Healing efficiency of oligosaccharides generated from almond gum (Prunus amygdalus) on dermal wounds of adult rats

Journal of Tissue Viability

Volumn 23, Issue 3, 2014, Pages 98-108

  Bouaziz, Fatma ^a   Ben Romdhane, Molka ^a   Boisset Helbert, Claire ^b   Buon, Laurine ^b   Bhiri, Fatma ^a   Bardaa, Sana ^c   Driss, Dorra ^a   Koubaa, Mohamed ^a   Fakhfakh, Akram ^a   Sahnoun, Zouhair ^c   Kallel, Fatma ^a   Zghal, Najiba ^c   Ellouz Chaabouni, Semia ^a  

^a UNIVERSITY OF SFAX   (Tunisia)

^b CENTRE DE RECHERCHES SUR LES MACROMOLÉCULES VÉGÉTALES CERMAV CNRS   (France)

^c UNIVERSITY OF SFAX   (Tunisia)

Author keywords

Almond gum; Arabinogalactan; Histopathology; Oligosaccharides; Wound healing

Indexed keywords

ARABINOSE; COLLAGEN; GALACTOSE; GLUCOSE; MANNOSE; OLIGOSACCHARIDE; RHAMNOSE; XYLOSE;

ADULT; ALMOND; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL DENSITY; CONTROLLED STUDY; FIBROBLAST; GAS CHROMATOGRAPHY; HISTOPATHOLOGY; IN VIVO STUDY; MASS SPECTROMETRY; MICROSCOPY; NONHUMAN; RAT; SKIN INJURY; WOUND CLOSURE; WOUND HEALING; AGING; ANIMAL; CHEMISTRY; CHROMATOGRAPHY; DRUG EFFECTS; INJURIES; ISOLATION AND PURIFICATION; SKIN; WISTAR RAT;

AGING; ANIMALS; CHROMATOGRAPHY; OLIGOSACCHARIDES; PRUNUS DULCIS; RATS; RATS, WISTAR; SKIN; WOUND HEALING;

EID: 84908126743     PISSN: 0965206X     EISSN: 18764746     Source Type: Journal    
DOI: 10.1016/j.jtv.2014.07.001     Document Type: Article

References (53)

1. C. Schmidt, M. Fronza, M. Goettert, F. Geller, S. Luik, and E.M.M. Flores Biological studies on Brazilian plants used in wound healing J Ethnopharmacol 122 2009 523 532
2. D.E. Tsala, N. Nga, M.N. Joseph, G.E. Kalandi, E. Jacques, and Z. Ze A dermal wound healing effect of water extract of the stem bark of Alafia multiflora Stapf Phytomedicine Int J Phytother Phytopharm 4 2012 114 122
3. K.R. Jones, K. Fennie, and A. Lenihan Evidence-based management of chronic wounds Adv Skin Wound Care 20 2007 591 600
4. B. Kumar, M. Vijayakumar, R. Govindarajan, and P. Pushpangadan Ethnopharmacological approaches to wound healing - exploring medicinal plants of India J Ethnopharmacol 114 2007 103 113
5. K. Von der Mark, J. Park, S. Bauer, and P. Schmuki Nanoscale engineering of biomimetic surfaces: cues from the extracellular matrix Cell Tissue Res 339 2010 131 153
6. P.B. Malafaya, G.A. Silva, and R.L. Reis Natural-origin polymers as carriers and scaffolds for biomolecules and cell delivery in tissue engineering applications Adv Drug Deliv Rev 59 2007 207 233
7. V. Gloaguen, P. Krausz, V. Brudieux, B. Closs, Y. Leroy, and Y. Guerardel Structural patterns of rhamnogalacturonans modulating Hsp-27 expression in cultured human keratinocytes Mol Basel Switz 13 2008 1207 1218
8. A.M. Deters, K.R. Schröder, T. Smiatek, and A. Hensel Ispaghula (Plantago ovata) seed husk polysaccharides promote proliferation of human epithelial cells (skin keratinocytes and fibroblasts) via enhanced growth factor receptors and energy production Planta Med 71 2005 33 39
9. A.M. Deters, K.R. Schröder, and A. Hensel Kiwi fruit (Actinidia chinensis L.) polysaccharides exert stimulating effects on cell proliferation via enhanced growth factor receptors, energy production, and collagen synthesis of human keratinocytes, fibroblasts, and skin equivalents J Cell Physiol 202 2005 717 722
10. C. Brunold, A. Deters, F. Knoepfel-Sidler, J. Hafner, B. Müller, and A. Hensel Polysaccharides from Hibiscus sabdariffa flowers stimulate proliferation and differentiation of human keratinocytes Planta Med 70 2004 370 373
11. J. Zippel, A. Deters, and A. Hensel Arabinogalactans from Mimosa tenuiflora (Willd.) Poiret bark as active principles for wound-healing properties: specific enhancement of dermal fibroblast activity and minor influence on HaCaT keratinocytes J Ethnopharmacol 124 2009 391 396
12. Y. Suzuki, Y. Okamoto, M. Morimoto, H. Sashiwa, H. Saimoto, and S.-i. Tanioka Influence of physico-chemical properties of chitin and chitosan on complement activation Carbohydr Polym 42 2000 307 310
13. S. Minami, M. Masuda, H. Suzuki, Y. Okamoto, A. Matsuhashi, and K. Kato Subcutaneous injected chitosan induces systemic activation in dogs Carbohydr Polym 33 1997 285 294
14. Y. Okamoto, M. Watanabe, K. Miyatake, M. Morimoto, Y. Shigemasa, and S. Minami Effects of chitin/chitosan and their oligomers/monomers on migrations of fibroblasts and vascular endothelium Biomaterials 23 2002 1975 1979
15. C.K. Chebbi, K. Kichenin, N. Amar, H. Nourry, J.M. Warnet, and D. Barritault Pilot study of a new matrix therapy agent (RGTA OTR4120) in treatment-resistant corneal ulcers and corneal dystrophy J Fr Ophtalmol 31 2008 465 471
16. V. Barbier-Chassefière, S. Garcia-Filipe, X.L. Yue, M.E. Kerros, E. Petit, and P. Kern Matrix therapy in regenerative medicine, a new approach to chronic wound healing J Biomed Mater Res A 90 2009 641 647
17. D. Barritault, and J.-P. Caruelle Regenerating agents (RGTAs): a new therapeutic approach Ann Pharm Fr 64 2006 135 144
18. Y. Ikeda, S. Charef, M.-O. Ouidja, V. Barbier-Chassefière, F. Sineriz, and A. Duchesnay Synthesis and biological activities of a library of glycosaminoglycans mimetic oligosaccharides Biomaterials 32 2011 769 776
19. H. Liu, P. Huang, P. Ma, Q. Liu, C. Yu, and Y. Du Chitosan oligosaccharides suppress LPS-induced IL-8 expression in human umbilical vein endothelial cells through blockade of p38 and Akt protein kinases Acta Pharmacol Sin 32 2011 478 486
20. C. Li, R. Fu, C. Yu, Z. Li, H. Guan, and D. Hu Silver nanoparticle/chitosan oligosaccharide/poly(vinyl alcohol) nanofibers as wound dressings: a preclinical study Int J Nanomedicine 8 2013 4131 4145
21. H.-R. Choi, Y.-A. Kang, J.-I. Na, S.Y. Huh, C.-H. Huh, and K.H. Kim Oligosaccharides of hyaluronic acid increased epidermal cell stemness by modulation of integrin expression J Cosmet Dermatol 11 2012 290 296
22. F. Gao, Y. Liu, Y. He, C. Yang, Y. Wang, and X. Shi Hyaluronan oligosaccharides promote excisional wound healing through enhanced angiogenesis Matrix Biol 29 2010 107 116
23. S. Smith, V.A. Ravnikar, and R.L. Barbieri Androgen and insulin response to an oral glucose challenge in hyperandrogenic women Fertil Steril 48 1987 72 77
24. S. Kalra, R.K. Sahay, O. Schnell, W.H.H. Sheu, W. Grzeszczak, and H. Watada Alpha-glucosidase inhibitor, acarbose, improves glycamic control and reduces body weight in type 2 diabetes: findings on indian patients from the pooled data analysis Indian J Endocrinol Metab 17 2013 S307 S309
25. S. Kalra, R.K. Sahay, O. Schnell, W.H.H. Sheu, W. Grzeszczak, and H. Watada Acarbose improves glycemic control and reduces body weight: subanalysis data of South Asia region Indian J Endocrinol Metab 17 2013 S304 S306
26. S. Karnjanapratum, and S. You Molecular characteristics of sulfated polysaccharides from Monostroma nitidum and their in vitro anticancer and immunomodulatory activities Int J Biol Macromol 48 2011 311 318
27. L. Masuelli, G. Tumino, M. Turriziani, A. Modesti, and R. Bei Topical use of sucralfate in epithelial wound healing: clinical evidences and molecular mechanisms of action Recent Pat Inflamm Allergy Drug Discov 4 2010 25 36
28. P.J. Gupta, P.S. Heda, S. Kalaskar, and V.P. Tamaskar Topical sucralfate decreases pain after hemorrhoidectomy and improves healing: a randomized, blinded, controlled study Dis Colon Rectum 51 2008 231 234
29. E. Rivera-Arce, M. Gattuso, R. Alvarado, E. Zárate, J. Agüero, and I. Feria Pharmacognostical studies of the plant drug Mimosae tenuiflorae cortex J Ethnopharmacol 113 2007 400 408
30. Council of European Communities Council instructions about the protection of living animals used in scientific investigations Off J Eur Communities 358 1986 1 28 JO 86609CEE
31. S. Jain, M. Parriche, H. Durand, and G. Tiraby Production of polysaccharidases by a cellulase-pectinase hyperproducing mutant (Pol6) of Penicillium occitanis Enzyme Microb Technol 12 1990 691 696
32. M. Mandels, and J. Weber The production of cellulases G.J. Hajny, E.T. Reese, Cell. their Appl. vol. 95 1969 American Chemical Society Washington, D. C. 391 414
33. S.E. Chaabouni, H. Belguith, I. Hassairi, K. M'Rad, and R. Ellouz Optimization of cellulase production by Penicillium occitanis Appl Microbiol Biotechnol 43 1995 267 269
34. M. Dubois, K.A. Gilles, J.K. Hamilton, P.A. Rebers, and F. Smith Colorimetric method for determination of sugars and related substances Anal Chem 28 1956 350 356
35. J.P. Kamerling, G.J. Gerwig, J.F. Vliegenthart, and J.R. Clamp Characterization by gas-liquid chromatography-mass spectrometry and proton-magnetic-resonance spectroscopy of pertrimethylsilyl methyl glycosides obtained in the methanolysis of glycoproteins and glycopeptides Biochem J 151 1975 491 495
36. S. Hakomori A rapid permethylation of glycolipid, and polysaccharide catalyzed by methylsulfinyl carbanion in dimethyl sulfoxide J Biochem (Tokyo) 55 1964 205 208
37. V. Kant, A. Gopal, N.N. Pathak, P. Kumar, S.K. Tandan, and D. Kumar Antioxidant and anti-inflammatory potential of curcumin accelerated the cutaneous wound healing in streptozotocin-induced diabetic rats Int Immunopharmacol 20 2014 322 330
38. H. Yu, L. Yuan, M. Xu, Z. Zhang, and H. Duan Sphingosine kinase 1 improves cutaneous wound healing in diabetic rats Injury 45 2014 1054 1058
39. D.R. Mehregan, and A.H. Mehregan Pinkus' guide to dermatohistopathology J Am Acad Dermatol 15 1986 719 720
40. M. Gabe Techniques histologiques Masson 1968
41. N. Mahfoudhi, M. Chouaibi, F. Donsì, G. Ferrari, and S. Hamdi Chemical composition and functional properties of gum exudates from the trunk of the almond tree (Prunus dulcis) Food Sci Technol Int 18 2012 241 250
42. F. Brown, E.L. Hirst, and J.D. Jones The structure of almond-tree gum; the constitution of the aldobionic acid derived from the gum J Chem Soc 3 1948 1677 1679
43. F.F. Simas, P.A.J. Gorin, R. Wagner, G.L. Sassaki, A. Bonkerner, and M. Iacomini Comparison of structure of gum exudate polysaccharides from the trunk and fruit of the peach tree (Prunus persica) Carbohydr Polym 71 2008 218 228
44. D.M.W. Anderson, and J.F. Stoddart Studies on uronic acid materials: part XV. The use of molecular-sieve chromatography in studies on acacia senegal gum (gum arabic) Carbohydr Res 2 1966 104 114
45. F.F. Simas-Tosin, R. Wagner, E.M.R. Santos, G.L. Sassaki, P.A.J. Gorin, and M. Iacomini Polysaccharide of nectarine gum exudate: comparison with that of peach gum Carbohydr Polym 76 2009 485 487
46. A. Grein, B.C. da Silva, C.F. Wendel, C.A. Tischer, M.R. Sierakowski, and A.B.D. Moura Structural characterization and emulsifying properties of polysaccharides of Acacia mearnsii de Wild gum Carbohydr Polym 92 2013 312 320
47. W.T. Lawrence Physiology of the acute wound Clin Plast Surg 25 1998 321 340
48. I. Gülçin, Z. Huyut, M. Elmastaş, and H.Y. Aboul-Enein Radical scavenging and antioxidant activity of tannic acid Arab J Chem 3 2010 43 53
49. R.F. Diegelmann, and M.C. Evans Wound healing: an overview of acute, fibrotic and delayed healing Front Biosci 9 2004 283 289
50. F. Buffoni, G. Banchelli, S. Cambi, G. Ignesti, R. Pirisino, and L. Raimondi Skin wound healing: some biochemical parameters in guinea-pig J Pharm Pharmacol 45 1993 784 790
51. P. Martin Wound healing - aiming for perfect skin regeneration Science 276 1997 75 81
52. G.F. Pierce, and T.A. Mustoe Pharmacologic enhancement of wound healing Annu Rev Med 46 1995 467 481
53. G.C. Jagetia, G.K. Rajanikant, and K.V.N. Mallikarjun Rao Ascorbic acid increases healing of excision wounds of mice whole body exposed to different doses of gamma-radiation Burns 33 2007 484 494