Contractile reserve but not tension is reduced in monocrotaline-induced right ventricular hypertrophy

The objective of this study was to evaluate the role of right ventricular hypertrophy on developed tension (Fdev) and contractile reserve of rat papillary muscle by using a model of monocrotaline (Mct)-induced pulmonary hypertension. Calcium handling and the influence of bicarbonate (symbol omitted)...

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Veröffentlicht in:American journal of physiology. Heart and circulatory physiology 2004-03, Vol.55 (3), p.H979-H984
Hauptverfasser: VERSLUIS, J. Pieter, HESLINGA, Johannes W, SIPKEMA, Pieter, WESTERHOF, Nico
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container_title American journal of physiology. Heart and circulatory physiology
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creator VERSLUIS, J. Pieter
HESLINGA, Johannes W
SIPKEMA, Pieter
WESTERHOF, Nico
description The objective of this study was to evaluate the role of right ventricular hypertrophy on developed tension (Fdev) and contractile reserve of rat papillary muscle by using a model of monocrotaline (Mct)-induced pulmonary hypertension. Calcium handling and the influence of bicarbonate (symbol omitted) were also addressed with the use of two different buffers ([symbol omitted] and HEPES). Wistar rats were injected with either Mct (40 mg/kg sc) or vehicle control (Con). Isometrically contracting right ventricular papillary muscles were studied at 80% of the length of maximal developed force. Contractile reserve (1 - Fdev/Fmax) was calculated from Fdev and maximal tension (Fmax). Calcium recirculation was determined with postextrasystolic potentiation. Both groups of muscles were superfused with either (symbol omitted) (Con-B and Mct-B, both n = 6) or HEPES (Con-H and Mct-H, both n = 6) buffer. With hypertrophy, contractions were slower but Fdev was not changed. However, Fmax was decreased (P < 0.05). With (symbol omitted), Fmax decreased from 23.8 +/- 6.5 mN x mm-2 in Con-B, to 13.7 +/- 3.3 mN x mm-2 in Mct-B. With HEPES, it decreased from 16.3 +/- 3.5 mN x mm-2 (n = 6, Con-H) to 8.3 +/- 1.6 mN x mm-2 (Mct-H). Contractile reserve during hypertrophy was therefore also decreased (P < 0.05). With (symbol omitted), it decreased from 0.73 +/- 0.03 (Con-B) to 0.55 +/- 0.04 (Mct-B). With HEPES, it decreased (P < 0.001) from 0.64 +/- 0.07 (Con-H) to 0.19 +/- 0.06 (Mct-H). The recirculation fraction decreased (P < 0.05) from 0.59 +/- 0.04 in Con-B to 0.44 +/- 0.04 in Mct-B. We conclude that contractile reserve and recirculation fraction are impaired during hypertrophy, with a stronger effect under HEPES than (formula omitted) superfusion. [PUBLICATION ABSTRACT]
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Pieter ; HESLINGA, Johannes W ; SIPKEMA, Pieter ; WESTERHOF, Nico</creator><creatorcontrib>VERSLUIS, J. Pieter ; HESLINGA, Johannes W ; SIPKEMA, Pieter ; WESTERHOF, Nico</creatorcontrib><description>The objective of this study was to evaluate the role of right ventricular hypertrophy on developed tension (Fdev) and contractile reserve of rat papillary muscle by using a model of monocrotaline (Mct)-induced pulmonary hypertension. Calcium handling and the influence of bicarbonate (symbol omitted) were also addressed with the use of two different buffers ([symbol omitted] and HEPES). Wistar rats were injected with either Mct (40 mg/kg sc) or vehicle control (Con). Isometrically contracting right ventricular papillary muscles were studied at 80% of the length of maximal developed force. Contractile reserve (1 - Fdev/Fmax) was calculated from Fdev and maximal tension (Fmax). Calcium recirculation was determined with postextrasystolic potentiation. Both groups of muscles were superfused with either (symbol omitted) (Con-B and Mct-B, both n = 6) or HEPES (Con-H and Mct-H, both n = 6) buffer. With hypertrophy, contractions were slower but Fdev was not changed. However, Fmax was decreased (P &lt; 0.05). With (symbol omitted), Fmax decreased from 23.8 +/- 6.5 mN x mm-2 in Con-B, to 13.7 +/- 3.3 mN x mm-2 in Mct-B. With HEPES, it decreased from 16.3 +/- 3.5 mN x mm-2 (n = 6, Con-H) to 8.3 +/- 1.6 mN x mm-2 (Mct-H). Contractile reserve during hypertrophy was therefore also decreased (P &lt; 0.05). With (symbol omitted), it decreased from 0.73 +/- 0.03 (Con-B) to 0.55 +/- 0.04 (Mct-B). With HEPES, it decreased (P &lt; 0.001) from 0.64 +/- 0.07 (Con-H) to 0.19 +/- 0.06 (Mct-H). The recirculation fraction decreased (P &lt; 0.05) from 0.59 +/- 0.04 in Con-B to 0.44 +/- 0.04 in Mct-B. We conclude that contractile reserve and recirculation fraction are impaired during hypertrophy, with a stronger effect under HEPES than (formula omitted) superfusion. [PUBLICATION ABSTRACT]</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>CODEN: AJPPDI</identifier><language>eng</language><publisher>Bethesda, MD: American Physiological Society</publisher><subject>Biological and medical sciences ; Fundamental and applied biological sciences. Psychology ; Heart ; Hypertension ; Muscular system ; Pulmonary arteries ; Rodents ; Vertebrates: cardiovascular system</subject><ispartof>American journal of physiology. 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Heart and circulatory physiology</title><description>The objective of this study was to evaluate the role of right ventricular hypertrophy on developed tension (Fdev) and contractile reserve of rat papillary muscle by using a model of monocrotaline (Mct)-induced pulmonary hypertension. Calcium handling and the influence of bicarbonate (symbol omitted) were also addressed with the use of two different buffers ([symbol omitted] and HEPES). Wistar rats were injected with either Mct (40 mg/kg sc) or vehicle control (Con). Isometrically contracting right ventricular papillary muscles were studied at 80% of the length of maximal developed force. Contractile reserve (1 - Fdev/Fmax) was calculated from Fdev and maximal tension (Fmax). Calcium recirculation was determined with postextrasystolic potentiation. Both groups of muscles were superfused with either (symbol omitted) (Con-B and Mct-B, both n = 6) or HEPES (Con-H and Mct-H, both n = 6) buffer. With hypertrophy, contractions were slower but Fdev was not changed. However, Fmax was decreased (P &lt; 0.05). With (symbol omitted), Fmax decreased from 23.8 +/- 6.5 mN x mm-2 in Con-B, to 13.7 +/- 3.3 mN x mm-2 in Mct-B. With HEPES, it decreased from 16.3 +/- 3.5 mN x mm-2 (n = 6, Con-H) to 8.3 +/- 1.6 mN x mm-2 (Mct-H). Contractile reserve during hypertrophy was therefore also decreased (P &lt; 0.05). With (symbol omitted), it decreased from 0.73 +/- 0.03 (Con-B) to 0.55 +/- 0.04 (Mct-B). With HEPES, it decreased (P &lt; 0.001) from 0.64 +/- 0.07 (Con-H) to 0.19 +/- 0.06 (Mct-H). The recirculation fraction decreased (P &lt; 0.05) from 0.59 +/- 0.04 in Con-B to 0.44 +/- 0.04 in Mct-B. We conclude that contractile reserve and recirculation fraction are impaired during hypertrophy, with a stronger effect under HEPES than (formula omitted) superfusion. 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Wistar rats were injected with either Mct (40 mg/kg sc) or vehicle control (Con). Isometrically contracting right ventricular papillary muscles were studied at 80% of the length of maximal developed force. Contractile reserve (1 - Fdev/Fmax) was calculated from Fdev and maximal tension (Fmax). Calcium recirculation was determined with postextrasystolic potentiation. Both groups of muscles were superfused with either (symbol omitted) (Con-B and Mct-B, both n = 6) or HEPES (Con-H and Mct-H, both n = 6) buffer. With hypertrophy, contractions were slower but Fdev was not changed. However, Fmax was decreased (P &lt; 0.05). With (symbol omitted), Fmax decreased from 23.8 +/- 6.5 mN x mm-2 in Con-B, to 13.7 +/- 3.3 mN x mm-2 in Mct-B. With HEPES, it decreased from 16.3 +/- 3.5 mN x mm-2 (n = 6, Con-H) to 8.3 +/- 1.6 mN x mm-2 (Mct-H). Contractile reserve during hypertrophy was therefore also decreased (P &lt; 0.05). With (symbol omitted), it decreased from 0.73 +/- 0.03 (Con-B) to 0.55 +/- 0.04 (Mct-B). With HEPES, it decreased (P &lt; 0.001) from 0.64 +/- 0.07 (Con-H) to 0.19 +/- 0.06 (Mct-H). The recirculation fraction decreased (P &lt; 0.05) from 0.59 +/- 0.04 in Con-B to 0.44 +/- 0.04 in Mct-B. We conclude that contractile reserve and recirculation fraction are impaired during hypertrophy, with a stronger effect under HEPES than (formula omitted) superfusion. [PUBLICATION ABSTRACT]</abstract><cop>Bethesda, MD</cop><pub>American Physiological Society</pub></addata></record>
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source American Physiological Society; EZB-FREE-00999 freely available EZB journals
subjects Biological and medical sciences
Fundamental and applied biological sciences. Psychology
Heart
Hypertension
Muscular system
Pulmonary arteries
Rodents
Vertebrates: cardiovascular system
title Contractile reserve but not tension is reduced in monocrotaline-induced right ventricular hypertrophy
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