skip to main content

Efek Kafein Dosis Bertingkat terhadap Epitelisasi dan Densitas Mikrovaskuler pada Penyembuhan Luka Full Thickness Skin Graft AutologusTikus Sprague Dawley

Fakultas Kedokteran, Universitas Diponegoro, Semarang, Indonesia

Received: 28 Dec 2018; Revised: 5 Feb 2020; Accepted: 20 Feb 2020; Published: 1 Apr 2020.
Open Access Copyright (c) 2020 MEDIA KESEHATAN MASYARAKAT INDONESIA under http://creativecommons.org/licenses/by-sa/4.0/.

Citation Format:
Abstract

Latar belakang : Skin graft saat ini menjadi salah satu terapi pilihan pada proses penyembuhan luka yang selalu berkembang. Proses epitelisasi dan pembentukan pembuluh darah baru memiliki peran penting dalam penyembuhan luka skin graft. Kandungan kafein (1,3,7 trimethylxanthine) sebagai antioksidan memiliki peran yang penting dalam penyembuhan luka. Tujuan dari penelitian ini adalah membuktikan efek kafein dalam berbagai dosis dalam meningkatkan densitas mikrovaskuler dan epitelisasi pada luka skin graft.

Metode : Penelitan ini adalah studi eksperimental dengan “Blinded randomized post test only controlled group design” terhadap 24 ekor tikus Sprague Dawley dilakukan skin graft autologous pada waktu yang bersamaan. Sampel dibagi secara acak menjadi 4 grup (K = tanpa pemberian kafein), (P1= Kafein 3 mg), (P2 = Kafein 6 mg), (P3 = Kafein 9 mg).Penilaian prosentase epitelisasi dan jumlah densitas mikrovaskuler jaringan dilakukan dengan pengecatan hematoxylin & eosin setelah hari ke 7 pasca skin graft.

Hasil : Analisis statistik perbandingan prosentase epitelisasi jaringan didapatkan didapatkan perbedaan yang bermakna antara kelompok kelompok K vs PI ( p = 0,003 ), K vs P2 (p = 0,001), K vsP3 (p = 0,001), P1 vs P2 (p = 0,001), P1 vs P3 (p = 0,001). Perbedaan yang tidak bermakna didapatkan antara kelompok P2 vs P3 (p = 0,669) dan pada jumlah densitas mikrovaskuler, didapatkan perbedaan yang bermakna antara kelompok K vs P2 (p = 0,010), K vs P3 (p = 0,008), P1 vs P2 (p = 0,009), P1 vs P3 (p = 0,007), P2 vs P3 (p = 0,008). Perbedaan yang tidak bermakna didapatkan antara kelompok K vs P1 (p = 0,343).

Kesimpulan :Kafeindapat meningkatkanprosentase epitelisasi dan jumlah densitas mikrovaskuler jaringan pada proses penyembuhan luka skin graft autologus tikus Sprague Dawley.

Kata Kunci : Kafein, skin graft autologus, epitelisasi, densitas mikrovaskuler

 

ABSTRACT

Title: Effects of Increased Dose Caffeine on Epithelialization and Microvascular Density in the Healing of Full Thickness Skin Graft Autologous Sprague Dawley Mouse

 

Background: Skin graft is currently one of the therapies of choice in the healing process of wounds that always develops. The process of epithelialization and formation of new blood vessels has an important role in healing skin graft wounds. Caffeine content (1,3,7 trimethylxanthine) as an antioxidant has an important role in wound healing. The aim of this study is to prove the effects of caffeine in various doses in increasing microvascular density and epithelialization in skin graft injuries.

Method: This research is an experimental study with a "Blinded randomized post test only controlled group design" of 24 Sprague Dawley rats by autologous skin graft at the same time. Samples were randomly divided into 4 groups (K = no caffeine), (P1 = Caffeine 3 mg), (P2 = Caffeine 6 mg), (P3 = Caffeine 9 mg). The assessment of the percentage of epithelialization and the amount of tissue microvascular density was done by painting hematoxylin & eosin after 7 days after skin graft.

Results: Statistical analysis of the comparison of tissue epithelialization percentage found significant differences between groups K vs PI (p = 0.003), K vs P2 (p = 0.001), K vsP3 (p = 0.001), P1 vs P2 (p = 0.001) , P1 vs P3 (p = 0.001). No significant difference was found between the P2 vs P3 group (p = 0.669) and in the total microvascular density, a significant difference was found between the K vs P2 group (p = 0.010), K vs P3 (p = 0.008), P1 vs P2 (p = 0.009), P1 vs P3 (p = 0.007), P2 vs P3 (p = 0.008). No significant difference was found between the K vs P1 groups (p = 0.343).

Conclusion: Caffeine can increase the percentage of epithelialization and the amount of tissue microvascular density in the healing process of autologous skin grafts of Sprague Dawley rats.

Keywords: Caffeine, autologous skin graft, epithelialization, microvascular density

Fulltext View|Download
Keywords: Kafein; skin graft autologus; epitelisasi; densitas mikrovaskuler

Article Metrics:

  1. Hidayat T, Noer M, Saputro I. Five years retrospective study of burns in Dr. Soetomo General Hospital Surabaya. PIT PERAPI; Medan: Department of Plastic Reconstructive and Aesthetic Surgery; 2012; 2-10
  2. Sjamsuhidajat, Jong D. Buku Ajar Ilmu Bedah. 4 ed. Jakarta: EGC; 2017;237
  3. Geoffrey C, Victor W. Wound Healing: Normal and Abnormal. In: Thorne CH, editor. Grabb and Smith's Plastic Surgery. 7 ed. Philadelphia: Lippincott Williams & Wilkins; 2014; 20-35
  4. Johnson K, Wilgus T. Vascular Endothelial Growth Factor and Angiogenesis in the Regulation of Cutaneous Wound Repair. Advances in Wound Care. 2014;3(10);77-86
  5. Hanahan D, Folkman J. Patterns and emerging mechanisms of the angiogenic switch during tumorigenesis. Cell. 1996;86(353);43-9
  6. Bonyanian Z, Rose'Meyer RB. Caffeine and its Potential Role in Attenuating Impaired Wound Healing in Diabetes. J Caff Research. 2015;5(4);1-8
  7. Ojeh N, Stojadinovic O, Pastar I, Sawaya A, Yin N, Tomic-Canic M. The effects of caffeine on wound healing. Int Wound J. 2016;13(5):605-13
  8. Liu P, Tong W, Liu K, Han S, Wang X, Badiavas E, et al. Liposome-mediated transfer of vascular endothelial growth factor cDNA augments survival of random-pattern skin flaps in the rat. Wound Repair Regen. 2004;12(80);45-51
  9. Galeano M, Deodato B, Altavilla D, Cucinotta D, Arsic N, Marini H, et al. Adeno-associated viral vector-mediated human vascular endothelial growth factor gene transfer stimulates angiogenesis and wound healing in the genetically diabetic mouse. Diabetologia. 2003;46(546);12-9
  10. Takahashi T, Kalka C, Masuda H, Chen D, Silver M, Kearney M, et al. Ischemia-and cytokine-induced mobilization of bone marrow-derived endothelial progenitor cells for neovascularization. Nat Med. 1999; 5(4);434-8
  11. Tepper O, Capla J, Galiano R, Ceradini D, Callaghan M, Kleinman M, et al. Adult vasculogenesis occurs through in situ recruitment, proliferation, and tubulization of circulating bone marrow-derived cells. Blood. 2005; 105(3);1068-7
  12. Pastar I, Stojadinovic O, Yin N, Ramirez H, Nusbaum A, Sawaya A, et al. Epithelialization in Wound Healing: A Comprehensive Review. Adv In Wound Care. 2014;3(7);30-9
  13. Barcelos R, Souza M, Amaral G, Stefanello S, Bresciani G, Fighera M, et al. Caffeine intake may modulate inflammation markers in trained rats. Nutrients. 2014;6(4):1678-90
  14. Feoktistov I, Biaggioni I, Cronstein BN. Adenosine receptors in wound healing, fibrosis and angiogenesis. Handb Exp Pharmacol. 2009(193):383-97
  15. Cronstein B. Adenosine receptors and fibrosis: a translational review. F1000 Biol Rep. 2011;3(21); 77-85
  16. Leibovich S, Chen J, Pinhal-Enfield G, Belem P, Elson G, Rosania A, et al. Synergistic up-regulation of vascular endothelial growth factor expression in murine macrophages by adenosine A(2A) receptor agonists and endotoxin. An H Pathol. 2002;160(6):2231-44
  17. Merighi S, Merighi S, Benini A, Mirandola P, Gessi S, Varani K, et al. Caffeine inhibits adenosine-induced accumulation of hypoxia-inducible factor-1Alpha, vascular endothelial growth factor, and interleukin 8 expression in hypoxic human colon cancer cells. Molecular Pharmacology. 2007;72:395-406
  18. Da Rocha LF, Junior S, Cerutti M, Santos A. Pharmacology of adenosine receptors and their signalling role in immunity and inflammation. Pharmacology and Therapeutics Journal. 2014;3:442-5
  19. Carmeliet P, Jain R. Molecular mechanisms and clinical applications of angiogenesis. Nature. 2011;473(7347);298-307

Last update:

No citation recorded.

Last update: 2024-11-24 07:20:04

No citation recorded.