<?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%">Víctor E. Villarreal-La Torre</style></author><author><style face="normal" font="default" size="100%">Juana E. Chávez-Flores</style></author><author><style face="normal" font="default" size="100%">Carmen R. Silva-Correa</style></author><author><style face="normal" font="default" size="100%">Abhel A. Calderón-Peña</style></author><author><style face="normal" font="default" size="100%">Cinthya L. Aspajo-Villalaz</style></author><author><style face="normal" font="default" size="100%">Julio Hilario-Vargas</style></author><author><style face="normal" font="default" size="100%">Maria J. Abanto-Vaella</style></author><author><style face="normal" font="default" size="100%">César D. Gamarra-Sánchez</style></author><author><style face="normal" font="default" size="100%">Yuri F. Curo-Vallejos</style></author><author><style face="normal" font="default" size="100%">Marco L. Salazar-Castillo</style></author><author><style face="normal" font="default" size="100%">Icela M. Rodriguez-Haro</style></author><author><style face="normal" font="default" size="100%">Flor Soriano-López</style></author><author><style face="normal" font="default" size="100%">Renato Cueva- Veneros</style></author><author><style face="normal" font="default" size="100%">José L. Cruzado-Razco</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of the Acute Toxicity of the Ethanolic Extract of the Rhizome of Zingiber officinale Roscoe 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%">Acute toxicity test</style></keyword><keyword><style  face="normal" font="default" size="100%">Biochemical parameters</style></keyword><keyword><style  face="normal" font="default" size="100%">Histopathology</style></keyword><keyword><style  face="normal" font="default" size="100%">Rats</style></keyword><keyword><style  face="normal" font="default" size="100%">Zingiber officinale</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%">April 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">323-331</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;Background: &lt;/strong&gt;Ginger has pharmacological activities such as anticancer, antidiabetic, antioxidant, antimicrobial, anti-neuroinflammatory, and chemotherapy-induced nausea and vomiting. &lt;strong&gt;Objective:&lt;/strong&gt; The research aims to evaluate the acute toxicity of the ethanolic extract of the rhizome of Zingiber officinale Roscoe in rats. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The extract was administrated at doses of 300 and 2000 mg/ Kg/day to female and male rats. Changes in body weight were determined during the 14-day treatment period, and on the last day of treatment, blood was drawn, and euthanasia was performed, removing organs for histological analysis. Biochemical parameters were measured. &lt;strong&gt;Results:&lt;/strong&gt; The body weight of the research specimens not show statistically significant variation. In the liver, mild lymphocytic portal inflammation and moderate hepatic steatosis occurred at doses of 2000 mg/kg/day. The kidneys exhibited a mild infiltration around the renal tubules and glomeruli at the same dose. The brain showed a slight increase in the count of astrocytes with focal glial reaction at the highest dose. The stomach and heart also showed mild inflammatory processes at the dose of 2000 mg/kg/day. In biochemical parameters, statistically significant differences were observed between the dose of 2000 mg/Kg/day and the control group. &lt;strong&gt;Conclusion: &lt;/strong&gt;The ethanolic extract of the rhizome of Z. officinale in rats revealed histopathological changes in the liver, kidneys, brain, stomach, and heart, besides changes in biochemical parameters at doses of 2000 mg/Kg/day.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">323</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Víctor E. Villarreal-La Torre&lt;sup&gt;1&lt;/sup&gt;, Juana E. Chávez-Flores&lt;sup&gt;2&lt;/sup&gt;, Carmen R. Silva-Correa&lt;sup&gt;1,*&lt;/sup&gt;, Abhel A. Calderón-Peña&lt;sup&gt;3&lt;/sup&gt;, Cinthya L. Aspajo-Villalaz&lt;sup&gt;3&lt;/sup&gt;, Julio Hilario- Vargas&lt;sup&gt;4&lt;/sup&gt;, Maria J. Abanto-Vaella&lt;sup&gt;4&lt;/sup&gt;, César D. Gamarra-Sánchez&lt;sup&gt;1&lt;/sup&gt;, Yuri F. Curo-Vallejos&lt;sup&gt;1&lt;/sup&gt;, Marco L. Salazar-Castillo&lt;sup&gt;3&lt;/sup&gt;, Icela M. Rodriguez- Haro&lt;sup&gt;3&lt;/sup&gt;, Flor Soriano-López&lt;sup&gt;3&lt;/sup&gt;, Renato Cueva-Veneros&lt;sup&gt;5&lt;/sup&gt;, José L. Cruzado-Razco&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Facultad de Farmacia y Bioquímica, Universidad Nacional de Trujillo, PERÚ.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Facultad de Farmacia y Bioquímica, Universidad Norbert Wiener, PERÚ.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Facultad de Ciencias Biológicas, Universidad Nacional de Trujillo, PERÚ.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;4&lt;/sup&gt;Facultad de Medicina, Universidad Nacional de Trujillo, PERÚ.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;5&lt;/sup&gt;Universidad Nacional de Frontera, PERÚ.&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%">Amr A. Fouad</style></author><author><style face="normal" font="default" size="100%">Moataz Mohamedalhasan Ali</style></author><author><style face="normal" font="default" size="100%">Mostafa Abdel-Hamid</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Punicalagin Opposes Gentamicin Nephrotoxicity in Rats: Role of Nrf2 and NF-κB Pathways</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%">Gentamicin</style></keyword><keyword><style  face="normal" font="default" size="100%">Kidney</style></keyword><keyword><style  face="normal" font="default" size="100%">Punicalagin</style></keyword><keyword><style  face="normal" font="default" size="100%">Rats</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 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">126-130</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;Background:&lt;/strong&gt; Oxidative stress, inflammation, and apoptosis are implicated in gentamicin (GEN)-induced nephrotoxicity. Punicalagin (PNG) possesses antioxidant, anti-inflammatory, and antiapoptotic effects. Objective: The aim of the present research was to investigate the possible defensive effect of PNG against nephrotoxicity caused by GEN in male Sprague-Dawley rats. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; GEN (80 mg/kg/day, i.p.) was administered for 8 days. Treatment with PNG (25 mg/kg/day, p.o.) for 10 days, began 2 days before GEN insult. &lt;strong&gt;Results: &lt;/strong&gt;PNG significantly decreased serum creatinine, and malondialdehyde, tumor necrosis factor-α, interleukin-6, inducible nitric oxide synthase, nuclear factor-κB p65 (NF- κB p65), and cleaved caspase-3 activity in the kidneys of GEN-challenged rats. PNG also significantly increased renal catalase, reduced glutathione, and nuclear factor erythroid 2-related factor 2 (Nrf2) in rats received GEN. Additionally, PNG markedly attenuated the histopathological kidney tissue injury caused by GEN. &lt;strong&gt;Conclusion: &lt;/strong&gt;PNG guarded against GEN-induced kidney damage in rats through its antioxidant, anti-inflammatory, and antiapoptotic effects, and by modulating the balance between Nrf2 and NF-κB pathways.&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%">126</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Amr A. Fouad&lt;sup&gt;1,&lt;/sup&gt;*, Moataz Mohamedalhasan Ali&lt;sup&gt;2&lt;/sup&gt;, Mostafa Abdel-Hamid&lt;sup&gt;3&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, Faculty of Medicine, Al-Baha University, Al-Baha, SAUDI ARABIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pathology, Faculty of Medicine, Al-Baha University, Al-Baha, Saudi Arabia &amp;amp; Department of Pathology, Faculty of Medicine, University of Elimam Elmahdi, SUDAN.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Anatomy and Embryology, Faculty of Medicine, Al-Baha University, Al- Baha, SAUDI ARABIA.&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%">Meilla Dwi Andrestian</style></author><author><style face="normal" font="default" size="100%">Rizal Damanik</style></author><author><style face="normal" font="default" size="100%">Faisal Anwar</style></author><author><style face="normal" font="default" size="100%">Nancy Dewi Yuliana</style></author><author><style face="normal" font="default" size="100%">Anwar Mallongi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Extract of Torbangun (Coleus amboinicus Lour) Leaves Inhibits  the Expression of PEPCK and G6Pase in Streptozotocin-Induced  Diabetic 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%">G6Pase</style></keyword><keyword><style  face="normal" font="default" size="100%">hyperglycemia</style></keyword><keyword><style  face="normal" font="default" size="100%">PEPCK</style></keyword><keyword><style  face="normal" font="default" size="100%">Rats</style></keyword><keyword><style  face="normal" font="default" size="100%">Torbangun</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%">December 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%">1116-1120</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; This study aimed to analyze the anti-hyperglycemic activity of Torbangun leaf extract (TLE) in hyperglycemic rats by observing its effect on blood glucose levels and &lt;em&gt;PEPCK &lt;/em&gt;and &lt;em&gt;G6Pase&lt;/em&gt; gene expression. &lt;strong&gt;Method:&lt;/strong&gt; This post-test-controlled group design study used a completely randomized design (CRD). Seven rats were separated as a normal group (N) and other rats were injected with streptozotocin (STZ). Hyperglycemia was characterized by fasting blood glucose (FBG) &amp;gt;126 mg/dl. Hyperglycemic rats were divided into three groups: H-IM (control drug metformin hydrochloride dose 62.5 mg/kg BW), H-IT (TLE dose 620mg/kg BB), and NG (negative control, hyperglycemic rats). Rats were given intervention for 14 days.&lt;strong&gt; Result:&lt;/strong&gt; The results showed a significant difference between initial and final FBG of the HI-IM group (p = 0.002, α = 0.01) and the H-IT group (p = 0.005, α = 0.01) and effect on the key gene expression of gluconeogenesis in the liver. The H-IT group showed a decrease in PEPCK gene expression 0.80 times and decreased G6Pase gene expression by 0.65 times compared to NG group. &lt;strong&gt;Conclusion:&lt;/strong&gt; The findings suggested the administration of TLE in STZ-induced hyperglycemic rats was able to reduce blood sugar levels and was involved in inhibiting the expression of PEPCK and G6Pase expression genes in the liver.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1116</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Meilla Dwi Andrestian&lt;sup&gt;1,*&lt;/sup&gt;, Rizal Damanik&lt;sup&gt;2,3&lt;/sup&gt;, Faisal Anwar&lt;sup&gt;2&lt;/sup&gt; , Nancy Dewi Yuliana&lt;sup&gt;4&lt;/sup&gt; , Anwar Mallongi&lt;sup&gt;5&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 Nutrition, Polytechnic of Health Ministry of Health Banjarmasin, Banjarbaru, South Kalimantan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Community Nutriton, Faculty of Human Ecology, IPB University, Bogor, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Southeast Asian Food and Agricultural Science and Technology (SEAFAST) Center Bogor, IPB University, Bogor, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Food Science, Faculty of Agricultural Agricultural Engineering and Technology, IPB University, Bogor, INDONESIA.&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%">Miloud Chakit</style></author><author><style face="normal" font="default" size="100%">Rezklah Boussekkour</style></author><author><style face="normal" font="default" size="100%">Aboubaker El Hessni</style></author><author><style face="normal" font="default" size="100%">Youssef Bahbiti</style></author><author><style face="normal" font="default" size="100%">Redouan Nakache</style></author><author><style face="normal" font="default" size="100%">Hicham El Mustaphi</style></author><author><style face="normal" font="default" size="100%">Abdelhalim Mesfioui</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antiurolithiatic Activity of Aqueous Extract of Ziziphus lotus on Ethylene Glycol-Induced Lithiasis 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%">Ethylene glycol</style></keyword><keyword><style  face="normal" font="default" size="100%">Rats</style></keyword><keyword><style  face="normal" font="default" size="100%">Urinary parameter</style></keyword><keyword><style  face="normal" font="default" size="100%">Urolithiasis</style></keyword><keyword><style  face="normal" font="default" size="100%">Ziziphus lotus</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">596-602</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;In Morocco, &lt;em&gt;Ziziphus lotus&lt;/em&gt; is commonly used as an urolithiatic agent in the traditional medicine. To confirm this effect, an aqueous extract of &lt;em&gt;Ziziphus lotus&lt;/em&gt; (AEZL) has been studied in ethylene glycolinduced urolithiasis model of rats. 30 male rats were randomly divided into five groups of six animals each. Group I served as a vehicle control and received distilled water (0.5 ml/100 g p.o.). All remaining groups received calculi inducing treatment for 28 days, comprised of 0.75% v/v ethylene glycol with 1% w/v ammonium chloride in drinking water ad libitum for 3 days followed by only 0.75% v/v ethylene glycol for 25 days. Group II served as lithiatic control and received distilled water (0.5 ml/100 g p.o.). Group III served as curative treatment group and received AEZL at doses of 150 mg/kg from 14&lt;sup&gt;th&lt;/sup&gt; day to 28&lt;sup&gt;th&lt;/sup&gt; day. Group VI served as preventive treatment group and received AEZL at doses of 150 mg/kg from 1st day to 28th day. Group V served as therapeutic and received a drug “Cystone” at dose of 750 mg/kg from 14&lt;sup&gt;th&lt;/sup&gt; day to 28&lt;sup&gt;th &lt;/sup&gt;day. The extract treatment decreased the levels of oxalate and calcium in urine. Crystalluria analysis showed that untreated rats excreted large CaOx monohydrate and few dihydrate crystals while treated animals excreted mostly small CaOx dihydrate crystals. Significant similarity was observed between preventive and therapeutic anti-urolithiatic effect of AEZL and anti-urolithiatic effect of cystone (P&amp;lt;0.001). These results demonstrated that AEZL have an anti-urolithiatic effect with preventive and therapeutic treatments in this experimental condition.&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%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">596</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Miloud Chakit*, Rezklah Boussekkour, Aboubaker El Hessni, Youssef Bahbiti, Redouan Nakache, Hicham El Mustaphi, Abdelhalim Mesfioui&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Biology and Health Laboratory, Faculty of Sciences, Ibn Tofail University, Kenitra, Morocco.&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%">Karnirius Harefa</style></author><author><style face="normal" font="default" size="100%">Delmi Sulastri</style></author><author><style face="normal" font="default" size="100%">Ellyza Nasrul</style></author><author><style face="normal" font="default" size="100%">Syafruddin Ilyas</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Analysis of Several Inflammatory Markers Expression in Obese Rats given Plectranthus amboinicus (Lour.) Spreng Ethanol Extract</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%">Enzyme-Linked Immunosorbent Assay</style></keyword><keyword><style  face="normal" font="default" size="100%">immunohistochemistry</style></keyword><keyword><style  face="normal" font="default" size="100%">Obese</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Rats</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">172-178</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;Oxidative stress is one of the inflammatory events caused by obesity. This condition is characterized by an increase in various inflammatory markers, such as intercellular adhesion molecule 1 (ICAM-1), vascular cell adhesion molecule 1 (VCAM-1), and a cluster of differentiation 40 (CD40). This study aimed to analyze the effect of Plectranthus amboinicus (Lour.) Spreng ethanol extract on ICAM-1, VCAM-1, and CD40 in obese rats. &lt;strong&gt;Methods: &lt;/strong&gt;The study used a pure experimental method with a completely randomized design. There were 6 groups, namely, C− (negative control), C+ (positive control), CMC (soluble control), EE300 (P. amboinicus ethanol extract, 300 mg/kg body weight [BW]), EE600 (P. amboinicus ethanol extract, 600 mg/kg BW) and EE900 groups (P. amboinicus ethanol extract, 900 mg/kg BW). &lt;strong&gt;Results: &lt;/strong&gt;The results showed low levels of ICAM-1 and VCAM-1 in the blood plasma, especially in the EE900 group, but the difference was not substantial. The same trend also occurred in the expression of CD40 in the tunica intima layer of the rat aorta. &lt;strong&gt;Conclusions:&lt;/strong&gt; Thus, the administration of 900 mg/kg BW P. amboinicus ethanol extract for 45 days has the potential to treat obesity in rats through the suppression of oxidative stress and inflammatory markers (ICAM-1, VCAM-1 and CD40).&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%">172</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Karnirius Harefa&lt;sup&gt;1&lt;/sup&gt;, Delmi Sulastri&lt;sup&gt;1&lt;/sup&gt;, Ellyza Nasrul&lt;sup&gt;1&lt;/sup&gt;, Syafruddin Ilyas&lt;sup&gt;2,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Study Programme of Biomedic, Faculty of Medicine, Universitas Andalas, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences,Universitas Sumatera Utara, Medan, INDONESIA.&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%">Amel CHOUABIA</style></author><author><style face="normal" font="default" size="100%">Samir DJEMLI</style></author><author><style face="normal" font="default" size="100%">Cherif ABDENNOUR</style></author><author><style face="normal" font="default" size="100%">Leila MALLEM</style></author><author><style face="normal" font="default" size="100%">Labiba KAHALERRAS</style></author><author><style face="normal" font="default" size="100%">Fatma Zohra ARKOUB</style></author><author><style face="normal" font="default" size="100%">Narimene BOUABDALLAH</style></author><author><style face="normal" font="default" size="100%">Abdelkrim TAHRAOUI</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Protective effect of Salvia officinalis against cypermethrininduced reprotoxicity in male Wistar 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%">Cypermethrin</style></keyword><keyword><style  face="normal" font="default" size="100%">Histology</style></keyword><keyword><style  face="normal" font="default" size="100%">Rats</style></keyword><keyword><style  face="normal" font="default" size="100%">Salvia officinalis</style></keyword><keyword><style  face="normal" font="default" size="100%">Spermatozoa</style></keyword><keyword><style  face="normal" font="default" size="100%">Toxicity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1413-1421</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;Background:&lt;/strong&gt; Medicinal plants are a reservoir of biologically active compounds with therapeutic properties that, over time, have been used for the treatment of various diseases. This study aims to evaluate the protective effect of the aqueous extract of the leaves of&lt;em&gt; Salvia officinalis &lt;/em&gt;against cypermethrin-induced toxicity. &lt;strong&gt;Methods: &lt;/strong&gt;30 male rats weighing approximately 240 g were divided into equal six groups; the control group received tap water, the positive control received the aqueous extract of sage leaves (SLE) at a dose of (0.5g/kg bw), the groups treated with cypermethrin (Cyp1) at 8.33 mg/kg bw and (Cyp2) at 25 mg/kg bw, and the groups treated by cypermethrin combined with aqueous extract of sage SLE+Cyp1 (0.5g/kg bw+8.33 mg/kg bw) and SLE+Cyp2 (0.5g/kg bw+25 mg/kg bw) for four days/week. After 4 weeks of oral administration, epididymal seminal fluid was analyzed via the CASA system, in addition to the histological study testis and epididymis. &lt;strong&gt;Results: &lt;/strong&gt;The obtained results showed a decrease in the absolute weight of the reproductive organs, with a significant decrease in sperm concentration, motility and speed in the cypermethrin-treated group compared to the control. Histological study of the testes and epididymis indicates an alteration in the stages of spermatogenesis in groups Cyp1 and Cyp2 compared to the control. However, the above-mentioned parameters were maintained almost normal in the groups that received the aqueous extract of sage with both doses of cypermethrin. &lt;strong&gt;Conclusion:&lt;/strong&gt; it can be demonstrated that SLE has been shown to protect rats from cypermethrin-induced reprotoxicity.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1413</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Amel CHOUABIA&lt;sup&gt;1&lt;/sup&gt;, Samir DJEMLI&lt;sup&gt;2&lt;/sup&gt;,*, Cherif ABDENNOUR&lt;sup&gt;1&lt;/sup&gt;, Leila MALLEM&lt;sup&gt;1&lt;/sup&gt;, Labiba KAHALERRAS&lt;sup&gt;1&lt;/sup&gt;, Fatma Zohra ARKOUB&lt;sup&gt;1&lt;/sup&gt;, Narimene BOUABDALLAH&lt;sup&gt;1&lt;/sup&gt;, Abdelkrim TAHRAOUI&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Sciences, Animal Ecophysiology Laboratory, Department of Biology, Badji Mokhtar University, Annaba, ALGERIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Sciences, Applied Neuroendocrinology Laboratory, Department of Biology, Badji Mokhtar University, Annaba, ALGERIA.&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%">K Sunand</style></author><author><style face="normal" font="default" size="100%">Mahipal Yellow</style></author><author><style face="normal" font="default" size="100%">P Naveen</style></author><author><style face="normal" font="default" size="100%">Yasho Deepika</style></author><author><style face="normal" font="default" size="100%">G Krishna Mohan</style></author><author><style face="normal" font="default" size="100%">Vasudha Bakshi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Betel Leaf Extract Amends Dehydroepiandrosterone Induced PCOS Related Hormonal Abnormality and Histopathological Alterations in Rat Model</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%">Anti-androgenic activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Betel Leaf</style></keyword><keyword><style  face="normal" font="default" size="100%">Clomiphene citrate</style></keyword><keyword><style  face="normal" font="default" size="100%">DHEA</style></keyword><keyword><style  face="normal" font="default" size="100%">PCOS</style></keyword><keyword><style  face="normal" font="default" size="100%">Rats</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%">November 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%">1442-1448</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;PCOS is a hormonal disorder with missed or irregular periods at the reproductive ages of women, which was mainly due to increased androgen levels. &lt;strong&gt;Objective:&lt;/strong&gt; To evaluate the antiandrogen activity of EEBL (ethanolic extract of betel leaf) in DHEA induced PCOS (polycystic ovary syndrome) and improving ovulation rate, consequently its effects on hormonal and biochemical profile of the blood serum and Histopathology of the ovary. &lt;strong&gt;Methods: &lt;/strong&gt;Divide the 30 immature (4-week-old) female Sprague Dawley rats into 5 groups. Four groups except the control group were injected each morning with dehydroepiandrosterone (DHEA) (6 mg/100 g body weight/0.2 ml sesame oil) for 20days. The control group was injected with 0.2ml sesame oil for 20days. Pretreatment completed after 21&lt;sup&gt;st &lt;/sup&gt;day then animals are subjected to posttreatment with EEBL (LD-100, HD-200mg/kg, p.o) and CC (100 μg/kg, p.o) from 21 to 41 days. After the treatment animals are subjected to biochemical, hormonal and histopathological examinations. &lt;strong&gt;Results:&lt;/strong&gt; In negative control group SOD, Catalase were decreased. Total protein, SGOT, SGPT, TG, LDL and cholesterol levels were increased than the control group. Hormones LH and Testosterone levels increased. FSH, estradiol, and progesterone levels were decreased when compared with the control group. Histopathology has revealed that the presence of cysts in the negative control group and recovery of cysts seen in treatment groups.&lt;strong&gt; Conclusion: &lt;/strong&gt;Treatment with EEBL is effectively attenuated to the DHEA induced PCOS and it is significant in comparison results with clomiphene citrate attributing its therapeutic potential towards the treatment of PCOS.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1442</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;K Sunand&lt;sup&gt;1,&lt;/sup&gt;*, Mahipal Yellow&lt;sup&gt;2&lt;/sup&gt;, P Naveen&lt;sup&gt;3&lt;/sup&gt;, Yasho Deepika&lt;sup&gt;3&lt;/sup&gt;, G Krishna Mohan&lt;sup&gt;4&lt;/sup&gt;, Vasudha Bakshi&lt;sup&gt;5&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty, Centre for Neuroscience, Dept. of Pharmacology, Anurag Group of Institutions, Hyderabad, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Student, Centre for Neuroscience, Dept. of Pharmacology, Anurag Group of Institutions, Hyderabad, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty, Centre for Neuroscience, Dept. of Pharmacology, Anurag Group of Institutions, Hyderabad, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Professor, Centre for Pharmaceutical Sciences, Institute of Science &amp;amp; Technology (IST), JNTUH, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Dean, Centre for Neuroscience, School of Pharmacy, Anurag Group of Institutions, Hyderabad, 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%">Nkiru Nwamaka Ezeani</style></author><author><style face="normal" font="default" size="100%">Udu Ama Ibiam</style></author><author><style face="normal" font="default" size="100%">Obasi Uche Orji</style></author><author><style face="normal" font="default" size="100%">Ikechuku Okorie Igwenyi</style></author><author><style face="normal" font="default" size="100%">Chinyere Aloke</style></author><author><style face="normal" font="default" size="100%">Esther Alum</style></author><author><style face="normal" font="default" size="100%">Partrick Mmaduabuchi Aja</style></author><author><style face="normal" font="default" size="100%">Okechukwu Paul Chima Ugwu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effects of Aqueous and Ethanol Root Extracts of Olax subscopioidea on Inflammatory Parameters in Complete Freund’s Adjuvant-Collagen Type II Induced Arthritic Albino 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%">Adjuvant</style></keyword><keyword><style  face="normal" font="default" size="100%">Arthritis</style></keyword><keyword><style  face="normal" font="default" size="100%">Indomethacine</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant extracts</style></keyword><keyword><style  face="normal" font="default" size="100%">Rats</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%">January 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%">16-25</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Aim/Background:&lt;/strong&gt; Rural and Urban dwellers in Nigeria claim to treat their arthritis with &lt;em&gt;Olax subscorpioidea&lt;/em&gt; root extracts. One of the reasons they chose this treatment is that it is effective and cost less than orthodox drugs with their accompanying side effects. Hence the aim of this study is to investigate the anti-arthritis effects of &lt;em&gt;Olax subscorpioidea &lt;/em&gt;Afzel ethanol and aqueous root extracts on chicken type II-Complete Freund’s adjuvant (CFA) induced arthritis rat model. &lt;strong&gt;Materials and Method:&lt;/strong&gt; The anti-arthritic potential of ethanol and aqueous root extracts of &lt;em&gt;Olax subscorpioidea&lt;/em&gt; was evaluated using the chicken type II-Complete Freund’s adjuvant model in 135 female wistar albino rats. The rats were treated with aqueous and ethanol root extracts of &lt;em&gt;Olax subscorpioidea&lt;/em&gt; at varying doses and standard indomethacine drug. &lt;strong&gt;Results:&lt;/strong&gt; The ethanol and aqueous root extracts of &lt;em&gt;Olax subscorpioidea &lt;/em&gt;showed significant anti-arthritic activity that was statistically similar to that of indomethacine. Our results suggest that the alcoholic extract of &lt;em&gt;Olax subscorpioidea &lt;/em&gt;showed significant (&lt;em&gt;P&lt;/em&gt;&amp;lt;0.05) anti-arthritic potential.&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%">16</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Nkiru Nwamaka Ezeani&lt;sup&gt;*&lt;/sup&gt;, Udu Ama Ibiam, Obasi Uche Orji, Ikechuku Okorie Igwenyi, Chinyere Aloke, Esther Alum, Partrick Mmaduabuchi Aja, Okechukwu Paul Chima Ugwu &lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;Department of Biochemistry, Ebonyi State University, Abakaliki, NIGERIA.&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%">Kusnandar Anggadiredja</style></author><author><style face="normal" font="default" size="100%">I Ketut Adnyana</style></author><author><style face="normal" font="default" size="100%">Dewi Safitri</style></author><author><style face="normal" font="default" size="100%">Siti Farah Rahmawati</style></author><author><style face="normal" font="default" size="100%">Tomi Hendrayana</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ethanol Extract of Gardenia augusta (L.) Merr. Flowers Produces Sleep Improvement in Rat Model</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%">Flowers</style></keyword><keyword><style  face="normal" font="default" size="100%">Gardenia augusta (L.) Merr.</style></keyword><keyword><style  face="normal" font="default" size="100%">Improvement</style></keyword><keyword><style  face="normal" font="default" size="100%">Rats</style></keyword><keyword><style  face="normal" font="default" size="100%">Sleep</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%">November 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%">1449-1454</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; Sleep disorder may have detrimental consequences on health and one of the treatments is the use of hypnotics. Unfortunately, hypnotics treatment may also be accompanied by side effects and lead to dependence. The present study aimed to investigate the sleep improving effects of ethanol extract of &lt;em&gt;Gardenia augusta&lt;/em&gt; (L.) Merr. flowers in rat model. &lt;strong&gt;Methods: &lt;/strong&gt;Rats were assigned into group receiving the extract (at 0.9 or 1.8 g/kg), the reference drug crocetin (at 0.9 mg/kg) or vehicle, once a day orally for 15 days. &lt;strong&gt;Results: &lt;/strong&gt;Tested on day 1 and 14 of treatment, the rats receiving 1.8 g/kg of the extract showed improvements in sleep latency, sleep duration, sleep efficiency, wake episodes, and sleep cycle, which were significantly different from crocetin. Furthermore, tested on day 2 and 15 of treatment, the rats treated with 1.8 g/kg extract demonstrated superior sedative rating scale compared to crocetin. &lt;strong&gt;Conclusions: &lt;/strong&gt;Results of the present study indicates the potential of Gardenia augusta (L.) Merr. flower extract to be used as an adjunct treatment for sleep disorder.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1449</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kusnandar Anggadiredja*, I Ketut Adnyana, Dewi Safitri, Siti Farah Rahmawati, Tomi Hendrayana&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Pharmacology and Clinical Pharmacy, School of Pharmacy Institut Teknologi Bandung, Jl. Ganesa 10 Bandung 40132, INDONESIA.&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%">Guenzet Akila,</style></author><author><style face="normal" font="default" size="100%">Krouf Djamil,</style></author><author><style face="normal" font="default" size="100%">Berzou Saadia</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Portulaca oleracea extract increases lecithin:cholesterol acyltransferase and paraoxonase 1 activities and enhances reverse cholesterol transport in streptozotocin-induced diabetic 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%">apo A-I</style></keyword><keyword><style  face="normal" font="default" size="100%">Cholesterol</style></keyword><keyword><style  face="normal" font="default" size="100%">LCAT</style></keyword><keyword><style  face="normal" font="default" size="100%">lipoprotein peroxidation</style></keyword><keyword><style  face="normal" font="default" size="100%">PON1</style></keyword><keyword><style  face="normal" font="default" size="100%">Portulaca oleracea</style></keyword><keyword><style  face="normal" font="default" size="100%">Rats</style></keyword><keyword><style  face="normal" font="default" size="100%">Streptozotocin</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%">1-9</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; Plant extracts are generally assumed to be more acceptable and less hazardous than synthetic compounds and could be alternative antidiabetic treatments. &lt;em&gt;Portula caoleracea&lt;/em&gt; has been used as one of the traditional edible and medicinal plant in Algeria to treat diabetes. The aim of the present study was to determine the effects of lyophilized aqueous extract of &lt;em&gt;Portulaca oleracea&lt;/em&gt; on high-density lipoproteins composition, paraoxonase (PON1) and lecithin:cholesterol acyltransferase (LCAT) activities in streptozotocin-induced diabetic rat. &lt;strong&gt;Methods:&lt;/strong&gt; Diabetes was induced intraperitonially by a single injection of streptozotocin (STZ) (60mg/kg bw). Twelve diabetic rats, weighing 263&amp;plusmn;5g, were divided into two groups fed a casein diet supplemented or not with&lt;em&gt; Portulaca oleracea&lt;/em&gt; extract (1g/kg bw), for 4 weeks.&lt;strong&gt; Results:&lt;/strong&gt; At d28, in&lt;em&gt; Portulaca oleracea&lt;/em&gt; treated vs untreated diabetic group, glycemia, serum total cholesterol (TC), triacylglycerols (TG) and phospholipids (PL) concentrations were decreased significantly (&lt;em&gt;p&lt;/em&gt;&amp;lt;0.05). The hypolipidemic effect induced by &lt;em&gt;Portulaca oleracea&lt;/em&gt; extract was due to the reduction of total cholesterol (TC) in LDL-HDL&lt;sub&gt;1&lt;/sub&gt; (-51%) and C-HDL&lt;sub&gt;3&lt;/sub&gt; (-21%).&lt;em&gt; Portulaca oleracea&lt;/em&gt; treatment improved PON1 and LCAT activities by 48%. HDL3-UC (acyl group acceptor) and -PL (enzyme substrate) were diminished respectively by 47% and 82%, whereas HDL&lt;sub&gt;2&lt;/sub&gt;-CE concentrations (product of LCAT reaction) were increased by 44%. Moreover, HDL-C levels were found to be positively correlated with PON1 activity (r=0.96, &lt;em&gt;p&lt;/em&gt;&amp;lt;0.05). Serum, LDL-HDL&lt;sub&gt;1&lt;/sub&gt;, HDL&lt;sub&gt;2&lt;/sub&gt; and HDL&lt;sub&gt;3&lt;/sub&gt; TBARS levels were respectively, 2.9-, 2.6-, 2.4- and 2.8-fold lower in &lt;em&gt;Portulaca oleracea&lt;/em&gt; treated than untreated diabetic groups. &lt;strong&gt;Conclusion:&lt;/strong&gt; These findings reflect the potential antihyperglycemic and hypolipidemic of &lt;em&gt;Portulaca oleracea&lt;/em&gt; extract, in STZ-induced diabetic rat. Moreover,&lt;em&gt; Portulaca oleracea&lt;/em&gt; extract restores PON1 and ameliorates the reverse cholesterol transport (RCT) by enhancing LCAT activity, therefore could prevent many diabetic complications by reducing dyslipidemia and oxidative damage.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words: &lt;/strong&gt;Rats, Streptozotocin, &lt;em&gt;Portulaca oleracea&lt;/em&gt;, Cholesterol, PON1, LCAT, apo A-I, lipoprotein peroxidation.&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;Guenzet Akila, Krouf Djamil and Berzou Saadia&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;Laboratoire de Nutrition Clinique et M&amp;eacute;tabolique, D&amp;eacute;partement de Biologie, Facult&amp;eacute; des Sciences de la Nature et de la Vie. Universit&amp;eacute; d&amp;rsquo;Oran. 31100 Oran, Alg&amp;eacute;rie.&lt;/p&gt;</style></auth-address></record></records></xml>