<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName>Faculty of Veterinary Medicine, Urmia University</PublisherName>
				<JournalTitle>Veterinary Research Forum</JournalTitle>
				<Issn>2008-8140</Issn>
				<Volume>17</Volume>
				<Issue>6</Issue>
				<PubDate PubStatus="epublish">
					<Year>2026</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Effectiveness of harmaline along with meglumine antimoniate on Leishmania major</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>423</FirstPage>
			<LastPage>430</LastPage>
			<ELocationID EIdType="pii">737240</ELocationID>
			
<ELocationID EIdType="doi">10.30466/vrf.2025.2054947.4685</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mahin</FirstName>
					<LastName>Ghafourzadeh</LastName>
<Affiliation>Department of Pathobiology, Faculty of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran</Affiliation>
<Identifier Source="ORCID">0000-0003-3364-1157</Identifier>

</Author>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Mirzaie</LastName>
<Affiliation>Department of Pathobiology, Faculty of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran</Affiliation>
<Identifier Source="ORCID">0000-0003-1829-1478</Identifier>

</Author>
<Author>
					<FirstName>Iraj</FirstName>
					<LastName>Sharifi</LastName>
<Affiliation>Leishmaniasis Research Center, Kerman University of Medical Sciences, Kerman, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-6894-6834</Identifier>

</Author>
<Author>
					<FirstName>Alireza</FirstName>
					<LastName>Keyani</LastName>
<Affiliation>Leishmaniasis Research Center, Kerman University of Medical Sciences, Kerman, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Ehsan</FirstName>
					<LastName>Salarkiya</LastName>
<Affiliation>Leishmaniasis Research Center, Kerman University of Medical Sciences, Kerman, Iran</Affiliation>
<Identifier Source="ORCID">0000-0001-6125-5101</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2025</Year>
					<Month>03</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>Leishmaniasis is a disease caused by Leishmania species and transmitted &lt;em&gt;via&lt;/em&gt; sandflies. Current control strategies against reservoir hosts and vectors are not eco-friendly. Using harmaline (HA) from Peganum harmala, and meglumine antimoniate (MA) could be a promising therapy. The study aimed to explore the potential treatment outcomes and action mechanisms of HA and MA against &lt;em&gt;Leishmania major&lt;/em&gt; stages by investigating their effectiveness through molecular docking, anti-leishmanial effects, safety assessment, and apoptotic profile evaluations. According to the molecular docking results, the protein-ligand interaction profiler identified that Bcl-2 interacts with HA mainly through hydrogen bonds, while Bax uses both hydrogen and hydrophobic interactions, indicating a stronger binding of HA to Bax compared to Bcl-2. The HA combined with MA (HA/MA) showed potent anti-leishmanial activity without toxicity. &lt;em&gt;In vitro&lt;/em&gt; studies significantly demonstrated that HA inhibited the growth of promastigotes and amastigotes. The HA/MA was more effective in inhibiting parasite growth. Based on the study findings, HA and HA/MA mixture can be considered a viable treatment option for cutaneous Leishmaniasis.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Harmaline</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Leishmania major</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Meglumine antimoniate</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://vrf.iranjournals.ir/article_737240_9fd448a19f1a7ca9489e273335beecc4.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
