EsturgeonV1, PascalFrancis, Curation, bibRecord, 000085

Glycemic responses in white sturgeon after oral administration of graded doses of D-glucose

Identifieur interne : 000085 ( PascalFrancis/Curation ); précédent : 000084; suivant : 000086

Glycemic responses in white sturgeon after oral administration of graded doses of D-glucose

Auteurs : Enric Gisbert [États-Unis, Espagne] ; Roberto D. Sainz [États-Unis] ; Silas S. O. Hung [États-Unis]

Source :

Aquaculture : (Amsterdam) [ 0044-8486 ] ; 2003.

RBID : Pascal:03-0383573

Descripteurs français

Pascal (Inist)
- Voie orale, Glucose, Hyperglycémie provoquée, Poids corporel, Modélisation, Absorption, Tube digestif, Glycémie, Pisces, Acipenser transmontanus.
Wicri :
- topic : Glucose.

English descriptors

KwdEn :
- Absorption, Acipenser transmontanus, Body weight, Digestive tract, Glucose, Glucose tolerance test, Glycemia, Modeling, Oral administration, Pisces.

Abstract

Oral glucose tolerance tests, using a technique that combined esophageal intubation, dorsal aorta cannulation and urinary catheterization, were performed to assess the ability of white sturgeon to utilize different doses of D-glucose (0, 250, 500, 750, 1000, 1250 and 1500 mg.kg^-1 body weight (BW)). In fish intubated with 0 mg glucose.kg^-1 BW, plasma glucose concentrations did not change significantly during the 24-h experimental period (4.3 ± 0.1 mmol.l^-1, mean ± S.E., n=40 (5 fish and 8 time points), P>0.05). Observed maximum plasma glucose concentrations (8.4 ± 0.4 and 10.1 ± 0.8 mmol.l^-1, n 5) were detected at 3-4 h post-intubation in fish given 1250 and 1500 mg glucose.kg^-1 BW, respectively (P<0.05). White sturgeon dosed with 500, 750, 1000, 1250 and 1500 mg glucose.kg BW^-1 showed a persistent hyperglycemia not corrected until 12-24 h post-intubation. Comparttnental modeling of plasma glucose kinetics indicated that the rate constant for glucose absorption from the digestive tract into the bloodstream was significantly reduced, indicating that glucose absorption into the circulation was non-linearly related to dose, and became saturated at higher dosages. In contrast, glucose clearance rate increased with increasing plasma glucose concentration, but the rate of gluconeogenesis appeared to decrease only slightly. The small reduction in gluconeogenesis may contribute to the prolonged hyperglycemia observed in sturgeon after a glucose load.

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A08	`01`	`1`	`ENG`	`@1 Glycemic responses in white sturgeon after oral administration of graded doses of D-glucose`
A11	`01`	`1`		`@1 GISBERT (Enric)`
A11	`02`	`1`		`@1 SAINZ (Roberto D.)`
A11	`03`	`1`		`@1 HUNG (Silas S. O.)`
A14	`01`			`@1 Department of Animal Science, University of California, One Shields Avenue @2 Davis, CA 95616-8521 @3 USA @Z 1 aut. @Z 2 aut. @Z 3 aut.`
A14	`02`			`@1 Laboratorio de Aciticultura, Facultat de Biologia, Universitat de Barcelona, Av. Diagonal, 625 @2 08028 Barcelona @3 ESP @Z 1 aut.`
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A23	`01`			`@0 ENG`
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A44				`@0 0000 @1 © 2003 INIST-CNRS. All rights reserved.`
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C01	`01`		`ENG`	@0 Oral glucose tolerance tests, using a technique that combined esophageal intubation, dorsal aorta cannulation and urinary catheterization, were performed to assess the ability of white sturgeon to utilize different doses of D-glucose (0, 250, 500, 750, 1000, 1250 and 1500 mg.kg^-1 body weight (BW)). In fish intubated with 0 mg glucose.kg^-1 BW, plasma glucose concentrations did not change significantly during the 24-h experimental period (4.3 ± 0.1 mmol.l^-1, mean ± S.E., n=40 (5 fish and 8 time points), P>0.05). Observed maximum plasma glucose concentrations (8.4 ± 0.4 and 10.1 ± 0.8 mmol.l^-1, n 5) were detected at 3-4 h post-intubation in fish given 1250 and 1500 mg glucose.kg^-1 BW, respectively (P<0.05). White sturgeon dosed with 500, 750, 1000, 1250 and 1500 mg glucose.kg BW^-1 showed a persistent hyperglycemia not corrected until 12-24 h post-intubation. Comparttnental modeling of plasma glucose kinetics indicated that the rate constant for glucose absorption from the digestive tract into the bloodstream was significantly reduced, indicating that glucose absorption into the circulation was non-linearly related to dose, and became saturated at higher dosages. In contrast, glucose clearance rate increased with increasing plasma glucose concentration, but the rate of gluconeogenesis appeared to decrease only slightly. The small reduction in gluconeogenesis may contribute to the prolonged hyperglycemia observed in sturgeon after a glucose load.
C02	`01`	`X`		`@0 002A36B03A`
C03	`01`	`X`	`FRE`	`@0 Voie orale @5 01`
C03	`01`	`X`	`ENG`	`@0 Oral administration @5 01`
C03	`01`	`X`	`SPA`	`@0 Vía oral @5 01`
C03	`02`	`X`	`FRE`	`@0 Glucose @2 NK @5 02`
C03	`02`	`X`	`ENG`	`@0 Glucose @2 NK @5 02`
C03	`02`	`X`	`SPA`	`@0 Glucosa @2 NK @5 02`
C03	`03`	`X`	`FRE`	`@0 Hyperglycémie provoquée @5 03`
C03	`03`	`X`	`ENG`	`@0 Glucose tolerance test @5 03`
C03	`03`	`X`	`SPA`	`@0 Hiperglicemia provocada @5 03`
C03	`04`	`X`	`FRE`	`@0 Poids corporel @5 05`
C03	`04`	`X`	`ENG`	`@0 Body weight @5 05`
C03	`04`	`X`	`SPA`	`@0 Peso corporal @5 05`
C03	`05`	`X`	`FRE`	`@0 Modélisation @5 07`
C03	`05`	`X`	`ENG`	`@0 Modeling @5 07`
C03	`05`	`X`	`SPA`	`@0 Modelización @5 07`
C03	`06`	`X`	`FRE`	`@0 Absorption @5 09`
C03	`06`	`X`	`ENG`	`@0 Absorption @5 09`
C03	`06`	`X`	`SPA`	`@0 Absorción @5 09`
C03	`07`	`X`	`FRE`	`@0 Tube digestif @5 10`
C03	`07`	`X`	`ENG`	`@0 Digestive tract @5 10`
C03	`07`	`X`	`SPA`	`@0 Tubo digestivo @5 10`
C03	`08`	`X`	`FRE`	`@0 Glycémie @5 11`
C03	`08`	`X`	`ENG`	`@0 Glycemia @5 11`
C03	`08`	`X`	`SPA`	`@0 Glucemia @5 11`
C03	`09`	`X`	`FRE`	`@0 Pisces @2 NS @5 55`
C03	`09`	`X`	`ENG`	`@0 Pisces @2 NS @5 55`
C03	`09`	`X`	`SPA`	`@0 Pisces @2 NS @5 55`
C03	`10`	`X`	`FRE`	`@0 Acipenser transmontanus @2 NS @5 56`
C03	`10`	`X`	`ENG`	`@0 Acipenser transmontanus @2 NS @5 56`
C03	`10`	`X`	`SPA`	`@0 Acipenser transmontanus @2 NS @5 56`
C07	`01`	`X`	`FRE`	`@0 Vertebrata @2 NS`
C07	`01`	`X`	`ENG`	`@0 Vertebrata @2 NS`
C07	`01`	`X`	`SPA`	`@0 Vertebrata @2 NS`
C07	`02`	`X`	`FRE`	`@0 Acipenseridae @2 NS @4 INC @5 71`
N21				`@1 272`
N82				`@1 PSI`

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Pascal:03-0383573

Le document en format XML

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<front><div type="abstract" xml:lang="en">Oral glucose tolerance tests, using a technique that combined esophageal intubation, dorsal aorta cannulation and urinary catheterization, were performed to assess the ability of white sturgeon to utilize different doses of D-glucose (0, 250, 500, 750, 1000, 1250 and 1500 mg.kg<sup>-1</sup>
 body weight (BW)). In fish intubated with 0 mg glucose.kg<sup>-1</sup>
 BW, plasma glucose concentrations did not change significantly during the 24-h experimental period (4.3 ± 0.1 mmol.l<sup>-1</sup>
, mean ± S.E., n=40 (5 fish and 8 time points), P>0.05). Observed maximum plasma glucose concentrations (8.4 ± 0.4 and 10.1 ± 0.8 mmol.l<sup>-1</sup>
, n 5) were detected at 3-4 h post-intubation in fish given 1250 and 1500 mg glucose.kg<sup>-1</sup>
 BW, respectively (P<0.05). White sturgeon dosed with 500, 750, 1000, 1250 and 1500 mg glucose.kg BW<sup>-1</sup>
 showed a persistent hyperglycemia not corrected until 12-24 h post-intubation. Comparttnental modeling of plasma glucose kinetics indicated that the rate constant for glucose absorption from the digestive tract into the bloodstream was significantly reduced, indicating that glucose absorption into the circulation was non-linearly related to dose, and became saturated at higher dosages. In contrast, glucose clearance rate increased with increasing plasma glucose concentration, but the rate of gluconeogenesis appeared to decrease only slightly. The small reduction in gluconeogenesis may contribute to the prolonged hyperglycemia observed in sturgeon after a glucose load.</div>
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<fA08 i1="01" i2="1" l="ENG"><s1>Glycemic responses in white sturgeon after oral administration of graded doses of D-glucose</s1>
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<fA14 i1="01"><s1>Department of Animal Science, University of California, One Shields Avenue</s1>
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<fC01 i1="01" l="ENG"><s0>Oral glucose tolerance tests, using a technique that combined esophageal intubation, dorsal aorta cannulation and urinary catheterization, were performed to assess the ability of white sturgeon to utilize different doses of D-glucose (0, 250, 500, 750, 1000, 1250 and 1500 mg.kg<sup>-1</sup>
 body weight (BW)). In fish intubated with 0 mg glucose.kg<sup>-1</sup>
 BW, plasma glucose concentrations did not change significantly during the 24-h experimental period (4.3 ± 0.1 mmol.l<sup>-1</sup>
, mean ± S.E., n=40 (5 fish and 8 time points), P>0.05). Observed maximum plasma glucose concentrations (8.4 ± 0.4 and 10.1 ± 0.8 mmol.l<sup>-1</sup>
, n 5) were detected at 3-4 h post-intubation in fish given 1250 and 1500 mg glucose.kg<sup>-1</sup>
 BW, respectively (P<0.05). White sturgeon dosed with 500, 750, 1000, 1250 and 1500 mg glucose.kg BW<sup>-1</sup>
 showed a persistent hyperglycemia not corrected until 12-24 h post-intubation. Comparttnental modeling of plasma glucose kinetics indicated that the rate constant for glucose absorption from the digestive tract into the bloodstream was significantly reduced, indicating that glucose absorption into the circulation was non-linearly related to dose, and became saturated at higher dosages. In contrast, glucose clearance rate increased with increasing plasma glucose concentration, but the rate of gluconeogenesis appeared to decrease only slightly. The small reduction in gluconeogenesis may contribute to the prolonged hyperglycemia observed in sturgeon after a glucose load.</s0>
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<fC02 i1="01" i2="X"><s0>002A36B03A</s0>
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<fC03 i1="01" i2="X" l="FRE"><s0>Voie orale</s0>
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<s2>NK</s2>
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<fC03 i1="02" i2="X" l="ENG"><s0>Glucose</s0>
<s2>NK</s2>
<s5>02</s5>
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<fC03 i1="02" i2="X" l="SPA"><s0>Glucosa</s0>
<s2>NK</s2>
<s5>02</s5>
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<fC03 i1="03" i2="X" l="FRE"><s0>Hyperglycémie provoquée</s0>
<s5>03</s5>
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<s5>03</s5>
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<fC03 i1="04" i2="X" l="FRE"><s0>Poids corporel</s0>
<s5>05</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Body weight</s0>
<s5>05</s5>
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<fC03 i1="04" i2="X" l="SPA"><s0>Peso corporal</s0>
<s5>05</s5>
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<s5>07</s5>
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<s5>07</s5>
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<fC03 i1="06" i2="X" l="FRE"><s0>Absorption</s0>
<s5>09</s5>
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<fC03 i1="06" i2="X" l="ENG"><s0>Absorption</s0>
<s5>09</s5>
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<s5>09</s5>
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<s5>10</s5>
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<fC03 i1="07" i2="X" l="SPA"><s0>Tubo digestivo</s0>
<s5>10</s5>
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<s5>11</s5>
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<fC03 i1="08" i2="X" l="ENG"><s0>Glycemia</s0>
<s5>11</s5>
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<fC03 i1="08" i2="X" l="SPA"><s0>Glucemia</s0>
<s5>11</s5>
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<fC03 i1="09" i2="X" l="FRE"><s0>Pisces</s0>
<s2>NS</s2>
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<s2>NS</s2>
<s5>55</s5>
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<fC03 i1="09" i2="X" l="SPA"><s0>Pisces</s0>
<s2>NS</s2>
<s5>55</s5>
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<fC03 i1="10" i2="X" l="FRE"><s0>Acipenser transmontanus</s0>
<s2>NS</s2>
<s5>56</s5>
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<fC03 i1="10" i2="X" l="ENG"><s0>Acipenser transmontanus</s0>
<s2>NS</s2>
<s5>56</s5>
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<fC03 i1="10" i2="X" l="SPA"><s0>Acipenser transmontanus</s0>
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{{Explor lien
   |wiki=    Wicri/Eau
   |area=    EsturgeonV1
   |flux=    PascalFrancis
   |étape=   Curation
   |type=    RBID
   |clé=     Pascal:03-0383573
   |texte=   Glycemic responses in white sturgeon after oral administration of graded doses of D-glucose
}}

This area was generated with Dilib version V0.6.27.
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Glycemic responses in white sturgeon after oral administration of graded doses of D-glucose

Glycemic responses in white sturgeon after oral administration of graded doses of D-glucose

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