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Antispasmodic, bronchodilator, vasorelaxant and cardiosuppressant effects of Buxus papillosa
BACKGROUND: The present research was carried out to investigate pharmacological properties of Buxus papillosa C.K. Schneid. (Buxaceae). METHODS: Buxus papillosa extracts of leaves (BpL), stem (BpS), roots (BpR) and BpL fractions: hexane (BpL-H), aqueous (BpL-A) also plant constituent, cyclomicrobuxi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241935/ https://www.ncbi.nlm.nih.gov/pubmed/28100216 http://dx.doi.org/10.1186/s12906-017-1558-x |
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author | Khan, Arif-ullah Ali, Shamsher Gilani, Anwarul-Hassan Ahmed, Manzoor Choudhary, Muhammad Iqbal |
author_facet | Khan, Arif-ullah Ali, Shamsher Gilani, Anwarul-Hassan Ahmed, Manzoor Choudhary, Muhammad Iqbal |
author_sort | Khan, Arif-ullah |
collection | PubMed |
description | BACKGROUND: The present research was carried out to investigate pharmacological properties of Buxus papillosa C.K. Schneid. (Buxaceae). METHODS: Buxus papillosa extracts of leaves (BpL), stem (BpS), roots (BpR) and BpL fractions: hexane (BpL-H), aqueous (BpL-A) also plant constituent, cyclomicrobuxine effect were studied in jejunum, atria, aorta and tracheal preparations from rabbit and guine-peg. RESULTS: Ca(++) antagonistic effect of BpS, BpR, BpL-H, BpL-A and cyclomicrobuxine were conclusively suggested, when spontaneous contractions of rabbit jejunal preparation was relaxed along with subsequent relaxation of potassium chloride (80 mM) induced contractions. Ca(++) antagonistic effect was further confirmed, when a prominent right shift like that of verapamil was observed in Ca(++) concentration-response curves, drawn in a tissue pretreated with BpL (0.3–1.0 mg/mL). In rabbit tracheal tissues BpL, BpS, BpR, BpL-H and BpL-A produced a prominent relaxation in contractions induced by potassium chloride (80 mM) and carbachol (1 μm). When tested in rabbit aortic rings, BpL, BpS, BpR, BpL-H and BpL-A showed concentration-dependent (0.1–3.0 mg/mL) vasorelaxant effect against phenylephrine (1 μM) and high K(+)-induced contractions. In isolated guinea-pig right atria, BpL, BpS, BpR, BpL-H and BpL-A suppressed atrial force of spontaneous contractions, with BpL-A being most potent. CONCLUSIONS: Our results reveal that Buxus papillosa possesses gut, airways and cardiovascular inhibitory actions. |
format | Online Article Text |
id | pubmed-5241935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52419352017-01-23 Antispasmodic, bronchodilator, vasorelaxant and cardiosuppressant effects of Buxus papillosa Khan, Arif-ullah Ali, Shamsher Gilani, Anwarul-Hassan Ahmed, Manzoor Choudhary, Muhammad Iqbal BMC Complement Altern Med Research Article BACKGROUND: The present research was carried out to investigate pharmacological properties of Buxus papillosa C.K. Schneid. (Buxaceae). METHODS: Buxus papillosa extracts of leaves (BpL), stem (BpS), roots (BpR) and BpL fractions: hexane (BpL-H), aqueous (BpL-A) also plant constituent, cyclomicrobuxine effect were studied in jejunum, atria, aorta and tracheal preparations from rabbit and guine-peg. RESULTS: Ca(++) antagonistic effect of BpS, BpR, BpL-H, BpL-A and cyclomicrobuxine were conclusively suggested, when spontaneous contractions of rabbit jejunal preparation was relaxed along with subsequent relaxation of potassium chloride (80 mM) induced contractions. Ca(++) antagonistic effect was further confirmed, when a prominent right shift like that of verapamil was observed in Ca(++) concentration-response curves, drawn in a tissue pretreated with BpL (0.3–1.0 mg/mL). In rabbit tracheal tissues BpL, BpS, BpR, BpL-H and BpL-A produced a prominent relaxation in contractions induced by potassium chloride (80 mM) and carbachol (1 μm). When tested in rabbit aortic rings, BpL, BpS, BpR, BpL-H and BpL-A showed concentration-dependent (0.1–3.0 mg/mL) vasorelaxant effect against phenylephrine (1 μM) and high K(+)-induced contractions. In isolated guinea-pig right atria, BpL, BpS, BpR, BpL-H and BpL-A suppressed atrial force of spontaneous contractions, with BpL-A being most potent. CONCLUSIONS: Our results reveal that Buxus papillosa possesses gut, airways and cardiovascular inhibitory actions. BioMed Central 2017-01-18 /pmc/articles/PMC5241935/ /pubmed/28100216 http://dx.doi.org/10.1186/s12906-017-1558-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Khan, Arif-ullah Ali, Shamsher Gilani, Anwarul-Hassan Ahmed, Manzoor Choudhary, Muhammad Iqbal Antispasmodic, bronchodilator, vasorelaxant and cardiosuppressant effects of Buxus papillosa |
title | Antispasmodic, bronchodilator, vasorelaxant and cardiosuppressant effects of Buxus papillosa |
title_full | Antispasmodic, bronchodilator, vasorelaxant and cardiosuppressant effects of Buxus papillosa |
title_fullStr | Antispasmodic, bronchodilator, vasorelaxant and cardiosuppressant effects of Buxus papillosa |
title_full_unstemmed | Antispasmodic, bronchodilator, vasorelaxant and cardiosuppressant effects of Buxus papillosa |
title_short | Antispasmodic, bronchodilator, vasorelaxant and cardiosuppressant effects of Buxus papillosa |
title_sort | antispasmodic, bronchodilator, vasorelaxant and cardiosuppressant effects of buxus papillosa |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241935/ https://www.ncbi.nlm.nih.gov/pubmed/28100216 http://dx.doi.org/10.1186/s12906-017-1558-x |
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