Effect of snail mucus on angiogenesis during wound healing
Open accessAbstract
Background: Angiogenesis is the process through which new blood vessels are formed from existing ones. This process plays an important role in supplying the oxygen and nutrients needed for cellular metabolism and eliminating cell debris during wound healing. Snail mucus can bind to several factors that stimulate angiogenesis, including vascular endothelial growth factor, platelet-derived growth factor, and fibroblast growth factor. The aim of this study is to observe changes in angiogenesis during the healing of wounds topically applied with snail mucus. Methods: Punch biopsy was performed on the back of male Wistar rats to obtain four wounds, and different concentrations of snail mucus were applied to each of these wounds. The animals were sacrificed on days 2, 4, and 7 to observe the extent of angiogenesis during wound healing by microscopy. Results: Two-way ANOVA showed differences in number of blood vessels formed (p = 0.00) and day of observation (p = 0.00) between groups. Post hoc Tukey’s HSD test showed that 24% snail mucus treatment does not significantly affect wound healing (p = 0.488); by contrast, treatment with 48% and 96% snail mucus demonstrated significant effects on angiogenesis (p = 0.01). Spearman’s test showed interactive effects between snail mucus concentration and day of observation on the extent of angiogenesis (p = 0.001, R = 0.946). Conclusion: Topical application of snail mucus gel can increase angiogenesis during wound healing in Wistar rat skin.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In male Wistar rats, 24% snail mucus did not significantly affect wound healing compared with negative control, while 48% and 96% snail mucus showed substantial effects on angiogenesis in papillary and reticular strata.
“Of the snail mucus, 24% did not significantly affect wound healing compared with the negative control, while 48% and 96% snail mucus showed substantial effects on angiogenesis in the papillary and reticular strata.”
From Chemical Variability and Biological Potential of Cornu aspersum Mucus as a Source for the Development of New Cosmetic and Pharmaceutical Products (2025) · cites this paper as [75]
Studies concerning angiogenesis indicate that snail mucus has different mechanisms of impact on the wound-healing process.
“In addition, the studies concerning angiogenesis [21,70,74,75,76] indicate that snail mucus has different mechanisms of impact on the wound-healing process.”
From Chemical Variability and Biological Potential of Cornu aspersum Mucus as a Source for the Development of New Cosmetic and Pharmaceutical Products (2025) · cites this paper as [75]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
No references could be resolved yet.
Research works printed but not linked: 52
- [1]Welsh JD: Medical History of Union Generals.OH: Kent State University Press. 2005. Reference Source
- [2]Politis C Schoenaers J Jacobs R: Wound healing problems in the mouth. Front Physiol. 2016; 7: 507. 10.3389/fphys.2016.00507 27853435 PMC5089986 · DOI
- [3]Gál P Toporcer T Vidinský B: Simple interrupted percutaneous suture versus intradermal running suture for wound tensile strength measurement in rats: a technical note. Eur Surg Res. 2009; 43(1): 61– 5. 10.1159/000219214 19451720 · DOI
- [4]Harlaar JJ van Ramshorst GH Nieuwenhuizen J: Small stitches with small suture distances increase laparotomy closure strength. Am J Surg. 2009; 198(3): 392– 5. 10.1016/j.amjsurg.2008.10.018 19285296 · DOI
- [5]Lee YS Yang HO Shin KH: Suppression of tumor growth by a new glycosaminoglycan isolated from the African giant snail Achatina fulica. Eur J Pharmacol. 2003; 465(1–2): 191– 8. 10.1016/s0014-2999(03)01458-4 12650849 · DOI
- [6]Macpherson N Lee S: Effect of different suture techniques on tension dispersion in cutaneous wounds: a pilot study. Australas J Dermatol. 2010; 51(4): 263– 7. 10.1111/j.1440-0960.2010.00691.x 21198523 · DOI
- [7]Azevedo LH de Sousa SC Correa L: Mast cell concentration in the wound healing process of incisions made by different instruments. Lasers Med Sci. 2009; 24(4): 585– 90. 10.1007/s10103-008-0616-5 18936870 · DOI
- [8]de Oliveira Gonzalez AC Costa TF de Araújo Andrade Z: Wound healing - A literature review. An Bras Dermatol. 2016; 91(5): 614– 20. 10.1590/abd1806-4841.20164741 27828635 PMC5087220 · DOI · Paper page
- [9]Krafts KP: Tissue repair: The hidden drama. Organogenesis. 2010; 6(4): 225– 33. 10.4161/org.6.4.12555 21220961 PMC3055648 · DOI
- [10]Velnar T Bailey T Smrkolj V: The wound healing process: an overview of the cellular and molecular mechanisms. J Int Med Res. 2009; 37(5): 1528– 42. 10.1177/147323000903700531 19930861 · DOI
- [11]Cañedo-Dorantes L Cañedo-Ayala M: Skin acute wound healing: A comprehensive review. Int J Inflam. 2019; 2019: 3706315. 10.1155/2019/3706315 31275545 PMC6582859 · DOI
- [12]Guo S Dipietro LA: Factors affecting wound healing. J Dent Res. 2010; 89(3): 219– 29. 10.1177/0022034509359125 20139336 PMC2903966 · DOI · Paper page
- [13]van der Laan AM Piek JJ van Royen N: Targeting angiogenesis to restore the microcirculation after reperfused MI. Nat Rev Cardiol. 2009; 6(8): 515– 23. 10.1038/nrcardio.2009.103 19528962 · DOI
- [14]Kumar V Abbas AK Fausto N: Robbins Basic Pathology. London: Elsevier. 2007. Reference Source
- [15]Bauer SM Bauer RJ Velazques OC: Angiogenesis, vasculogenesis, and induction of healing in chronic wounds. Vasc Endovascular Surg. 2005; 39(4): 293– 305. 10.1177/153857440503900401 16079938 · DOI
- [16]Szpaderska AM Walsh CG Steinberg MJ: Distinct patterns of angiogenesis in oral and skin wounds. J Dent Res. 2005; 84(4): 309– 14. 10.1177/154405910508400403 15790734 · DOI
- [17]Sivamani RK Ma BR Wehrli LN: Phytochemicals and naturally derived substances for wound healing. Adv Wound Care (New Rochelle). 2012; 1(5): 213– 7. 10.1089/wound.2011.0330 24527308 PMC3839002 · DOI
- [18]Yuan H Ma Q Ye L: The traditional medicine and modern medicine from natural products. Molecules. 2016; 21(5): 559. 10.3390/molecules21050559 27136524 PMC6273146 · DOI
- [20]Cilia G Fratini F: Antimicrobial properties of terrestrial snail and slug mucus. J Complement Integr Med. 2018; 15(3). 10.1515/jcim-2017-0168 29596054 · DOI
- [21]Shim JY Lee YS Jung SH: Pharmacological activities of a new glycosaminoglycan, acharan sulfate isolated from the giant African snail Achatina fulica. Arch Pharm Res. 2002; 25(6): 889– 94. 10.1007/BF02977010 12510844 · DOI
- [22]Jeong J Toida T Muneta Y: Localization and characterization of acharan sulfate in the body of the giant African snail Achatina fulica. Comp Biochem Physiol B Biochem Mol Biol. 2001; 130(4): 513– 9. 10.1016/s1096-4959(01)00468-7 11691628 · DOI
- [23]Pomin VH Mulloy B: Glycosaminoglycans and proteoglycans. Pharmaceuticals (Basel). 2018; 11(1): 27. 10.3390/ph11010027 29495527 PMC5874723 · DOI
- [24]Kim HS Lee YH Lee YR: Activation of professional antigen presenting cells by Acharan sulfate isolated from giant African snail, achatina fulica. Arch Pharm Res. 2007; 30(7): 866– 70. 10.1007/BF02978838 17703739 · DOI
- [25]Kim HJ Ulagessan S: Antibacterial and antifungal activities of proteins extracted from seven different snails. Appl Sci. 2018; 8(8): 1362. 10.3390/app8081362 · DOI
- [26]Gurtner GC Werner S Barrandon Y: Wound repair and regeneration. Nature. 2008; 453(7193): 314– 21. 10.1038/nature07039 18480812 · DOI · Paper page
- [27]Zeng Z Zhu BH: Arnebin-1 promotes the angiogenesis of human umbilical vein endothelial cells and accelerates the wound healing process in diabetic rats. J Ethnopharmacol. 2014; 154(3): 653– 62. 10.1016/j.jep.2014.04.038 24794013 · DOI
- [28]Prasojo S Rahajoe PS Hasan CY: Effect of Snail Mucus (Achatina fulica) on Increased Angiogenesis in Skin Incision Wounds of Mice (Mus musculus) (Immunohistochemical Study CD34). Thesis. Universitas Gadjah Mada. 2018.
- [29]Harti AS Murharyati A Sulisetyawati DS: The effectiveness of snail mucus (Achatina fulica) and chitosan toward limfosit proliferation in vitro. Asian J Pharm Clin Res. 2018; 11(15): 85– 88. 10.22159/ajpcr.2018.v11s3.30041 · DOI
- [30]van Wijk XMR van Kuppevelt TH: Heparan sulfate in angiogenesis: a target for therapy. Angiogenesis. Springer 2014; 17(3): 443– 62. 10.1007/s10456-013-9401-6 24146040 · DOI
- [31]Ucuzian AA Gassman AA East AT: Molecular mediators of angiogenesis. J Burn Care Res. 2010; 31(1): 158– 75. 10.1097/BCR.0b013e3181c7ed82 20061852 PMC2818794 · DOI
- [32]Fuster MM Wang L: Endothelial heparan sulfate in angiogenesis. Prog Mol Biol Transl Sci. 2010; 93: 179– 212. 10.1016/S1877-1173(10)93009-3 20807646 PMC3703633 · DOI
- [34]Lamalice L Le Boeuf F Huot J: Endothelial cell migration during angiogenesis. Circ Res. 2007; 100(6): 782– 94. 10.1161/01.RES.0000259593.07661.1e 17395884 · DOI
- [35]Vieira TCRG, Costa-Filho A Salgado NC: Acharan sulfate, the new glycosaminoglycan from Achatina fulica Bowdich 1822. Structural heterogeneity, metabolic labeling and localization in the body, mucus and the organic shell matrix. Eur J Biochem. 2004; 271(4): 845– 54. 10.1111/j.1432-1033.2004.03989.x 14764101 · DOI
- [37]Ingber DE: Mechanical signaling and the cellular response to extracellular matrix in angiogenesis and cardiovascular physiology. Circ Res. 2002; 91(10): 877– 87. 10.1161/01.res.0000039537.73816.e5 12433832 · DOI
- [38]Norton KA Popel AS: Effects of endothelial cell proliferation and migration rates in a computational model of sprouting angiogenesis. Sci Rep. 2016; 6: 36992. 10.1038/srep36992 27841344 PMC5107954 · DOI
- [39]Mardiyantoro F Prasetyaningrum N Rahmastuti HT: Histopathological characteristics of dental socket healing on collagen density following use of pangas catfish (Pangasius djambal) gelatin. Majalah Kedokteran Gigi Indonesia. 2019; 5(3): 120– 5. 10.22146/majkedgiind.39830 · DOI
- [40]Fermillian A Agustina D Subagyo G: The effect of papaya leaf extract (Carica papaya L.) on healing process of buccal traumatic ulcer in Wistar rats. MKGI. 2019; 5(1): 15– 22. 10.22146/majkedgiind.37026 · DOI
- [41]Adair TH Montani JP: Angiogenesis.San Rafael: Morgan & Claypool Life Sciences. 2010. 21452444
- [42]Khakoo AY Finkel T: Endothelial progenitor cells. Annu Rev Med. 2005; 56: 79– 101. 10.1146/annurev.med.56.090203.104149 15660503 · DOI
- [43]Milkiewicz M Ispanovic E Doyle JL: Regulators of angiogenesis and strategies for their therapeutic manipulation. Int J Biochem Cell Biol. 2006; 38(3): 333– 57. 10.1016/j.biocel.2005.10.006 16309946 · DOI
- [44]Fidler IJ Ellis LM: Neoplastic angiogenesis--not all blood vessels are created equal. N Engl J Med. 2004; 351(3): 215– 6. 10.1056/NEJMp048080 15254281 · DOI
- [45]Kalangi SJR: The role of collagen in wound healing. Dexa Media. 2004; 17(4): 168– 74.
- [46]Jimmy S Elmarakby D Gazia MA: The role of hepatic stellate cells and angiogenesis in liver regeneration following partial hepatectomy in adult male albino rats: histological and immunohistochemical study. Egyptian Journal of Histology. 2019; 42(4): 1070– 1095. 10.21608/ejh.2019.9692.1087 · DOI
- [47]Eldien HMS Mostafa NA ElTawab OA: Effect of hematopoietic stem cells and platelet-rich plasma on the healing of experimental skin burned tissues: A comparative study in adult male mice. Egyptian Journal of Histology. 2019; 42(3): 740– 754. 10.21608/ejh.2019.8023.1083 · DOI
- [48]Towheed TE Maxwell L Anastassiades TP: Glucosamine therapy for treating osteoarthritis. Cochrane Database Syst Rev. 2005; 18(2): CD002946. 10.1002/14651858.CD002946.pub2 15846645 PMC8459392 · DOI
- [49]Ricard N Tu L Le Hiress M: Increased pericyte coverage mediated by endothelial-derived fibroblast growth Factor-2 and interleukin-6 is a source of smooth muscle-like cells in pulmonary hypertension. Circulation. 2014; 129(15): 1586– 97. 10.1161/CIRCULATIONAHA.113.007469 24481949 · DOI · Paper page
- [50]Honnegowda TM Kumar P Udupa EGP: Role of angiogenesis and angiogenic factors in acute and chronic wound healing. Plast Aesthet Res. 2015; 2: 243– 9. 10.4103/2347-9264.165438 · DOI
- [51]DiPietro LA: Angiogenesis and wound repair: when enough is enough. J Leukoc Biol. 2016; 100(5): 979– 984. 10.1189/jlb.4MR0316-102R 27406995 PMC6608066 · DOI
- [52]Attia G Atef H Elmansy R: Autologous platelet rich plasma enhances satellite cells expression of MyoD and exerts angiogenic and antifibrotic effects in experimental rat model of traumatic skeletal muscle injury. Egyptian Journal of Histology. 2017; 40(4): 443– 458. 10.21608/ejh.2017.5686 · DOI
- [53]Kelly-Goss MR Sweat RS Stapor PC: Targeting pericytes for angiogenic therapies. Microcirculation. 2014; 21(4): 345– 57. 10.1111/micc.12107 24267154 PMC4079092 · DOI
- [54]Dulmovits BM Herman IM: Microvascular remodeling and wound healing: a role for pericytes. Int J Biochem Cell Biol. 2012; 44(11): 1800– 12. 10.1016/j.biocel.2012.06.031 22750474 PMC3455116 · DOI
- [55]Wietecha MS Król MJ Michalczyk ER: Pigment epithelium-derived factor as a multifunctional regulator of wound healing. Am J Physiol Heart Circ Physiol. 2015; 309(5): H812– 26. 10.1152/ajpheart.00153.2015 26163443 PMC4591402 · DOI
Cited by
Sorted by citations
Hudz, N., Turkina, V., Alyokhina, T., Motyka, O., Chemerys, N., Rumynska, T., Lozynskyi, A., Jasicka-Misiak, I., & Kobylinska, L. (2025) · Molecules · doi:10.3390/molecules30214197 · Cited by 4 · see citing works
- Authors
- Rosanto, Y. B., Hasan, C. Y., Rahardjo, R., & Pangestiningsih, T. W.
- Affiliations
- Universitas Gadjah Mada (ID)
- Corresponding author
- Hasan, Cahya Yustisia
- Venue
- F1000Research
- Publisher
- F1000 Research Ltd
- Published
- 2021-05-21
- Volume
- 10
- Pages
- 181
- ISSN
- 2046-1402 (ISSN-L)
- PMC
- PMC11190653
- OpenAlex
- W3134523492
- Cited by
- 15
- References
- 0
- Citations by year
- 2026: 1 · 2025: 7 · 2024: 2 · 2023: 2 · 2022: 2 · 2021: 1
- FWCI
- 0.92
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- F1000Research (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Topics
- Health Sciences › Medicine › Rehabilitation › Wound Healing and Treatments
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Phytochemistry and biological activity of medicinal plants
- Life Sciences › Agricultural and Biological Sciences › Insect Science › Bee Products Chemical Analysis
- Keywords
- snail mucus, angiogenesis, wound healing, topical application, vascular endothelial growth factor, platelet-derived growth factor, fibroblast growth factor, skin wounds, growth factor binding
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review