Phosphodiesterases type 2, 3 and 4 promote vascular tone in mesenteric arteries from rats with heart failure
Phosphodiesterases (PDE) type 3 and 4 promote vasoconstriction by hydrolysing cAMP. In experimental heart failure (HF), PDE3 makes PDE4 redundant in aorta, but it is not known if this occurs in resistance vessels, such as mesenteric artery. As PDE2 is increased in the failing myocardium, its possibl...
Ausführliche Beschreibung
Autor*in: |
Wang, Liting [verfasserIn] Hubert, Fabien [verfasserIn] Idres, Sarah [verfasserIn] Belacel-Ouari, Milia [verfasserIn] Domergue, Valérie [verfasserIn] Domenichini, Séverine [verfasserIn] Lefebvre, Florence [verfasserIn] Mika, Delphine [verfasserIn] Fischmeister, Rodolphe [verfasserIn] Leblais, Véronique [verfasserIn] Manoury, Boris [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2023 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: European journal of pharmacology - New York, NY [u.a.] : Elsevier, 1967, 944 |
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Übergeordnetes Werk: |
volume:944 |
DOI / URN: |
10.1016/j.ejphar.2023.175562 |
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Katalog-ID: |
ELV009321071 |
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245 | 1 | 0 | |a Phosphodiesterases type 2, 3 and 4 promote vascular tone in mesenteric arteries from rats with heart failure |
264 | 1 | |c 2023 | |
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520 | |a Phosphodiesterases (PDE) type 3 and 4 promote vasoconstriction by hydrolysing cAMP. In experimental heart failure (HF), PDE3 makes PDE4 redundant in aorta, but it is not known if this occurs in resistance vessels, such as mesenteric artery. As PDE2 is increased in the failing myocardium, its possible role in the vasculature also needs to be addressed. Here, the function of PDE2, PDE3 and PDE4 in rat mesenteric arteries was characterized in experimental HF. | ||
650 | 4 | |a Phosphodiesterase inhibitor | |
650 | 4 | |a Vascular tone | |
650 | 4 | |a Mesenteric artery | |
650 | 4 | |a Heart failure | |
650 | 4 | |a Nitric oxide (NO) | |
700 | 1 | |a Hubert, Fabien |e verfasserin |4 aut | |
700 | 1 | |a Idres, Sarah |e verfasserin |4 aut | |
700 | 1 | |a Belacel-Ouari, Milia |e verfasserin |4 aut | |
700 | 1 | |a Domergue, Valérie |e verfasserin |4 aut | |
700 | 1 | |a Domenichini, Séverine |e verfasserin |4 aut | |
700 | 1 | |a Lefebvre, Florence |e verfasserin |4 aut | |
700 | 1 | |a Mika, Delphine |e verfasserin |4 aut | |
700 | 1 | |a Fischmeister, Rodolphe |e verfasserin |4 aut | |
700 | 1 | |a Leblais, Véronique |e verfasserin |4 aut | |
700 | 1 | |a Manoury, Boris |e verfasserin |0 (orcid)0000-0001-7305-5633 |4 aut | |
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912 | |a GBV_ILN_4334 | ||
912 | |a GBV_ILN_4338 | ||
912 | |a GBV_ILN_4393 | ||
912 | |a GBV_ILN_4700 | ||
936 | b | k | |a 44.38 |j Pharmakologie |
951 | |a AR | ||
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allfields |
10.1016/j.ejphar.2023.175562 doi (DE-627)ELV009321071 (ELSEVIER)S0014-2999(23)00073-0 DE-627 ger DE-627 rda eng 610 DE-600 PHARM DE-84 fid 44.38 bkl Wang, Liting verfasserin aut Phosphodiesterases type 2, 3 and 4 promote vascular tone in mesenteric arteries from rats with heart failure 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Phosphodiesterases (PDE) type 3 and 4 promote vasoconstriction by hydrolysing cAMP. In experimental heart failure (HF), PDE3 makes PDE4 redundant in aorta, but it is not known if this occurs in resistance vessels, such as mesenteric artery. As PDE2 is increased in the failing myocardium, its possible role in the vasculature also needs to be addressed. Here, the function of PDE2, PDE3 and PDE4 in rat mesenteric arteries was characterized in experimental HF. Phosphodiesterase inhibitor Vascular tone Mesenteric artery Heart failure Nitric oxide (NO) Hubert, Fabien verfasserin aut Idres, Sarah verfasserin aut Belacel-Ouari, Milia verfasserin aut Domergue, Valérie verfasserin aut Domenichini, Séverine verfasserin aut Lefebvre, Florence verfasserin aut Mika, Delphine verfasserin aut Fischmeister, Rodolphe verfasserin aut Leblais, Véronique verfasserin aut Manoury, Boris verfasserin (orcid)0000-0001-7305-5633 aut Enthalten in European journal of pharmacology New York, NY [u.a.] : Elsevier, 1967 944 Online-Ressource (DE-627)300897340 (DE-600)1483526-5 (DE-576)081952627 1879-0712 nnns volume:944 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-PHARM SSG-OLC-PHA SSG-OPC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.38 Pharmakologie AR 944 |
spelling |
10.1016/j.ejphar.2023.175562 doi (DE-627)ELV009321071 (ELSEVIER)S0014-2999(23)00073-0 DE-627 ger DE-627 rda eng 610 DE-600 PHARM DE-84 fid 44.38 bkl Wang, Liting verfasserin aut Phosphodiesterases type 2, 3 and 4 promote vascular tone in mesenteric arteries from rats with heart failure 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Phosphodiesterases (PDE) type 3 and 4 promote vasoconstriction by hydrolysing cAMP. In experimental heart failure (HF), PDE3 makes PDE4 redundant in aorta, but it is not known if this occurs in resistance vessels, such as mesenteric artery. As PDE2 is increased in the failing myocardium, its possible role in the vasculature also needs to be addressed. Here, the function of PDE2, PDE3 and PDE4 in rat mesenteric arteries was characterized in experimental HF. Phosphodiesterase inhibitor Vascular tone Mesenteric artery Heart failure Nitric oxide (NO) Hubert, Fabien verfasserin aut Idres, Sarah verfasserin aut Belacel-Ouari, Milia verfasserin aut Domergue, Valérie verfasserin aut Domenichini, Séverine verfasserin aut Lefebvre, Florence verfasserin aut Mika, Delphine verfasserin aut Fischmeister, Rodolphe verfasserin aut Leblais, Véronique verfasserin aut Manoury, Boris verfasserin (orcid)0000-0001-7305-5633 aut Enthalten in European journal of pharmacology New York, NY [u.a.] : Elsevier, 1967 944 Online-Ressource (DE-627)300897340 (DE-600)1483526-5 (DE-576)081952627 1879-0712 nnns volume:944 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-PHARM SSG-OLC-PHA SSG-OPC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.38 Pharmakologie AR 944 |
allfields_unstemmed |
10.1016/j.ejphar.2023.175562 doi (DE-627)ELV009321071 (ELSEVIER)S0014-2999(23)00073-0 DE-627 ger DE-627 rda eng 610 DE-600 PHARM DE-84 fid 44.38 bkl Wang, Liting verfasserin aut Phosphodiesterases type 2, 3 and 4 promote vascular tone in mesenteric arteries from rats with heart failure 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Phosphodiesterases (PDE) type 3 and 4 promote vasoconstriction by hydrolysing cAMP. In experimental heart failure (HF), PDE3 makes PDE4 redundant in aorta, but it is not known if this occurs in resistance vessels, such as mesenteric artery. As PDE2 is increased in the failing myocardium, its possible role in the vasculature also needs to be addressed. Here, the function of PDE2, PDE3 and PDE4 in rat mesenteric arteries was characterized in experimental HF. Phosphodiesterase inhibitor Vascular tone Mesenteric artery Heart failure Nitric oxide (NO) Hubert, Fabien verfasserin aut Idres, Sarah verfasserin aut Belacel-Ouari, Milia verfasserin aut Domergue, Valérie verfasserin aut Domenichini, Séverine verfasserin aut Lefebvre, Florence verfasserin aut Mika, Delphine verfasserin aut Fischmeister, Rodolphe verfasserin aut Leblais, Véronique verfasserin aut Manoury, Boris verfasserin (orcid)0000-0001-7305-5633 aut Enthalten in European journal of pharmacology New York, NY [u.a.] : Elsevier, 1967 944 Online-Ressource (DE-627)300897340 (DE-600)1483526-5 (DE-576)081952627 1879-0712 nnns volume:944 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-PHARM SSG-OLC-PHA SSG-OPC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.38 Pharmakologie AR 944 |
allfieldsGer |
10.1016/j.ejphar.2023.175562 doi (DE-627)ELV009321071 (ELSEVIER)S0014-2999(23)00073-0 DE-627 ger DE-627 rda eng 610 DE-600 PHARM DE-84 fid 44.38 bkl Wang, Liting verfasserin aut Phosphodiesterases type 2, 3 and 4 promote vascular tone in mesenteric arteries from rats with heart failure 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Phosphodiesterases (PDE) type 3 and 4 promote vasoconstriction by hydrolysing cAMP. In experimental heart failure (HF), PDE3 makes PDE4 redundant in aorta, but it is not known if this occurs in resistance vessels, such as mesenteric artery. As PDE2 is increased in the failing myocardium, its possible role in the vasculature also needs to be addressed. Here, the function of PDE2, PDE3 and PDE4 in rat mesenteric arteries was characterized in experimental HF. Phosphodiesterase inhibitor Vascular tone Mesenteric artery Heart failure Nitric oxide (NO) Hubert, Fabien verfasserin aut Idres, Sarah verfasserin aut Belacel-Ouari, Milia verfasserin aut Domergue, Valérie verfasserin aut Domenichini, Séverine verfasserin aut Lefebvre, Florence verfasserin aut Mika, Delphine verfasserin aut Fischmeister, Rodolphe verfasserin aut Leblais, Véronique verfasserin aut Manoury, Boris verfasserin (orcid)0000-0001-7305-5633 aut Enthalten in European journal of pharmacology New York, NY [u.a.] : Elsevier, 1967 944 Online-Ressource (DE-627)300897340 (DE-600)1483526-5 (DE-576)081952627 1879-0712 nnns volume:944 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-PHARM SSG-OLC-PHA SSG-OPC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.38 Pharmakologie AR 944 |
allfieldsSound |
10.1016/j.ejphar.2023.175562 doi (DE-627)ELV009321071 (ELSEVIER)S0014-2999(23)00073-0 DE-627 ger DE-627 rda eng 610 DE-600 PHARM DE-84 fid 44.38 bkl Wang, Liting verfasserin aut Phosphodiesterases type 2, 3 and 4 promote vascular tone in mesenteric arteries from rats with heart failure 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Phosphodiesterases (PDE) type 3 and 4 promote vasoconstriction by hydrolysing cAMP. In experimental heart failure (HF), PDE3 makes PDE4 redundant in aorta, but it is not known if this occurs in resistance vessels, such as mesenteric artery. As PDE2 is increased in the failing myocardium, its possible role in the vasculature also needs to be addressed. Here, the function of PDE2, PDE3 and PDE4 in rat mesenteric arteries was characterized in experimental HF. Phosphodiesterase inhibitor Vascular tone Mesenteric artery Heart failure Nitric oxide (NO) Hubert, Fabien verfasserin aut Idres, Sarah verfasserin aut Belacel-Ouari, Milia verfasserin aut Domergue, Valérie verfasserin aut Domenichini, Séverine verfasserin aut Lefebvre, Florence verfasserin aut Mika, Delphine verfasserin aut Fischmeister, Rodolphe verfasserin aut Leblais, Véronique verfasserin aut Manoury, Boris verfasserin (orcid)0000-0001-7305-5633 aut Enthalten in European journal of pharmacology New York, NY [u.a.] : Elsevier, 1967 944 Online-Ressource (DE-627)300897340 (DE-600)1483526-5 (DE-576)081952627 1879-0712 nnns volume:944 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-PHARM SSG-OLC-PHA SSG-OPC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.38 Pharmakologie AR 944 |
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Wang, Liting ddc 610 fid PHARM bkl 44.38 misc Phosphodiesterase inhibitor misc Vascular tone misc Mesenteric artery misc Heart failure misc Nitric oxide (NO) Phosphodiesterases type 2, 3 and 4 promote vascular tone in mesenteric arteries from rats with heart failure |
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610 DE-600 PHARM DE-84 fid 44.38 bkl Phosphodiesterases type 2, 3 and 4 promote vascular tone in mesenteric arteries from rats with heart failure Phosphodiesterase inhibitor Vascular tone Mesenteric artery Heart failure Nitric oxide (NO) |
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Phosphodiesterases type 2, 3 and 4 promote vascular tone in mesenteric arteries from rats with heart failure |
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Phosphodiesterases type 2, 3 and 4 promote vascular tone in mesenteric arteries from rats with heart failure |
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Wang, Liting Hubert, Fabien Idres, Sarah Belacel-Ouari, Milia Domergue, Valérie Domenichini, Séverine Lefebvre, Florence Mika, Delphine Fischmeister, Rodolphe Leblais, Véronique Manoury, Boris |
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phosphodiesterases type 2, 3 and 4 promote vascular tone in mesenteric arteries from rats with heart failure |
title_auth |
Phosphodiesterases type 2, 3 and 4 promote vascular tone in mesenteric arteries from rats with heart failure |
abstract |
Phosphodiesterases (PDE) type 3 and 4 promote vasoconstriction by hydrolysing cAMP. In experimental heart failure (HF), PDE3 makes PDE4 redundant in aorta, but it is not known if this occurs in resistance vessels, such as mesenteric artery. As PDE2 is increased in the failing myocardium, its possible role in the vasculature also needs to be addressed. Here, the function of PDE2, PDE3 and PDE4 in rat mesenteric arteries was characterized in experimental HF. |
abstractGer |
Phosphodiesterases (PDE) type 3 and 4 promote vasoconstriction by hydrolysing cAMP. In experimental heart failure (HF), PDE3 makes PDE4 redundant in aorta, but it is not known if this occurs in resistance vessels, such as mesenteric artery. As PDE2 is increased in the failing myocardium, its possible role in the vasculature also needs to be addressed. Here, the function of PDE2, PDE3 and PDE4 in rat mesenteric arteries was characterized in experimental HF. |
abstract_unstemmed |
Phosphodiesterases (PDE) type 3 and 4 promote vasoconstriction by hydrolysing cAMP. In experimental heart failure (HF), PDE3 makes PDE4 redundant in aorta, but it is not known if this occurs in resistance vessels, such as mesenteric artery. As PDE2 is increased in the failing myocardium, its possible role in the vasculature also needs to be addressed. Here, the function of PDE2, PDE3 and PDE4 in rat mesenteric arteries was characterized in experimental HF. |
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Hubert, Fabien Idres, Sarah Belacel-Ouari, Milia Domergue, Valérie Domenichini, Séverine Lefebvre, Florence Mika, Delphine Fischmeister, Rodolphe Leblais, Véronique Manoury, Boris |
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