Effect of taurine on vascular dysfunction in an in vitro ischemia-reperfusion model of rat thoracic aorta

The primary objective of this study was to evaluate the protective effect of taurine on endothelial dysfunction in a vascular ischemia-reperfusion (IR) model. Thoracic aortas of 9 male Sprague-Dawley rats (350-500 g) were cut into rings and randomized into control (n = 7), IR (n = 8), IR + taurine 1...

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Published in:General thoracic and cardiovascular surgery
Main Authors: Teimoori, Ariyan, Orhan, Halit Güner, Demirtaş, Elif, Zeynalova, Nargiz, Efe, Oğuzhan Ekin, Emre Aydıngöz, Selda
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Language:English
Published: Japan 30-09-2024
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Abstract The primary objective of this study was to evaluate the protective effect of taurine on endothelial dysfunction in a vascular ischemia-reperfusion (IR) model. Thoracic aortas of 9 male Sprague-Dawley rats (350-500 g) were cut into rings and randomized into control (n = 7), IR (n = 8), IR + taurine 1 mM (n = 7), IR + taurine 10 mM (n = 8), IR + taurine 30 mM (n = 8), and IR + taurine 100 mM (n = 5) groups. Aortic rings in the IR group were stored in 0.9% saline at 4 °C for 24 h, placed in Krebs-Henseleit solution gassed with 95%O  + 5%CO at 37 °C, and exposed to sodium hypochlorite (200 μM) for 30 min. Responses to KCl (80 mM), phenylephrine (10 -10  M), acetylcholine (10 -10  M), and sodium nitroprusside (SNP, 10 -10  M) were recorded. E (maximum response) and pD (negative logarithm of concentration producing half-maximum response) were calculated. IR decreased KCl contraction (control 1047 ± 176 mg, IR 682 ± 128 mg, p = 0.0007), which was reversed by 30 and 100 mM taurine (960 ± 313 mg, p = 0.02 and 1066 ± 488 mg, p = 0.02, respectively). IR impaired phenylephrine, acetylcholine, and SNP responses (p < 0.0001). Taurine did not affect IR-impaired phenylephrine contractions. IR decreased both pD (control, 7.1 ± 0.1; IR, 6.0 ± 0.2; p < 0.01) and E (control, 83.5 ± 2.7%; IR, 26.8 ± 2.5%; p < 0.0001) of acetylcholine relaxation, both of which were reversed by 100 mM taurine (pD 7.2 ± 0.1; p < 0.001; E 45.4 ± 2.6%; p < 0.0001). For SNP relaxation, IR decreased pD (control 8.2 ± 0.1, IR 7.7 ± 0.1, p < 0.01), which was reversed by 100 mM taurine (8.5 ± 0.1, p < 0.0001). Taurine protects endothelial function after IR injury. Further studies should explore the mechanism of this effect and the potential of adding taurine to vascular graft storage solutions.
AbstractList The primary objective of this study was to evaluate the protective effect of taurine on endothelial dysfunction in a vascular ischemia-reperfusion (IR) model. Thoracic aortas of 9 male Sprague-Dawley rats (350-500 g) were cut into rings and randomized into control (n = 7), IR (n = 8), IR + taurine 1 mM (n = 7), IR + taurine 10 mM (n = 8), IR + taurine 30 mM (n = 8), and IR + taurine 100 mM (n = 5) groups. Aortic rings in the IR group were stored in 0.9% saline at 4 °C for 24 h, placed in Krebs-Henseleit solution gassed with 95%O  + 5%CO at 37 °C, and exposed to sodium hypochlorite (200 μM) for 30 min. Responses to KCl (80 mM), phenylephrine (10 -10  M), acetylcholine (10 -10  M), and sodium nitroprusside (SNP, 10 -10  M) were recorded. E (maximum response) and pD (negative logarithm of concentration producing half-maximum response) were calculated. IR decreased KCl contraction (control 1047 ± 176 mg, IR 682 ± 128 mg, p = 0.0007), which was reversed by 30 and 100 mM taurine (960 ± 313 mg, p = 0.02 and 1066 ± 488 mg, p = 0.02, respectively). IR impaired phenylephrine, acetylcholine, and SNP responses (p < 0.0001). Taurine did not affect IR-impaired phenylephrine contractions. IR decreased both pD (control, 7.1 ± 0.1; IR, 6.0 ± 0.2; p < 0.01) and E (control, 83.5 ± 2.7%; IR, 26.8 ± 2.5%; p < 0.0001) of acetylcholine relaxation, both of which were reversed by 100 mM taurine (pD 7.2 ± 0.1; p < 0.001; E 45.4 ± 2.6%; p < 0.0001). For SNP relaxation, IR decreased pD (control 8.2 ± 0.1, IR 7.7 ± 0.1, p < 0.01), which was reversed by 100 mM taurine (8.5 ± 0.1, p < 0.0001). Taurine protects endothelial function after IR injury. Further studies should explore the mechanism of this effect and the potential of adding taurine to vascular graft storage solutions.
The primary objective of this study was to evaluate the protective effect of taurine on endothelial dysfunction in a vascular ischemia-reperfusion (IR) model.OBJECTIVEThe primary objective of this study was to evaluate the protective effect of taurine on endothelial dysfunction in a vascular ischemia-reperfusion (IR) model.Thoracic aortas of 9 male Sprague-Dawley rats (350-500 g) were cut into rings and randomized into control (n = 7), IR (n = 8), IR + taurine 1 mM (n = 7), IR + taurine 10 mM (n = 8), IR + taurine 30 mM (n = 8), and IR + taurine 100 mM (n = 5) groups. Aortic rings in the IR group were stored in 0.9% saline at 4 °C for 24 h, placed in Krebs-Henseleit solution gassed with 95%O2 + 5%CO2 at 37 °C, and exposed to sodium hypochlorite (200 μM) for 30 min. Responses to KCl (80 mM), phenylephrine (10-10-10-4 M), acetylcholine (10-10-10-4 M), and sodium nitroprusside (SNP, 10-11-10-5 M) were recorded. Emax (maximum response) and pD2 (negative logarithm of concentration producing half-maximum response) were calculated.METHODSThoracic aortas of 9 male Sprague-Dawley rats (350-500 g) were cut into rings and randomized into control (n = 7), IR (n = 8), IR + taurine 1 mM (n = 7), IR + taurine 10 mM (n = 8), IR + taurine 30 mM (n = 8), and IR + taurine 100 mM (n = 5) groups. Aortic rings in the IR group were stored in 0.9% saline at 4 °C for 24 h, placed in Krebs-Henseleit solution gassed with 95%O2 + 5%CO2 at 37 °C, and exposed to sodium hypochlorite (200 μM) for 30 min. Responses to KCl (80 mM), phenylephrine (10-10-10-4 M), acetylcholine (10-10-10-4 M), and sodium nitroprusside (SNP, 10-11-10-5 M) were recorded. Emax (maximum response) and pD2 (negative logarithm of concentration producing half-maximum response) were calculated.IR decreased KCl contraction (control 1047 ± 176 mg, IR 682 ± 128 mg, p = 0.0007), which was reversed by 30 and 100 mM taurine (960 ± 313 mg, p = 0.02 and 1066 ± 488 mg, p = 0.02, respectively). IR impaired phenylephrine, acetylcholine, and SNP responses (p < 0.0001). Taurine did not affect IR-impaired phenylephrine contractions. IR decreased both pD2 (control, 7.1 ± 0.1; IR, 6.0 ± 0.2; p < 0.01) and Emax (control, 83.5 ± 2.7%; IR, 26.8 ± 2.5%; p < 0.0001) of acetylcholine relaxation, both of which were reversed by 100 mM taurine (pD2, 7.2 ± 0.1; p < 0.001; Emax, 45.4 ± 2.6%; p < 0.0001). For SNP relaxation, IR decreased pD2 (control 8.2 ± 0.1, IR 7.7 ± 0.1, p < 0.01), which was reversed by 100 mM taurine (8.5 ± 0.1, p < 0.0001).RESULTSIR decreased KCl contraction (control 1047 ± 176 mg, IR 682 ± 128 mg, p = 0.0007), which was reversed by 30 and 100 mM taurine (960 ± 313 mg, p = 0.02 and 1066 ± 488 mg, p = 0.02, respectively). IR impaired phenylephrine, acetylcholine, and SNP responses (p < 0.0001). Taurine did not affect IR-impaired phenylephrine contractions. IR decreased both pD2 (control, 7.1 ± 0.1; IR, 6.0 ± 0.2; p < 0.01) and Emax (control, 83.5 ± 2.7%; IR, 26.8 ± 2.5%; p < 0.0001) of acetylcholine relaxation, both of which were reversed by 100 mM taurine (pD2, 7.2 ± 0.1; p < 0.001; Emax, 45.4 ± 2.6%; p < 0.0001). For SNP relaxation, IR decreased pD2 (control 8.2 ± 0.1, IR 7.7 ± 0.1, p < 0.01), which was reversed by 100 mM taurine (8.5 ± 0.1, p < 0.0001).Taurine protects endothelial function after IR injury. Further studies should explore the mechanism of this effect and the potential of adding taurine to vascular graft storage solutions.CONCLUSIONTaurine protects endothelial function after IR injury. Further studies should explore the mechanism of this effect and the potential of adding taurine to vascular graft storage solutions.
Author Efe, Oğuzhan Ekin
Zeynalova, Nargiz
Teimoori, Ariyan
Demirtaş, Elif
Orhan, Halit Güner
Emre Aydıngöz, Selda
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  givenname: Halit Güner
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  fullname: Orhan, Halit Güner
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  organization: Department of Medical Pharmacology, Başkent University Faculty of Medicine, Ankara, Turkey
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  givenname: Oğuzhan Ekin
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  email: seldaemre71@yahoo.com
  organization: Department of Medical Pharmacology, Başkent University Faculty of Medicine, Ankara, Turkey. seldaemre71@yahoo.com
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Keywords Taurine
Ischemia‒reperfusion
Rat
Organ bath
In vitro
Language English
License 2024. The Author(s), under exclusive licence to The Japanese Association for Thoracic Surgery.
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Snippet The primary objective of this study was to evaluate the protective effect of taurine on endothelial dysfunction in a vascular ischemia-reperfusion (IR) model....
The primary objective of this study was to evaluate the protective effect of taurine on endothelial dysfunction in a vascular ischemia-reperfusion (IR)...
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Title Effect of taurine on vascular dysfunction in an in vitro ischemia-reperfusion model of rat thoracic aorta
URI https://www.ncbi.nlm.nih.gov/pubmed/39349917
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