<?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%">Saugi Abduh</style></author><author><style face="normal" font="default" size="100%">Purwanto Bambang</style></author><author><style face="normal" font="default" size="100%">Dirgahayu Paramasari</style></author><author><style face="normal" font="default" size="100%">Soetrisno</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Cardioprotective Effects of Thymoquinone on Myocardial Fibrosis</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%">Cardiac Fibrosis</style></keyword><keyword><style  face="normal" font="default" size="100%">Lipopolysaccharide</style></keyword><keyword><style  face="normal" font="default" size="100%">Nigella sativa</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxidative stress.</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%">October 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%">924-927</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; Thymoquinone (TQ) is one of the active ingredients in herbal plants such as &lt;em&gt;Nigella sativa &lt;/em&gt;which has antioxidant and anti-inflammatory properties thus may inhibits cardiac fibrosis formation. This study aims to determine the effectiveness of Thymoquinone as a cardioprotective agent in suppressing the extent of fibrosis in Wistar rats induced with lipopolysaccharide (LPS). &lt;strong&gt;Methods&lt;/strong&gt;: This post-test only control study used 30 Wistar rats which were divided into 5 groups: saline, LPS-induced cardiac fibrosis, LPS-induced cardiac fibrosis treated with TQ 10 mg/mL, LPS-induced cardiac fibrosis treated with TQ 20 mg/mL, and LPS-induced cardiac fibrosis treated with TQ 40 mg/mL. Serum IL-6, GSH, and cTnT levels were measured using ELISA, and Mason's trichrome staining was used to assess myocardial fibrosis. &lt;strong&gt;Results:&lt;/strong&gt; The LPS10+TQ20 and LPS10+TQ40 groups exhibited significantly lower levels of IL-6 compared to the LPS10+TQ10 group (p &amp;lt; 0.05). GSH levels did not show a significant decrease in the TQ groups across different doses (p=0.771). The TQ-treated group demonstrated lower cTnT levels compared to the LPS-only group (p&amp;lt;0.05). Thymoquinone treatment resulted in reduced fibrosis area compared to the LPS10 group (p&amp;lt;0.05). &lt;strong&gt;Conclusions: &lt;/strong&gt;TQ has a promising cardioprotective effect on the formation of cardiac fibrosis in Wistar rats induced with LPS.&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%">924</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Saugi Abduh&lt;sup&gt;1,2,*&lt;/sup&gt;, Purwanto Bambang&lt;sup&gt;3&lt;/sup&gt;, Dirgahayu Paramasari&lt;sup&gt;4&lt;/sup&gt;, Soetrisno&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;Doctoral Student in Medical Science, Faculty of Medicine, Sebelas Maret University, Surakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Division of Cardiology, Department of Internal Medicine, Sultan Agung Islamic University, Semarang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Division of Nephrology and Hypertension, Department of Internal Medicine, Sebelas Maret University, Surakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Parasitology, Sebelas Maret University, Surakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Obstetrics and Gynecology, Sebelas Maret University, Surakarta, 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%">Rasio Putra Hutama</style></author><author><style face="normal" font="default" size="100%">Alpha Fardah Athiyyah</style></author><author><style face="normal" font="default" size="100%">I.G.M. Reza Gunadi Ranuh</style></author><author><style face="normal" font="default" size="100%">Andy Darma</style></author><author><style face="normal" font="default" size="100%">Khadijah Rizky Sumitro</style></author><author><style face="normal" font="default" size="100%">Wibi Riawan</style></author><author><style face="normal" font="default" size="100%">Ingrid S. Surono</style></author><author><style face="normal" font="default" size="100%">Subijanto Marto Sudarmo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Lactobacillus Plantarum IS-10506 on Paneth Cell Regeneration in the Ileum of 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%">DEFA-6</style></keyword><keyword><style  face="normal" font="default" size="100%">Escherichia coli O55:B5</style></keyword><keyword><style  face="normal" font="default" size="100%">Lactobacillus plantarum IS-10506</style></keyword><keyword><style  face="normal" font="default" size="100%">Lipopolysaccharide</style></keyword><keyword><style  face="normal" font="default" size="100%">MATH-1.</style></keyword><keyword><style  face="normal" font="default" size="100%">Paneth cells</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%">October 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%">928-932</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;Pathogenic &lt;em&gt;Escherichia coli &lt;/em&gt;(E. coli) is the most common infectious agent among children in developing countries. Indigenous probiotics are not widely used to treat diarrhea and intestinal infections. This study aims to investigate the cell regeneration process of paneth cells after administration of &lt;em&gt;Lactobacillus plantarum&lt;/em&gt; IS-10506 due to damage caused by Lipopolysaccharide (LPS) &lt;em&gt;E. coli&lt;/em&gt; O55:B5, through the expression of MATH-1 and DEFA-6. &lt;strong&gt;Methods: &lt;/strong&gt;This study used 64 paraffin blocks from Rattus norvegicus strain Sprague-Dawley divided into four groups. There were three treatments, KN, KL, KP and KPR groups, The KN group represent the administration of placebo. The KL group received LPS &lt;em&gt;E. coli &lt;/em&gt;O55:B5 on day one. The KP group received LPS &lt;em&gt;E. coli&lt;/em&gt; O55:B5 on the first day and &lt;em&gt;Lactobacillus plantarum&lt;/em&gt; IS-10506 on the second day until six-day. The KPR group were administered &lt;em&gt;Lactobacillus plantarum&lt;/em&gt; IS- 10506 six days prior to receiving LPS &lt;em&gt;E. coli&lt;/em&gt; O55:B5, respectively. All groups, except KN, received LPS at a dose of 250 μg/kg body weight once, and Lactobacillus plantarum IS-10506 at a dose of 2.86x1010 CFU/ day. Evaluating paneth cell regeneration, DEFA-6, and MATH-1 expression immunohistochemistry was conducted on all tissues. &lt;strong&gt;Results:&lt;/strong&gt; The expression of DEFA-6 and MATH-1 in the KP and KPR groups on day three of observation was significantly higher from the KL group. Even though the KL group achieved significant growth, the results of this expansion were significantly smaller than KP and KPR groups. &lt;strong&gt;Conclusion:&lt;/strong&gt; After mucosal injury caused by LPS &lt;em&gt;E. coli &lt;/em&gt;O55:B5, administration of probiotic &lt;em&gt;Lactobacillus plantarum&lt;/em&gt; IS-10506 may increase paneth cell regeneration through differentiation and cell number.&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%">928</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Rasio Putra Hutama&lt;sup&gt;1&lt;/sup&gt;, Alpha Fardah Athiyyah&lt;sup&gt;1,*&lt;/sup&gt;, I.G.M. Reza Gunadi Ranuh&lt;sup&gt;1&lt;/sup&gt;, Andy Darma&lt;sup&gt;1&lt;/sup&gt;, Khadijah Rizky Sumitro&lt;sup&gt;1&lt;/sup&gt;, Wibi Riawan&lt;sup&gt;2&lt;/sup&gt;, Ingrid S. Surono&lt;sup&gt;3&lt;/sup&gt;, Subijanto Marto Sudarmo&lt;sup&gt;1&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 Child Health, Faculty of Medicine Universitas Airlangga. Dr. Soetomo General Academic Teaching Hospital, Mayjend. Prof. Dr. Moestopo No. 6-8, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Laboratory of Biochemistry and Biomolecular Universitas Brawijaya, Veteran Street, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Food Technology Department, Faculty of Engineering, Bina Nusantara University, Jakarta 11480, 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%">Thriveni Vasanthkumar</style></author><author><style face="normal" font="default" size="100%">Manjunatha Hanumanthappa</style></author><author><style face="normal" font="default" size="100%">Prabhakar BT</style></author><author><style face="normal" font="default" size="100%">Santhosh Kondajji Hanumanthappa</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hepatoprotective Effect of Curcumin and Capsaicin against Lipopolysaccharide Induced Liver Damage in Mice</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%">ALP.</style></keyword><keyword><style  face="normal" font="default" size="100%">Capsaicin</style></keyword><keyword><style  face="normal" font="default" size="100%">Curcumin</style></keyword><keyword><style  face="normal" font="default" size="100%">Hepatoprotective activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Lipopolysaccharide</style></keyword><keyword><style  face="normal" font="default" size="100%">SGOT</style></keyword><keyword><style  face="normal" font="default" size="100%">SGPT</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/201</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">947-951</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;Objective:&lt;/strong&gt; The present study was undertaken to evaluate the possible ameliorative role of curcumin, capsaicin and their combination against lipopolysaccharide (LPS) induced hepatic toxicity in mice. &lt;strong&gt;Methods:&lt;/strong&gt; Animals were distributed into five experimental groups: Normal control, vehicle control, curcumin, capsaicin and combined curcumin and capsaicin treatment groups respectively, for 7 days prior to LPS induced liver toxicity (3 mg/kg b.w. in saline). Hepatoprotective effect of individual and combined spice principles were evidenced by the measurement of serum marker enzyme activities such as, SGPT, ALP and TB and it was further confirmed by histopathological observation of liver tissue section. &lt;strong&gt;Results:&lt;/strong&gt; The administration of LPS increased serum nonspecific enzymes (SGOT; 174.2&amp;plusmn;3.79 IU/L, SGPT; 124.0&amp;plusmn;3.14 IU/L, ALP; 320.15&amp;plusmn;3.88 IU/L and total bilirubin level; 2.32&amp;plusmn;1.23 mg/dL), however dietary curcumin and capsaicin decreased the activities of these non&amp;ndash;specific serum enzymes including total bilirubin indicating amelioration of the severe LPS induced hepatotoxicity, while the combined spice principles were more significant as shown by the levels of enzymes activities SGOT; 89.9&amp;plusmn;1.39 IU/L, SGPT; 85.9&amp;plusmn;1.83 IU/L, ALP; 138.4&amp;plusmn;2.05 IU/L including total bilirubin level; 0.86&amp;plusmn;0.03 mg/dL. &lt;strong&gt;Conclusion:&lt;/strong&gt; Dietary curcumin and capsaicin individually are protective to LPS induced hepatotoxicity, the beneficial effect was found to be more when the two compounds were fed in combination.&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%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">947</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Thriveni Vasanthkumar&lt;sup&gt;1&lt;/sup&gt;, Manjunatha Hanumanthappa&lt;sup&gt;1&lt;/sup&gt;, Prabhakar BT&lt;sup&gt;2&lt;/sup&gt;, Santhosh Kondajji Hanumanthappa&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biotechnology, Kuvempu University, Shankaraghatta - 577 451 Shimoga, Karnataka (St), INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Molecular biomedicine laboratory, Postgraduate department of studies and research in biotechnology, Sahyadri science college, Kuvempu University, Shimoga-577203, Karnataka (St), INDIA.&lt;/p&gt;</style></auth-address></record></records></xml>