<ici-import>
	<journal issn="1409-7621"/>
	<issue number="1" volume="42" year="2019" publicationDate="2019-03-15T09:00:00" coverDate="March 2019" coverUrl="https://macvetrev.mk/Files/Issues/Vol%2042/1/2019cover-42-1.png" numberOfArticles="12">
	<article externalId="2018-0023">
			<type>ORIGINAL_ARTICLE</type>
			<languageVersion language="en">
				<title>Immunohistomorphometric changes of the pituitary gonadotropic cells after testosterone application in a rat model of the andropause</title>
				<abstract>Andropause, the culminating phase of male ageing, is characterized by deregulation of the hypothalamic-pituitarygonadal axis and low circulating free testosterone. The aim of this study was to investigate the immunohistomorphometric characteristics of the pituitary gonadotropic i.e. follicle-stimulating hormone (FSH) and the luteinizing hormone (LH) producing cells after testosterone application in a rat model of the andropause. Middle-aged Wistar rats were divided into orchidectomized (ORX; n=8) and testosterone treated orchidectomized (ORX+T; n=8) groups. Testosterone propionate (5 mg/kg b.m. /day) was administered for three weeks, while the ORX group received the vehicle alone. Immunohistochemically stained FSH and LH cells underwent morphometric and optical density-related analysis, while circulating concentrations of the sex steroids were measured by immunoassays. Serum concentrations of testosterone and estradiol were significantly (p &lt; 0.05) increased by 24 and 2.7 fold respectively, compared to the ORX group. The volume of FSH and LH cells was significantly (p &lt; 0.05) decreased by 51.3% and 56.6% respectively, in comparison with ORX rats. Relative volume density of FSH and LH cells was also significantly (p &lt; 0.05) decreased by 54.0% and 72.8% respectively, compared to the ORX group. Results related to the optical density of gonadotropic cells (reflecting their hormonal content) were in line with the morphometric findings i.e. this parameter of FSH and LH cells was significantly (p &lt; 0.05) decreased by 25.7% and 16.2% respectively, in comparison with ORX rats. Conclusion: In conclusion, applied testosterone increased the serum concentrations of sex steroids, as well as it decreased morphometric parameters and optical density of gonadotropic cells in ORX rats.</abstract>
				<pdfFileUrl>https://macvetrev.mk/Files/Article/2020/10.2478/macvetrev-2018-0023/macvetrev-2018-0023.pdf</pdfFileUrl>
				<publicationDate>2019-03-15T09:00:00</publicationDate>
				<pageFrom>5</pageFrom>
				<pageTo>13</pageTo>
				<doi>10.2478/macvetrev-2018-0023</doi>
				<keywords>
					<keyword>andropause</keyword>
					<keyword>testosterone</keyword>
					<keyword>gonadotropic cells</keyword>
					<keyword>immunohistomorphometry</keyword>
					<keyword>optical density</keyword>
				</keywords>
			</languageVersion>
			<authors>
				<author>
					<name>Nataša</name>
					<name2></name2>
					<surname>Ristić</surname>
					<email>negicn@ibiss.bg.ac.rs</email>
					<polishAffiliation>false</polishAffiliation>
					<order>1</order>
					<instituteAffiliation>Department of Cytology, Institute for Biological Research “Siniša Stanković”, University of Belgrade, Despot Stefan Blvd., 142, 11060 Belgrade, Serbia</instituteAffiliation>
					<role>LEAD_AUTHOR</role>
				</author>
				<author>
					<name>Vladimir</name>
					<name2></name2>
					<surname>Ajdžanović</surname>
					<email></email>
					<polishAffiliation>false</polishAffiliation>
					<order>2</order>
					<instituteAffiliation>Department of Cytology, Institute for Biological Research “Siniša Stanković”, University of Belgrade, Despot Stefan Blvd., 142, 11060 Belgrade, Serbia</instituteAffiliation>
					<role>AUTHOR</role>
				</author>
				<author>
					<name>Dragana</name>
					<name2></name2>
					<surname>Petrović-Kosanović</surname>
					<email></email>
					<polishAffiliation>false</polishAffiliation>
					<order>3</order>
					<instituteAffiliation>Department of Cytology, Institute for Biological Research “Siniša Stanković”, University of Belgrade, Despot Stefan Blvd., 142, 11060 Belgrade, Serbia</instituteAffiliation>
					<role>AUTHOR</role>
				</author>
				<author>
					<name>Marko</name>
					<name2></name2>
					<surname>Miler</surname>
					<email></email>
					<polishAffiliation>false</polishAffiliation>
					<order>4</order>
					<instituteAffiliation>Department of Cytology, Institute for Biological Research “Siniša Stanković”, University of Belgrade, Despot Stefan Blvd., 142, 11060 Belgrade, Serbia</instituteAffiliation>
					<role>AUTHOR</role>
				</author>
				<author>
					<name>Gordana</name>
					<name2></name2>
					<surname>Ušćebrka</surname>
					<email></email>
					<polishAffiliation>false</polishAffiliation>
					<order>5</order>
					<instituteAffiliation>Department of Veterinary Medicine, Faculty of Agriculture, University of Novi Sad, Trg Dositeja Obradovića 8, Novi Sad, Serbia</instituteAffiliation>
					<role>AUTHOR</role>
				</author>
				<author>
					<name>Verica</name>
					<name2></name2>
					<surname>Milošević</surname>
					<email></email>
					<polishAffiliation>false</polishAffiliation>
					<order>6</order>
					<instituteAffiliation>Department of Cytology, Institute for Biological Research “Siniša Stanković”, University of Belgrade, Despot Stefan Blvd., 142, 11060 Belgrade, Serbia</instituteAffiliation>
					<role>AUTHOR</role>
				</author>
			</authors>
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		</article>
		</issue>
</ici-import>