<?xml version="1.0" encoding="utf-8"?>
 <journal>
 <language>En</language>
 <journal_id_issn>1680-6433</journal_id_issn>
 <journal_id_issn_online>2008-2177</journal_id_issn_online>
 <journal_id_pubmed></journal_id_pubmed>
 <journal_id_pii></journal_id_pii>
 <journal_id_doi></journal_id_doi>
 <journal_id_isnet></journal_id_isnet>
 <journal_id_iranmedex></journal_id_iranmedex>
 <journal_id_magiran></journal_id_magiran>
 <journal_id_sid></journal_id_sid>

 <pubdate>
	<type>jalali</type>
	<year>1387</year>
	<month>8</month>
	<day>12</day>
 </pubdate>
 <pubdate>
	<type>gregorian</type>
	<year>2008</year>
	<month>11</month>
	<day>2</day>
 </pubdate>
 <volume>6</volume>
 <number>4</number>

 <publish_type>online</publish_type>
 <publish_edition>1</publish_edition>
 <article_type>fulltext</article_type>

<articleset>
	<article>
	<language>En</language>
	<article_id_issn>1680-6433</article_id_issn>
	<article_id_issn_online>2008-2177</article_id_issn_online>
	<article_id_pubmed></article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_isnet></article_id_isnet>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	
	<title_fa>Antispasmodic effect of Physalis alkekengi fruit extract</title_fa>
	<title>Antispasmodic effect of Physalis alkekengi fruit extract</title>
	<subject_fa/>
	<subject/>
	
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	
	
	<abstract_fa>Background: Studies have shown that Physalis alkekengi reduces implantation and
induces antifertility in rat. In Iranian traditional medicine it is believed that this plant
has abortifacient and antifertility activities.
Objective: The goal of this study was to evaluate the effect of Physalis alkekengi ripe
fruit hydroalcoholic extract (PFE) on uterine contractility and its possible
mechanism(s).
Materials and Methods: Extraction of Physalis alkekengi fruit was carried out by
maceration method (70% alcohol). Uterus was dissected out from adult non-pregnant rat
(Wistar) and contracted by KCl (60mM) or oxytocin (10mU/ml) in an organ bath
containing De Jalon solution and the effect of PFE on the uterine contractions was
investigated. Furthermore, the role of Î±- and Î²-adrenoceptors, opioid receptors, nitric
oxide and cyclic guanosine monophosphate synthesis inhibitors on the extract effects
were evaluated.
Results: KCl- and oxytocin-induced uterine contractions were inhibited (p&amp;amp;lt;0.001) by
the cumulative concentrations of the extract in a concentration dependent manner.
Incubation of uterus with propranolol (1Î¼M) and L-NAME (100Î¼M) attenuated the PFE
antispasmodic effect (p&amp;amp;lt;0.05). But the PFE effect was unaffected by phentolamine
(1Î¼M), naloxone (1Î¼M) or methylene blue (10Î¼M). In Ca2+-free with high potassium
(60mM) De Jalon solution, cumulative concentrations of CaCl2 (0.1-0.5mM) induced
uterine contraction concentration-dependently (p&amp;amp;lt;0.001). Uterus incubation (5min) with
PFE (0.25-1.75mg/ml) attenuated the CaCl2â€“induced contractions (p&amp;amp;lt;0.05).
Conclusion: It seems that the extract induced antispasmodic effect mainly via calcium
influx blockade and partially through blocking Î²-adrenoceptors and nitric oxide (NO)
synthesis. However, neither Î±-adrenoceptors nor opioid receptors or cGMP synthesis
were involved.</abstract_fa>
	<abstract>Background: Studies have shown that Physalis alkekengi reduces implantation and
induces antifertility in rat. In Iranian traditional medicine it is believed that this plant
has abortifacient and antifertility activities.
Objective: The goal of this study was to evaluate the effect of Physalis alkekengi ripe
fruit hydroalcoholic extract (PFE) on uterine contractility and its possible
mechanism(s).
Materials and Methods: Extraction of Physalis alkekengi fruit was carried out by
maceration method (70% alcohol). Uterus was dissected out from adult non-pregnant rat
(Wistar) and contracted by KCl (60mM) or oxytocin (10mU/ml) in an organ bath
containing De Jalon solution and the effect of PFE on the uterine contractions was
investigated. Furthermore, the role of Î±- and Î²-adrenoceptors, opioid receptors, nitric
oxide and cyclic guanosine monophosphate synthesis inhibitors on the extract effects
were evaluated.
Results: KCl- and oxytocin-induced uterine contractions were inhibited (p&amp;amp;lt;0.001) by
the cumulative concentrations of the extract in a concentration dependent manner.
Incubation of uterus with propranolol (1Î¼M) and L-NAME (100Î¼M) attenuated the PFE
antispasmodic effect (p&amp;amp;lt;0.05). But the PFE effect was unaffected by phentolamine
(1Î¼M), naloxone (1Î¼M) or methylene blue (10Î¼M). In Ca2+-free with high potassium
(60mM) De Jalon solution, cumulative concentrations of CaCl2 (0.1-0.5mM) induced
uterine contraction concentration-dependently (p&amp;amp;lt;0.001). Uterus incubation (5min) with
PFE (0.25-1.75mg/ml) attenuated the CaCl2â€“induced contractions (p&amp;amp;lt;0.05).
Conclusion: It seems that the extract induced antispasmodic effect mainly via calcium
influx blockade and partially through blocking Î²-adrenoceptors and nitric oxide (NO)
synthesis. However, neither Î±-adrenoceptors nor opioid receptors or cGMP synthesis
were involved.</abstract>

	<keyword_fa>Rat, Uterus, Physalis alkekengi, Antispasmodic.</keyword_fa>
	<keyword>Rat, Uterus, Physalis alkekengi, Antispasmodic.</keyword>
	<start_page>193</start_page>
	<end_page>198</end_page>
	<web_url></web_url>
	<web_url></web_url>
	<author_list>
	<author>
		<first_name>Mohammad Kazem</first_name>
		<middle_name/>
		<last_name> Gharib Naseri</last_name>
		<suffix/>
		<affiliation></affiliation>
		<first_name_fa>Mohammad Kazem</first_name_fa>
		<middle_name_fa></middle_name_fa>
		<last_name_fa> Gharib Naseri</last_name_fa>
		<suffix_fa/>
		<email>Gharibnaseri_m@yahoo.com</email>
		<code></code>
		<coreauthor>No</coreauthor>
		<affiliation_fa></affiliation_fa>
	</author>
	<author>
		<first_name>Maryam </first_name>
		<middle_name/>
		<last_name>Mohammadian</last_name>
		<suffix/>
		<affiliation></affiliation>
		<first_name_fa>Maryam </first_name_fa>
		<middle_name_fa></middle_name_fa>
		<last_name_fa>Mohammadian</last_name_fa>
		<suffix_fa/>
		<email></email>
		<code></code>
		<coreauthor>No</coreauthor>
		<affiliation_fa></affiliation_fa>
	</author>
	<author>
		<first_name>Zahra</first_name>
		<middle_name/>
		<last_name>Gharib Naseri Pharm</last_name>
		<suffix/>
		<affiliation></affiliation>
		<first_name_fa>Zahra</first_name_fa>
		<middle_name_fa></middle_name_fa>
		<last_name_fa>Gharib Naseri Pharm</last_name_fa>
		<suffix_fa/>
		<email></email>
		<code></code>
		<coreauthor>No</coreauthor>
		<affiliation_fa></affiliation_fa>
	</author>
	</author_list>
</article>
</articleset></journal>
  
