Smith P L, Chiossone D C, McCafferty G P
Department of Drug Delivery, Smith Kline and French Laboratories, King of Prussia, PA 19406-0939.
Naunyn Schmiedebergs Arch Pharmacol. 1990 Jan-Feb;341(1-2):94-100. doi: 10.1007/BF00195064.
The effects of peptidoleukotriene C4 (LTC4) on electrical properties and Na+ and Cl- fluxes in the presence or absence of the LTD4/LTE4 antagonist, 2(S)-hydroxy-3-(R)-carboxyethylthio)-3-[2-(8-phenyloctyl)phe nyl] propanoic acid (SK&F 104353) were investigated in stripped ileal mucosa from rabbits placed in Ussing chambers. Results from this study demonstrate that serosal addition of LTC4 produced a dose-dependent increase in short-circuit current (Isc) which is not affected by pretreatment of the tissue with SK&F 104353 (0.1 microM). The concentration of LTC4 which produced an increase in Isc of 4 mu Eq/h.cm2 was 181 nM in the absence of SK&F 104353 and this value did not differ significantly from the value of 212 nM in the presence of SK&F 104353 (0.1 microM). SK&F 104353 (0.1 microM) reduced the increase in Isc elicited by LTD4 and LTE4 by greater than 95%. Mucosal addition of LTC4 failed to alter Isc. The time course of the increase in Isc in response to LTC4 is qualitatively similar to that seen with both LTD4 and LTE4. Increases in Isc produced by LTC4 are not inhibited by removal of Ca2+ from the serosal bathing solution but are inhibited by pretreatment of the tissue with indomethacin (1 microM). The histamine receptor antagonist, mepyramine, reduced the change in Isc resulting from stimulation with LTC4 by 20% while the cholinergic antagonist, atropine, and the excitable tissue Na+ channel blocker, tetrodotoxin, were without effect. Measurement of unidirectional and net Na+ and Cl- fluxes revealed that LTC4 reduces Na+ and Cl- absorption and that subsequent addition of PGE1 produced no further decrease.(ABSTRACT TRUNCATED AT 250 WORDS)
在置于尤斯灌流小室的兔离体回肠黏膜中,研究了肽白三烯C4(LTC4)在存在或不存在白三烯D4/白三烯E4拮抗剂2(S)-羟基-3-(R)-羧乙基硫基)-3-[2-(8-苯基辛基)苯基]丙酸(SK&F 104353)的情况下,对电特性以及钠和氯通量的影响。本研究结果表明,向浆膜侧添加LTC4会使短路电流(Isc)呈剂量依赖性增加,而用SK&F 104353(0.1微摩尔)预处理组织对此无影响。在不存在SK&F 104353时,使Isc增加4微当量/小时·平方厘米的LTC4浓度为181纳摩尔,此值与存在SK&F 104353(0.1微摩尔)时的212纳摩尔值无显著差异。SK&F 104353(0.1微摩尔)使白三烯D4和白三烯E4引起的Isc增加降低超过95%。向黏膜侧添加LTC4未能改变Isc。LTC4引起的Isc增加的时间进程在定性上与白三烯D4和白三烯E4所见相似。LTC4引起的Isc增加不受从浆膜浴液中去除钙离子的抑制,但受吲哚美辛(1微摩尔)预处理组织的抑制。组胺受体拮抗剂美吡拉敏使LTC4刺激引起的Isc变化降低20%,而胆碱能拮抗剂阿托品和可兴奋组织钠通道阻滞剂河豚毒素则无作用。单向和净钠及氯通量的测量表明,LTC4减少钠和氯的吸收,随后添加前列腺素E1未进一步降低吸收。(摘要截短于250字)