Inducible nitric oxide synthase expression by peritoneal macrophages in endometriosis-associated infertility

被引:81
作者
Osborn, BH
Haney, AF
Misukonis, MA
Weinberg, JB
机构
[1] Duke Univ, Med Ctr, Dept Obstet & Gynecol, Div Reprod Endocrinol & Infertil, Durham, NC 27705 USA
[2] Vet Affairs Med Ctr, Durham, NC 27705 USA
关键词
human infertility; endometriosis; inflammation; monocytes; macrophages; nitric oxide; reproductive immunology;
D O I
10.1016/S0015-0282(01)02940-5
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: Determine whether peritoneal macrophages from women with endometriosis-associated infertility express more inducible nitric oxide synthase (NOS2) and produce more NO than fertile controls. Design: Unblinded clinical study. Patient(s): Nine infertile women with endometriosis and nine normal fertile women undergoing laparoscopy. Intervention(s): Peritoneal fluid and macrophages were collected. Cells were also cultured with the NOS2 inducers interferon-alpha (IFN-alpha) or IFN-gamma plus lipopolysaccharide (LPS). Main Outcome Measure(s): Peritoneal fluid NO levels. peritoneal macrophage NOS activity, and peritoneal macrophage NOS2 protein expression. Result(s): NOS enzyme activity was higher in peritoneal macrophages from endometriosis patients. Immunoblots demonstrated NOS2 protein only in peritoneal macrophages from women with endometriosis. Peritoneal fluid NO concentration was similar in the two groups, but total peritoneal fluid NO content was higher in endometriosis patients. After 3 days' culture, peritoneal macrophages from women with endometriosis produced more NO in response to IFN-alpha or IFN-gamma plus LPS than controls. Conclusion(s): Peritoneal macrophages from women with endometriosis-associated infertility express higher levels of NOS2, have higher NOS enzyme activity, and produce more NO in response to immune stimulation in vitro. As high levels of NO adversely affect sperm, embryos, implantation, and oviductal function, reducing peritoneal fluid NO production or blocking NO effects may improve fertility in women with endometriosis. (Fertil Steril(R) 2002;77:46-51. (C) 2002 by American Society for Reproductive Medicine.).
引用
收藏
页码:46 / 51
页数:6
相关论文
共 41 条
[1]   Nitric oxide inhibits development of embryos and implantation in mice [J].
Barroso, RP ;
Osuamkpe, C ;
Nagamani, M ;
Yallampalli, C .
MOLECULAR HUMAN REPRODUCTION, 1998, 4 (05) :503-507
[2]  
Brannstrom M, 1997, HUM REPROD, V12, P51
[3]  
DMOWSKI WP, 1994, ACTA OBSTET GYN SCAN, V73, P7
[4]   Evidence for nitric oxide mediation of contractile activity in isolated strips of the human Fallopian tube [J].
Ekerhovd, E ;
Brannstrom, M ;
Alexandersson, M ;
Norstrom, A .
HUMAN REPRODUCTION, 1997, 12 (02) :301-305
[5]   Nitric oxide as a regulator of embryonic development [J].
Gouge, RC ;
Marshburn, P ;
Gordan, BE ;
Nunley, W ;
Huet-Hudson, YM .
BIOLOGY OF REPRODUCTION, 1998, 58 (04) :875-879
[6]   EARLY EMBRYO LOSS IS ASSOCIATED WITH LOCAL PRODUCTION OF NITRIC-OXIDE BY DECIDUAL MONONUCLEAR-CELLS [J].
HADDAD, EK ;
DUCLOS, AJ ;
BAINES, MG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (04) :1143-1151
[7]   Modulation of adenovirus-mediated gene transfer by nitric oxide [J].
Haddad, IY ;
Sorscher, EJ ;
Garver, RI ;
Hong, J ;
Tzeng, E ;
Matalon, S .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1997, 16 (05) :501-509
[8]   ALTERED MATURATION AND FUNCTION OF PERITONEAL-MACROPHAGES - POSSIBLE ROLE IN PATHOGENESIS OF ENDOMETRIOSIS [J].
HALME, J ;
BECKER, S ;
HASKILL, S .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1987, 156 (04) :783-789
[9]  
HANEY AF, 1983, FERTIL STERIL, V39, P310
[10]  
HANEY AF, 1981, FERTIL STERIL, V35, P696