<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>International Journal of Radiation Research</title>
<title_fa>نشریه پرتو پژوه</title_fa>
<short_title>Int J Radiat Res</short_title>
<subject>Basic Sciences</subject>
<web_url>http://ijrr.com</web_url>
<journal_hbi_system_id>79</journal_hbi_system_id>
<journal_hbi_system_user>journal79</journal_hbi_system_user>
<journal_id_issn>2322-3243</journal_id_issn>
<journal_id_issn_online>2345-4229</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.61882/ijrr</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1398</year>
	<month>7</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2019</year>
	<month>10</month>
	<day>1</day>
</pubdate>
<volume>17</volume>
<number>4</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Topically applied melatonin ameliorates radiation-induced skin fibrosis in mice
</title>
	<subject_fa>Radiation Biology</subject_fa>
	<subject>Radiation Biology</subject>
	<content_type_fa>تحقيق بديع</content_type_fa>
	<content_type>Original Research</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;div style=&quot;text-align: justify;&quot;&gt;Background: We investigated whether topical administration of melatonin ameliorates radiation-induced skin fibrosis (RISF) and inhibits the expression of profibrogenic genes in mice. Materials and Methods: Forty-eight female BALB/c mice were randomly divided into three groups: topically applied 5% ethanol (Control), topically applied 5% ethanol plus irradiation (IR), and topically applied melatonin plus irradiation (Mel+IR). The right hind legs of the IR and Mel+IR group mice were exposed to two fractions of electron beam radiation (20 Gy &amp;times; 2). For 4 weeks, melatonin solution (10 mg/day) was topically applied to Mel+IR group mice. Fourteen days after IR, the relative levels of transforming growth factor (TGF)-&amp;beta;1 mRNA expression and TGF-&amp;beta;1 protein in skin specimens were analyzed by real-time quantitative PCR and immunohistochemical staining. Dermal thickness and tissue collagen accumulation were measured at 100 days post irradiation. Results: The Radiation caused a 2.2-fold increase in TGF-&amp;beta;1 mRNA expression relative to that in control group, which was decreased by 37% following melatonin treatment (P = 0.024). We also observed substantial reduction of TGF-&amp;beta;1 expression in immunohistochemical studies. The mean values of dermal thickness were 105 &amp;plusmn; 11 &amp;mu;m (Control), 195 &amp;plusmn; 21 &amp;mu;m (IR), and 148 &amp;plusmn; 19 &amp;mu;m (Mel+IR). Dermal thickness and collagen accumulation, which increased in the IR group, was significantly reduced by topically applied melatonin.&amp;nbsp; Conclusion: Topical administration of melatonin successfully attenuated RISF.&lt;/div&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Melatonin, Radiation, Fibrosis, Transforming growth factor-β, Topical application.</keyword>
	<start_page>617</start_page>
	<end_page>624</end_page>
	<web_url>http://ijrr.com/browse.php?a_code=A-10-1-824&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>D.H. </first_name>
	<middle_name></middle_name>
	<last_name>Kim</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>7900319475328460014009</code>
	<orcid>7900319475328460014009</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Radiation Oncology, Otorhinolaryngology, and Hemato-oncology, Biomedical Research Institute, Pusan National University Hospital and Pusan National University School of Medicine, Pusan National University, Busan, Korea</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Y.M. </first_name>
	<middle_name></middle_name>
	<last_name>Choi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>7900319475328460014010</code>
	<orcid>7900319475328460014010</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Radiation Oncology, DongA University Hospital, Busan, Korea</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Y.K. </first_name>
	<middle_name></middle_name>
	<last_name>Ki</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>7900319475328460014011</code>
	<orcid>7900319475328460014011</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Radiation Oncology, Pusan National University Yangsan Hospital and Pusan National University School of Medicine, Yangsan, Korea</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>K.S. </first_name>
	<middle_name></middle_name>
	<last_name>Cho</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>7900319475328460014012</code>
	<orcid>7900319475328460014012</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Radiation Oncology, Otorhinolaryngology, and Hemato-oncology, Biomedical Research Institute, Pusan National University Hospital and Pusan National University School of Medicine, Pusan National University, Busan, Korea</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Y.J. </first_name>
	<middle_name></middle_name>
	<last_name>Choi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>7900319475328460014013</code>
	<orcid>7900319475328460014013</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Radiation Oncology, Otorhinolaryngology, and Hemato-oncology, Biomedical Research Institute, Pusan National University Hospital and Pusan National University School of Medicine, Pusan National University, Busan, Korea</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>W.T. </first_name>
	<middle_name></middle_name>
	<last_name>Kim</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>rokwt@hanmail.net </email>
	<code>7900319475328460014014</code>
	<orcid>7900319475328460014014</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Radiation Oncology, Otorhinolaryngology, and Hemato-oncology, Biomedical Research Institute, Pusan National University Hospital and Pusan National University School of Medicine, Pusan National University, Busan, Korea</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
