Source:http://linkedlifedata.com/resource/pubmed/id/16157513
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2005-11-8
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pubmed:abstractText |
Ginger is a world known food plant which is equally reputed for its medicinal properties. We report here the hypotensive, endothelium-dependent and independent vasodilator and cardio-suppressant and stimulant effects of its aqueous extract (Zo.Cr). Zo.Cr, which tested positive for saponins, flavonoids, amines, alkaloids and terpenoids, induced a dose-dependent (3.0-10.0 mg/kg) fall in the arterial blood pressure (BP) of anaesthetized rats which was partially blocked by atropine (1 mg/kg). In isolated endothelium-intact rat aorta, Zo.Cr (0.01-5.0 mg/ml) relaxed the phenylephrine (1 microM)-induced contractions, effect partially blocked by atropine (1 microM). Zo.Cr inhibited the K+ (80 mM)-induced contractions and also shifted the Ca++ dose-response curves to the right, similar to verapamil, indicating Ca++ antagonist activity. An atropine-resistant and l-NAME-sensitive vasodilator activity was also noted from ginger phenolic constituents 6-, 8- and 10-gingerol, while 6-shogaol showed a mild vasodilator effect. In guinea-pig atria, Zo.Cr (0.1-5.0 mg/ml) inhibited the force and rate of atrial contractions. Pretreatment with atropine blocked the inhibitory effect and a stimulatory effect was unmasked which was resistant to propranolol and verapamil but sensitive to ryanodine, blocker of Ca++ release from intracellular stores. Later at doses >or=1.0 mg/ml, the extract completely suppressed the atrial tissue, effect resistant to glibenclamide, pyrilamine, aminophylline and L-NAME. These data indicate that the aqueous ginger extract lowers BP through a dual inhibitory effect mediated via stimulation of muscarinic receptors and blockade of Ca++ channels and this study provides sound mechanistic basis for the use of ginger in hypertension and palpitations.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Cardiovascular Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Catechols,
http://linkedlifedata.com/resource/pubmed/chemical/Fatty Alcohols,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide,
http://linkedlifedata.com/resource/pubmed/chemical/Phenols,
http://linkedlifedata.com/resource/pubmed/chemical/Plant Extracts,
http://linkedlifedata.com/resource/pubmed/chemical/gingerol,
http://linkedlifedata.com/resource/pubmed/chemical/shogaol
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1537-1891
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
43
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
234-41
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16157513-Anesthesia,
pubmed-meshheading:16157513-Animals,
pubmed-meshheading:16157513-Aorta, Thoracic,
pubmed-meshheading:16157513-Blood Pressure,
pubmed-meshheading:16157513-Calcium,
pubmed-meshheading:16157513-Cardiovascular Agents,
pubmed-meshheading:16157513-Catechols,
pubmed-meshheading:16157513-Chromatography, Thin Layer,
pubmed-meshheading:16157513-Dose-Response Relationship, Drug,
pubmed-meshheading:16157513-Fatty Alcohols,
pubmed-meshheading:16157513-Female,
pubmed-meshheading:16157513-Ginger,
pubmed-meshheading:16157513-Guinea Pigs,
pubmed-meshheading:16157513-Male,
pubmed-meshheading:16157513-Nitric Oxide,
pubmed-meshheading:16157513-Phenols,
pubmed-meshheading:16157513-Plant Extracts,
pubmed-meshheading:16157513-Plant Roots,
pubmed-meshheading:16157513-Rats
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pubmed:year |
2005
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pubmed:articleTitle |
Cardiovascular effects of ginger aqueous extract and its phenolic constituents are mediated through multiple pathways.
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pubmed:affiliation |
Department of Biological and Biomedical Sciences, The Aga Khan University Medical College, Karachi 74800, Pakistan.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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