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. 2020 Jun 10;13(6):1045–1049. doi: 10.14202/vetworld.2020.1045-1049

Histopathological evaluation of latex of Bellaco-Caspi, Himatanthus sucuuba (Spruce) Woodson on wound healing effect in BALB/C mice

Lisbeth Lucia Calero-Armijos 1, Oscar Herrera-Calderon 2,, Jorge Luis Arroyo-Acevedo 3, Juan Pedro Rojas-Armas 3, Renán Dilton Hañari-Quispe 4, Linder Figueroa-Salvador 5
PMCID: PMC7396333  PMID: 32801553

Abstract

Background and Aim:

Himatanthus sucuuba (Spruce) Woodson (Apocynaceae) is a medicinal plant known as “Bellaco-Caspi” widely distributed in Loreto, Peru. In the Peruvian traditional medicine, the latex of the plant is used for the treatment of wounds, inflammation, ulcers, and other ailments. This study aims to evaluate the wound healing effect of the latex of H. sucuuba in BALB/C albino mice.

Materials and Methods:

Thirty BALB/C male mice were used for wound healing study. In the experimental procedures, wound skin incision was performed at 2.0 cm in length until subcutaneous on the paravertebral of each animal. Under locally anesthetized with procaine cream, the treatment was conducted. All the mice were divided into three groups, the control group (A), zinc oxide cream (B), and H. sucuuba latex (C). The entire surface of the wound was treated for all the groups, and the treatments were performed daily for 15 days. The experiments were stopped on days 1, 7, and 15, respectively.

Results:

The histopathological study of tissues revealed significant changes in wound healing effect in H. sucuuba latex compared to the control and B groups. Consequently, the mice treated with latex showed a significant reduction in epithelialization time and collagen formation. Furthermore, the latex showed a dose-dependent significant reduction of inflammation in the first 24 h of treatment.

Conclusion:

BALB/C mice treated with the latex of H. sucuuba possess a wound healing effect that can scientifically prove the traditional use of the plant as a wound healing agent.

Keywords: Apocynaceae, BALB/C mice, latex, pathology, regeneration, wound healing

Introduction

The skin is the body’s first line of immune defense against physical, chemical, or biological aggression from the external environment [1]. Vasoconstriction is the immediate response to physical aggression, which is caused by prostaglandins and thromboxanes; platelets adhere to exposed collagen and the content is released into granules, while tissue factor activates the coagulation cascade and platelets [2]. All body tissues are capable of healing by regeneration or repair mechanisms [3,4]. The process of wound healing is divided into three phases: (a) Inflammation process, (b) proliferation, and (c) tissue remodeling. The inflammation phase includes activation of the innate immune system. During this phase, the differentiation of macrophages, monocytes, lymphocytes, and neutrophils infiltrates the wound site and hemostasis [5]. In addition, pathogens and foreign materials are removed from the wound and prevent damage in a localized area. [6]. The proliferative phase is characterized by angiogenesis, collagen deposition, epithelialization, and wound contraction. Angiogenesis involves the growth of new blood vessels from endothelial cells and these are presented in the tissue remodeling phase. Fibroblasts activate collagen and fibronectin to form a new extracellular matrix in fibroplasia and granulation tissue formation [7].

Plants have an important history in wound healing, as they contain a wide variety of botanical compounds [8]. Medicines derived from plants have been the first line of defense to maintain health and fight diseases [9]. These natural agents provide tissue healing and renewal through multiple mechanisms [10]. Members of the Apocynaceae family constitute an important source of pharmacological discoveries, as they are used for centuries in ethnic and traditional medicine. Himatanthus sucuuba (Spruce) Woodson is a shrub plant belonging to the Apocynaceae family, which grows in the Amazon regions of Brazil, Peru, and Colombia, which is known as “janaguba,” “sucuba,” “sucuuba,” and “Bellaco-Caspi” [11]. It is used in common medicine as a vermifuge, antitumor, antifungal, analgesic, anti-ulcer, and anti-arthritic [12]. The practice of traditional medicine has stayed in the majority of the Amazon population and H. sucuuba is claimed and commonly used for wound healing purposes, which require scientific validation in Peru.

This study aims to evaluate the wound healing effect of the latex of H. sucuuba on wounds induced in BALB/C mice.

Materials and Methods

Ethical approval

The Ethical Committee at the Faculty of Medicine of the Universidad Nacional Mayor de San Marcos (UNMSM) (Project N° 0206-FFB-UPG-2018) reviewed and approved this study.

Study period and Plant material

Leaves of H. sucuuba (Spruce) Woodson were collected in Iquitos, Department of Loreto, Peru, in December 2018. In the Herbarium of the UNMSM (Lima, Peru), a voucher was deposited with N° 010-USM-2019.

The latex used in this study acquired a break of H. sucuuba stems, which were procured from local farmyard areas of Iquitos. The latex was collected in the morning with a break of stems into a sterile bottle and was stored until further use at 8°C.

Phytochemical analysis

For the phytochemical screening of H. sucuuba latex, different types of reagents were used; the identification results were presented as positive and negative. The amount of sample taken was 1 mL of latex with five drops of each reagent [13].

Animals

In this study, 30 male mice (Mus musculus: BALB/C) aged 12 weeks old and weighing 30-40 g from the Bioterio of the National Institute of Health (INS) were used. All the mice were maintained individually in cages at the Laboratory of Pharmacology, Faculty of Medicine, UNMSM. Pelletized food (Ratonina®) and water were given to ad libitum for 2 weeks, under controlled conditions of temperature (24°C), relative humidity (70%), and with a photoperiod of 12 h of light cycle and 12 h of darkness. The research was done in the Bioterio of the Faculty of Medicine in the UNMSM (Lima, Peru).

Experimental design

Thirty adult mice were divided into three groups. The animal’s skin wound was done by means of surgical procedures as explained by Salim et al. [14]. The mice were locally anesthetized by topical cream containing lidocaine 25 mg and procaine 25 mg. The control group (A) had no treatment, the standard group (B) applied a commercial cream containing zinc oxide and the latex group (H. sucuuba latex) (C). The study was experimental and the dorsal area of the mouse was shaved with a Depile® cream where a transverse incision was made with an N° 20 scalpel on the dorsal-cervical part of 7 mm in length. The effect of H. sucuuba latex was observed in the wound area, and the presence of inflammation and re-epithelialization was pointed as markers of wound healing [15]. The treatments were applied once a day with a swab in sufficient quantity to cover the incision. Furthermore, the respective euthanasia was performed on days 2, 7, and 15, using an intraperitoneal dose of sodium pentobarbital [16].

Histopathological analysis

Through surgical precision, a 1 cm×1 cm tissue sample was taken from the dorsocervical area after the euthanasia. The fixation of the sample was performed with 10% neutral formalin buffer, processed by the classical paraffin inclusion technique. The samples were cut to a thickness of 5–8 μm, staining with hematoxylin-eosin. Histopathological observations were made by light microscopy at two magnifications: 10× and 40×. The captured images were allowed to evaluate the re-epithelialization, presence of fibroblasts, granulation tissue, and inflammatory tissue response. For the diagnosis of the healing study, the qualification criteria proposed by Nguyen et al. were used as a reference [17].

Statistical analysis

The data analyses were expressed by the IBM SPSS Statistics 20.0 (IBM Corp., NY, USA). For the histopathology analysis, the Mann–Whitney U-test was used. p<0.01 was considered statistically significant, which is equivalent to a confidence level of 95%.

Results

Table-1 shows the phytochemical analysis of H. sucuuba latex. The presence of each metabolite was considered as positive or negative by a change of color or any precipitation. More so, free amino groups, phenolic compounds, alkaloids, flavonoids, quinones, saponins, terpenes, and steroids were confirmed.

Table-1.

Phytochemical constituents of Himatanthus sucuuba latex (Spruce ex Müll. Arg.) Woodson.

Test Results Phytochemicals
Ninhydrin + Free amino groups
Ferric chloride + Phenolic compounds
Dragendorff’s + Alkaloids
Mayer + Alkaloids
Hager + Alkaloids
Shinoda Flavonoids
Bornträger + Quinones
Foam test + Saponins
Liebermann–Burchard + Terpenes and steroids

+=Positive, −=Negative

Table-2 shows the qualification of the histopathological index of the wound on days 1, 7, and 15; for the negative control, the positive control (commercial cream), and H. sucuuba latex.

Table-2.

Qualitative analysis of the histological evaluation on wound healing effect of Himatanthus sucuuba latex.

Treatment Results
Day 1 Negative control Inflammation: Severe Reepithelialization: Mild Granulation tissue: Thin
Positive control (commercial cream) Inflammation: Moderate Reepithelialization: Mild Granulation tissue: Thin
Himatanthus sucuuba latex Inflammation: Mild Reepithelialization: Moderate Granulation tissue: Moderate
Day 7 Negative control Inflammation: Severe Reepithelialization: Mild Granulation tissue: Thin
Positive control (commercial cream) Inflammation: Mild Reepithelialization: Moderate Granulation tissue: Moderate
Himatanthus sucuuba latex Inflammation: Mild Reepithelialization: Complete Granulation tissue: Moderate
Day 15 Negative control Inflammation: Moderate Reepithelialization: Moderate Granulation tissue: Thin
Positive control (commercial cream) Inflammation: Mild Reepithelialization: Moderate Granulation tissue: Moderate
Himatanthus sucuuba latex Inflammation: Mild Reepithelialization: Complete Granulation tissue: Abundant

The latex of H. sucuuba reduced the time required for epithelialization of the excised wound in mice. A significant (p<0.001) reduction of epithelialization time was observed in mice treated with 100% (w/w) latex, as compared to the negative control group (Table-2).

New vessel formation with scattered inflammatory cells and epithelialization was observed in latex treated mice in the histopathological evaluation of excised skin for 15 days. In fact, when the latex group is compared to the sections from the positive control group (commercial drug), the latex treated mice exhibited a higher number of collagen fibers and fibroblasts. Excised skin of the control group showed an incomplete epithelialization and high grade of inflammation, large ulcers in tissue matrix indicating incomplete wound healing at the end of the treatment.

Figures-1-3 show that the latex has a good healing process with very significant differences in the different groups; evidence-based treatment of mild inflammation, complete re-epithelialization, and abundant granulation tissue compared to the positive control (commercial cream) reflecting mild inflammation, mild re-epithelialization, and moderate granulation tissue.

Figure-1.

Figure-1

Healing process of the control group with hematoxylin and eosin staining (H and E stain, 40×). (a) Day 1: Loss of epithelium with bleeding and fibrinoid exudate, dense infiltrate of polymorphonuclear leukocytes at the level of the dermoepidermal junction. (b) Day 7: Inflammatory reaction filtered by polymorphonuclear leukocytes and eosinophils, which spread from the superficial dermis to the deepest dermis. (c) Day 15: A large inflammatory reaction to polymorphonuclear leukocytes and eosinophils, which spread from the superficial dermis to the deepest dermis.

Figure-2.

Figure-2

Healing process of the positive control group (cream) with hematoxylin and eosin staining (H and E stain, 40×). (a) Day 1: Inflammatory reaction to polymorphonuclear leukocytes, slightly less intense, but also with injury. (b) Day 7: The treated skin appears normal; absence of annexes (hairs and sebaceous glands), which would be atrophy due to the injury performed. (c) Day 15: Preserved skin, decreased skin attachments (hair and glands), and an inflammatory infiltrate of mononuclear cells, such as lymphocytes and macrophages, indicating less intense, chronic inflammation.

Figure-3.

Figure-3

Healing process of the Himatanthus sucuuba latex group (H and E stain, 40×). (a) Day 1: Dense inflammatory reaction, but the epithelium is better preserved, two rows of keratinocytes are observed below the superficial infiltrate. Less severe inflammation in the deep dermis. (b) Day 7: An area with fewer adnexa (hairs and sebaceous glands) than in the rest of the skin, and a little more collagen (fibers or thicker). The treated skin appears normal. (c) Day 15: The skin is within normal limits. There is no scar, which would be a fibrous area, with a decrease in skin attachments.

Discussion

Peru has a rich tradition of plant-based knowledge on health care with a large number of medicinal plants for wound healing and others. H. sucuuba contains several medically active compounds such as plumericin, plumericin C, isoplumericin, both bioactive spirolactone iridoids, and four known pentacyclic triterpenes: Lupeol acetate, lupeol cinnamate, lupeol b-phenyl propionate, and a-amyrin cinnamate, which have been isolated from the bark and latex [18]. A study has shown that the bark has a greater antifungal effect than a control drug (nystatin), this action has been attributed to the triterpenic esters found in the bark [19].

H. sucuuba is the most studied species, with a record of the chemical composition of the latex, bark, leaves, and roots. The identification of plumericin attributed as a potent new inhibitor of the NF-kB ­pathway provides a solid scientific rationale for the traditional use of extracts of H. sucuuba as herbal medicines for the treatment of inflammatory diseases [20]. As shown in Table-1, terpenoids were determined and are considered promising anticancer drugs due to their diverse pharmacological activities, including antiangiogenic, anti-inflammatory, antioxidant effects, and the ability to increase cell differentiation [21].

Latex is used in skin conditions, such as antipyretic, healing of ulcers or wounds on the skin and gastric ulcers, against low back pain, in gastritis, against hernias, herpes, in inflammations of the uterus, malaria, rheumatism, tuberculosis, and tumors [22]. The treated skin with latex appears normal, fairly preserved skin, while the control group decreased its skin attachments (hair and glands), and an infiltrate of mononuclear cells, such as lymphocytes and macrophages, which indicate less intensity and damage in the chronic inflammation. de Miranda et al. [23] determined the hexane fraction of H. sucuuba inhibited in the edema formation by 35.9% at a dose of 200 mg/kg (p.o.). These results indicate a greater advantage in wound healing of the latex in relation to the positive control.

In addition, the proliferative phase is characterized by angiogenesis, collagen deposition, epithelialization, and wound contraction. Angiogenesis involves the growth of new blood vessels from endothelial cells. Fibroblasts activate collagen and fibronectin to form a new extracellular matrix in fibroplasia and granulation tissue formation [24]. In another report, latex of H. sucuuba increased tumor nuclear factor-α, nitric oxide, and decreased transforming growth factor-β production in macrophages which could be involved in its wound healing mechanism [25]. More so, macrophages are the critical key in the wound healing process and provide a useful therapeutic target for wound healing disorders in aging and diabetes, or excessive wound healing in fibrosis [26,27].

There are no toxic, abortive, or birth defects reported in latex of H. sucuuba. However, it is necessary to establish its toxic dose or concentrations in the future.

Conclusion

This study has shown that H. sucuuba latex has properties that promote a wound healing and anti-inflammatory effect on BALB/C mice; therefore, further research on latex derivatives could lead to its application as a treatment for post-surgical wounds.

Authors’ Contributions

LLC and OH conceived the study designed. JLA and LLC performed the experiment. OH and RDH analyzed the data. LF, JPR, and OH drafted and revised the manuscript. All authors read and approved the final manuscript.

Acknowledgments

The authors are thankful to Universidad Nacional Mayor de San Marcos, Peru for providing necessary facilities for this study. This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Competing Interests

The authors declare that they have no competing interests.

Publisher’s Note

Veterinary World remains neutral with regard to jurisdictional claims in published institutional affiliation.

References

  • 1.Rodrigues M, Kosaric N, Bonham C.A, Gurtner G.C. Wound healing:A cellular perspective. Physiol. Rev. 2019;99(1):665–706. doi: 10.1152/physrev.00067.2017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Asadi S.Y, Parsaei P, Karimi M, Ezzati S, Zamiri A, Mohammadizadeh F, Rafieian-kopaei M. Effect of green tea (Camellia sinensis) extract on healing process of surgical wounds in rat. Int. J. Surg. 2013;11(4):332–337. doi: 10.1016/j.ijsu.2013.02.014. [DOI] [PubMed] [Google Scholar]
  • 3.Bhaskar A, Nithya V. Evaluation of the wound-healing activity of Hibiscus rosasinensis L (Malvaceae) in Wistar albino rats. Indian. J. Pharmacol. 2012;44(6):694. doi: 10.4103/0253-7613.103252. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Bhat P.B, Hegde S, Upadhya V, Hegde G.R, Habbu P.V, Mulgund G.S. Evaluation of wound healing property of Caesalpinia mimosoid es Lam. J. Ethnopharmacol. 2016;193:712–724. doi: 10.1016/j.jep.2016.10.009. [DOI] [PubMed] [Google Scholar]
  • 5.Ibrahim N, Wong S.K, Mohamed I.N, Mohamed N, Chin K.Y, Ima-Nirwana S, Shuid A.N. Wound healing properties of selected natural products. Int. J. Environ. Res. Public. Health. 2018;15(11):2360. doi: 10.3390/ijerph15112360. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Lindley L.E, Stojadinovic O, Pastar I, Tomic-Canic M. Biology and biomarkers for wound healing. Plast. Reconstr. Surg. 2016;138(3 Suppl):18S–28S. doi: 10.1097/PRS.0000000000002682. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Chen J, Jayachandran M, Xu B, Yu Z. Sea bass (Lateolabrax maculatus) accelerates wound healing:A transition from inflammation to proliferation. J. Ethnopharmacol. 2019;236 doi: 10.1016/j.jep.2019.03.012. [DOI] [PubMed] [Google Scholar]
  • 8.Shedoeva A, Leavesley D, Upton Z, Fan C. Wound healing and the use of medicinal plants. Evid. Based Complement. Alternat. Med. 2019;2019:2684108. doi: 10.1155/2019/2684108. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Shah A, Amini-Nik S. The role of phytochemicals in the inflammatory phase of wound healing. Int. J. Mol. Sci. 2017;18(5):1068. doi: 10.3390/ijms18051068. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Klein K.C, Guha S.C. Cutaneous wound healing:Current concepts and advances in wound care. Indian. J. Plast. Surg. 2014;47(3):303–317. doi: 10.4103/0970-0358.146574. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Soares F.P, Cavalcante L.F, Romero N.R, Bandeira M.A. Himatanthus Willd ex Schult. (Apocynaceae):Review Pharmacogn. Rev. 2016;10(19):6–10. doi: 10.4103/0973-7847.176549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Luziatelli G, Sørensen M, Theilade I, Mølgaard P. Asháninka medicinal plants:A case study from the native community of Bajo Quimiriki, Junín, Peru. J. Ethnobiol. Ethnomed. 2010;6:21. doi: 10.1186/1746-4269-6-21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Aliyu R.M, Abubakar M.B, Kasarawa A.B, Dabai Y.U, Lawal N, Bello M.B, Fardami A.Y. Efficacy and phytochemical analysis of latex of Calotropis procera against selected dermatophytes. J. Intercult. Ethnopharmacol. 2015;4(4):314–317. doi: 10.5455/jice.20151012012909. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Salim M.N, Masyitha D, Harris A, Balqis U, Iskandar C.D, Hambal M. Darmawi Anti-inflammatory activity of Jatropha curcas Linn latex in cream formulation on CD68 expression in mice skin wound. Vet. World. 2018;11(2):99–103. doi: 10.14202/vetworld.2018.99-103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Gebrehiwot M, Asres K, Bisrat D, Mazumder A, Lindemann P, Bucar F. Evaluation of the wound healing property of Commiphora guidottii Chiov ex. Guid. BMC Complement. Med. Ther. 2015;15:282. doi: 10.1186/s12906-015-0813-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Dwivedi D, Dwivedi M, Malviya S, Singh V. Evaluation of wound healing, anti-microbial and antioxidant potential of Pongamia pinnata in wistar rats. J. Tradit. Complement. Med. 2016;7(1):79–85. doi: 10.1016/j.jtcme.2015.12.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Nguyen V.L, Truong C.T, Nguyen B, Vo T.V, Dao T.T, Nguyen V.D, Trinh D.T, Huynh H.K, Bui C.B. Anti-inflammatory and wound healing activities of calophyllolide isolated from Calophyllum inophyllum Linn. PLoS One. 2017;12(10):e0185674. doi: 10.1371/journal.pone.0185674. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Wood C.A, Lee K, Vaisberg A.J, Kingston D.G.I, Neto C.C, Hammond G.B. A bioactive spirolactone iridoid and triterpenoids from Himatanthus sucuuba. Chem. Pharm. Bull. 2001;49(11):1477–1478. doi: 10.1248/cpb.49.1477. [DOI] [PubMed] [Google Scholar]
  • 19.Lucetti D.L, Lucetti E.C, Bandeira M.A, Veras H.N, Silva A.H, Leal L.K, Lopes A.A, Alves V.C, Silva G.S, Brito G.A, Viana G.B. Anti-inflammatory effects and possible mechanism of action of lupeol acetate isolated from Himatanthus drasticus (Mart.) Plumel. J. Inflamm (Lond) 2010;7:60. doi: 10.1186/1476-9255-7-60. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Waltenberger B, Rollinger J.M, Griesser U.J, Stuppner H, Gelbrich T. Plumeridoid C from the Amazonian traditional medicinal plant Himatanthus sucuuba. Acta Crystallogr. C. 2011;67(pt 10):409–412. doi: 10.1107/S0108270111035761. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Fakhrudin N, Waltenberger B, Cabaravdic M, Atanasov A.G, Malainer C, Schachner D, Heiss E.H, Liu R, Noha S.M, Grzywacz A.M, Mihaly-Bison J, Awad E.M, Schuster D, Breuss J.M, Rollinger J.M, Bochkov V, Stuppner H, Dirsch V.M. Identification of plumericin as a potent new inhibitor of the NF-kB pathway with anti-inflammatory activity in vitro and in vivo. Br. J. Pharmacol. 2014;171(7):1676–1686. doi: 10.1111/bph.12558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Saleem M. Lupeol, a novel anti-inflammatory and anti-cancer dietary triterpene. Cancer Lett. 2009;285(2):109–115. doi: 10.1016/j.canlet.2009.04.033. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.de Miranda A.L.P, Silva J.R, Rezende C.M, Neves J.S, Parrini S.C, Pinheiro M.L, Cordeiro M.C, Tamborini E, Pinto A.C. Anti-inflammatory and analgesic activities of the latex containing triterpenes from Himatanthus sucuuba. Planta Med. 2000;66(3):284–286. doi: 10.1055/s-2000-8572. [DOI] [PubMed] [Google Scholar]
  • 24.Landén N.X, Li D, Ståhle M. Transition from inflammation to proliferation:A critical step during wound healing. Cell. Mol. Life Sci. 2016;73(20):3861–3885. doi: 10.1007/s00018-016-2268-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Soares D.C, Andrade A.L, Delorenzi J.C, Silva J.R, Freire-de-Lima L, Falcão C.A, Pinto A.C, Rossi-Bergmann B, Saraiva E.M. Leishmanicidal activity of Himatanthus sucuuba latex against Leishmania amazonensis. Parasitol. Int. 2010;59(2):173–177. doi: 10.1016/j.parint.2010.01.002. [DOI] [PubMed] [Google Scholar]
  • 26.Pastar I, Stojadinovic O, Yin N.C, Ramirez H, Nusbaum A.G, Sawaya A, Patel S.B, Khalid L, Isseroff R.R, Tomic-Canic M. Epithelialization in wound healing:A comprehensive review. Adv. Wound Care (New Rochelle) 2014;3(7):445–464. doi: 10.1089/wound.2013.0473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Kim S.Y, Nair M.G. Macrophages in wound healing:Activation and plasticity. Immunol. Cell Biol. 2019;97(3):258–267. doi: 10.1111/imcb.12236. [DOI] [PMC free article] [PubMed] [Google Scholar]

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