<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Urmila M Aswar</style></author><author><style face="normal" font="default" size="100%">Savita R. Nimse</style></author><author><style face="normal" font="default" size="100%">Prasad A. Thakurdesai</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Androgenic Efficacy and Mechanism of Glycosides-Based  Standardized Fenugreek Seeds Extract Through Aromatase And  5-Alpha Reductase Inhibition</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Androgenic</style></keyword><keyword><style  face="normal" font="default" size="100%">Fenugreek extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Glycosides</style></keyword><keyword><style  face="normal" font="default" size="100%">Sexual Behavior</style></keyword><keyword><style  face="normal" font="default" size="100%">Spermatogenic</style></keyword><keyword><style  face="normal" font="default" size="100%">Testosterone</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">09-19</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Fenugreek seeds glycosides content have many health benefits. &lt;strong&gt;Objective:&lt;/strong&gt; To evaluate the androgenic efficacy and probable mechanism of glycosides-based standardized fenugreek seed extract (SFSE-G) in laboratory rats. &lt;strong&gt;Methods:&lt;/strong&gt; Male Wistar rats were administrated with 28-days of once-daily oral administration of SFSE-G (10 or 35 mg/kg) on sexual and orientational behavior with female rats, serum testosterone concentrations, weights of reproductive system-related organs (seminal vesicles, prostate, levator ani), nitric oxide level in penis homogenate, sperm count in the cauda epididymis, and testis histology were evaluated. Separate groups of rats with a positive control (testosterone propionate (10 mg/ kg, s.c. bi-weekly) and vehicle control (distilled water) were maintained. In addition, the safety of acute intravenous administration of SFSE-G (1 mg/kg) on cardiovascular function parameters was evaluated. Moreover, the inhibitory potential of SFSE-G against aromatase and 5-alpha-reductase enzymes was evaluated in vitro. &lt;strong&gt;Results:&lt;/strong&gt; Subacute administration of SFSE-G (35 mg/kg, oral) to male rats showed androgenic efficacy in sexual behavior (increased mounting and intromission latency and rearing), with increased weights of seminal vehicles, prostate and levator ani muscles, serum testosterone levels, sperm count, and penile NO concentration, while preserving the normal architecture of the testes. Acute intravenous administration of SFSE-G to rats increased intracavernous pressure but retained normal cardiovascular parameters, such as blood pressure, heart rate, and corrected QT interval (QTc). SFSE-G showed significant inhibition of aromatase and 5-alpha-reductase in vitro. &lt;strong&gt;Conclusion:&lt;/strong&gt; SFFE-G exhibited significant androgenic and spermatogenic efficacy, mediated through testosterone metabolism inhibition, without affecting the cardiovascular system in laboratory rats.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">09</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Urmila M Aswar&lt;sup&gt;1&lt;/sup&gt;, Savita R. Nimse&lt;sup&gt;2&lt;/sup&gt;, Prasad A. Thakurdesai&lt;sup&gt;2&lt;/sup&gt;,&lt;sup&gt;*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, Poona College of Pharmacy, Bharati Vidyapeeth Deemed University, Pune, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Scientific affairs, Indus Biotech Limited, 1, Rahul Residency, Off Salunke Vihar Road, Kondhwa, Pune 411048, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Saba Khair Alddin Ibrahim</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Assessment of Serum Irisin and Vaspin in Women with Polycystic Ovary Syndrome in Mosul City</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">FSH</style></keyword><keyword><style  face="normal" font="default" size="100%">Insulin</style></keyword><keyword><style  face="normal" font="default" size="100%">Irisin</style></keyword><keyword><style  face="normal" font="default" size="100%">LH</style></keyword><keyword><style  face="normal" font="default" size="100%">PCOS.</style></keyword><keyword><style  face="normal" font="default" size="100%">Testosterone</style></keyword><keyword><style  face="normal" font="default" size="100%">Vaspin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">212-215</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Patients with “polycystic ovary syndrome” (PCOS) may have changes in adipokine levels due to obesity rather than PCOS per se. This should be taken into account as there is a correlation between adipokine levels and BMI. The objective of the subsequent investigation was to measure serum levels of irisin and vaspin in women with PCOS. In the following study, overall, 140 sample size was selected for the evaluation. These 140 were divided into two groups in which 70 women were on the one group which was the intervention group, and 70 women were in control group. The control group of the study were the women who reportedly had regular and normal menstrual cycle. The results indicated high values of vaspin and irisin. The results of this study and previously published literature suggest that both adipocytokines are associated with high blood glucose levels and higher BMI, and finally, both values remain higher in women with PCOS. Vaspin and irisin could be considered as a biomarker for prognosis and therapy followup in patients with PCOS.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">212</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Saba Khair Alddin Ibrahim*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Basic Science, Dentistry College, Environmental Researches Center, University of Mosul, Mosul, IRAQ.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Robert Palomino-De-La-Gala</style></author><author><style face="normal" font="default" size="100%">Hugo Justil-Guerrero</style></author><author><style face="normal" font="default" size="100%">Jorge Arroyo-Acevedo</style></author><author><style face="normal" font="default" size="100%">Juan Rojas-Armas</style></author><author><style face="normal" font="default" size="100%">Cristian Aguilar-Carranza</style></author><author><style face="normal" font="default" size="100%">Jaime Martínez-Heredia</style></author><author><style face="normal" font="default" size="100%">Edwin Cieza-Macedo</style></author><author><style face="normal" font="default" size="100%">Carlos García-Bustamante</style></author><author><style face="normal" font="default" size="100%">Oscar Herrera-Calderon</style></author><author><style face="normal" font="default" size="100%">Edwin Enciso-Roca</style></author><author><style face="normal" font="default" size="100%">Roberto Chávez- Asmat</style></author><author><style face="normal" font="default" size="100%">Lester Dominguez-Huarcaya</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Protective Effect of the Ethanolic Extracts of Leaves of Chuquiraga spinosa Less and Baccharis genistelloides on Benign Prostatic Hyperplasia in Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Baccharis genistelloides</style></keyword><keyword><style  face="normal" font="default" size="100%">Benign prostatic hyperplasia</style></keyword><keyword><style  face="normal" font="default" size="100%">Chuquiraga spinosa</style></keyword><keyword><style  face="normal" font="default" size="100%">Dutasteride</style></keyword><keyword><style  face="normal" font="default" size="100%">Testosterone</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">858-865</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Benign prostatic hyperplasia (BPH) is one of the most common conditions affecting middle-aged men, with oxidative stress postulated as an important factor in its development.&lt;strong&gt; Objective:&lt;/strong&gt; To evaluate the protective effect of the association of the ethanolic extract of &lt;em&gt;Chuquiraga spinosa &lt;/em&gt;(ChS) and &lt;em&gt;Baccharis genistelloides&lt;/em&gt; (BaG) on benign prostatic hyperplasia in rats. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Sixty-six male rats were randomized into groups: 1) Inductor Group: Testosterone enanthate (ET) 25 mg/Kg on days 8 and 14 intramuscularly. 2) Group P80: Polysorbate-80 3% 10 mL / Kg. 3) Positive Group: ET + Dutasteride (DU) 0.5 mg / Kg, 4) ET + ChS 250, 5) ET + ChS 500, 6) ET + BaG250, 7) ET + BaG 500, 8) ET + ChS 250 + BaG 250, 9) ET + ChS 500 + BaG 500, 10) ET + ChS 250 + BaG 500, 11) ET + ChS 500 + BaG250. PSA, nitric oxide (NO) and malondialdehyde (MDA), prostate dimensions by ultrasound and histopathological findings were quantified as main markers. &lt;strong&gt;Results:&lt;/strong&gt; Lower levels of NO, MDA and PSA were observed in all groups treated with extract compared to the Inductor group (&lt;em&gt;p&lt;/em&gt; &amp;lt;0.01), with the reductive capacity of the mixture ChS 250 + BaG 500 and ChS 500 + BaG 250 compared with Dutasteride (&lt;em&gt;p&lt;/em&gt; &amp;lt;0.05). The volume of the prostate was lower in the Dutasteride, P80 and ChS250 + BaG500 groups compared to the inducer (&lt;em&gt;p&lt;/em&gt; &amp;lt;0.05). Regarding the histopathological study, it was observed that the association of variable doses (ChS250 + BaG500 and ChS500 + BaG250) had a better protective effect. &lt;strong&gt;Conclusion:&lt;/strong&gt; Under experimental conditions, the association of the extracts of &lt;em&gt;Chuquiraga spinosa&lt;/em&gt; and &lt;em&gt;Baccharis genistelloides &lt;/em&gt;has an effect in the protection of BPH induced with testosterone, which could be linked to its antioxidant capacity of the extracts.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">858</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Robert Palomino-De-La- Gala&lt;sup&gt;1,2&lt;/sup&gt;, Hugo Justil-Guerrero&lt;sup&gt;1,2&lt;/sup&gt;, Jorge Arroyo-Acevedo&lt;sup&gt;1,2&lt;/sup&gt;, Juan Rojas-Armas&lt;sup&gt;1,2&lt;/sup&gt;, Cristian Aguilar-Carranza&lt;sup&gt;3&lt;/sup&gt;, Jaime Martínez-Heredia&lt;sup&gt;1,2&lt;/sup&gt;, Edwin Cieza-Macedo&lt;sup&gt;1,2&lt;/sup&gt;, Carlos García- Bustamante&lt;sup&gt;1,2&lt;/sup&gt;, Oscar Herrera- Calderon&lt;sup&gt;4&lt;/sup&gt;, Edwin Enciso-Roca&lt;sup&gt;5&lt;/sup&gt;, Roberto Chávez- Asmat&lt;sup&gt;6&lt;/sup&gt;, Lester Dominguez-Huarcaya&lt;sup&gt;7&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Institute of Clinical Research, Universidad Nacional Mayor de San Marcos, Lima, PERU.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmacology Laboratory, Faculty of Medicine, Universidad Nacional Mayor de San Marcos, Lima, PERU.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pathology, Instituto Nacional Cardiovascular, Lima, PERU.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Faculty of Pharmacy and Biochemistry, Universidad Nacional Mayor de San Marcos, Lima, PERU.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Faculty of Health Sciences, Universidad Nacional de San Cristóbal de Huamanga, Ayacucho, PERU.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Association for the Development of Student Research in Health Sciences (ADIECS), Lima, PERU.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Physiology laboratory. Faculty of Medicine, Universidad Nacional Mayor de San Marcos, Lima, PERU.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Imad M Al-Ani</style></author><author><style face="normal" font="default" size="100%">Norsidah Ku-Zaifah</style></author><author><style face="normal" font="default" size="100%">Fakhria A. Al-Joufi</style></author><author><style face="normal" font="default" size="100%">Rafidah H.Mokhtar</style></author><author><style face="normal" font="default" size="100%">Norlelawati A. Talib</style></author><author><style face="normal" font="default" size="100%">Ghasak Ghazi Faisal</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Protective Role of Eurycoma longifolia Jack Root Extract Against High-Fat Diet Induced Testicular Damage in Sprague-Dawley Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Eurycoma Longifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">High-Fat-Diet</style></keyword><keyword><style  face="normal" font="default" size="100%">Seminiferous Tubules Tongkat Ali</style></keyword><keyword><style  face="normal" font="default" size="100%">Testis</style></keyword><keyword><style  face="normal" font="default" size="100%">Testosterone</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">808-811</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective: &lt;/strong&gt;The aims of this study were to investigate the adverse effects of the high-fat-diet (HFD) on the testosterone level and testicular structure of male rats as well as to examine whether &lt;em&gt;Eurycoma longifolia&lt;/em&gt; (EL) is able to ameliorate these effects. &lt;strong&gt;Methods:&lt;/strong&gt; Twenty-four male Sprague-Dawley (SD) rats were divided into four groups each containing 6 rats. Group ND was given only normal diet, group NDEL was given normal diet and EL extracts (15 mg/ kg) dissolved in distilled water, group HFD was given only high-fat-diet and group HFDEL was given high-fat-diet and EL extracts (15 mg/kg). EL was administered orally for 12 weeks. The animal’s testosterone level was measured at week 0, 6 and 12. The rats were sacrificed at the end of 12&lt;sup&gt;th &lt;/sup&gt;weeks and the testes samples were processed for histological examination&lt;strong&gt; Results: &lt;/strong&gt;The testosterone level was significantly increased (&lt;em&gt;p&lt;/em&gt; &amp;lt; 0.05) in the in the treated rats with EL (NDEL and HFDEL) compared with ND and HFD groups. Treatment with HFD revealed a marked degeneration of the seminiferous tubule epithelium and disruption of interstitial cells of the testis thereby interfering with spermatogenesis. Treatment of HFD rats with El reduced the adverse effects of HFD and improved the morphological structure of the seminiferous tubules. &lt;strong&gt;Conclusion: &lt;/strong&gt;These findings revealed that EL has ameliorative effects against the testicular damage caused by high-fat-diet.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">808</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Imad M Al-Ani&lt;sup&gt;1&lt;/sup&gt;, Norsidah Ku-Zaifah&lt;sup&gt;2&lt;/sup&gt;, Fakhria A. Al- Joufi&lt;sup&gt;3&lt;/sup&gt;, Rafidah H.Mokhtar&lt;sup&gt;4&lt;/sup&gt;, Norlelawati A. Talib&lt;sup&gt;5&lt;/sup&gt;, Ghasak Ghazi Faisal&lt;sup&gt;6,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Dentistry, Al-Hikmah University College, Al-Yarmook, Baghdad, IRAQ.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Basic Medical Sciences, Kulliyyah of Medicine, International Islamic University, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;College of Pharmacy, Al Jouf University, Aljouf, Skaka KSA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Faculty of Medicine, Universiti Sains Islam Malaysia, Nilai, Negeri Sembilan, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Pathology and Laboratory Medicine, Kulliyyah of Medicine, International Islamic University, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Fundamental Dental and Medical sciences, Kulliyyah of Dentistry, International Islamic University, MALAYSIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pratik Kumar Chatterjee</style></author><author><style face="normal" font="default" size="100%">Vinodini Nithyananda Madom Anantharaya</style></author><author><style face="normal" font="default" size="100%">Rashmi Kaup Shiva</style></author><author><style face="normal" font="default" size="100%">Nayanatara Arun Kumar</style></author><author><style face="normal" font="default" size="100%">Sneha Bhoja Shetty</style></author><author><style face="normal" font="default" size="100%">Suman Veerappa Budihal</style></author><author><style face="normal" font="default" size="100%">Mangalore Ramesh Bhat</style></author><author><style face="normal" font="default" size="100%">Kunal</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pre and Post-Treatment Effects: Estimation of Serum Testosterone and Lipid Peroxidation Levels on Moringa olifera Extract Induced Cadmium Exposed Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cadmium</style></keyword><keyword><style  face="normal" font="default" size="100%">MDA</style></keyword><keyword><style  face="normal" font="default" size="100%">Morniga olifera extract.</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxidative stress</style></keyword><keyword><style  face="normal" font="default" size="100%">Testosterone</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/185</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">846-849</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Cadmium (Cd), is a toxic metal which affects various organs including testis. It produces oxidative stress leading to male infertility. Moringa tree, is a natural plant with a great therapeutic value and hence it is found to be effective both in prevention and treatment of various conditions including reducing toxicity of hazardous materials. The aim of the present study was to examine the effects of Pre-and Post-treatment with &lt;em&gt;Moringa oliefera&lt;/em&gt; leaf extract (MoE) on testis in cadmium exposed rats. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The present study was conducted at the Department of Physiology, Kasturba Medical College (KMC), Mangalore, Manipal University (MU), Karnataka, India, between (2011-2013). This prospective study consisted a total of 30 rats. These were divided into 5 groups with group I being the control. Data were presented as mean &amp;plusmn;SD. student&amp;rsquo;s t test was used as statistical tool, &lt;em&gt;p&lt;/em&gt;&amp;lt;0.05 considered statistically significant. Group IV and V were pre-and post-MoE treated groups respectively. Serum testosterone and tissue lipid peroxidation levels were estimated.&lt;strong&gt; Results:&lt;/strong&gt; Treatment with MoE prior and after administration of cadmium, respectively showed an increase significantly in the testosterone levels and a decrease in the tissue lipid peroxidation as compared to the group treated with cadmium. However, the pre-treatment showed better results in combatting the toxic effects of cadmium. &lt;strong&gt;Conclusion:&lt;/strong&gt; This study shows that &lt;em&gt;Moringa olifera&lt;/em&gt; leaf extract altered the testosterone and tissue lipid peroxidation levels. Also, pre-treatment showed better outcome.&lt;/p&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; contenteditable=&quot;true&quot; aria-hidden=&quot;true&quot;&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;Background: Cadmium (Cd), is a toxic metal which affects various organs including testis.&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;It produces oxidative stress leading to male infertility. Moringa tree, is a natural plant with&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;a great therapeutic value and hence it is found to be effective both in prevention and treatment&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;of various conditions including reducing toxicity of hazardous materials. The aim of the&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;present study was to examine the effects of Pre-and Post-treatment with Moringa oliefera&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;leaf extract (MoE) on testis in cadmium exposed rats. Materials and Methods: The present&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;study was conducted at the Department of Physiology, Kasturba Medical College (KMC),&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;Mangalore, Manipal University (MU), Karnataka, India, between (2011-2013). This prospective&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;study consisted a total of 30 rats. These were divided into 5 groups with group I being&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;the control. Data were presented as mean &amp;plusmn;SD. student&amp;rsquo;s t test was used as statistical tool,&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;p&amp;lt;0.05 considered statistically significant. Group IV and V were pre-and post-MoE treated&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;groups respectively. Serum testosterone and tissue lipid peroxidation levels were estimated.&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;Results: Treatment with MoE prior and after administration of cadmium, respectively showed&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;an increase significantly in the testosterone levels and a decrease in the tissue lipid peroxidation&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;as compared to the group treated with cadmium. However, the pre-treatment showed&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;better results in combatting the toxic effects of cadmium. Conclusion: This study shows that&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;Moringa olifera leaf extract altered the testosterone and tissue lipid peroxidation levels. Also,&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;pre-treatment showed better outcome.&lt;/div&gt;
&lt;/div&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">846</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Pratik Kumar Chatterjee, Vinodini Nithyananda Madom Anantharaya, Rashmi Kaup Shiva, Nayanatara Arun Kumar, Sneha Bhoja Shetty, Suman Veerappa Budihal, Mangalore Ramesh Bhat, Kunal &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Department of Physiology, Kasturba Medical College (KMC), Mangalore-575004, Manipal University (MU), Karnataka, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Manuj Kr Bharali,</style></author><author><style face="normal" font="default" size="100%">Luk Bahadur Chetry</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Aqueous Methanolic Bark Extract of Oroxylum indicum Inhibited Testosterone induced Prostate Hyperplasia in Rat</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Benign Prostate Hyperplasia</style></keyword><keyword><style  face="normal" font="default" size="100%">Finasteride</style></keyword><keyword><style  face="normal" font="default" size="100%">Oroxylum indicum</style></keyword><keyword><style  face="normal" font="default" size="100%">Rat</style></keyword><keyword><style  face="normal" font="default" size="100%">Testosterone</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">8th April 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">79-85</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;Oroxylum indicum is a frequently reported traditional medicinal plant known to possess antiproliferative and antitumor activity. The present study investigated the effect of crude methanolic bark extract of Oroxylum indicum on testosterone induced benign prostate hyperplasia (BPH) in rat. Adult male rats were given either corn oil or testosterone dissolved in corn oil and testosterone with aqueous methanolic bark extracts of Oroxylum indicum (10, 50 and 100 mg/kg/day) for 14 days. The inhibitory effect of Oroxylum indicum on testosterone induced hyperplasia was evaluated by prostatic index and histopathological examination. Serum marker of liver injury (alanine aminotransferase, ALT and aspartate aminotransferase, AST) and liver histopathological examination were also conducted. Compared with testosterone induced BPH model group, Oroxylum indicum extract treated groups exhibited significant reduction in the prostatic index. Oroxylum indicum treated group also exhibited reduced hyperplasia of prostatic epithelium likewise finasteride treated group. Aqueous methanolic extract of Oroxylum indicum significantly inhibited testosterone induced prostate hyperplasia thus indicated the presence of efficient ingredients which can be used for the treatment of BPH.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Benign Prostate Hyperplasia, Oroxylum indicum, Testosterone, Finasteride, Rat.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Manuj Kr Bharali&lt;sup&gt;*&lt;/sup&gt; and Luk Bahadur Chetry&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;Cell and Molecular Biology Section, Department of Zoology, Rajiv Gandhi University, Rono Hills, Doimukh: 791112, Arunachal Pradesh, India.&lt;/p&gt;</style></auth-address></record></records></xml>