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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">87</journal-id>
      <journal-id journal-id-type="index">urn:lsid:arphahub.com:pub:A116C711-4C18-5A38-8F1E-5E97753A8A64</journal-id>
      <journal-title-group>
        <journal-title xml:lang="en">Folia Medica</journal-title>
        <abbrev-journal-title xml:lang="en">FM</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="ppub">0204-8043</issn>
      <issn pub-type="epub">1314-2143</issn>
      <publisher>
        <publisher-name>Plovdiv Medical University</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.3897/folmed.64.e62272</article-id>
      <article-id pub-id-type="publisher-id">62272</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Original Article</subject>
        </subj-group>
        <subj-group subj-group-type="scientific_subject">
          <subject>Dermatology</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Effect of earthworm oil on formation of collagen type III during wound healing process in BALB/c mice</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author" xlink:type="simple" corresp="no">
          <name name-style="western">
            <surname>Afshar</surname>
            <given-names>Mohammad</given-names>
          </name>
          <xref ref-type="aff" rid="A1">1</xref>
          <xref ref-type="aff" rid="A2">2</xref>
        </contrib>
        <contrib contrib-type="author" xlink:type="simple" corresp="no">
          <name name-style="western">
            <surname>Hassanzadeh-Taheri</surname>
            <given-names>Mohammadmehdi</given-names>
          </name>
          <xref ref-type="aff" rid="A1">1</xref>
          <xref ref-type="aff" rid="A3">3</xref>
        </contrib>
        <contrib contrib-type="author" xlink:type="simple" corresp="no">
          <name name-style="western">
            <surname>Zardast</surname>
            <given-names>Mahmood</given-names>
          </name>
          <xref ref-type="aff" rid="A4">4</xref>
        </contrib>
        <contrib contrib-type="author" xlink:type="simple" corresp="yes">
          <name name-style="western">
            <surname>Naderi</surname>
            <given-names>Zahra</given-names>
          </name>
          <xref ref-type="aff" rid="A1">1</xref>
          <email xlink:type="simple">zahra.naderi1993@gmail.com</email>
        </contrib>
      </contrib-group>
      <aff id="A1">
        <label>1</label>
        <addr-line content-type="verbatim">Department of Anatomy, Faculty of Medicine, Birjand University of Medical Sciences, Birjand, Iran</addr-line>
        <institution>Birjand University of Medical Sciences</institution>
        <addr-line content-type="city">Birjand</addr-line>
        <country>Iran</country>
      </aff>
      <aff id="A2">
        <label>2</label>
        <addr-line content-type="verbatim">Medical Toxicology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran</addr-line>
        <institution>Mashhad University of Medical Sciences</institution>
        <addr-line content-type="city">Mashhad</addr-line>
        <country>Iran</country>
      </aff>
      <aff id="A3">
        <label>3</label>
        <addr-line content-type="verbatim">Birjand Cellular and Molecular Research Center, University of Medical Sciences, Birjand, Iran</addr-line>
        <institution>Birjand University of Medical Sciences</institution>
        <addr-line content-type="city">Birjand</addr-line>
        <country>Iran</country>
      </aff>
      <aff id="A4">
        <label>4</label>
        <addr-line content-type="verbatim">Department of Pathology, Birjand University of Medical Sciences, Birjand, Iran</addr-line>
        <institution>Mashhad University of Medical Sciences</institution>
        <addr-line content-type="city">Mashhad</addr-line>
        <country>Iran</country>
      </aff>
      <author-notes>
        <fn fn-type="corresp">
          <p>Corresponding author: Zahra Naderi, Department of Anatomy, Faculty of Medicine, Birjand University of Medical Sciences, Birjand, Iran; Email: <email xlink:type="simple">zahra.naderi1993@gmail.com</email>; Tel.: +98-5154225023</p>
        </fn>
      </author-notes>
      <pub-date pub-type="collection">
        <year>2022</year>
      </pub-date>
      <pub-date pub-type="epub">
        <day>30</day>
        <month>04</month>
        <year>2022</year>
      </pub-date>
      <volume>64</volume>
      <issue>2</issue>
      <fpage>267</fpage>
      <lpage>274</lpage>
      <uri content-type="arpha" xlink:href="http://openbiodiv.net/28EA8475-ADA4-5066-BD9A-9274C660EC6F">28EA8475-ADA4-5066-BD9A-9274C660EC6F</uri>
      <history>
        <date date-type="received">
          <day>20</day>
          <month>12</month>
          <year>2020</year>
        </date>
        <date date-type="accepted">
          <day>15</day>
          <month>04</month>
          <year>2021</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>Mohammad Afshar, Mohammadmehdi Hassanzadeh-Taheri, Mahmood Zardast, Zahra Naderi</copyright-statement>
        <license license-type="creative-commons-attribution" xlink:href="http://creativecommons.org/licenses/by/4.0/" xlink:type="simple">
          <license-p>This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
        </license>
      </permissions>
      <abstract>
        <p>
          <bold>Abstract</bold>
        </p>
        <p><bold>Introduction</bold>: <italic>Eisenia fetida</italic> is a species of earthworm. The oil extracted from this species has been found to have antimicrobial and antioxidant characteristics as well as omega-3, omega-6, and omega-9 fatty acids in its contents. The regenerative properties of this compound are very impressive.</p>
        <p><bold>Aim</bold>: This study aimed to evaluate the effect of earthworm oil on wound healing based on collagen type III formation in the BALB/c mice.</p>
        <p><bold>Materials and methods</bold>: The present experimental study was conducted in Birjand, Iran, in 2019. Forty-eight male adults BALB/c mice were divided into 4 groups (12 mice in each group). The intervention group received earthworm oil, the negative and positive control groups received sesame oil and 1% nitrofurazone cream, respectively, whereas the sham group received no treatment at al. A full-thickness excision wound with a 5-mm disposable surgical punch was made on the dorsal skin of all mice after anesthesia. The wounds in groups 1, 2, and 3 were dressed twice a day. At days 4, 7, 10, and 14 after wounding, excisional biopsy was performed and the sample was examined histologically and immunohistochemically using the ImageJ software. Data were analysed by ANOVA and Tukey tests using SPSS software version 22.</p>
        <p><bold>Results</bold>: In the tissue samples treated with earthworm oil, the number of fibroblast cells and granulation tissue formation and epithelialization significantly increased; the thickness of type III collagen fibers in this group predominantly increased in comparison to other control groups.</p>
        <p><bold>Conclusions</bold>: This study has demonstrated that the earthworm oil has a positive effect on the wound healing process, especially by promoting the collagen synthesis.</p>
      </abstract>
      <kwd-group>
        <label>Keywords</label>
        <kwd>collagen formation</kwd>
        <kwd>earthworm oil</kwd>
        <kwd>mice</kwd>
        <kwd>wound healing</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec sec-type="Introduction" id="SECID0EFF">
      <title>Introduction</title>
      <p>A wound is a tissue injury that might be formed due to various factors such as trauma, burns, surgery, and other destructive events. Wound healing can be considered as a dynamic response to injury that is complex and regular and involves interaction among different types of cells, growth factors, and structural proteins.<sup>[<xref ref-type="bibr" rid="B1">1</xref>]</sup> Annually, chronic wounds affect 6.5 million patients in the United States, with an estimated cost of over $25 million.<sup>[<xref ref-type="bibr" rid="B2">2</xref>]</sup> Many factors, including the blood flow of the wound area, the presence of foreign microorganisms, age, and poor nutrition status, can affect the speed of wound healing. Wound healing is a physiological response to the injured skin. It consists of three complex interactive phases: 1) hemostasis – inflammation phase that starts immediately after injury with the launch of hemostatic mechanisms to stop bleeding immediately and migration of inflammatory cells to injured tissue, 2) proliferation phase in which many important events are formed such as the production of collagens, proteoglycan and fibronectin for the formation of extracellular matrix (ECM), new epithelium and angiogenesis<sup>[<xref ref-type="bibr" rid="B3">3</xref>]</sup>, and 3) remodelling phase in which the ECM is organized to produce new functional tissue and mature collagen fibres<sup>[<xref ref-type="bibr" rid="B4">4</xref>]</sup>. However, the fibroblasts producing the matrix and collagen fibers are the dominant cells in the second stage and are responsible for the synthesis of collagen types. The two dominant types of collagen in wound repair are collagen I and III. Type III collagen is fibrillar-forming collagen that plays some important roles in fibrillogenesis and determines the fibril diameter of collagen I.<sup>[<xref ref-type="bibr" rid="B3">3</xref>]</sup> It has been reported that accelerating the wound healing process is an important part of the field of healing.<sup>[<xref ref-type="bibr" rid="B5">5</xref>]</sup></p>
      <p>Nowadays, there is a tendency to use traditional drugs to heal wounds as they are known to be more cost-effective and have fewer side effects in comparison with the chemical drugs used for the purpose.<sup>[<xref ref-type="bibr" rid="B5">5</xref>]</sup> However, one of the challenges in medical research is how a traditional compound can be made to be useful.<sup>[<xref ref-type="bibr" rid="B5">5</xref>,6]</sup> Recently, essential oils have been studied and used by the pharmaceutical and food industries because these compounds have been shown to have a variety of therapeutic effects.<sup>[<xref ref-type="bibr" rid="B7">7</xref>,8]</sup> Earthworms have been used in the traditional medicine of many countries such as Iran, China, Japan, and Indonesia for many therapeutic purposes and have been also known in eastern medicine as anti-inflammatory, analgesic, and antipyretic agents.<sup>[<xref ref-type="bibr" rid="B9">9</xref>]</sup></p>
      <p>The healing property of the earthworm is very impressive. In Iran, earthworm oil is extracted from the species <italic>Eisenia fetida</italic> which contains omega-3, omega-6, and omega-9 fatty acids.<sup>[<xref ref-type="bibr" rid="B10">10</xref>]</sup> The inflammatory impacts of earthworm oil result from the omega fatty acids which are components of the earthworm oil.<sup>[<xref ref-type="bibr" rid="B11">11</xref>]</sup></p>
      <p>The alcoholic extract of the worm also has a strong antimicrobial activity.<sup>[<xref ref-type="bibr" rid="B10">10</xref>]</sup> Studies have shown that the macromolecular mixture with glycoprotein 90 (G90) extracted from earthworms has antibacterial and antioxidants effects.<sup>[<xref ref-type="bibr" rid="B12">12</xref>]</sup> On the other hand, the anti-inflammatory and angiogenic effects of omega-3 fatty acids have been confirmed by many studies.<sup>[<xref ref-type="bibr" rid="B10">10</xref>]</sup> There are also lymphokines in the body of these worms which with their fibrinolytic effects can be involved in further developing the blood supply of the organs.<sup>[<xref ref-type="bibr" rid="B8">8</xref>]</sup> Hence, this oil may modify many of the potential mechanisms involved in wound healing and improve it.<sup>[<xref ref-type="bibr" rid="B13">13</xref>]</sup></p>
      <p>To date, only few studies have focused on finding the wound healing effects of this oil.</p>
    </sec>
    <sec sec-type="Aim" id="SECID0EIBAC">
      <title>Aim</title>
      <p>Therefore, the present study was designed to examine the healing effect of earthworm oil based on collagen type III formation in the wounds identified in the skin of BALB/c mice.</p>
    </sec>
    <sec sec-type="materials|methods" id="SECID0ENBAC">
      <title>Materials and methods</title>
      <sec sec-type="methods" id="SECID0ERBAC">
        <title>Methods</title>
        <sec sec-type="Animals" id="SECID0EVBAC">
          <title>
            <italic>Animals</italic>
          </title>
          <p>This experimental study was performed on 48 adult male BALB/C mice (25±5 g), which were provided by the Experimental Medical Research Center of Birjand University of Medical Sciences (Ethical Code: IR.BUMS.REC.1397.003). The animals were housed in clean individual cages (12:12 hour light/dark cycle, at a temperature of 22°–24°C) and provided free access to standard food and water.</p>
        </sec>
        <sec sec-type="Preparing earthworm oil" id="SECID0E4BAC">
          <title>
            <italic>Preparing earthworm oil</italic>
          </title>
          <p><italic>Eisenia fetida</italic> (<italic>Annelida, Lumbricidae</italic>) was purchased from an earthworm breeding farm in Mashhad (Iran). The species of the earthworm was identified by a zoologist at Ferdowsi University (Mashhad, Iran). The worms were washed with tap water to remove the soil particles from the bodies of earthworms. They were then soaked in normal saline for 24 hours to clean the earthworm gut. After drying the worms with an incubator, 500 grams of <italic>Eisenia fetida</italic> powder was mixed in a litre of sesame oil, and then exposed to sunlight for 40 days.</p>
        </sec>
        <sec sec-type="Excisional dermal wound technique" id="SECID0EMCAC">
          <title>
            <italic>Excisional dermal wound technique</italic>
          </title>
          <p>The mice were first anesthetized with intraperitoneal injection of ketamine hydrochloride (70 mg/kg) and xylazine (13.4 mg/kg), then the skin on the mice backs was shaved and two symmetrical full-thickness excisional wounds were created beside the midline (at least 2 cm apart) using 5 disposable surgical punches.<sup>[<xref ref-type="bibr" rid="B14">14</xref>]</sup> The mice were randomly divided into 4 groups (n=12). The intervention group was treated with earthworm oil (group 1), the negative control group received sesame oil (group 2), the positive control group received nitrofurazone 0.2% (group 3)<sup>[<xref ref-type="bibr" rid="B7">7</xref>]</sup> and the sham group received no treatment (group 4). The animals received topical treatment twice a day at a 12-h interval (at 8:00 a.m. and 8:00 p.m.)<sup>[<xref ref-type="bibr" rid="B7">7</xref>]</sup> for 14 consecutive days from baseline (day 0, the day the wound was made). During the study, if a mouse had a skin infection, it was discarded from the study. Digital imaging studies of the wound was performed (on days 4, 7, 10, and 14) using a digital camera (Mavica FD91, Sony). On days 4, 7, 10, and 14 post-wounding, three mice of each group were sacrificed and the excisional wound areas were removed for routine histological and immunohistochemical studies.</p>
        </sec>
        <sec sec-type="Histopathological analysis" id="SECID0EKDAC">
          <title>
            <italic>Histopathological analysis</italic>
          </title>
          <p>Biopsy specimens were obtained from the wound area and fixed in formalin 10% (48 hours), then the samples were prepared for tissue processing and were finally serially sectioned (5 µm) using a microtome. Sections (n=10) from each group were stained with H&amp;E, also specific stainings including Masson’s trichrome stain and immunohistochemistry (IHC) were performed to assess the morphological details and the density of collagen types I and III.<sup>[<xref ref-type="bibr" rid="B15">15</xref>]</sup> For each specimen, epidermal parameters (i.e. re-epithelization) and dermal parameters including inflammatory cells (i.e. lymphocytes and neutrophils), granulation, and collagen synthesis were evaluated by ImageJ software. To perform IHC, 5-µm sections (n=20) were placed on charged slides and rehydrated. The sections were washed in 0.1 M phosphate-buffered saline (PBS) (pH=7.4). Endogenous peroxidase activity was blocked by 0.3% (v/v) H<sub>2</sub>O<sub>2</sub>. The samples were then incubated in PBS (0.01 M) with Triton X100 (0.025%) for 10 min at room temperature. Samples were incubated in goat serum 10% with 1% BSA in 0.01 M PBS for 30 min. Primary antibody (Abcam Ab7778 Anti-Collagen III Antibody) with concentration (1.55% BSA1%) was poured on the samples for 12 h (overnight). Slides were washed with PBS containing Triton X100 (0.025%) in two successive 5-min steps. Secondary antibody (Abcam Ab7090 Goat Anti-Rabbit IgG H&amp;L (HRP)) was diluted to 1.000% BSA1% and incubated on the samples at room temperature for 2 hours. PBS containing Triton X100 (0.025%) was used for 5 min to wash on the slides. A mixture of two solutions, DAB (0.03%, Sigma Aldrich) of and H<sub>2</sub>O<sub>2</sub> (0.01%) dissolved in PBS (0.01 M), was added to the samples for 30 min. Then, slides were washed with distilled water (3 min) to eliminate DAB from non-specific locations. Mayer hematoxylin staining (for 10 seconds) was the next step. After final washing, the slides were dehydrated and mounted. Images were obtained using an Olympus SZX microscope fitted with Pixera digital camera.</p>
        </sec>
      </sec>
      <sec sec-type="Statistical analysis" id="SECID0ECEAC">
        <title>Statistical analysis</title>
        <p>Data were analysed using SPSS statistical software (version 22). One-way ANOVA test was used to intergroup comparisons and Tukey test was used to compare data obtained from all groups of the study. The quantitative data were expressed as mean ± standard deviation (SD). Results with <italic>p</italic>&lt;0.05 were considered statistically significant.</p>
      </sec>
    </sec>
    <sec sec-type="Results" id="SECID0EKEAC">
      <title>Results</title>
      <sec sec-type="Histopathological analysis" id="SECID0EOEAC">
        <title>Histopathological analysis</title>
        <p>All data related to the inflammatory cells, granulation area, fibroblast, and collagenisation are shown in <bold>Table <xref ref-type="table" rid="T1">1</xref></bold>. On day 4 of the study, the average number of inflammatory cells in the intervention group (earthworm oil) was significantly less than that number in the other control groups (groups 2, 3, 4). During the wound healing, there was no evidence of proliferation of fibroblastic cells, granulation, angiogenesis, and synthesis of collagen fibers on the mentioned day (<italic>p</italic>&gt;0.05). Interestingly, the findings 7 days after wounding showed that the number of inflammatory cells (mononuclear and polymorph) significantly decreased in the mice treated with earthworm oil compared to those treated with nitrofurazone, sesame oil, and the sham group (groups 2, 3, 4) (<italic>p</italic>=0.001) <bold>(Table <xref ref-type="table" rid="T1">1</xref>)</bold>. Also, a significant increase was observed in the treated group with earthworm compared to other control groups (groups 2, 3, 4) when the mean number of fibroblasts was analysed (<italic>p</italic>=0). Furthermore, the rate of granulation tissue formation and angiogenesis were significantly higher in the earthworm oil-treated group than in the control groups (groups 2, 3, 4) (<italic>p</italic>=0.00). On the other hand, on day 10, the average number of inflammatory cells significantly decreased in the earthworm oil-treated group compared to the nitrofurazone-treated, the sesame oil-treated, and the control groups (<italic>p</italic>=0), while the mean number of fibroblasts, the granulation area, and epithelization were found to be greatly increased in the earthworm oil-treated group compared to the other groups (groups 2, 3, 4) (<italic>p</italic>=0, <italic>p</italic>=0.042, and <italic>p</italic>=0, respectively) <bold>(Fig. <xref ref-type="fig" rid="F1">1</xref>)</bold>. Also, in the nitrofurazone-treated group, the mean number of whole fibroblasts and granulation area showed a significant difference in comparison with the control sham group (group 4)(<italic>p</italic>=0.009, p=0.001). The overall average collagen fibers density in the earthworm oil group was significantly higher than in the other groups (groups 2, 3, 4) (<italic>p</italic>=0). The density of collagen fibers in the nitrofurazone-treated group also showed a significant increase compared to the sham and sesame oil groups (groups 3, 4) (<italic>p</italic>=0). The score of type III collagen synthesis in two groups – the earthworm oil and the nitrofurazone-treated groups – was higher than that of the negative and sham control groups (groups 3, 4) (<italic>p</italic>=0, <italic>p</italic>=0.001) <bold>(Fig. <xref ref-type="fig" rid="F2">2</xref>)</bold>. At the end of day 14, in the group treated with earthworm oil, the mean number of fibroblast cells significantly increased compared to the sesame oil and nitrofurazone groups (groups 2, 3) (<italic>p</italic>=0.005). Also, in the nitrofurazone group, the number of fibroblast cells increased compared to the negative and sham control groups (groups 3, 4) (<italic>p</italic>=0.012) <bold>(Table <xref ref-type="table" rid="T1">1</xref>)</bold>. Moreover, the granulation area was significantly increased in the group treated with earthworm oil compared to the sham group (group 4) (<italic>p</italic>=0.00), and in the nitrofurazone-treated group compared to the other groups (groups 3, 4) (<italic>p</italic>=0) <bold>(Fig. <xref ref-type="fig" rid="F1">1</xref>)</bold>. Also, the mean total density of collagen fibers was significantly higher in the earthworm oil group than in the sham, the nitrofurazone, and the sesame oil groups (groups 2, 3, 4) (<italic>p</italic>=0). In this regard, collagen fibers density was significantly increased in the nitrofurazone group when compared with the other control groups (groups 3, 4) (<italic>p</italic>=0.001). In the earthworm oil-treated group, the score of collagen type III synthesis and the mean of epithelialization was higher than in the other groups (groups 2, 3, 4) (<italic>p</italic>=0, <italic>p</italic>=0) <bold>(Table <xref ref-type="table" rid="T2">2</xref>)</bold>.</p>
        <fig id="F1" position="float" orientation="portrait">
          <object-id content-type="arpha">199978D5-1957-57F5-855D-8E1B17A3C960</object-id>
          <label>Figure 1.</label>
          <caption>
            <p>(<bold>i</bold>) Total inflammatory cells infiltration in <bold>a</bold>. (earthworm oil), <bold>b</bold>. (nit), <bold>c</bold>. (sesame oil), and <bold>d</bold>. (sham), Trichrome staining, magnification ×400 in 257/55×334/65 μm<sup>2</sup> at day 10; (<bold>ii</bold>) Collagenization in <bold>a</bold>. (earthworm oil), <bold>b</bold>. (nit), <bold>c</bold>. (sesame oil), <bold>d</bold>. (sham), Trichrome staining, magnification ×400 in 257/55×334/65 μm<sup>2</sup> at day 10; (<bold>iii</bold>) The area of granulation in <bold>a</bold>. (earthworm oil), <bold>b</bold>. (nit), <bold>c</bold>. (sesame oil), <bold>d</bold>. (sham), Trichrome staining, magnification ×400 in 3204/12×2401/34 μm<sup>2</sup> at day 10.</p>
          </caption>
          <graphic xlink:href="foliamedica-64-2-e62272-g001.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_684592.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/684592</uri>
          </graphic>
        </fig>
        <table-wrap id="T1" position="float" orientation="portrait">
          <label>Table 1.</label>
          <caption>
            <p>The effect of earthworm oil on dermal and epidermal parameters in wound healing</p>
          </caption>
          <table id="TID0EFJAE" rules="all">
            <tbody>
              <tr>
                <td rowspan="1" colspan="1"/>
                <td rowspan="1" colspan="1">
                  <bold>Day</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Earthworm oil</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Nitrofurazone</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Sesame oil</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Sham</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold><italic>P</italic>-value<sup>1</sup></bold>
                </td>
              </tr>
              <tr>
                <td rowspan="3" colspan="1">Inflammatory cells</td>
                <td rowspan="1" colspan="1">4</td>
                <td rowspan="1" colspan="1">22.00±4.83 <sup>a,b</sup></td>
                <td rowspan="1" colspan="1">29.50±3.89 <sup>a</sup></td>
                <td rowspan="1" colspan="1">32.7±3.8</td>
                <td rowspan="1" colspan="1">34.8±7.08</td>
                <td rowspan="1" colspan="1">&lt;0.001</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">7</td>
                <td rowspan="1" colspan="1">30.20±4.13 <sup>a,b</sup></td>
                <td rowspan="1" colspan="1">41.4±2.36 <sup>a</sup></td>
                <td rowspan="1" colspan="1">47.8±5.99</td>
                <td rowspan="1" colspan="1">50.60±4.19</td>
                <td rowspan="1" colspan="1">&lt;0.001</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">10</td>
                <td rowspan="1" colspan="1">18.9±3.51 <sup>a,b</sup></td>
                <td rowspan="1" colspan="1">24.4±4.24 <sup>a</sup></td>
                <td rowspan="1" colspan="1">31.5±3.34</td>
                <td rowspan="1" colspan="1">34.4±3.7</td>
                <td rowspan="1" colspan="1">&lt;0.001</td>
              </tr>
              <tr>
                <td rowspan="3" colspan="1">Granulation</td>
                <td rowspan="1" colspan="1">7</td>
                <td rowspan="1" colspan="1">1883603.474±312649.66 <sup>a,b</sup></td>
                <td rowspan="1" colspan="1">1077241.91±551699.52</td>
                <td rowspan="1" colspan="1">1036133.59±201206.95</td>
                <td rowspan="1" colspan="1">120902.47±375595.26</td>
                <td rowspan="1" colspan="1">0.002</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">10</td>
                <td rowspan="1" colspan="1">1688831.86±709933.136 <sup>a</sup></td>
                <td rowspan="1" colspan="1">211386.421±605012.67 <sup>a</sup></td>
                <td rowspan="1" colspan="1">1767479.59±339268.36</td>
                <td rowspan="1" colspan="1">925183.86±155969.78</td>
                <td rowspan="1" colspan="1">0.042</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">14</td>
                <td rowspan="1" colspan="1">1302440.497 <sup>a</sup> ±231688.6405</td>
                <td rowspan="1" colspan="1">1438549.87±191935.661 <sup>a</sup></td>
                <td rowspan="1" colspan="1">1239835.689±237112.4971</td>
                <td rowspan="1" colspan="1">742293.2522±131162.5436</td>
                <td rowspan="1" colspan="1">&lt;0.001</td>
              </tr>
              <tr>
                <td rowspan="2" colspan="1">Collagenization</td>
                <td rowspan="1" colspan="1">10</td>
                <td rowspan="1" colspan="1">0.33±0.016 <sup>a,b</sup></td>
                <td rowspan="1" colspan="1">0.29470±0.16</td>
                <td rowspan="1" colspan="1">0.25570±0.12</td>
                <td rowspan="1" colspan="1">0.24319±0.01</td>
                <td rowspan="1" colspan="1">&lt;0.001</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">14</td>
                <td rowspan="1" colspan="1">0.5871±0.030 <sup>a,b</sup></td>
                <td rowspan="1" colspan="1">0.49503±0.029 <sup>a</sup></td>
                <td rowspan="1" colspan="1">0.5387±0.033</td>
                <td rowspan="1" colspan="1">0.46570±0.21</td>
                <td rowspan="1" colspan="1">&lt;0.001</td>
              </tr>
              <tr>
                <td rowspan="3" colspan="1">Fibroblast</td>
                <td rowspan="1" colspan="1">7</td>
                <td rowspan="1" colspan="1">27.9±2.02 <sup>a,b</sup></td>
                <td rowspan="1" colspan="1">21.30±2.26</td>
                <td rowspan="1" colspan="1">22.1±3.95</td>
                <td rowspan="1" colspan="1">19.50±1.58</td>
                <td rowspan="1" colspan="1">&lt;0.001</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">10</td>
                <td rowspan="1" colspan="1">50.8±2.52 <sup>a,b</sup></td>
                <td rowspan="1" colspan="1">42.6±4.14 <sup>a</sup></td>
                <td rowspan="1" colspan="1">36±4.15</td>
                <td rowspan="1" colspan="1">36.5±4.90</td>
                <td rowspan="1" colspan="1">&lt;0.001</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">14</td>
                <td rowspan="1" colspan="1">34.80±4.82 <sup>a</sup></td>
                <td rowspan="1" colspan="1">30.10±2.42 <sup>a</sup></td>
                <td rowspan="1" colspan="1">25.90±6.04</td>
                <td rowspan="1" colspan="1">20.20±3.25</td>
                <td rowspan="1" colspan="1">&lt;0.001</td>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn>
              <p><italic>P</italic>-value<sup>1</sup>: <sup>a</sup>: compared with the sham control group; <sup>b</sup>: compared with the nitrofurazone group</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
        <fig id="F2" position="float" orientation="portrait">
          <object-id content-type="arpha">7EB592AC-D130-5560-B734-7594AB5D58F0</object-id>
          <label>Figure 2.</label>
          <caption>
            <p>Comparative collagen type III images at days 10 and 14: samples in the studied groups. Magnification ×400 in 257/55×334/65 μm<sup>2</sup> (IHC staining).</p>
          </caption>
          <graphic xlink:href="foliamedica-64-2-e62272-g002.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_684593.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/684593</uri>
          </graphic>
        </fig>
        <table-wrap id="T2" position="float" orientation="portrait">
          <label>Table 2.</label>
          <caption>
            <p>The effect of earthworm oil on type III collagen synthesis in wound healing</p>
          </caption>
          <table id="TID0EDYAE" rules="all">
            <tbody>
              <tr>
                <td rowspan="1" colspan="1">
                  <bold>Collagenization</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Day</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Earthworm oil</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Nitrofurazone</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Sesame oil</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Sham</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold><italic>P</italic>-value<sup>1</sup></bold>
                </td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">Collagen type III</td>
                <td rowspan="1" colspan="1">10</td>
                <td rowspan="1" colspan="1">0.22516±0.018 <sup>a,b</sup></td>
                <td rowspan="1" colspan="1">0.17864±0.020 <sup>a</sup></td>
                <td rowspan="1" colspan="1">0.15977±0.019</td>
                <td rowspan="1" colspan="1">0.14342±0.029</td>
                <td rowspan="1" colspan="1">&lt;0.001</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1"/>
                <td rowspan="1" colspan="1">14</td>
                <td rowspan="1" colspan="1">0.17334±0.023 <sup>a,b</sup></td>
                <td rowspan="1" colspan="1">0.16265±0.19 <sup>a</sup></td>
                <td rowspan="1" colspan="1">0.13128±0.11</td>
                <td rowspan="1" colspan="1">0.12476±0.02</td>
                <td rowspan="1" colspan="1">&lt;0.001</td>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn>
              <p><sup>a</sup>: compared with the sham control group; <sup>b</sup>: compared with the nitrofurazone group</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
      </sec>
    </sec>
    <sec sec-type="Discussion" id="SECID0EOHAC">
      <title>Discussion</title>
      <p>Earthworm oil has been reported to have several biological activities including anti-oxidative, anti-microbial, and anti-coagulative functions. Also, the benefits it has for tissue regeneration and wound healing have been recently proved.</p>
      <p>The results of our study showed that earthworm oil exerts positive effects on different stages of wound healing, especially on the process of collagen type III formation. Wound healing is a natural response of injured skins that consists of three interactive phases including inflammation, proliferation, and remodelling.<sup>[<xref ref-type="bibr" rid="B3">3</xref>]</sup> The inflammatory phase starts immediately after injury and is characterized by the influx of two important leukocytes, lymphocytes, and neutrophils.<sup>[<xref ref-type="bibr" rid="B16">16</xref>]</sup> In the present study, the results obtained in days 4, 7, and 10 showed that treatment with earthworm oil could decrease inflammation and infiltration of inflammatory cells. Mathur et al. showed that petroleum ether fraction of earthworm extract had a comparable anti-inflammatory effect to that of aspirin.<sup>[<xref ref-type="bibr" rid="B17">17</xref>]</sup> In another study, the anti-inflammatory activity of <italic>Eutyphoeus gammiei</italic> (a type of earthworm species) was assessed in the carrageenan-induced animal model and the results of this study confirmed the previous study.<sup>[<xref ref-type="bibr" rid="B18">18</xref>]</sup> Moreover, Balamurugan et al. reported similar results in their study.<sup>[<xref ref-type="bibr" rid="B19">19</xref>]</sup></p>
      <p>On the other hand, the proliferative or repair phase is characterized by granulation tissue formation, angiogenesis, wound contraction, and epithelialization.<sup>[<xref ref-type="bibr" rid="B3">3</xref>]</sup> Fibroblasts, as the main cell type in granulation tissue formation, are involved in the proliferation process and produce matrix components, including hyaluronan, fibronectin, proteoglycans, and procollagen (types I and III).<sup>[<xref ref-type="bibr" rid="B3">3</xref>]</sup> The results of days 7, 10, and 14 of our study revealed that treatment with earthworm oil could increase the mean number of fibroblast cells and the thickness of the granulation tissue. Yang et al. investigated the therapeutic effects of earthworm extract (G-90´), which was separated from the head tissue of <italic>Eisenia fetida</italic>, on the wound healing process in vitro and in vivo; their results showed the bioactive proteins (ES2) in G-90´ enhanced the proliferative phase in the acute wound healing process.<sup>[<xref ref-type="bibr" rid="B20">20</xref>]</sup> Their results have been considered as a new concept in using such a natural material in wound healing. Furthermore, Grdiša et al. investigated the efficacy of a glycolipoprotein tissue homogenate extracted from <italic>Eisenia fetida</italic> (G-90) to activate signal transduction pathways, which are involved in wound healing.<sup>[<xref ref-type="bibr" rid="B21">21</xref>]</sup> Their results showed that treatment with G-90 could stimulate the synthesis of the epidermal growth factor (EGF, 10-fold elevations) and fibroblast growth factor (FGF, 5-fold elevations) in the wound compared to the healthy skin.<sup>[<xref ref-type="bibr" rid="B21">21</xref>]</sup> EGF and FGF by increasing the proliferation of epithelial cells and promoting angiogenesis and growth of fibroblast cells, respectively, could promote the rate of wound healing.<sup>[<xref ref-type="bibr" rid="B21">21</xref>]</sup> However, it seems that one of the causes of fibroblast proliferation is related to the FGF level. We strongly suggest that the levels of FGF and EGF should be investigated in future studies.</p>
      <p>The final step of wound healing is the maturation phase. In this stage, the granulation tissue is converted into mature connective tissue regeneration.<sup>[<xref ref-type="bibr" rid="B3">3</xref>]</sup> The normal skin contains about 80% type I collagen and 20% type III collagen. Collagen type III, which is involved in fibrillogenesis and determination of the fibril diameter of collagen I, is made by myofibroblasts during the early stages of granulation tissue formation.<sup>[<xref ref-type="bibr" rid="B3">3</xref>]</sup> Moreover, in the early stages of healing, the expression of collagen type III increases relative to collagen I, resulting in an increased ratio between the two collagen subtypes from 20% up to 50% collagen III, but during maturation of the scar, this ratio backs to the normal levels.<sup>[<xref ref-type="bibr" rid="B3">3</xref>]</sup></p>
      <p>In the present study, on days 10 and 14, treatment with earthworm oil increased the density of collagen fibers. Heydari et al., by evaluating the comparative effects of earthworm extract and phenytoin sodium on suture wound healing in Goldfish (Carassiusauratus), reported that the earthworm extract could produce better collagen fibers, increase the formation of granulation tissues, angiogenesis, and fibroblast proliferation, and also could decrease lipid peroxidation (LPO) in fish serum.<sup>[<xref ref-type="bibr" rid="B22">22</xref>]</sup> Wound contraction has been considered as a good factor for evaluating the rate of wound healing.<sup>[<xref ref-type="bibr" rid="B3">3</xref>]</sup> The contraction of the wound is done by differentiated myofibroblasts from migrating fibroblasts in granulation tissue.<sup>[<xref ref-type="bibr" rid="B3">3</xref>]</sup> Differentiated myofibroblasts lead to the formation of pseudopodia, which are involved in attaching to fibronectin and collagen in the ECM.<sup>[<xref ref-type="bibr" rid="B23">23</xref>]</sup> The process of wound contraction is initiated by this attachment.<sup>[<xref ref-type="bibr" rid="B23">23</xref>]</sup></p>
      <p>The results of this study showed that treatment with earthworm oil led to complete re-epithelization of the epidermal layer with a higher percentage of wound contraction. Earthworm oil contains omega-3, omega-6, and omega-9 fatty acids; hence, it seems that these fatty acids, through their anti-inflammatory and angiogenic properties, could modify many of the potential mechanisms involved in reducing the diameter of the wound and finally improve wound healing. Cardoso et al. showed that omega-6 had better effects on wound healing in mice compared to omega-3 and omega-9.<sup>[<xref ref-type="bibr" rid="B24">24</xref>]</sup> On the other hand, it has been reported that omega-6 (30 µM treatment with omega-6) could decrease cyclooxygenase-2 (COX-2) level and also induce the expression of collagen type III. Furthermore, this study also showed that omega-3 fatty acid is involved in the early closure of open wounds, but not as much as the oleic acid.<sup>[<xref ref-type="bibr" rid="B24">24</xref>,25]</sup> Administration of the COX-2 inhibitor delayed re-epithelialization in the early phase of wound healing and also inhibited angiogenesis.<sup>[<xref ref-type="bibr" rid="B25">25</xref>]</sup></p>
    </sec>
    <sec sec-type="Conclusions" id="SECID0EZMAC">
      <title>Conclusions</title>
      <p>The study presented the results about the role of earthworm oil in the wound healing process by a significant proliferation of fibroblast and collagen type III synthesis.</p>
    </sec>
  </body>
  <back>
    <ack>
      <title>Conflict of Interests</title>
      <p>The authors declare that there is no conflict of interests.</p>
      <p>
        <bold>Acknowledgments</bold>
      </p>
      <p>The current study was extracted from an MSc thesis (455454) in anatomical science by Zahra Naderi at Birjand University of Medical Sciences, Birjand, Iran.</p>
    </ack>
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</article>
