Soory M, Gower D B
Department of Periodontology, GKT Dental Institute, King's College Hospital, London.
J Periodontal Res. 1998 Nov;33(8):439-47. doi: 10.1111/j.1600-0765.1998.tb02342.x.
The aim of this investigation was to study the effects of prostaglandins E1 and E2 (PGE1 and PGE2) on the accumulation, release and metabolism of C19 steroids by human gingival fibroblasts (HGF) and gingivae, due to their anabolic potential in inflammatory repair. For the accumulation studies, HGF were incubated with 14C-testosterone at timed intervals and the cell-digests analysed for label uptake. The release of 5 alpha-dihydrotestosterone (DHT) by HGF was studied by preincubating the cells with 14C-DHT and reincubating with cold steroid to quantify its release at timed intervals. For the metabolic studies, HGF/gingival tissue were incubated with 14C-testosterone and serial concentrations of PGE1 and PGE2 to study their effects on the synthesis of DHT. The incubations were terminated at 24 h and extracted metabolites were analysed and quantified. The accumulation of 14C-testosterone by human gingival fibroblasts was elevated 3-fold at 24 h by PGE1 (n = 3, p < 0.001; 1-way ANOVA). The release of 14C-DHT was enhanced nearly 2-fold by PGE1 (n = 3, p < 0.001), compared with controls. Both PGE1 and PGE2 caused 2-fold increases in DHT synthesis by HGF and 3-fold increases in 4-androstenedione formation (n = 4, p < 0.001). With the tissue incubations PGE1/PGE2 caused 3-4 fold increases in DHT synthesis (n = 5, p < 0.005; Wilcoxon signed rank statistic for paired observations). Direct stimulation of the accumulation/release and metabolism of these steroids by prostaglandins in gingivae may contribute to the anabolic potential of androgens in inflammatory periodontal disease.
本研究的目的是探讨前列腺素E1和E2(PGE1和PGE2)对人牙龈成纤维细胞(HGF)和牙龈中C19类固醇的积累、释放和代谢的影响,因为它们在炎症修复中具有合成代谢潜力。在积累研究中,将HGF与14C-睾酮在不同时间间隔孵育,并对细胞消化物进行标记摄取分析。通过将细胞与14C-DHT预孵育,然后与冷类固醇再孵育,以在不同时间间隔定量其释放,来研究HGF对5α-二氢睾酮(DHT)的释放。在代谢研究中,将HGF/牙龈组织与14C-睾酮以及不同浓度的PGE1和PGE2孵育,以研究它们对DHT合成的影响。孵育在24小时终止,对提取的代谢物进行分析和定量。PGE1使24小时时人牙龈成纤维细胞对14C-睾酮的积累增加了3倍(n = 3,p < 0.001;单因素方差分析)。与对照组相比,PGE1使14C-DHT的释放增加了近2倍(n = 3,p < 0.001)。PGE1和PGE2均使HGF合成DHT增加2倍,使4-雄烯二酮的形成增加3倍(n = 4,p < 0.001)。在组织孵育中,PGE1/PGE2使DHT合成增加3-4倍(n = 5,p < 0.005;配对观察的Wilcoxon符号秩统计量)。前列腺素对牙龈中这些类固醇的积累/释放和代谢的直接刺激可能有助于雄激素在炎症性牙周病中的合成代谢潜力。