Efek Kadar Serum Estradiol Fase Bleeding Siklus Menstruasi Pada Aktivitas Fibroblas Dermis Manusia
DOI:
https://doi.org/10.33820/mdvi.v45i1.6Abstract
Pembedahan elektif selama fase bleeding siklus menstruasi sering dihindari terkait gangguan koagulasi. Salah satu hormon yang berhubungan dengan proses penyembuhan luka adalah estrogen. Kadar estrogen berfluktuasi sepanjang siklus menstruasi dan berada pada kadar terendah selama fase bleeding. Penelitian eksperimental ex vivo dilakukan pada 16 perempuan berusia 18–40 tahun yang memiliki siklus menstruasi teratur. Darah vena subjek diambil sebanyak 5ml pada fase bleeding dan ovulasi. Kemampuan penyembuhan luka dari masing-masing serum dinilai dengan mengukur proliferasi fibroblas dan deposisi kolagen fibroblas kulit. Ovulasi ditentukan dengan uji pakis saliva, kadar estradiol serum diukur menggunakan Cobas Elecsys®, proliferasi fibroblas menggunakan MTT assay, dan deposisi kolagen dengan sirius red. Hasil penelitian menunjukkan rerata kadar serum estradiol pada fase bleeding dan ovulasi berturut-turut adalah 29,6±10,5pg/dl dan 180,1±164,5pg/dl. Rerata indeks proliferasi fibroblas yang dipajankan pada fase bleeding dan ovulasi adalah 1,09±0,63 dan 1,44±0,66. Rerata densitas optik kolagen fibroblas yang terpajan serum fase bleeding dan ovulasi adalah 0,47±0,2 dan 0,54±0,14. Seluruhnya menunjukkan perbedaan yang bermakna secara statistik (p<0,05). Serum fase bleeding memiliki kemampuan penyembuhan luka yang lebih rendah dibandingkan dengan serum fase ovulasi. Kebijakan untuk tidak melakukan pembedahan elektif selama fase bleeding, selain terkait dengan gangguan pembekuan darah juga terkait dengan proses penyembuhan luka.
Kata Kunci:Â menstruasi, estradiol, ovulasi, proliferasi fibroblas, deposisi kolagen, penyembuhan luka
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References
2. Sharief LA, Lawrie AS, Mackie IJ, Halimeh IJ, Kappert G, Smith C, dkk. Plasma factor XIII level variations during menstrual cycle. Blood Coagul Fibrinolysis.2016;20;26:5.
3. Hanci V, AyoÄŸlu H, Yilmaz M, Yurtlu S, Okyay RD, ErdoÄŸan G, dkk. Effect of menstrual cycle on the injection pain due to propofol. Eur J Anaesthesiol. 2010;27:425-7.
4. Rahimi M, Kalani P. The effects of the menstrual cycle on the hemodynamic responsse to laryngoscopy and tracheal intubation [abstract]. Eur J Anaesthesiol.2014;31:55.
5. Philips N, Devaney J. Beneficial regulation of type I collagen and matrixmetalloproteinase-1 expression by estrogen, progesterone, and its combination in skin fibroblast. J Am Aging Assoc. 2003;26:59-62.
6. Markiewicz M, Znoyko S, Stawski L, Ghatnekar A, Gilkeson G, Trojanowska M. A role for estrogen receptor-α and estrogen receptor-β in collagen biosynthesis in mouse skin. J Invest Dermatol.2013;133:120-7.
7. Qu LD, Abe M, Yokoyama Y, Ishikawa O. Effects of 17β-estradiol on matrix metalloproteinase-1 synthesis by human dermal fibroblasts. Maturitas. 2006;54:39-46.
8. Bottai G, Mancina R, Muratori M, Di Gennaro P, Lotti T. 17β-estradiol protects human skin fibroblasts and keratinocytes against oxidative damage. J Eur Acad Dermatol Venereol. 2013;27:1236-43.
9. James TJ, Hughes MA, Cherry GW, Taylor RP. Evidence of oxidative stress in chronic venous ulcers. Wound Repair Regen. 2003;11:172-6.
10. Wlaschek M, Scharffetter-Kochanek K. Oxidative stress in chronic venous leg ulcers. Wound Repair Regen. 2005;13:452-61.
11. Hall G, Phillips TJ. Estrogen and skin: the effects of estrogen, menopause, and hormone replacement therapy on the skin. J Am Acad Dermatol. 2005;53:555-68.
12. Stricker R, Eberhart R, Chevailler MC, Quinn FA, Bischof P, Stricker R. 2006, Establishment of detailed reference values for luteinizing hormone, follicle stimulating hormone, estradiol, and progesterone during different phases of the menstrual cycle on the Abbot ARCHITECT® analyzer. Clin Chem Lab Med. 2006;44:883-7.
13. Henriet P, Gaide Chevronnay HP, Marbaix E. The endocrine and paracrine control of menstruation. Mol Cell Endocrinol. 2012;358:197-207.
14. Adkins JN, Vamum SM, Auberry KJ, Moore RJ, Angell NH, Smith RD, dkk. Toward a human blood serum proteome. Mol Cell Proteomics. 2002;1:947-55.
15. Dighe AS, Sluss PM. Improved detection of serum estradiol after sample extraction procedure. Clin Chem. 2004;50:764-6.
16. Li Y, Fan J, Chen M, Woodley DT. Transforming growth factor-alpha: a major human serum factor that promotes human keratinocyte migration. J Invest Dermatol. 2006;126:2096-105.
17. Brincat MP, Baron YM, Galea R. Estrogens and the skin. Climacteric. 2005;8:110-23.
18. Son ED, Lee JY, Lee S, Kim SM, Lee BG, Chang IS, dkk. Topical application of 17β-estradiol increases extracellular matrix protein synthesis by stimulating TGF-β signaling in aged human skin in vivo. J Invest Dermatol. 2005;124:1149-61.
19. Stevenson S, Nelson LD, Sharpe DT. 17β-estradiol regulates the secretion of TGF- β by cultured human dermal fibroblasts. J Biomater Sci Polym Ed. 2008;19:1097-109.
20. Thornton MJ. Estrogens and aging skin. Dermato-Endocrinol. 2013;5:264-70.
21. Stevenson S, Thornton J. Effect of estrogens on skin aging and the potential role of SERMs. Clin Interv Aging. 2007;2:283-97.
22. Stevenson S, Nelson LD, Huq S, Sharpe DT, Thornton MJ. Oestrogens and wound healing: migration, proliferation and secretion of paracrine factors by human dermal fibroblasts in vitro [Online]. 2005 [citated August 2016]. Presented at 196th Meeting of the Society for Endocrinology and Society for Endocrinology joint Endocrinology and Diabetes Day. 2005, London, UK. Endocrine Abstracts 10 P80. Available from URL: http://www.endocrine-abstracts.org/ea/0010/ea0010P80.htm
23. Ashcroft GS, Dodsworth J, van Boxtel E, Tarnuzzer RW, Horan MA, Schultz GS, dkk. Estrogen accelerates cutaneous wound healing associated with an increase in TGF-β1 levels. Nat Med. 1997;3:1209-15.
24. Lal BK, Saito S, Pappas PJ, Padberg PJ, Cerveira JJ, Hobson RW, dkk. Altered proliferative responsses of dermal fibroblasts to TGF-β1 may contribute to chronic venous stasis ulcer. J Vasc Surg. 2003;37:1285-93.
25. Ashcroft GS, Greenwell-Wild T, Horan MA, Wahl SM, Ferguson MWJ. Topical estrogen accelerates cutaneous wound healing in aged human associated with an altered inflammatory responsse. Am J Pathol. 1999;155:1137-46.
26. Strudwick X, Powell BC, Cowin AJ. Role of sex hormones in acute and chronic wound healing. Primary Intention. 2006;14:35-8.
27. Emmerson E, Hardman MJ. The role of estrogen deficiency in skin ageing and wound healing. Biogerontology. 2012;13:3-20.
28. Velarde MC. Mitochondrial and sex steroid hormone crosstalk during aging. Longev Healthspan. 2014;3:2.
29. Ashcroft GS, Mills SJ, Lei KJ, Gibbons L, Jeong MJ, Taniguchi M, dkk. Estrogen modulates cutaneous wound healing by downregulating macrophage migration inhibitory factor. J Clin Invest. 2003;111:1309-18.
30. Hardman MJ, Ashcroft GS. Hormonal influences on wound healing: A review of current experimental data. Wounds. [Online]. 2005 [citated March 2016]. Available from URL: http://www.woundsresearch.com/article/4908.