ParkinsonFranceV1, PascalFrancis, Corpus, bibRecord, 001736

Effects of iron complexes on brain calcium homeostasis

Identifieur interne : 001736 ( PascalFrancis/Corpus ); précédent : 001735; suivant : 001737

Effects of iron complexes on brain calcium homeostasis

Auteurs : L. J. Anghileri ; P. Thouvenot ; A. Bertrand

Source :

Annals of clinical and laboratory science [ 0091-7370 ] ; 1997.

RBID : Pascal:97-0299238

Descripteurs français

Pascal (Inist)
- Parkinson maladie, Homéostasie phosphocalcique, Calcium, Fer complexe, In vivo, Pathogénie, Animal, Souris, Rat, In vitro, Culture cellulaire.

English descriptors

KwdEn :
- Animal, Calcium, Cell culture, In vitro, In vivo, Iron complex, Mouse, Parkinson disease, Pathogenesis, Phosphocalcic homeostasis, Rat.

Abstract

The effects of two physiological low molecular weight iron complexes, ferric lactate and ferric adenosine triphosphate (ATP) on brain Ca²⁺ homeostasis modification, have been studied in vitro and in vivo. In vitro ferric ATP complex shows a higher efficiency as modifier of Ca²⁺ homeostasis. This higher reactivity and the in vivo observed effect of increased brain uptake of iron from ferric lactate provoked by the presence of ATP, corroborate in vitro results showing an iron transfer from ferric lactate to ATP, as well as the mediator role of ATP in the iron-induced cellular Ca²⁺ homeostasis modification process. The possible role of this process in Parkinson's disease is discussed.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A02	`01`			`@0 ACLSCP`
A03		`1`		`@0 Ann. clin. lab. sci.`
A05				`@2 27`
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A08	`01`	`1`	`ENG`	`@1 Effects of iron complexes on brain calcium homeostasis`
A11	`01`	`1`		`@1 ANGHILERI (L. J.)`
A11	`02`	`1`		`@1 THOUVENOT (P.)`
A11	`03`	`1`		`@1 BERTRAND (A.)`
A14	`01`			`@1 Biophysics Laboratory, Medical Faculty, University of Nancy @2 Nancy @3 FRA @Z 1 aut.`
A14	`02`			`@1 Nuclear Medicine Department, University of Nancy Medical Center @2 Nancy @3 FRA @Z 2 aut. @Z 3 aut.`
A20				`@1 210-215`
A21				`@1 1997`
A23	`01`			`@0 ENG`
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A44				`@0 0000 @1 © 1997 INIST-CNRS. All rights reserved.`
A45				`@0 18 ref.`
A47	`01`	`1`		`@0 97-0299238`
A60				`@1 P`
A61				`@0 A`
A64	`01`	`1`		`@0 Annals of clinical and laboratory science`
A66	`01`			`@0 USA`
C01	`01`		`ENG`	@0 The effects of two physiological low molecular weight iron complexes, ferric lactate and ferric adenosine triphosphate (ATP) on brain Ca²⁺ homeostasis modification, have been studied in vitro and in vivo. In vitro ferric ATP complex shows a higher efficiency as modifier of Ca²⁺ homeostasis. This higher reactivity and the in vivo observed effect of increased brain uptake of iron from ferric lactate provoked by the presence of ATP, corroborate in vitro results showing an iron transfer from ferric lactate to ATP, as well as the mediator role of ATP in the iron-induced cellular Ca²⁺ homeostasis modification process. The possible role of this process in Parkinson's disease is discussed.
C02	`01`	`X`		`@0 002B17G`
C03	`01`	`X`	`FRE`	`@0 Parkinson maladie @5 01`
C03	`01`	`X`	`ENG`	`@0 Parkinson disease @5 01`
C03	`01`	`X`	`SPA`	`@0 Parkinson enfermedad @5 01`
C03	`02`	`X`	`FRE`	`@0 Homéostasie phosphocalcique @5 04`
C03	`02`	`X`	`ENG`	`@0 Phosphocalcic homeostasis @5 04`
C03	`02`	`X`	`SPA`	`@0 Homeostasia fosfocálcica @5 04`
C03	`03`	`X`	`FRE`	`@0 Calcium @2 NC @2 FR @5 05`
C03	`03`	`X`	`ENG`	`@0 Calcium @2 NC @2 FR @5 05`
C03	`03`	`X`	`GER`	`@0 Calcium @2 NC @2 FR @5 05`
C03	`03`	`X`	`SPA`	`@0 Calcio @2 NC @2 FR @5 05`
C03	`04`	`X`	`FRE`	`@0 Fer complexe @5 07`
C03	`04`	`X`	`ENG`	`@0 Iron complex @5 07`
C03	`04`	`X`	`GER`	`@0 Eisenkomplex @5 07`
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C03	`08`	`X`	`SPA`	`@0 Ratón @5 21`
C03	`09`	`X`	`FRE`	`@0 Rat @5 22`
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C03	`10`	`X`	`FRE`	`@0 In vitro @5 23`
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C03	`10`	`X`	`SPA`	`@0 In vitro @5 23`
C03	`11`	`X`	`FRE`	`@0 Culture cellulaire @5 24`
C03	`11`	`X`	`ENG`	`@0 Cell culture @5 24`
C03	`11`	`X`	`SPA`	`@0 Cultivo celular @5 24`
C07	`01`	`X`	`FRE`	`@0 Rodentia @2 NS`
C07	`01`	`X`	`ENG`	`@0 Rodentia @2 NS`
C07	`01`	`X`	`SPA`	`@0 Rodentia @2 NS`
C07	`02`	`X`	`FRE`	`@0 Mammalia @2 NS`
C07	`02`	`X`	`ENG`	`@0 Mammalia @2 NS`
C07	`02`	`X`	`SPA`	`@0 Mammalia @2 NS`
C07	`03`	`X`	`FRE`	`@0 Vertebrata @2 NS`
C07	`03`	`X`	`ENG`	`@0 Vertebrata @2 NS`
C07	`03`	`X`	`SPA`	`@0 Vertebrata @2 NS`
C07	`04`	`X`	`FRE`	`@0 Système nerveux pathologie @5 37`
C07	`04`	`X`	`ENG`	`@0 Nervous system diseases @5 37`
C07	`04`	`X`	`SPA`	`@0 Sistema nervioso patología @5 37`
C07	`05`	`X`	`FRE`	`@0 Système nerveux central pathologie @5 38`
C07	`05`	`X`	`ENG`	`@0 Central nervous system disease @5 38`
C07	`05`	`X`	`SPA`	`@0 Sistema nervosio central patología @5 38`
C07	`06`	`X`	`FRE`	`@0 Encéphale pathologie @5 39`
C07	`06`	`X`	`ENG`	`@0 Cerebral disorder @5 39`
C07	`06`	`X`	`SPA`	`@0 Encéfalo patología @5 39`
C07	`07`	`X`	`FRE`	`@0 Extrapyramidal syndrome @5 40`
C07	`07`	`X`	`ENG`	`@0 Extrapyramidal syndrome @5 40`
C07	`07`	`X`	`SPA`	`@0 Extrapiramidal síndrome @5 40`
C07	`08`	`X`	`FRE`	`@0 Maladie dégénérative @5 41`
C07	`08`	`X`	`ENG`	`@0 Degenerative disease @5 41`
C07	`08`	`X`	`SPA`	`@0 Enfermedad degenerativa @5 41`
N21				`@1 167`

Format Inist (serveur)

NO :	PASCAL 97-0299238 INIST
ET :	Effects of iron complexes on brain calcium homeostasis
AU :	ANGHILERI (L. J.); THOUVENOT (P.); BERTRAND (A.)
AF :	Biophysics Laboratory, Medical Faculty, University of Nancy/Nancy/France (1 aut.); Nuclear Medicine Department, University of Nancy Medical Center/Nancy/France (2 aut., 3 aut.)
DT :	Publication en série; Niveau analytique
SO :	Annals of clinical and laboratory science; ISSN 0091-7370; Coden ACLSCP; Etats-Unis; Da. 1997; Vol. 27; No. 3; Pp. 210-215; Bibl. 18 ref.
LA :	Anglais
EA :	The effects of two physiological low molecular weight iron complexes, ferric lactate and ferric adenosine triphosphate (ATP) on brain Ca²⁺ homeostasis modification, have been studied in vitro and in vivo. In vitro ferric ATP complex shows a higher efficiency as modifier of Ca²⁺ homeostasis. This higher reactivity and the in vivo observed effect of increased brain uptake of iron from ferric lactate provoked by the presence of ATP, corroborate in vitro results showing an iron transfer from ferric lactate to ATP, as well as the mediator role of ATP in the iron-induced cellular Ca²⁺ homeostasis modification process. The possible role of this process in Parkinson's disease is discussed.
CC :	002B17G
FD :	Parkinson maladie; Homéostasie phosphocalcique; Calcium; Fer complexe; In vivo; Pathogénie; Animal; Souris; Rat; In vitro; Culture cellulaire
FG :	Rodentia; Mammalia; Vertebrata; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative
ED :	Parkinson disease; Phosphocalcic homeostasis; Calcium; Iron complex; In vivo; Pathogenesis; Animal; Mouse; Rat; In vitro; Cell culture
EG :	Rodentia; Mammalia; Vertebrata; Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease
GD :	Calcium; Eisenkomplex
SD :	Parkinson enfermedad; Homeostasia fosfocálcica; Calcio; Hierro complejo; In vivo; Patogenia; Animal; Ratón; Rata; In vitro; Cultivo celular
LO :	INIST-16904.354000065519320060
ID :	97-0299238

Links to Exploration step

Pascal:97-0299238

Le document en format XML

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<front><div type="abstract" xml:lang="en">The effects of two physiological low molecular weight iron complexes, ferric lactate and ferric adenosine triphosphate (ATP) on brain Ca<sup>2+</sup>
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 homeostasis. This higher reactivity and the in vivo observed effect of increased brain uptake of iron from ferric lactate provoked by the presence of ATP, corroborate in vitro results showing an iron transfer from ferric lactate to ATP, as well as the mediator role of ATP in the iron-induced cellular Ca<sup>2+</sup>
 homeostasis modification process. The possible role of this process in Parkinson's disease is discussed.</div>
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<fC07 i1="02" i2="X" l="FRE"><s0>Mammalia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Mammalia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Mammalia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Système nerveux pathologie</s0>
<s5>37</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>37</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Système nerveux central pathologie</s0>
<s5>38</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>38</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>38</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Encéphale pathologie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>39</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>41</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>41</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>41</s5>
</fC07>
<fN21><s1>167</s1>
</fN21>
</pA>
</standard>
<server><NO>PASCAL 97-0299238 INIST</NO>
<ET>Effects of iron complexes on brain calcium homeostasis</ET>
<AU>ANGHILERI (L. J.); THOUVENOT (P.); BERTRAND (A.)</AU>
<AF>Biophysics Laboratory, Medical Faculty, University of Nancy/Nancy/France (1 aut.); Nuclear Medicine Department, University of Nancy Medical Center/Nancy/France (2 aut., 3 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Annals of clinical and laboratory science; ISSN 0091-7370; Coden ACLSCP; Etats-Unis; Da. 1997; Vol. 27; No. 3; Pp. 210-215; Bibl. 18 ref.</SO>
<LA>Anglais</LA>
<EA>The effects of two physiological low molecular weight iron complexes, ferric lactate and ferric adenosine triphosphate (ATP) on brain Ca<sup>2+</sup>
 homeostasis modification, have been studied in vitro and in vivo. In vitro ferric ATP complex shows a higher efficiency as modifier of Ca<sup>2+</sup>
 homeostasis. This higher reactivity and the in vivo observed effect of increased brain uptake of iron from ferric lactate provoked by the presence of ATP, corroborate in vitro results showing an iron transfer from ferric lactate to ATP, as well as the mediator role of ATP in the iron-induced cellular Ca<sup>2+</sup>
 homeostasis modification process. The possible role of this process in Parkinson's disease is discussed.</EA>
<CC>002B17G</CC>
<FD>Parkinson maladie; Homéostasie phosphocalcique; Calcium; Fer complexe; In vivo; Pathogénie; Animal; Souris; Rat; In vitro; Culture cellulaire</FD>
<FG>Rodentia; Mammalia; Vertebrata; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative</FG>
<ED>Parkinson disease; Phosphocalcic homeostasis; Calcium; Iron complex; In vivo; Pathogenesis; Animal; Mouse; Rat; In vitro; Cell culture</ED>
<EG>Rodentia; Mammalia; Vertebrata; Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease</EG>
<GD>Calcium; Eisenkomplex</GD>
<SD>Parkinson enfermedad; Homeostasia fosfocálcica; Calcio; Hierro complejo; In vivo; Patogenia; Animal; Ratón; Rata; In vitro; Cultivo celular</SD>
<LO>INIST-16904.354000065519320060</LO>
<ID>97-0299238</ID>
</server>
</inist>
</record>

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	La maladie de Parkinson en France (serveur d'exploration)
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La maladie de Parkinson en France (serveur d'exploration)

Effects of iron complexes on brain calcium homeostasis

Effects of iron complexes on brain calcium homeostasis

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