Changes in molecular weight of hyaluronan and hyaluronidase activity in uterine cervical mucus in cervical ripening

References

• von Maillot VK, Stuhlsatz HW, Mohanaradhakrishnan V, Greiling H. Changes in the glycosaminoglycans distribution pattern in the human uterine cervix during pregnancy and labor. Am J Obstet Gynecol 1979; 135: 503–6.
   Google Scholar
• Osmers R, Rath W, Pflanz MA, Kuhn W, Stuhlsatz HW, Szeverenyi M. Glycosaminoglycans in cervical connective tissue during pregnancy and parturition. Obstet Gynecol 1996; 81: 88–92.
   Google Scholar
• West DC, Hampson IN, Arnold F, Kumar S. Angiogenesis induced by degradation products of hyaluronic acid. Science 1985; 228: 1324–6.
   Google Scholar
• Hiro D, Ito A, Mori Y. Hyaluronic acid is an endogenous inducer of interleukin-1 production by human monocytes and rabbit macrophages. Biochem Biophys Res Commun 1986; 140: 715–22.
   Google Scholar
• Kobayashi H, Terao T. Hyaluronic acid-specific regulation of cytokines by human uterine fibroblasts. Am J Physiol 1997; 2734 Pt 1 c1: 151–9.
   Google Scholar
• El Maradny E, Kanayama N, Kobayashi H, Hossain B, Khatun S, Liping S et al. The role of hyaluronic acid as a mediator and regulator of cervical ripening. Hum Reprod 1997; 12: 1080–8.
   Google Scholar
• McKee CM, Lowenstein CJ, Horton MR, Wu J, Bao C, Chin BY et al. Hyaluronan fragments induce nitric-oxide synthase in murine macrophages through a nuclear factor kappaB-dependent mechanism. J Biol Chem 1997; 272: 8013–18.
   Google Scholar
• Li Z. [Clinical study on uterine cervix ripening with hyaluronidase and animal experimentation on mechanism of action] (Chinese with English abstract). Chung Hua Fu Chan Ko Tsa Chih 1993; 28: 592–4.
   Google Scholar
• Li WJ, Li ZL, Ha KW. Effect of hyaluronidase on cervical ripening. Chin Med J Engl 1994; 10: 552–3.
   Google Scholar
• Gupta T, Verma NK, Sood A. Effects of intracervical injection of hyaluronidase in primigravidae during labour. J Indian Med Assoc 1994; 92: 47–8.
   Google Scholar
• Ogawa M, Hirano H, Tsubaki H, Kodama H, Tanaka T. The role of cytokines in cervical ripening: correlations between the concentrations of cytokines and hyaluronic acid in cervical mucus and the induction of hyaluronic acid production by inflammatory cytokines by human cervical fibroblasts. Am J Obstet Gynecol 1998; 179: 105–10.
   Google Scholar
• Ogamo A, Matsuzaki K, Uchiyama H, Nagasawa K. Preparation and properties of fluorescent glycosaminoglycuronans labeled with 5-aminofluorescein. Carbohydr Res 1982; 105: 69–85.
   Google Scholar
• Titus JA, Haugland R, Sharrow SO, Segal DM. Texas Red, a hydrophilic, red-emitting fluorophore for use with fluorescein in dual parameter flow microfluorometric and fluorescence microscopic studies. J Immunol Methods 1982; 50: 193–204.
   Google Scholar
• Miyauchi S, Morita M, Kuramoto K, Horie K. Hyaluron- an and chondroitin sulfate in rabbit tears. Curr Eye Res 1996; 15: 131–5.
   Google Scholar
• Obara M, Hirano H, Ogawa M, Tsubaki H, Yoshida Y et al. Does chondroitin sulfate defend the human uterine cervix against ripening in threatened premature labor? Am J Obstet Gynecol 2000; 182: 334–9.
   Google Scholar
• Tanaka K, Nakamura T, Takagaki K, Funahashi M, Saito Y, Endo M. Regulation of hyaluronate metabolism by progesterone in cultured fibroblasts from the human uterine cervix. FEBS Lett 1997; 402: 223–6.
   Google Scholar
• Sampson PM, Rochester CL, Freundlich B, Elias JA. Cytokine regulation of human lung fibroblast hyaluronan (hyaluronic acid) production. Evidence for cytokine-regulated hyaluronan (hyaluronic acid) degradation and human lung fibroblast-derived hyaluronidase. J Clin Invest 1992; 90: 1492–503.
   Google Scholar
• Konttinen YT, Saari H, Nordstrom DC. Effect of interleukin-1 on hyaluronate synthesis by synovial fibroblastic cells. Clin Rheumatol 1991; 10: 151–4.
   Google Scholar