Nagao T, Ito M, Suzuki Y
Department of Pharmacology, Faculty of Pharmacy, Meijo University.
Nihon Jinzo Gakkai Shi. 1991 Nov;33(11):1071-9.
The present study was designed to examine the suppressive action of Lipo PGE1 on the development of accelerated passive Heymann nephritis in rats. Lipo PGE1, given i.v. twice a day at 20, 40 and 80 micrograms/kg from the day after immunization with rabbit gamma-globulin (gamma-G) (the 1st day), remarkably inhibited the urinary protein excretion as well as glomerular histopathological changes such as thickening of basement membrane and spike formation. Lipo PGE1 at doses which the development of nephritis was suppressed, significantly inhibited the elevation of plasma antibody titer against rabbit gamma-G from the day before the appearance of the heavy proteinuria and apparently reduced the deposition of rat IgG in glomeruli. In addition, a single i. v. administration of Lipo PGE1 remarkably recovered the diminished renal blood flow induced by nephritis. These results suggest that intravenous Lipo PGE1 is effective in suppressing the development of the experimental membranous nephropathy. This agent may mainly prevent the development of nephritis by reducing the deposition of rat IgG in glomeruli via the suppression of host antibody formation. Furthermore, the increasing action of Lipo PGE1 on renal blood flow may be also in part related to a beneficial effect of this agent.
本研究旨在探讨前列腺素E1脂质体(Lipo PGE1)对大鼠被动型Heymann肾炎加速发展的抑制作用。从用兔γ球蛋白(γ-G)免疫后的第二天(第1天)开始,以20、40和80微克/千克的剂量每天静脉注射Lipo PGE1两次,显著抑制了尿蛋白排泄以及肾小球组织病理学变化,如基底膜增厚和钉突形成。在抑制肾炎发展的剂量下,Lipo PGE1从重度蛋白尿出现前一天开始,显著抑制了抗兔γ-G血浆抗体滴度的升高,并明显减少了大鼠IgG在肾小球中的沉积。此外,单次静脉注射Lipo PGE1可显著恢复由肾炎引起的肾血流量减少。这些结果表明,静脉注射Lipo PGE1对抑制实验性膜性肾病的发展有效。该药物可能主要通过抑制宿主抗体形成,减少大鼠IgG在肾小球中的沉积来预防肾炎的发展。此外,Lipo PGE1对肾血流量的增加作用也可能部分与其有益作用有关。