Myers S I, Haley-Russell D, Bartula L L, Nabzdyk W
Department of Surgery, University of Texas Medical School, Houston 77030.
Prostaglandins. 1990 Aug;40(2):165-85. doi: 10.1016/0090-6980(90)90082-7.
Gallbladder prostanoid (PG) synthesis and histologic inflammatory changes were compared after 6, 24, and 72 hours of bile duct ligation (BDL) or cystic duct ligation (CDL) in the male rabbit. At each time interval the gallbladder was scored for degree of acute inflammation, examined by radiochromatography for endogenous PG synthesis and analyzed by ANOVA. BDL induced progressive increases in acute inflammation whereas prostanoid synthesis significantly increased only after the 6 and 72 hour groups. Indomethacin treatment inhibited PG synthesis in all BDL groups but only decreased the inflammation score in the 6 and 24 hour BDL groups. CDL did not induce progressive gallbladder inflammatory changes or prostanoid synthesis. These data show that prostanoids are intimately involved with the development of early acute gallbladder inflammation following BDL. Inhibition of PG synthesis could attenuate or retard the progression of early acute gallbladder inflammation if started prior to development of established disease.
在雄性兔中,比较胆管结扎(BDL)或胆囊管结扎(CDL)6、24和72小时后胆囊前列腺素(PG)合成及组织学炎症变化。在每个时间间隔,对胆囊的急性炎症程度进行评分,通过放射色谱法检测内源性PG合成,并进行方差分析。BDL导致急性炎症进行性加重,而前列腺素合成仅在6小时和72小时组后显著增加。吲哚美辛治疗抑制了所有BDL组的PG合成,但仅降低了6小时和24小时BDL组的炎症评分。CDL未诱导胆囊炎症进行性变化或前列腺素合成。这些数据表明,前列腺素与BDL后早期急性胆囊炎症的发展密切相关。如果在疾病确立之前开始抑制PG合成,可能会减轻或延缓早期急性胆囊炎症的进展。