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Comparison of sarcoplasmic reticulum calcium content in atrial and ventricular myocytes of three fish species

Identifieur interne : 000081 ( PascalFrancis/Curation ); précédent : 000080; suivant : 000082

Comparison of sarcoplasmic reticulum calcium content in atrial and ventricular myocytes of three fish species

Auteurs : Jaakko Haverinen [Finlande] ; Matti Vornanen [Finlande]

Source :

RBID : Pascal:09-0420924

Descripteurs français

English descriptors

Abstract

Ryanodine (Ry) sensitivity of cardiac contraction differs between teleost species, between atrium and ventricle, and according to the thermal history of the fish. The hypothesis that variability in Ry sensitivity of contraction is due to species-specific, chamber-specific, and temperature-related differences in the sarcoplasmic reticulum (SR) Ca2+ content, was tested by comparing steady-state (SS) and maximal (Max) Ca2+ loads of the SR in three teleost fish, rainbow trout (Oncorhynchus mykiss), burbot (Lota lota), and crucian carp (Carassius carassius), which differ in the extent of SR contribution to excitation-contraction coupling. Fish were acclimated at 4°C (cold-acclimation, CA) or 18°C (warm-acclimation, WA), and SR Ca2+ content was released by a rapid application of 10 mM caffeine to single cardiac myocytes; its amount was determined from the Na+-Ca2+ exchange current at 18°C. SS Ca2+ load was larger in atrial (304-915 μmol/l) than ventricular (224-540 μmol/l) myocytes in all fish species (P < 0.05), and the same was true for Max SR Ca2+ content: 550-1,522 μmol/l and 438-840 μmol/l for atrial and ventricular myocytes, respectively (P < 0.05). Consistent with the hypothesis, acclimation to cold increased Ca2+ load of the cardiac SR in the burbot heart, but contrary to the hypothesis, temperature acclimation did not affect SR Ca2+ content in rainbow trout and crucian carp hearts. Furthermore, there was an inverse relation between SR Ca2+ content and Ry sensitivity of contraction force: the species with the smallest SR Ca2+ content (burbot) is most sensitive to Ry. Collectively, these findings show that SR Ca2+ content of fish cardiac myocytes is several times larger than that in mammalian cardiac SR.
pA  
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A03   1    @0 Am. j. physiol., Regul. integr. comp. physiol.
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A06       @2 4
A08 01  1  ENG  @1 Comparison of sarcoplasmic reticulum calcium content in atrial and ventricular myocytes of three fish species
A11 01  1    @1 HAVERINEN (Jaakko)
A11 02  1    @1 VORNANEN (Matti)
A14 01      @1 University of Joensuu, Faculty of Biosciences @2 Joensuu @3 FIN @Z 1 aut. @Z 2 aut.
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A66 01      @0 USA
C01 01    ENG  @0 Ryanodine (Ry) sensitivity of cardiac contraction differs between teleost species, between atrium and ventricle, and according to the thermal history of the fish. The hypothesis that variability in Ry sensitivity of contraction is due to species-specific, chamber-specific, and temperature-related differences in the sarcoplasmic reticulum (SR) Ca2+ content, was tested by comparing steady-state (SS) and maximal (Max) Ca2+ loads of the SR in three teleost fish, rainbow trout (Oncorhynchus mykiss), burbot (Lota lota), and crucian carp (Carassius carassius), which differ in the extent of SR contribution to excitation-contraction coupling. Fish were acclimated at 4°C (cold-acclimation, CA) or 18°C (warm-acclimation, WA), and SR Ca2+ content was released by a rapid application of 10 mM caffeine to single cardiac myocytes; its amount was determined from the Na+-Ca2+ exchange current at 18°C. SS Ca2+ load was larger in atrial (304-915 μmol/l) than ventricular (224-540 μmol/l) myocytes in all fish species (P < 0.05), and the same was true for Max SR Ca2+ content: 550-1,522 μmol/l and 438-840 μmol/l for atrial and ventricular myocytes, respectively (P < 0.05). Consistent with the hypothesis, acclimation to cold increased Ca2+ load of the cardiac SR in the burbot heart, but contrary to the hypothesis, temperature acclimation did not affect SR Ca2+ content in rainbow trout and crucian carp hearts. Furthermore, there was an inverse relation between SR Ca2+ content and Ry sensitivity of contraction force: the species with the smallest SR Ca2+ content (burbot) is most sensitive to Ry. Collectively, these findings show that SR Ca2+ content of fish cardiac myocytes is several times larger than that in mammalian cardiac SR.
C02 01  X    @0 002A22C
C02 02  X    @0 002A23B
C03 01  X  FRE  @0 Réticulum sarcoplasmique @5 01
C03 01  X  ENG  @0 Sarcoplasmic reticulum @5 01
C03 01  X  SPA  @0 Retículo sarcoplásmico @5 01
C03 02  X  FRE  @0 Calcium @2 NC @2 FR @5 02
C03 02  X  ENG  @0 Calcium @2 NC @2 FR @5 02
C03 02  X  SPA  @0 Calcio @2 NC @2 FR @5 02
C03 03  X  FRE  @0 Myocyte @5 03
C03 03  X  ENG  @0 Myocyte @5 03
C03 03  X  SPA  @0 Miocito @5 03
C03 04  X  FRE  @0 Ryanodine @5 04
C03 04  X  ENG  @0 Ryanodine @5 04
C03 04  X  SPA  @0 Ryanodina @5 04
C03 05  X  FRE  @0 Sensibilité @5 05
C03 05  X  ENG  @0 Sensitivity @5 05
C03 05  X  SPA  @0 Sensibilidad @5 05
C03 06  X  FRE  @0 Oreillette @5 06
C03 06  X  ENG  @0 Atrium @5 06
C03 06  X  SPA  @0 Orejuela @5 06
C03 07  X  FRE  @0 Variabilité @5 07
C03 07  X  ENG  @0 Variability @5 07
C03 07  X  SPA  @0 Variabilidad @5 07
C03 08  X  FRE  @0 Température @5 08
C03 08  X  ENG  @0 Temperature @5 08
C03 08  X  SPA  @0 Temperatura @5 08
C03 09  X  FRE  @0 Régime permanent @5 10
C03 09  X  ENG  @0 Steady state @5 10
C03 09  X  SPA  @0 Régimen permanente @5 10
C03 10  X  FRE  @0 Charge @5 11
C03 10  X  ENG  @0 Load @5 11
C03 10  X  SPA  @0 Carga @5 11
C03 11  X  FRE  @0 Truite @5 13
C03 11  X  ENG  @0 Trout @5 13
C03 11  X  SPA  @0 Trucha @5 13
C03 12  X  FRE  @0 Carpe @5 14
C03 12  X  ENG  @0 Carp @5 14
C03 12  X  SPA  @0 Carpa @5 14
C03 13  X  FRE  @0 Oncorhynchus mykiss @2 NS @5 54
C03 13  X  ENG  @0 Oncorhynchus mykiss @2 NS @5 54
C03 13  X  SPA  @0 Oncorhynchus mykiss @2 NS @5 54
C03 14  X  FRE  @0 Carassius carassius @2 NS @5 55
C03 14  X  ENG  @0 Carassius carassius @2 NS @5 55
C03 14  X  SPA  @0 Carassius carassius @2 NS @5 55
C07 01  X  FRE  @0 Facteur milieu @5 20
C07 01  X  ENG  @0 Environmental factor @5 20
C07 01  X  SPA  @0 Factor medio @5 20
C07 02  X  FRE  @0 Appareil circulatoire @5 21
C07 02  X  ENG  @0 Circulatory system @5 21
C07 02  X  SPA  @0 Aparato circulatorio @5 21
C07 03  X  FRE  @0 Pisces @2 NS
C07 03  X  ENG  @0 Pisces @2 NS
C07 03  X  SPA  @0 Pisces @2 NS
C07 04  X  FRE  @0 Vertebrata @2 NS
C07 04  X  ENG  @0 Vertebrata @2 NS
C07 04  X  SPA  @0 Vertebrata @2 NS
N21       @1 306
N44 01      @1 OTO
N82       @1 OTO

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Pascal:09-0420924

Le document en format XML

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<term>Régime permanent</term>
<term>Charge</term>
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<div type="abstract" xml:lang="en">Ryanodine (Ry) sensitivity of cardiac contraction differs between teleost species, between atrium and ventricle, and according to the thermal history of the fish. The hypothesis that variability in Ry sensitivity of contraction is due to species-specific, chamber-specific, and temperature-related differences in the sarcoplasmic reticulum (SR) Ca
<sup>2+</sup>
content, was tested by comparing steady-state (SS) and maximal (Max) Ca
<sup>2+</sup>
loads of the SR in three teleost fish, rainbow trout (Oncorhynchus mykiss), burbot (Lota lota), and crucian carp (Carassius carassius), which differ in the extent of SR contribution to excitation-contraction coupling. Fish were acclimated at 4°C (cold-acclimation, CA) or 18°C (warm-acclimation, WA), and SR Ca
<sup>2+</sup>
content was released by a rapid application of 10 mM caffeine to single cardiac myocytes; its amount was determined from the Na
<sup>+</sup>
-Ca
<sup>2+</sup>
exchange current at 18°C. SS Ca
<sup>2+</sup>
load was larger in atrial (304-915 μmol/l) than ventricular (224-540 μmol/l) myocytes in all fish species (P < 0.05), and the same was true for Max SR Ca
<sup>2+</sup>
content: 550-1,522 μmol/l and 438-840 μmol/l for atrial and ventricular myocytes, respectively (P < 0.05). Consistent with the hypothesis, acclimation to cold increased Ca
<sup>2+</sup>
load of the cardiac SR in the burbot heart, but contrary to the hypothesis, temperature acclimation did not affect SR Ca
<sup>2+</sup>
content in rainbow trout and crucian carp hearts. Furthermore, there was an inverse relation between SR Ca
<sup>2+</sup>
content and Ry sensitivity of contraction force: the species with the smallest SR Ca
<sup>2+</sup>
content (burbot) is most sensitive to Ry. Collectively, these findings show that SR Ca
<sup>2+</sup>
content of fish cardiac myocytes is several times larger than that in mammalian cardiac SR.</div>
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<sup>2+</sup>
content, was tested by comparing steady-state (SS) and maximal (Max) Ca
<sup>2+</sup>
loads of the SR in three teleost fish, rainbow trout (Oncorhynchus mykiss), burbot (Lota lota), and crucian carp (Carassius carassius), which differ in the extent of SR contribution to excitation-contraction coupling. Fish were acclimated at 4°C (cold-acclimation, CA) or 18°C (warm-acclimation, WA), and SR Ca
<sup>2+</sup>
content was released by a rapid application of 10 mM caffeine to single cardiac myocytes; its amount was determined from the Na
<sup>+</sup>
-Ca
<sup>2+</sup>
exchange current at 18°C. SS Ca
<sup>2+</sup>
load was larger in atrial (304-915 μmol/l) than ventricular (224-540 μmol/l) myocytes in all fish species (P < 0.05), and the same was true for Max SR Ca
<sup>2+</sup>
content: 550-1,522 μmol/l and 438-840 μmol/l for atrial and ventricular myocytes, respectively (P < 0.05). Consistent with the hypothesis, acclimation to cold increased Ca
<sup>2+</sup>
load of the cardiac SR in the burbot heart, but contrary to the hypothesis, temperature acclimation did not affect SR Ca
<sup>2+</sup>
content in rainbow trout and crucian carp hearts. Furthermore, there was an inverse relation between SR Ca
<sup>2+</sup>
content and Ry sensitivity of contraction force: the species with the smallest SR Ca
<sup>2+</sup>
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<s5>13</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Trucha</s0>
<s5>13</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE">
<s0>Carpe</s0>
<s5>14</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Carp</s0>
<s5>14</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Carpa</s0>
<s5>14</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE">
<s0>Oncorhynchus mykiss</s0>
<s2>NS</s2>
<s5>54</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG">
<s0>Oncorhynchus mykiss</s0>
<s2>NS</s2>
<s5>54</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA">
<s0>Oncorhynchus mykiss</s0>
<s2>NS</s2>
<s5>54</s5>
</fC03>
<fC03 i1="14" i2="X" l="FRE">
<s0>Carassius carassius</s0>
<s2>NS</s2>
<s5>55</s5>
</fC03>
<fC03 i1="14" i2="X" l="ENG">
<s0>Carassius carassius</s0>
<s2>NS</s2>
<s5>55</s5>
</fC03>
<fC03 i1="14" i2="X" l="SPA">
<s0>Carassius carassius</s0>
<s2>NS</s2>
<s5>55</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Facteur milieu</s0>
<s5>20</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Environmental factor</s0>
<s5>20</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Factor medio</s0>
<s5>20</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Appareil circulatoire</s0>
<s5>21</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Circulatory system</s0>
<s5>21</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Aparato circulatorio</s0>
<s5>21</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Pisces</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Pisces</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Pisces</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fN21>
<s1>306</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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