quareticctivity of Solidago canadensiscultivated ingypt and etermination of theostioactiveraction
Despite the traditional use of Solidago canadensis L. ( Asteraceae ) as a diuretic drug, there is a scarcity in scientific data concerning the activity of its different extracts and fractions as well as the class of constituents responsible for this diuretic action. A comparative study was carried o...
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Veröffentlicht in: | Iranian journal of pharmaceutical research : IJPR 2019-01, Vol.18 (2), p.922-937 |
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creator | Abdel Baki, Passent Mahmoud El-Sherei, Moshera Mohamed Khaleel, Amal Elsayed Abdel Motaal, Amira Ahmed Ibrahim Abdallah, Heba Mohammed |
description | Despite the traditional use of
Solidago canadensis
L. (
Asteraceae
) as a diuretic drug, there is a scarcity in scientific data concerning the activity of its different extracts and fractions as well as the class of constituents responsible for this diuretic action. A comparative study was carried out for the diuretic activities of the different standardized extracts and fractions of the flowering aerial parts of
S. canadensis,
as well as isolation of compounds from the most biologically active fraction. The ethanol extract and its ethyl acetate fraction (EA) showed the highest aquaretic activities (91 and 58% at a dose of 400 mg/Kg b.wt., respectively) compared to 100% of furosemide at 20 mg/Kg b.wt.. Their activities were higher than Cystinol® and spironolactone reference standards (74% and 59% of furosemide, respectively). EA showed the highest total phenolic and flavonoid contents among the tested fractions of the ethanol and aqueous extracts (9.38 ± 0.004 g GAE and 39.75 ± 0.005 g RE/100 g dried extract, respectively). Eight flavonoids, 2 phenolic acids and 1 nucleoside were isolated from EA. This is the first report of a comparative study between the aquaretic activities of the different extracts, fractions and essential oil of
S. canadensis
, as well as isolation of thyimidine
(1)
, isorhamnetin-3-
O
-
β
-ᴅ-glucopyranoside (
2
), kaempferol-3-
O
-(6”-
O
-acetyl)-
β
-ᴅ-glucopyranoside (
4
), quercetin-3-
O
-(6”-
O
-acetyl)-
β
-ᴅ-glucopyranoside (
5
), and kaempferol-3-
O
-
β
-ᴅ-apiofuranoside (
7
) from genus
Solidago
. |
doi_str_mv | 10.22037/ijpr.2019.2390 |
format | Article |
fullrecord | <record><control><sourceid>pubmedcentral</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6706705</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>pubmedcentral_primary_oai_pubmedcentral_nih_gov_6706705</sourcerecordid><originalsourceid>FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_67067053</originalsourceid><addsrcrecordid>eNqljD9PwzAUxC0EouXPzOovkPBsN0mzsCAQe9mth-2mr0rsYDuV8u1JJBZmpJN-dzrdMfYkoJQSVPNM5zGWEkRbStXCFduKRtZFvW_hevWqKkDJ_YbdpXQGqOp2B7dso0SlBDS7LcPvCaPLZEymC-WZhyM_hJ4sdoEb9GidT5TM1C89Zmc5-W4eM0dvucsuDuQxU_DrMJ9cSEvA9czFFcE_sJsj9sk9_vKevby_fb5-FOP0NThrnM8Rez1GGjDOOiDpv42nk-7CRdcNLKrUvw9-ANmsZzU</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>quareticctivity of Solidago canadensiscultivated ingypt and etermination of theostioactiveraction</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Abdel Baki, Passent Mahmoud ; El-Sherei, Moshera Mohamed ; Khaleel, Amal Elsayed ; Abdel Motaal, Amira Ahmed ; Ibrahim Abdallah, Heba Mohammed</creator><creatorcontrib>Abdel Baki, Passent Mahmoud ; El-Sherei, Moshera Mohamed ; Khaleel, Amal Elsayed ; Abdel Motaal, Amira Ahmed ; Ibrahim Abdallah, Heba Mohammed</creatorcontrib><description>Despite the traditional use of
Solidago canadensis
L. (
Asteraceae
) as a diuretic drug, there is a scarcity in scientific data concerning the activity of its different extracts and fractions as well as the class of constituents responsible for this diuretic action. A comparative study was carried out for the diuretic activities of the different standardized extracts and fractions of the flowering aerial parts of
S. canadensis,
as well as isolation of compounds from the most biologically active fraction. The ethanol extract and its ethyl acetate fraction (EA) showed the highest aquaretic activities (91 and 58% at a dose of 400 mg/Kg b.wt., respectively) compared to 100% of furosemide at 20 mg/Kg b.wt.. Their activities were higher than Cystinol® and spironolactone reference standards (74% and 59% of furosemide, respectively). EA showed the highest total phenolic and flavonoid contents among the tested fractions of the ethanol and aqueous extracts (9.38 ± 0.004 g GAE and 39.75 ± 0.005 g RE/100 g dried extract, respectively). Eight flavonoids, 2 phenolic acids and 1 nucleoside were isolated from EA. This is the first report of a comparative study between the aquaretic activities of the different extracts, fractions and essential oil of
S. canadensis
, as well as isolation of thyimidine
(1)
, isorhamnetin-3-
O
-
β
-ᴅ-glucopyranoside (
2
), kaempferol-3-
O
-(6”-
O
-acetyl)-
β
-ᴅ-glucopyranoside (
4
), quercetin-3-
O
-(6”-
O
-acetyl)-
β
-ᴅ-glucopyranoside (
5
), and kaempferol-3-
O
-
β
-ᴅ-apiofuranoside (
7
) from genus
Solidago
.</description><identifier>ISSN: 1735-0328</identifier><identifier>EISSN: 1726-6890</identifier><identifier>DOI: 10.22037/ijpr.2019.2390</identifier><identifier>PMID: 31531074</identifier><language>eng</language><publisher>Tehran, Iran: Shaheed Beheshti University of Medical Sciences</publisher><subject>Original</subject><ispartof>Iranian journal of pharmaceutical research : IJPR, 2019-01, Vol.18 (2), p.922-937</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706705/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706705/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids></links><search><creatorcontrib>Abdel Baki, Passent Mahmoud</creatorcontrib><creatorcontrib>El-Sherei, Moshera Mohamed</creatorcontrib><creatorcontrib>Khaleel, Amal Elsayed</creatorcontrib><creatorcontrib>Abdel Motaal, Amira Ahmed</creatorcontrib><creatorcontrib>Ibrahim Abdallah, Heba Mohammed</creatorcontrib><title>quareticctivity of Solidago canadensiscultivated ingypt and etermination of theostioactiveraction</title><title>Iranian journal of pharmaceutical research : IJPR</title><description>Despite the traditional use of
Solidago canadensis
L. (
Asteraceae
) as a diuretic drug, there is a scarcity in scientific data concerning the activity of its different extracts and fractions as well as the class of constituents responsible for this diuretic action. A comparative study was carried out for the diuretic activities of the different standardized extracts and fractions of the flowering aerial parts of
S. canadensis,
as well as isolation of compounds from the most biologically active fraction. The ethanol extract and its ethyl acetate fraction (EA) showed the highest aquaretic activities (91 and 58% at a dose of 400 mg/Kg b.wt., respectively) compared to 100% of furosemide at 20 mg/Kg b.wt.. Their activities were higher than Cystinol® and spironolactone reference standards (74% and 59% of furosemide, respectively). EA showed the highest total phenolic and flavonoid contents among the tested fractions of the ethanol and aqueous extracts (9.38 ± 0.004 g GAE and 39.75 ± 0.005 g RE/100 g dried extract, respectively). Eight flavonoids, 2 phenolic acids and 1 nucleoside were isolated from EA. This is the first report of a comparative study between the aquaretic activities of the different extracts, fractions and essential oil of
S. canadensis
, as well as isolation of thyimidine
(1)
, isorhamnetin-3-
O
-
β
-ᴅ-glucopyranoside (
2
), kaempferol-3-
O
-(6”-
O
-acetyl)-
β
-ᴅ-glucopyranoside (
4
), quercetin-3-
O
-(6”-
O
-acetyl)-
β
-ᴅ-glucopyranoside (
5
), and kaempferol-3-
O
-
β
-ᴅ-apiofuranoside (
7
) from genus
Solidago
.</description><subject>Original</subject><issn>1735-0328</issn><issn>1726-6890</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqljD9PwzAUxC0EouXPzOovkPBsN0mzsCAQe9mth-2mr0rsYDuV8u1JJBZmpJN-dzrdMfYkoJQSVPNM5zGWEkRbStXCFduKRtZFvW_hevWqKkDJ_YbdpXQGqOp2B7dso0SlBDS7LcPvCaPLZEymC-WZhyM_hJ4sdoEb9GidT5TM1C89Zmc5-W4eM0dvucsuDuQxU_DrMJ9cSEvA9czFFcE_sJsj9sk9_vKevby_fb5-FOP0NThrnM8Rez1GGjDOOiDpv42nk-7CRdcNLKrUvw9-ANmsZzU</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Abdel Baki, Passent Mahmoud</creator><creator>El-Sherei, Moshera Mohamed</creator><creator>Khaleel, Amal Elsayed</creator><creator>Abdel Motaal, Amira Ahmed</creator><creator>Ibrahim Abdallah, Heba Mohammed</creator><general>Shaheed Beheshti University of Medical Sciences</general><scope>5PM</scope></search><sort><creationdate>20190101</creationdate><title>quareticctivity of Solidago canadensiscultivated ingypt and etermination of theostioactiveraction</title><author>Abdel Baki, Passent Mahmoud ; El-Sherei, Moshera Mohamed ; Khaleel, Amal Elsayed ; Abdel Motaal, Amira Ahmed ; Ibrahim Abdallah, Heba Mohammed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_67067053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Original</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abdel Baki, Passent Mahmoud</creatorcontrib><creatorcontrib>El-Sherei, Moshera Mohamed</creatorcontrib><creatorcontrib>Khaleel, Amal Elsayed</creatorcontrib><creatorcontrib>Abdel Motaal, Amira Ahmed</creatorcontrib><creatorcontrib>Ibrahim Abdallah, Heba Mohammed</creatorcontrib><collection>PubMed Central (Full Participant titles)</collection><jtitle>Iranian journal of pharmaceutical research : IJPR</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abdel Baki, Passent Mahmoud</au><au>El-Sherei, Moshera Mohamed</au><au>Khaleel, Amal Elsayed</au><au>Abdel Motaal, Amira Ahmed</au><au>Ibrahim Abdallah, Heba Mohammed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>quareticctivity of Solidago canadensiscultivated ingypt and etermination of theostioactiveraction</atitle><jtitle>Iranian journal of pharmaceutical research : IJPR</jtitle><date>2019-01-01</date><risdate>2019</risdate><volume>18</volume><issue>2</issue><spage>922</spage><epage>937</epage><pages>922-937</pages><issn>1735-0328</issn><eissn>1726-6890</eissn><abstract>Despite the traditional use of
Solidago canadensis
L. (
Asteraceae
) as a diuretic drug, there is a scarcity in scientific data concerning the activity of its different extracts and fractions as well as the class of constituents responsible for this diuretic action. A comparative study was carried out for the diuretic activities of the different standardized extracts and fractions of the flowering aerial parts of
S. canadensis,
as well as isolation of compounds from the most biologically active fraction. The ethanol extract and its ethyl acetate fraction (EA) showed the highest aquaretic activities (91 and 58% at a dose of 400 mg/Kg b.wt., respectively) compared to 100% of furosemide at 20 mg/Kg b.wt.. Their activities were higher than Cystinol® and spironolactone reference standards (74% and 59% of furosemide, respectively). EA showed the highest total phenolic and flavonoid contents among the tested fractions of the ethanol and aqueous extracts (9.38 ± 0.004 g GAE and 39.75 ± 0.005 g RE/100 g dried extract, respectively). Eight flavonoids, 2 phenolic acids and 1 nucleoside were isolated from EA. This is the first report of a comparative study between the aquaretic activities of the different extracts, fractions and essential oil of
S. canadensis
, as well as isolation of thyimidine
(1)
, isorhamnetin-3-
O
-
β
-ᴅ-glucopyranoside (
2
), kaempferol-3-
O
-(6”-
O
-acetyl)-
β
-ᴅ-glucopyranoside (
4
), quercetin-3-
O
-(6”-
O
-acetyl)-
β
-ᴅ-glucopyranoside (
5
), and kaempferol-3-
O
-
β
-ᴅ-apiofuranoside (
7
) from genus
Solidago
.</abstract><cop>Tehran, Iran</cop><pub>Shaheed Beheshti University of Medical Sciences</pub><pmid>31531074</pmid><doi>10.22037/ijpr.2019.2390</doi><oa>free_for_read</oa></addata></record> |
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subjects | Original |
title | quareticctivity of Solidago canadensiscultivated ingypt and etermination of theostioactiveraction |
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