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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>14</Volume><Issue>4</Issue></Journal><ArticleTitle>17β-estradiol and progesterone upregulate cyclooxygenase-2 expression in the human gingival fibroblasts</ArticleTitle><FirstPage>190</FirstPage><LastPage>196</LastPage><AuthorList><Author><FirstName></FirstName><LastName>Ostad S. N.</LastName></Author><Author><FirstName></FirstName><LastName>Motahhary P.</LastName></Author><Author><FirstName></FirstName><LastName>Beshkar M.</LastName></Author><Author><FirstName></FirstName><LastName>Ghahremani M.H.</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>10</Month><Day>06</Day></PubDate></History><Abstract>Gingivitis is associated with 60-75% of all pregnancies and elevated levels of 17&amp;#946;-estradiol and progesterone is known to increase gingival inflammation and the proinflammatory prostaglandins in the human gingiva. Since cyclooxygenase-2 (COX-2) is an inducible enzyme responsible for the production of prostaglandins at the sites of inflammation, it is plausible to hypothesize that 17&amp;#946;- estradiol and progesterone could contribute to gingival inflammation by upregulation of COX-2 expression and subsequent prostaglandin formation. To examine this hypothesis, primary cultures of human gingival fibroblasts (HGFs) from either sex were established. The cells were treated with different concentrations (10-5, 10-7, and 10-9 M) of 17&amp;#946;-estradiol and progesterone, and expression of COX-2 protein was detected immunocytochemically. The growth potential and proliferation of these cells were studied using trypan blue exclusion method and MTT assay. The results show that both 17&amp;#946;-estradiol and progesterone upregulate COX-2 expression in the HGFs significantly. In addition, progesterone is more effective than 17&amp;#946;-estradiol to induce COX-2 expression at 10-5M but not at lower concentration (10-9M). Furthermore, cells prepared from either sex do not show any difference in COX-2 expression following hormone treatment and neither hormones show any changes in proliferation of these cells. In conclusion, the results of this investigation clearly illustrate significant regulatory effects of 17&amp;#946;-estradiol and progesterone on COX-2 expression in the cultured HGFs. Thus, one possible pathogenetic mechanism of the female sex hormone-associated gingivitis in vivo may be the synthesis of proinflammatory prostaglandins via upregulation of COX-2 expression by gingiva in response to elevated levels of circulating estrogens and progesterone.</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/288</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/288/288</pdf_url></Article></Articles>
