Riley R T, Norred W P, Dorner J W, Cole R J
J Toxicol Environ Health. 1985;15(6):779-88. doi: 10.1080/15287398509530704.
Pig kidney renal epithelial cells (LLC-PK1) in culture were used to determine the effects of cyclopiazonic acid (CPA) on the uptake of the transmembrane potential probe, [3H]tetraphenylphosphonium bromide (TPP+). CPA had a significant stimulatory effect on TPP+ accumulation, which occurred in a dose-related manner. TPP+ accumulation in the presence of CPA was significantly reduced by high-potassium media (HK) and carbonylcyanide m-chlorophenylhydrazone (CCCP), but neither HK nor the protonophore CCCP, could completely abolish the stimulatory effect of CPA. The apparent transmembrane potential difference (delta psi), calculated based on the difference in accumulation of TPP+ in low-potassium and HK media, ranged from -55.9 to -85.7 mV for control cells and -89.4 to -109.0 mV for CPA-treated cells (20 mg CPA/I). The mechanism of CPA stimulation of TPP+ accumulation was not known. However, it was hypothesized that the effect could be a result of alterations in ion pumps or altered membrane permeability. The fact that the stimulatory effect could not be completely abolished by high potassium or CCCP suggested that there was some interaction between CPA and TPP+ or there were sites of TPP+ accumulation that were insensitive to K+ and H+ permeability.
培养的猪肾肾上皮细胞(LLC-PK1)被用于确定环匹阿尼酸(CPA)对跨膜电位探针[3H]四苯基溴化膦(TPP+)摄取的影响。CPA对TPP+的积累有显著的刺激作用,且呈剂量相关。在高钾培养基(HK)和羰基氰化物间氯苯腙(CCCP)存在的情况下,CPA存在时TPP+的积累显著减少,但HK和质子载体CCCP均不能完全消除CPA的刺激作用。根据低钾和HK培养基中TPP+积累的差异计算出的表观跨膜电位差(δψ),对照细胞为-55.9至-85.7 mV,CPA处理的细胞(20 mg CPA/I)为-89.4至-109.0 mV。CPA刺激TPP+积累的机制尚不清楚。然而,据推测,这种作用可能是离子泵改变或膜通透性改变的结果。高钾或CCCP不能完全消除刺激作用这一事实表明,CPA与TPP+之间存在某种相互作用,或者存在对K+和H+通透性不敏感的TPP+积累位点。