<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>2340-9894</journal-id>
<journal-title><![CDATA[Ars Pharmaceutica (Internet)]]></journal-title>
<abbrev-journal-title><![CDATA[Ars Pharm]]></abbrev-journal-title>
<issn>2340-9894</issn>
<publisher>
<publisher-name><![CDATA[Universidad de Granada]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2340-98942020000300006</article-id>
<article-id pub-id-type="doi">10.30827/ars.v61i3.13634</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Phytochemical screening and hepatoprotective potential of Niphidium albopunctatissimum Lellinger on alcoholic hepatoxicity induced in albino rats]]></article-title>
<article-title xml:lang="es"><![CDATA[Tamizaje fitoquímico y potencial hepatoprotector de Niphidium albopunctatissimum Lellinger en la hepatoxicidad alcohólica inducida en ratas albinas]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Chávez-Alcántara]]></surname>
<given-names><![CDATA[Leyly]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cabanillas-Vargas]]></surname>
<given-names><![CDATA[Yesica]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ruiz-Reyes]]></surname>
<given-names><![CDATA[Segundo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Guevara-Vásquez]]></surname>
<given-names><![CDATA[Ana María]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Nacional de Trujillo Facultad de Farmacia y Bioquímica Departamento de Farmacología]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Peru</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad Nacional de Trujillo Facultad de Farmacia y Bioquímica Departamento de Farmacotecnia]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Peru</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>09</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>09</month>
<year>2020</year>
</pub-date>
<volume>61</volume>
<numero>3</numero>
<fpage>187</fpage>
<lpage>192</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_arttext&amp;pid=S2340-98942020000300006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_abstract&amp;pid=S2340-98942020000300006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_pdf&amp;pid=S2340-98942020000300006&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  Objectives:  To identify the phytoconstituents and determine the effect of Niphidium albopunctatissimum Lellinger on alcoholic hepatoxicity induced in albino rats.  Methods:  Phytochemical screening was performed using the drop Test. For hepatoxicity study, albino rats were randomized into 5 groups of 6 each. Healthy group: without hepatoxicity; Control group: hepatotoxicity; Curative group: hepatotoxicity plus fluid extract of N. albopunctatissimum Lellinger; Standard group: hepatotoxicity plus silymarin; Preventive group: Fluid extract of N. albopunctatissimum Lellinger for one week, then hepatotoxicity. Hepatotoxicity was induced with 56% (w / v) ethanol at doses of 7.6 mL / kg p.c every 12 hours for 7 days. Glutamic pyruvic transaminase (GPT) values were determined at baseline, 7 days after induction and 14 days after. A histopathological study of the livers was performed.  Results:  Phytochemical screening revealed the presence of polyphenols, anthocyanidins, saponins, flavonoids and tannins. The preventive and standard groups showed a very significant decrease in serum GPT levels compared to control group (p &lt;0.01), and curative group did so significantly (p &lt;0.05). Histopathological analysis showed in curative group some degenerating hepatocytes, many with normal-looking cytoplasm; the preventive and standard groups presented hepatocytes with normal architecture and some in degeneration, unlike the evident degeneration and necrosis in control group.  Conclusión: Niphidium albopunctatissimum Lellinger may have hepatoprotective potential against alcoholic toxicity induced in albino rats.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  Objetivos:  Identificar los fitoconstituyentes y determinar el efecto de Niphidium albopunctatissimum Lellinger en la hepatoxicidad alcohólica inducida en ratas albinas.  Métodos:  El tamizaje fitoquímico se realizó mediante la Prueba de la gota. Para el efecto en la hepatoxicidad, las ratas albinas fueron distribuidas al azar en 5 grupos de 6 cada uno, Grupo sano: Sin hepatoxicidad, Grupo Control: hepatotoxicidad, Grupo Curativo: hepatotoxicidad más extracto fluído de N. albopunctatissimum Lellinger, Grupo Patrón: hepatotoxicidad más silimarina y Grupo Preventivo: extracto fluido de N. albopunctatissimum Lellinger por una semana, luego hepatotoxicidad. La hepatotoxicidad se indujo con etanol 56% (p/v) en dosis de 7,6 mL/kg p.c cada 12 horas por 7 días. Se determinaron valores de Glutámico pirúvica transaminasa (GPT) al inicio, a los 7 días de inducción y a los 14 días. Se realizó el estudio histopatológico a los hígados.  Resultados:  El tamizaje fitoquímico reveló presencia de polifenoles, antocianidinas, saponinas, flavonoides y taninos. Los grupos preventivo y patrón evidenciaron disminución muy significativa de niveles séricos de GPT en comparación con el grupo control (p&lt; 0,01), y el grupo curativo lo hizo de manera significativa (p&lt;0,05). El análisis histopatológico evidenció en el grupo curativo algunos hepatocitos en degeneración, muchos con citoplasma de aspecto normal; los grupos preventivo y patrón presentaron hepatocitos con arquitectura normal y algunos en degeneración, a diferencia de la evidente degeneración y necrosis en el grupo control.  Conclusión: Niphidium albopunctatissimum Lellinger puede tener potencial hepatoprotector frente a la toxicidad alcohólica inducida en ratas albinas.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Phytochemicals]]></kwd>
<kwd lng="en"><![CDATA[Liver]]></kwd>
<kwd lng="en"><![CDATA[Plant extracts]]></kwd>
<kwd lng="en"><![CDATA[Ethanol]]></kwd>
<kwd lng="es"><![CDATA[Fitoquímicos]]></kwd>
<kwd lng="es"><![CDATA[Hígado]]></kwd>
<kwd lng="es"><![CDATA[Extractos vegetales]]></kwd>
<kwd lng="es"><![CDATA[Etanol]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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