主要作用部位似乎都是中枢神经系统。一些使用大鼠大脑皮层切片的生化研究表明,三甲基铅和三丙基铅会抑制葡萄糖的氧化,而在这方面四甲基铅和四丙基铅的活性要低一百倍。