Loading…
Moderate-Intensity Exercise Training Reduces Vasorelaxation of Mesenteric Arteries: Role of BKCa Channels and Nitric Oxide
Exercise training (ET) is well established to induce vascular adaptations on the metabolically active muscles. These adaptations include increased function of vascular potassium channels and enhanced endothelium-dependent relaxations. However, the available data on the effect of ET on vasculatures t...
Saved in:
Published in: | Physiological research 2022-03, Vol.71 (1), p.67-77 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c327t-3f5bbe8540f8783bca114fb218375c0dbb4682d5dcc63cb8ae16de36a90d9bf63 |
---|---|
cites | cdi_FETCH-LOGICAL-c327t-3f5bbe8540f8783bca114fb218375c0dbb4682d5dcc63cb8ae16de36a90d9bf63 |
container_end_page | 77 |
container_issue | 1 |
container_start_page | 67 |
container_title | Physiological research |
container_volume | 71 |
creator | AL-DHUHLI, F AL-SIYABI, S AL-MAAMARI, H AL-FARSI, S ALBARWANI, S |
description | Exercise training (ET) is well established to induce vascular adaptations on the metabolically active muscles. These adaptations include increased function of vascular potassium channels and enhanced endothelium-dependent relaxations. However, the available data on the effect of ET on vasculatures that normally constrict during exercise, such as mesenteric arteries (MA), are scarce and not conclusive. Therefore, this study hypothesized that 10 weeks of moderate-intensity ET would result in adaptations towards more vasoconstriction or/and less vasodilatation of MA. Young Fischer 344 rats were randomly assigned to a sedentary group (SED; n=24) or exercise training group (EXE; n=28). The EXE rats underwent a progressive treadmill ET program for 10 weeks. Isometric tensions of small (SED; 252.9±29.5 µm, EXE; 248.6±34.4 µm) and large (SED; 397.7±85.3 µm, EXE; 414.0±86.95 µm) MA were recorded in response to cumulative phenylephrine concentrations (PE; 0-30 µM) in the presence and absence of the BKCa channel blocker, Iberiotoxin (100 nM). In another set of experiments, tensions in response to cumulative concentration-response curves of acetylcholine (ACh) or sodium nitroprusside (SNP) were obtained, and pEC50s were compared. Immunoblotting was performed to measure protein expression levels of the BKCa channel subunits and eNOS. ET did not alter the basal tension of small and large MA but significantly increased their responses to PE, and reduced the effect of BKCa channels in opposing the contractile responses to PE without changes in the protein expression level of BKCa subunits. ET also elicited a size-dependent functional adaptations that involved reduced endothelium-independent and endothelium-dependent relaxations. In large MA the sensitivity to SNP was decreased more than in small MA suggesting impaired nitric oxide (NO)-dependent mechanisms within the vascular smooth muscle cells of ET group. Whereas the shift in pEC50 of ACh-induced relaxation of small MA would suggest more effect on the production of NO within the endothelium, which is not changed in large MA of ET group. However, the eNOS protein expression level was not significantly changed between the ET and SED groups. In conclusion, our results indicate an increase in contraction and reduced relaxation of MA after 10 weeks of ET, an adaptation that may help shunt blood flow to metabolically active tissues during acute exercise. |
doi_str_mv | 10.33549/physiolres.934671 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8997679</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2646987370</sourcerecordid><originalsourceid>FETCH-LOGICAL-c327t-3f5bbe8540f8783bca114fb218375c0dbb4682d5dcc63cb8ae16de36a90d9bf63</originalsourceid><addsrcrecordid>eNpVUU1P4zAUtBBoKWX_ACdLnMM6sWM7HJCgKgvioxJi92r544UaBbvYKWr59aQU7YrTHGbevNEMQkclOaG0Zs2vxXydfewS5JOGMi7KHTQqJamKphF0F42I5FUhGZH76CDnZ0IqQQT9gfZpTRjlrB6h97voIOkeiuvQQ8i-X-PpCpL1GfBj0j748IQfwC0tZPxX55ig0yvd-xhwbPEdZBgOk7f4PG0Q8il-iB1syIubicaTuQ4Buox1cPje9xvpbOUdHKK9VncZfn7hGP25nD5Ororb2e_ryfltYWkl-oK2tTEga0ZaKSQ1Vpcla01VSipqS5wxjMvK1c5aTq2RGkrugHLdENeYltMxOtv6LpbmBZwd8ibdqUXyLzqtVdRefWeCn6un-KbkUCMXzWBw_GWQ4usScq-e4zKFIbOqOOONFFSQQVVtVTbFnBO0_z6URH3upf7vpbZ70Q_Wfo3R</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2646987370</pqid></control><display><type>article</type><title>Moderate-Intensity Exercise Training Reduces Vasorelaxation of Mesenteric Arteries: Role of BKCa Channels and Nitric Oxide</title><source>PubMed Central</source><creator>AL-DHUHLI, F ; AL-SIYABI, S ; AL-MAAMARI, H ; AL-FARSI, S ; ALBARWANI, S</creator><creatorcontrib>AL-DHUHLI, F ; AL-SIYABI, S ; AL-MAAMARI, H ; AL-FARSI, S ; ALBARWANI, S</creatorcontrib><description>Exercise training (ET) is well established to induce vascular adaptations on the metabolically active muscles. These adaptations include increased function of vascular potassium channels and enhanced endothelium-dependent relaxations. However, the available data on the effect of ET on vasculatures that normally constrict during exercise, such as mesenteric arteries (MA), are scarce and not conclusive. Therefore, this study hypothesized that 10 weeks of moderate-intensity ET would result in adaptations towards more vasoconstriction or/and less vasodilatation of MA. Young Fischer 344 rats were randomly assigned to a sedentary group (SED; n=24) or exercise training group (EXE; n=28). The EXE rats underwent a progressive treadmill ET program for 10 weeks. Isometric tensions of small (SED; 252.9±29.5 µm, EXE; 248.6±34.4 µm) and large (SED; 397.7±85.3 µm, EXE; 414.0±86.95 µm) MA were recorded in response to cumulative phenylephrine concentrations (PE; 0-30 µM) in the presence and absence of the BKCa channel blocker, Iberiotoxin (100 nM). In another set of experiments, tensions in response to cumulative concentration-response curves of acetylcholine (ACh) or sodium nitroprusside (SNP) were obtained, and pEC50s were compared. Immunoblotting was performed to measure protein expression levels of the BKCa channel subunits and eNOS. ET did not alter the basal tension of small and large MA but significantly increased their responses to PE, and reduced the effect of BKCa channels in opposing the contractile responses to PE without changes in the protein expression level of BKCa subunits. ET also elicited a size-dependent functional adaptations that involved reduced endothelium-independent and endothelium-dependent relaxations. In large MA the sensitivity to SNP was decreased more than in small MA suggesting impaired nitric oxide (NO)-dependent mechanisms within the vascular smooth muscle cells of ET group. Whereas the shift in pEC50 of ACh-induced relaxation of small MA would suggest more effect on the production of NO within the endothelium, which is not changed in large MA of ET group. However, the eNOS protein expression level was not significantly changed between the ET and SED groups. In conclusion, our results indicate an increase in contraction and reduced relaxation of MA after 10 weeks of ET, an adaptation that may help shunt blood flow to metabolically active tissues during acute exercise.</description><identifier>ISSN: 0862-8408</identifier><identifier>EISSN: 1802-9973</identifier><identifier>DOI: 10.33549/physiolres.934671</identifier><identifier>PMID: 35043645</identifier><language>eng</language><publisher>Praha: Institute of Physiology</publisher><subject>Adaptation ; Arteries ; Blood flow ; Blood pressure ; Blood vessels ; Endothelium ; Exercise ; Fitness equipment ; Fitness training programs ; Heart rate ; Immunoblotting ; Laboratory animals ; Muscle contraction ; Nitric oxide ; Phenylephrine ; Physical training ; Physiology ; Potassium ; Potassium channels (calcium-gated) ; Protein expression ; Proteins ; Smooth muscle ; Sodium nitroprusside ; Vasoconstriction ; Vasodilation ; Veins & arteries</subject><ispartof>Physiological research, 2022-03, Vol.71 (1), p.67-77</ispartof><rights>Copyright Institute of Physiology 2022</rights><rights>2022 Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c327t-3f5bbe8540f8783bca114fb218375c0dbb4682d5dcc63cb8ae16de36a90d9bf63</citedby><cites>FETCH-LOGICAL-c327t-3f5bbe8540f8783bca114fb218375c0dbb4682d5dcc63cb8ae16de36a90d9bf63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997679/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997679/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids></links><search><creatorcontrib>AL-DHUHLI, F</creatorcontrib><creatorcontrib>AL-SIYABI, S</creatorcontrib><creatorcontrib>AL-MAAMARI, H</creatorcontrib><creatorcontrib>AL-FARSI, S</creatorcontrib><creatorcontrib>ALBARWANI, S</creatorcontrib><title>Moderate-Intensity Exercise Training Reduces Vasorelaxation of Mesenteric Arteries: Role of BKCa Channels and Nitric Oxide</title><title>Physiological research</title><description>Exercise training (ET) is well established to induce vascular adaptations on the metabolically active muscles. These adaptations include increased function of vascular potassium channels and enhanced endothelium-dependent relaxations. However, the available data on the effect of ET on vasculatures that normally constrict during exercise, such as mesenteric arteries (MA), are scarce and not conclusive. Therefore, this study hypothesized that 10 weeks of moderate-intensity ET would result in adaptations towards more vasoconstriction or/and less vasodilatation of MA. Young Fischer 344 rats were randomly assigned to a sedentary group (SED; n=24) or exercise training group (EXE; n=28). The EXE rats underwent a progressive treadmill ET program for 10 weeks. Isometric tensions of small (SED; 252.9±29.5 µm, EXE; 248.6±34.4 µm) and large (SED; 397.7±85.3 µm, EXE; 414.0±86.95 µm) MA were recorded in response to cumulative phenylephrine concentrations (PE; 0-30 µM) in the presence and absence of the BKCa channel blocker, Iberiotoxin (100 nM). In another set of experiments, tensions in response to cumulative concentration-response curves of acetylcholine (ACh) or sodium nitroprusside (SNP) were obtained, and pEC50s were compared. Immunoblotting was performed to measure protein expression levels of the BKCa channel subunits and eNOS. ET did not alter the basal tension of small and large MA but significantly increased their responses to PE, and reduced the effect of BKCa channels in opposing the contractile responses to PE without changes in the protein expression level of BKCa subunits. ET also elicited a size-dependent functional adaptations that involved reduced endothelium-independent and endothelium-dependent relaxations. In large MA the sensitivity to SNP was decreased more than in small MA suggesting impaired nitric oxide (NO)-dependent mechanisms within the vascular smooth muscle cells of ET group. Whereas the shift in pEC50 of ACh-induced relaxation of small MA would suggest more effect on the production of NO within the endothelium, which is not changed in large MA of ET group. However, the eNOS protein expression level was not significantly changed between the ET and SED groups. In conclusion, our results indicate an increase in contraction and reduced relaxation of MA after 10 weeks of ET, an adaptation that may help shunt blood flow to metabolically active tissues during acute exercise.</description><subject>Adaptation</subject><subject>Arteries</subject><subject>Blood flow</subject><subject>Blood pressure</subject><subject>Blood vessels</subject><subject>Endothelium</subject><subject>Exercise</subject><subject>Fitness equipment</subject><subject>Fitness training programs</subject><subject>Heart rate</subject><subject>Immunoblotting</subject><subject>Laboratory animals</subject><subject>Muscle contraction</subject><subject>Nitric oxide</subject><subject>Phenylephrine</subject><subject>Physical training</subject><subject>Physiology</subject><subject>Potassium</subject><subject>Potassium channels (calcium-gated)</subject><subject>Protein expression</subject><subject>Proteins</subject><subject>Smooth muscle</subject><subject>Sodium nitroprusside</subject><subject>Vasoconstriction</subject><subject>Vasodilation</subject><subject>Veins & arteries</subject><issn>0862-8408</issn><issn>1802-9973</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpVUU1P4zAUtBBoKWX_ACdLnMM6sWM7HJCgKgvioxJi92r544UaBbvYKWr59aQU7YrTHGbevNEMQkclOaG0Zs2vxXydfewS5JOGMi7KHTQqJamKphF0F42I5FUhGZH76CDnZ0IqQQT9gfZpTRjlrB6h97voIOkeiuvQQ8i-X-PpCpL1GfBj0j748IQfwC0tZPxX55ig0yvd-xhwbPEdZBgOk7f4PG0Q8il-iB1syIubicaTuQ4Buox1cPje9xvpbOUdHKK9VncZfn7hGP25nD5Ororb2e_ryfltYWkl-oK2tTEga0ZaKSQ1Vpcla01VSipqS5wxjMvK1c5aTq2RGkrugHLdENeYltMxOtv6LpbmBZwd8ibdqUXyLzqtVdRefWeCn6un-KbkUCMXzWBw_GWQ4usScq-e4zKFIbOqOOONFFSQQVVtVTbFnBO0_z6URH3upf7vpbZ70Q_Wfo3R</recordid><startdate>20220325</startdate><enddate>20220325</enddate><creator>AL-DHUHLI, F</creator><creator>AL-SIYABI, S</creator><creator>AL-MAAMARI, H</creator><creator>AL-FARSI, S</creator><creator>ALBARWANI, S</creator><general>Institute of Physiology</general><general>Institute of Physiology of the Czech Academy of Sciences</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BYOGL</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope></search><sort><creationdate>20220325</creationdate><title>Moderate-Intensity Exercise Training Reduces Vasorelaxation of Mesenteric Arteries: Role of BKCa Channels and Nitric Oxide</title><author>AL-DHUHLI, F ; AL-SIYABI, S ; AL-MAAMARI, H ; AL-FARSI, S ; ALBARWANI, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c327t-3f5bbe8540f8783bca114fb218375c0dbb4682d5dcc63cb8ae16de36a90d9bf63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adaptation</topic><topic>Arteries</topic><topic>Blood flow</topic><topic>Blood pressure</topic><topic>Blood vessels</topic><topic>Endothelium</topic><topic>Exercise</topic><topic>Fitness equipment</topic><topic>Fitness training programs</topic><topic>Heart rate</topic><topic>Immunoblotting</topic><topic>Laboratory animals</topic><topic>Muscle contraction</topic><topic>Nitric oxide</topic><topic>Phenylephrine</topic><topic>Physical training</topic><topic>Physiology</topic><topic>Potassium</topic><topic>Potassium channels (calcium-gated)</topic><topic>Protein expression</topic><topic>Proteins</topic><topic>Smooth muscle</topic><topic>Sodium nitroprusside</topic><topic>Vasoconstriction</topic><topic>Vasodilation</topic><topic>Veins & arteries</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>AL-DHUHLI, F</creatorcontrib><creatorcontrib>AL-SIYABI, S</creatorcontrib><creatorcontrib>AL-MAAMARI, H</creatorcontrib><creatorcontrib>AL-FARSI, S</creatorcontrib><creatorcontrib>ALBARWANI, S</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>East Europe, Central Europe Database</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Physiological research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>AL-DHUHLI, F</au><au>AL-SIYABI, S</au><au>AL-MAAMARI, H</au><au>AL-FARSI, S</au><au>ALBARWANI, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Moderate-Intensity Exercise Training Reduces Vasorelaxation of Mesenteric Arteries: Role of BKCa Channels and Nitric Oxide</atitle><jtitle>Physiological research</jtitle><date>2022-03-25</date><risdate>2022</risdate><volume>71</volume><issue>1</issue><spage>67</spage><epage>77</epage><pages>67-77</pages><issn>0862-8408</issn><eissn>1802-9973</eissn><abstract>Exercise training (ET) is well established to induce vascular adaptations on the metabolically active muscles. These adaptations include increased function of vascular potassium channels and enhanced endothelium-dependent relaxations. However, the available data on the effect of ET on vasculatures that normally constrict during exercise, such as mesenteric arteries (MA), are scarce and not conclusive. Therefore, this study hypothesized that 10 weeks of moderate-intensity ET would result in adaptations towards more vasoconstriction or/and less vasodilatation of MA. Young Fischer 344 rats were randomly assigned to a sedentary group (SED; n=24) or exercise training group (EXE; n=28). The EXE rats underwent a progressive treadmill ET program for 10 weeks. Isometric tensions of small (SED; 252.9±29.5 µm, EXE; 248.6±34.4 µm) and large (SED; 397.7±85.3 µm, EXE; 414.0±86.95 µm) MA were recorded in response to cumulative phenylephrine concentrations (PE; 0-30 µM) in the presence and absence of the BKCa channel blocker, Iberiotoxin (100 nM). In another set of experiments, tensions in response to cumulative concentration-response curves of acetylcholine (ACh) or sodium nitroprusside (SNP) were obtained, and pEC50s were compared. Immunoblotting was performed to measure protein expression levels of the BKCa channel subunits and eNOS. ET did not alter the basal tension of small and large MA but significantly increased their responses to PE, and reduced the effect of BKCa channels in opposing the contractile responses to PE without changes in the protein expression level of BKCa subunits. ET also elicited a size-dependent functional adaptations that involved reduced endothelium-independent and endothelium-dependent relaxations. In large MA the sensitivity to SNP was decreased more than in small MA suggesting impaired nitric oxide (NO)-dependent mechanisms within the vascular smooth muscle cells of ET group. Whereas the shift in pEC50 of ACh-induced relaxation of small MA would suggest more effect on the production of NO within the endothelium, which is not changed in large MA of ET group. However, the eNOS protein expression level was not significantly changed between the ET and SED groups. In conclusion, our results indicate an increase in contraction and reduced relaxation of MA after 10 weeks of ET, an adaptation that may help shunt blood flow to metabolically active tissues during acute exercise.</abstract><cop>Praha</cop><pub>Institute of Physiology</pub><pmid>35043645</pmid><doi>10.33549/physiolres.934671</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0862-8408 |
ispartof | Physiological research, 2022-03, Vol.71 (1), p.67-77 |
issn | 0862-8408 1802-9973 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8997679 |
source | PubMed Central |
subjects | Adaptation Arteries Blood flow Blood pressure Blood vessels Endothelium Exercise Fitness equipment Fitness training programs Heart rate Immunoblotting Laboratory animals Muscle contraction Nitric oxide Phenylephrine Physical training Physiology Potassium Potassium channels (calcium-gated) Protein expression Proteins Smooth muscle Sodium nitroprusside Vasoconstriction Vasodilation Veins & arteries |
title | Moderate-Intensity Exercise Training Reduces Vasorelaxation of Mesenteric Arteries: Role of BKCa Channels and Nitric Oxide |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T22%3A22%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Moderate-Intensity%20Exercise%20Training%20Reduces%20Vasorelaxation%20of%20Mesenteric%20Arteries:%20Role%20of%20BKCa%20Channels%20and%20Nitric%20Oxide&rft.jtitle=Physiological%20research&rft.au=AL-DHUHLI,%20F&rft.date=2022-03-25&rft.volume=71&rft.issue=1&rft.spage=67&rft.epage=77&rft.pages=67-77&rft.issn=0862-8408&rft.eissn=1802-9973&rft_id=info:doi/10.33549/physiolres.934671&rft_dat=%3Cproquest_pubme%3E2646987370%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c327t-3f5bbe8540f8783bca114fb218375c0dbb4682d5dcc63cb8ae16de36a90d9bf63%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2646987370&rft_id=info:pmid/35043645&rfr_iscdi=true |