Biological Activity of Catfish (Clarias gariepinus) Mucus Gel on the Wistar Rats (Rattus norvegicus) Wound Healing Process http://.www.doi.org/10.26538/tjnpr/v7i2.12
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Abstract
Clarias gariepinus (North African catfish) is a preferred freshwater fish for consumption in Indonesia. Catfish mucus by-product is considered to have no economic value and is not optimally utilized. Even though, recent studies have shown that the mucus contains various bioactive molecules that support fish immunity. The purpose of this study was to determine the effect of C. gariepinus catfish strain Mutiara mucus gel on the Wistar rat wound healing process. This study was conducted by formulating catfish mucus into a gel preparation. Mucus gel was evaluated for physicochemical characteristics and organoleptics. Mucus gel was applied in vivo to the incision wound of rats for 14 days and compared with the positive control using povidone iodine and placebo control using gel base. Wound morphology and length were observed every day, whereas wound histology and immunohistochemistry were observed once on the 15th day. The qualitative data was analyzed descriptively. The physicochemical characteristics of the gel revealed that the gel has a low viscosity, an effective adhesion time, and a neutral pH. Based on organoleptic evaluation, it has a moderate texture, a fishy and strong aroma, and a cloudy color, making it less favorable to the panelists. In an in vivo study, catfish mucus gel significantly accelerated woundclosure and increased epithelial tissue thickness but had no significant effect on increasing fibroblast and blood vessel numbers, and VEGF-A expression. More in-depth studies of the catfish mucus gel is needed for further development.
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Aquarista F, Subhan U. Giving probiotic with carrier zeolit on enlargment dumbo catfish (Clarias gariepinus). JPK. 2012; 7(4):1–25.
Gustiano R, Prakoso VA, Radona D, Dewi RRSPS, Saputra A, Nurhidayat. A sustainable aquaculture model in Indonesia: multi-biotechnical approach in Clarias farming. IOP Conf. Ser.: Earth Environ. Sci. 2021; 718012039.
Indonesia Central Bureau of Statistics. Production and production value of aquaculture by province and main commodity, 2020. [Online]. 2019 [cited 2021 Apr 14]. Available from: https://www.bps.go.id/indikator/indikator/view_data_pub/0000/api_pubNGFxSy9BUVlUN0RrVklTNjU3UnJBdz09/da_05/1.
Ministry of Marine Affairs and FisheriesRepublic of Indonesia. Subsektor perikanan budidaya sepanjang tahun 2017 menunjukkan kinerja positif. [Online]. 2018 [cited 2021 Apr 11]. Available from: https://kkp.go.id/djpb/artikel/3113-subsektor-perikananbudidaya-sepanjang-tahun-2017-.
Wang S, Wang Y, Ma J, Ding Y, Zhang S. Phosvitin plays a critical role in the immunity of zebrafish embryos via acting as a pattern recognition receptor and an antimicrobial effector. J. Biol. Chem. 2011; 286(25):22653–22664. Doi: 10.1074/jbc.M111.247635 v
Esteban ÁM. An overview of the immunological defenses in fish skin. Int. Sch. Res. Notices Immunol. 2012; 1–29.
Astuti RD. Activity of pearl catfish (Clarias gariepinus) mucus as antibacterial against MRSA (Methicillin Resistant Staphylococcus aureus) and Pseudomonas aeruginosaATCC 27853 bacteria in vitro. Undergraduate Thesis, Department of Biology Sebelas Maret University. 2022.
Reverter M, Tapissier-Bontemps N, Lecchini D, Banaigs B, Sasal P. Biological and ecological roles of external fish mucus: a review. Fishes. 2018; 3(4):41. https://www.mdpi.com/2410-3888/3/4/41
Ellis AE. Innate host defense mechanisms of fish against viruses and bacteria. Dev. Comp. Immunol. 2001; 25(8–9):827–839.
Brinchmann MF, Patel DM, Pinto N, Iversen MH. Functional aspects of fish mucosal lectins interaction with non-self. Molecules. 2018; 23(5):1–12.
Dash S, Das SK, Samal J, Thatoi HN. Epidermal mucus, a major determinant in fish health: A review. Iran. J. Vet.Res.2018; 19(2):72–81.
Shoemaker C, Xu DH, LaFrentz B, LaPatra S. Overview of fish immune system and infectious diseases. In: Dietary nutrients, additives, and fish health (eds. CS Lee, C Lim, DM Gatlin and CD Webster). 2015. https://doi.org/10.1002/9781119005568.ch1.
Rusli N, Yeniati N. Formulation of gel lele fish mucus (Clarias gariepinus L) as wound healing with various basis of carbopol 934. MS. 2019; 3(2):131–138.
Safaruddin, Safitri NAA, Yuliana B, Firman I. Gel formulation of snakehead fish (Channa striata) mucus and effectiveness test on rabbit (Oryctolagus cuniculus) burn wound. Proceeding of National Seminars on Science, Technology, and Social Humanities Universitas Indonesia
Timur. 2019; 1(1):248–254.
Afianti HP, Murrukmihadi M. Influence of variation levels hpmc as gelling agent against physical properties and antibacterial activity of preparation gel ethanolic extract of basil leaves (Ocimum basilicum L. forma citratum Back.). Majalah Farmaseutik. 2015; 11(2):307-315. https://doi.org/10.22146/farmaseutik.v11i2.24121
Dewi C, Saleh A, Awaliyah NH, Hasnawati H. Evaluation of snail (Achatina fulica) mucus emulgel formula and antibacterial activity test against acne-causing bacteria, Staphylococcus epidermidis. JMPI, 2018; 4(02):122–134.
National Standardization Agency of Indonesia. SNI 01-2346-2006: Instructions for organoleptic and sensory testing. BSN, 2006. 137p.
Setiawan A. The effect of eel (Monopterus albus) mucus on the number of blood vessels in wound healing in Wistar male rats. Undergraduate Thesis, Faculty of Medicine Unissula. 2016.
Hakim RF, Fakhrurrazi F, Rezeki S, Sari LM, Marfirah Z. Hemostatic and wound healing effects of Gracilaria verrucosa extract gel in albino rats. Trop. J. Nat. Prod. Res.2020; 4(11):912–917.
Widhihastuti YS, Kaelan C, Wahid S. Correlations between the immunoexpresionof Vascular Endothelial Growth Factor A (VEGF A) and the histopathological grade and metastatic potency of ovarian cancer. MPI. 2011; 20(1):1–5.
Atik N, Iwan J. The differences between topical aplication of the aloe vera gel with the povidone iodine solutio for skin wound healing in mice (Mus musculus). MKB. 2009; 41(2):29–36.
Garg A, Aggarwal D, Garg S, Singla AK. Spreading of semisolid formulations: an update. Pharm. Technol. N. Am. 2002; 26(9):84–105.
Yusuf AL, Nurawaliah E, Harun N. The effectiveness test of gel of ethanol extract of Moringa oleifera leaves as antifungal of Malassezia furfur. KJIF. 2017; 5(2):62-67
Song JJ, Salcido R, Erdman W. Use of honey in wound care. Adv. Skin Wound Care. 2011; 24(1):45–46.
Tracy LE, Minasian RA, Caterson EJ. Extracellular matrix and dermal fibroblast function in the healing wound. Adv Wound Care. 2016; 5(3):119–136.
Olayemi O, Adenike K. Charaterization of galactose-specific lectin from the skin mucus of African catfish Clarias gariepinus. Sci. Res. Essays. 2014; 9(20):869–879.
Okella H, Ikiriza H, Ochwo S, Ajayi CO, Ndekezi C, Nkamwesiga J, Aber J, Mtewa AG, Odongo S. Identification of antimicrobial peptides isolated from the skin mucus of african catfish, Clarias gariepinus (Burchell , 1822). Front Microbiol. 2021; 12: 794631.
Abdel-Shafi S, Osman A, Al-Mohammadi AR, Enan G, Kamal N, Sitohy M. Biochemical, biological characteristics and antibacterial activity of glycoprotein extracted from the epidermal mucus of African catfish (Clarias gariepinus). Int. J. Biol. Macromol. 2019; 138:773–780.
Bao P, Kodra A, Tomic-Canic M, Golinko M, Ehrlich P, Brem H. The role of vascular endothelial growth factor in wound healing. J. Surg. Res. 2009; 153(2):347–358.
Bayer G, Grasselli S, Malchiodi A, Bayer IS. Antiseptic povidone-iodine encapsulating edible phospholipid gels. Colloids Surf. A Physicochem. Eng. Asp. 2021; 619(2021):126537.