Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

Moderate-intensity exercise training reduces vasorelaxation of mesenteric arteries: role of BKCa channels and nitric oxide

F. Al-Dhuhli, S. Al-Siyabi, H. Al-Maamari, S. Al-Farsi, S. Albarwani

. 2022 ; 71 (1) : 67-77. [pub] 20220119

Language English Country Czech Republic

Document type Journal Article

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 microm, EXE; 248.6+/-34.4 microm) and large (SED; 397.7+/-85.3 microm, EXE; 414.0+/-86.95 microm) MA were recorded in response to cumulative phenylephrine concentrations (PE; 0-30 microM) 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.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc22009487
003      
CZ-PrNML
005      
20230331094442.0
007      
ta
008      
220419s2022 xr d f 000 0|eng||
009      
AR
024    7_
$a 10.33549/physiolres.934671 $2 doi
035    __
$a (PubMed)35043645
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xr
100    1_
$a Al-Dhuhli, Farid $u Department of Physiology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman
245    10
$a Moderate-intensity exercise training reduces vasorelaxation of mesenteric arteries: role of BKCa channels and nitric oxide / $c F. Al-Dhuhli, S. Al-Siyabi, H. Al-Maamari, S. Al-Farsi, S. Albarwani
520    9_
$a 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 microm, EXE; 248.6+/-34.4 microm) and large (SED; 397.7+/-85.3 microm, EXE; 414.0+/-86.95 microm) MA were recorded in response to cumulative phenylephrine concentrations (PE; 0-30 microM) 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.
650    _2
$a zvířata $7 D000818
650    _2
$a cévní endotel $x metabolismus $7 D004730
650    _2
$a arteriae mesentericae $7 D008638
650    12
$a oxid dusnatý $x metabolismus $7 D009569
650    _2
$a nitroprusid $x farmakologie $7 D009599
650    _2
$a krysa rodu Rattus $7 D051381
650    _2
$a vazokonstrikce $7 D014661
650    12
$a vazodilatace $7 D014664
655    _2
$a časopisecké články $7 D016428
700    1_
$a Al-Siyabi, Sultan $u Department of Physiology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman
700    1_
$a Al-Maamari, Hamed $u Department of Physiology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman
700    1_
$a Al-Farsi, Said $u Department of Physiology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman
700    1_
$a Albarwani, Sulayma $u Department of Physiology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman
773    0_
$w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 71, č. 1 (2022), s. 67-77
856    41
$u https://pubmed.ncbi.nlm.nih.gov/35043645 $y Pubmed
910    __
$a ABA008 $b A 4120 $c 266 $y p $z 0
990    __
$a 20220419 $b ABA008
991    __
$a 20230331094436 $b ABA008
999    __
$a ok $b bmc $g 1796995 $s 1160685
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2022 $b 71 $c 1 $d 67-77 $e 20220119 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
LZP    __
$b NLK198 $a Pubmed-20220419

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...