Hassall C D, Gandolfi A J, Brendel K
Toxicology. 1983 Mar-Apr;26(3-4):285-94. doi: 10.1016/0300-483x(83)90089-6.
Addition of halogenated vinyl cysteine conjugates to isolated rabbit kidney tubule suspensions resulted in a decrease in the active transport of para-aminohippuric acid (PAH) and tetraethylammonium bromide (TEA). At 10(-5) M vinyl cysteine conjugate, tubule to medium accumulation ratios (T/M) were similar to those of controls while at 10(-3) M the T/M values decreased to 1, indicating complete inhibition of active accumulation of PAH or TEA. The decreased active transport was not caused by inhibition of mitochondrial oxidation since incubations in the presence of 10(-3) M halogenated vinyl cysteine did not inhibit tubule O2 utilization or production of 14CO2 from [14C]glucose or [14C]succinate. A mechanism is proposed whereby toxicity may result from covalent binding of an active intermediate, produced by enzyme cleavage, to membrane associated nucleophilic groups thereby decreasing active transport.
向分离的兔肾小管悬浮液中添加卤化乙烯基半胱氨酸缀合物会导致对氨基马尿酸(PAH)和溴化四乙铵(TEA)的主动转运减少。在10⁻⁵ M乙烯基半胱氨酸缀合物时,肾小管与培养基的积累比(T/M)与对照组相似,而在10⁻³ M时,T/M值降至1,表明PAH或TEA的主动积累被完全抑制。主动转运的降低不是由线粒体氧化抑制引起的,因为在10⁻³ M卤化乙烯基半胱氨酸存在下孵育不会抑制肾小管对氧气的利用或[¹⁴C]葡萄糖或[¹⁴C]琥珀酸产生¹⁴CO₂。提出了一种机制,即毒性可能源于酶裂解产生的活性中间体与膜相关亲核基团的共价结合,从而降低主动转运。