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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Metabolismo glicídico em ratos submetidos à imobilização por desnervação do músculo esquelético /

Nunes, Wilton Marlindo Santana. January 2005 (has links)
Orientador: Maria Alice Rostom de Mello / Banca: Eliete Luciano / Banca: Carlos Alberto da Silva / Banca: Maria Esméria C. do Amaral. / Banca: Silvia Cristina Crepaldi Alves / Resumo: Este estudo visou analisar o metabolismo da glicose no músculo sóleo de ratos submetidos a desnervação bem como a resposta do animal como um todo à insulina exógena e ao exercício. Os animais foram tratados de acordo com o Guide for care use of laboratory animals. (National Research Council, 1996). Para isso foram realizados 3 experimentos. No primeiro, ratos adultos (3 a 5 meses) foram submetidos à secção do nervo isquiático da pata direita. Observou-se redução da captação de glicose pelo músculo sóleo isolado da pata desnervada após 3 e 7 dias mas não após 28 dias em relação a animais controles íntegros. Não houve diferença após 3 e 7 dias na captação de glicose pelo músculo sóleo da pata contralateral em relação ao animal controle. Houve aumento da captação de glicose na pata contralateral 28 dias após a desnervação. Verificou-se que após 28 dias de desnervação, não houve reinervação do nervo isquiático. A taxa de remoção da glicose em resposta à insulina exógena após 28 dias de desnervação foi superior à de animais controle íntegros e aquela observada após 3 e 7 dias de desnervação. No segundo, ratos nas mesmas condições, após 48 h de desnervação iniciaram programa de natação 1h/dia, 5dias/semana, durante 28 dias. Ratos desnervados submetidos ao exercício mostraram maior taxa de remoção da glicose sangüínea em resposta à insulina exógena comparados aos sedentários e a animais controle íntegros. O exercício elevou a captação e a oxidação da glicose pelo músculo contralateral e pelo desnervado assim como pelo músculo de animais controles íntegros. Esses resultados sugerem que alterações restritas do metabolismo glicídico muscular influenciam a homeostase glicêmica do animal. Além disso, o exercício melhora o aporte e a utilização da glicose no músculo desnervado... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: This study aimed to analyze the metabolism of glucose in the soleus muscle of rats submitted to denervation, as well as the response of the animal as a whole to exogenous insulin and to exercise. To do this, 3 experiments were carried out. In the first, adult rats (3 to 5 months old) were submitted to section of the sciatic nerve in the right paw. A reduction was observed in the uptake of glucose by the isolated soleum muscle of the denervated paw after 3 and 7 days, but not after 28 days in relation to the whole control animals. There was no difference after 3 and 7 days in glucose uptake by the soleum muscle of the opposite paw in relation to the control animal. There was increased glucose uptake in this same paw 28 days after denervation. The rate of glucose removal in response to exogenous insulin after 28 days of denervation was higher than that of whole control animals and those observed after 3 and 7 days of denervation. In the second experiment, rats in the same conditions, after 48 h of denervation started a swimming program 1h/day, 5day/week, for 28 days. The denerved rats submitted to exercise showed a higher blood glucose removal rate in response to exogenous insulin compared to the sedentary and whole control animals. Exercise raised the uptake and oxidation of glucose by the opposite muscle and by the denervated one, as well as by the muscles of the whole control animals. These results suggest that restricted alterations of the muscular glucose metabolism influenced the glycemic homeostasis of the animal. Furthermore, exercise improved the uptake and use of glucose in the denerved muscle. In the third experiment, adult rats in the same conditions as in the first study, had an assessment made of their insulin secretion by isolated pancreatic islets, incubated in the presence of growing concentrations of glucose (2.8; 5.6; 8.3 and 16.7 mM)... (Complete abstract, access undermentioned electronic address) / Doutor
2

Metabolismo glicídico em ratos submetidos à imobilização por desnervação do músculo esquelético

Nunes, Wilton Marlindo Santana [UNESP] 29 April 2005 (has links) (PDF)
Made available in DSpace on 2014-06-11T19:30:52Z (GMT). No. of bitstreams: 0 Previous issue date: 2005-04-29Bitstream added on 2014-06-13T21:01:30Z : No. of bitstreams: 1 nunes_wms_dr_rcla.pdf: 627562 bytes, checksum: 28c76e2045589f985d1f281f264eb449 (MD5) / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / Este estudo visou analisar o metabolismo da glicose no músculo sóleo de ratos submetidos a desnervação bem como a resposta do animal como um todo à insulina exógena e ao exercício. Os animais foram tratados de acordo com o Guide for care use of laboratory animals. (National Research Council, 1996). Para isso foram realizados 3 experimentos. No primeiro, ratos adultos (3 a 5 meses) foram submetidos à secção do nervo isquiático da pata direita. Observou-se redução da captação de glicose pelo músculo sóleo isolado da pata desnervada após 3 e 7 dias mas não após 28 dias em relação a animais controles íntegros. Não houve diferença após 3 e 7 dias na captação de glicose pelo músculo sóleo da pata contralateral em relação ao animal controle. Houve aumento da captação de glicose na pata contralateral 28 dias após a desnervação. Verificou-se que após 28 dias de desnervação, não houve reinervação do nervo isquiático. A taxa de remoção da glicose em resposta à insulina exógena após 28 dias de desnervação foi superior à de animais controle íntegros e aquela observada após 3 e 7 dias de desnervação. No segundo, ratos nas mesmas condições, após 48 h de desnervação iniciaram programa de natação 1h/dia, 5dias/semana, durante 28 dias. Ratos desnervados submetidos ao exercício mostraram maior taxa de remoção da glicose sangüínea em resposta à insulina exógena comparados aos sedentários e a animais controle íntegros. O exercício elevou a captação e a oxidação da glicose pelo músculo contralateral e pelo desnervado assim como pelo músculo de animais controles íntegros. Esses resultados sugerem que alterações restritas do metabolismo glicídico muscular influenciam a homeostase glicêmica do animal. Além disso, o exercício melhora o aporte e a utilização da glicose no músculo desnervado... / This study aimed to analyze the metabolism of glucose in the soleus muscle of rats submitted to denervation, as well as the response of the animal as a whole to exogenous insulin and to exercise. To do this, 3 experiments were carried out. In the first, adult rats (3 to 5 months old) were submitted to section of the sciatic nerve in the right paw. A reduction was observed in the uptake of glucose by the isolated soleum muscle of the denervated paw after 3 and 7 days, but not after 28 days in relation to the whole control animals. There was no difference after 3 and 7 days in glucose uptake by the soleum muscle of the opposite paw in relation to the control animal. There was increased glucose uptake in this same paw 28 days after denervation. The rate of glucose removal in response to exogenous insulin after 28 days of denervation was higher than that of whole control animals and those observed after 3 and 7 days of denervation. In the second experiment, rats in the same conditions, after 48 h of denervation started a swimming program 1h/day, 5day/week, for 28 days. The denerved rats submitted to exercise showed a higher blood glucose removal rate in response to exogenous insulin compared to the sedentary and whole control animals. Exercise raised the uptake and oxidation of glucose by the opposite muscle and by the denervated one, as well as by the muscles of the whole control animals. These results suggest that restricted alterations of the muscular glucose metabolism influenced the glycemic homeostasis of the animal. Furthermore, exercise improved the uptake and use of glucose in the denerved muscle. In the third experiment, adult rats in the same conditions as in the first study, had an assessment made of their insulin secretion by isolated pancreatic islets, incubated in the presence of growing concentrations of glucose (2.8; 5.6; 8.3 and 16.7 mM)... (Complete abstract, access undermentioned electronic address)
3

Polymérisation anionique de l'épichlorhydrine par activation du monomère : synthèse de (co)polymères fonctionnels et applications

Doutaz, Stéphane 08 December 2010 (has links)
L'association d'halogénure de tétraoctylammonium et de triisobutylaluminium permet de réaliser la polymérisation anionique de divers époxydes par activation du monomère. Ces systèmes catalytiques ont été appliqués à la (co)polymérisation de l'épichlorhydrine. Cette méthode qui a permis d'obtenir des poly(épichlorhydrine)s de masses molaires contrôlées jusqu'à 100 000 g/mol, a été étendue ensuite à la synthèse de copolymères, statistiques et à blocs, associant l'épichlorhydrine à divers oxiranes substitués : oxyde de propylène, éther tert-butyl glycidique et éther allyl glycidique. Dans le but d'élargir le domaine d'application de ces polyéthers ω-hydroxylés, l'introduction de groupements fonctionnels en tête de chaine a été étudiée. L'influence des substituants du dérivé aluminique et la nature de l'amorceur sur l'efficacité et la spécificité de l'amorçage ont été examinés. / Association of tetraoctylammonium halide and triisobutylaluminium allows anionic polymerization of epoxides by an activated monomer mechanism. This catalytic system was applied to the synthesis of (co)polymers of epichlorohydrin. The synthesis of poly(epichlorohydrin) was achieved in a controlled manner allowing the preparation of polymers with molar masses up to 100 000 g/mol. This approach was extended to the synthesis of statistic and block copolymers of epichlorohydrin with various substituted oxirane : propylene oxide, tert-butyl glycidyl ether and allyl glycidyl ether.In order to extend the application field of this ω-hydroxyl polyether, we have investigated the introduction of functional groups at the beginning of the polymer chain. For this purpose, the influence of the substituted group on the aluminium and the nature of the initiator were examined on the efficiency and the specificity of the initiation step.
4

Optisch aktive Heterocyclen durch Ringtransformation von Oxiran-2-carbonsäurederivaten

Woydowski, Karsten 20 April 1999 (has links)
Heterocyclen mit einer a-Hydroxycarbonyl-Einheit wie 3-Hydroxy-[1,5]-benzothiazepin-4-one oder 3-Hydroxychroman-4-one sind von Interesse, da sie Bestandteil von Pharmazeutika (z. B. Diltiazem®) oder Naturstoffen (z.B. die Flavonoide) sind. Ringtransformationen von optisch aktiven Glycidaten mit Binucleophilen stellen eine nützliche Synthesemethode zur Darstellung solcher Produkte dar. In Abhängigkeit von der Position des Angriffes des Nucleophiles am Oxiranring (a- oder b-Angriff) werden zwei Produkttypen mit verschiedenen Ringgrößen gebildet. Der Ablauf der Reaktion hängt vom Binucleophil, von den Substituenten am Oxiran und von den Reaktionsbedingungen ab. 4-Hydroxypyrazolidin-3-one werden bei der Reaktion von Glycidaten mit Hydrazinen gebildet. Reaktionen mit 1-Amino-2-mercapto-Verbindungen geben ausschließlich [1,4]-Thiazin-3-one. Gelenkt durch die Substituenten am Oxiran reagieren Glycidate mit o-Phenylendiaminen entweder zu Tetrahydro-chinoxalin-2-onen oder zu 3-Hydroxy-[1,5]-benzodiazepin-2-onen. Bei der Bildung der Tetrahydro-chinoxalin-2-one aus unsymmetrisch substituierten o-Phenylendiaminen wird eine hohe Regioselektivität beobachtet. Epoxyamide, gebildet aus Glycidsäuren und o-Aminophenol, cyclisieren unter basischen Bedingungen zu 1,4-Benzoxazin-3-onen, während in Gegenwart einer Lewis-Säure 3-Hydroxy-[1,5]-oxazepin-4-one gebildet werden. Reaktionen von Oxiran-carbonsäureamiden mit o-lithiierten Phenolderivaten führen zu Epoxyketonen, die zu 2-Alkyliden-cumaranonen oder 3-Hydroxychroman-4-onen transformiert werden können. Ohne Inanspruchnahme der Carbonylgruppe sind [1,4]-Benzoxazine durch die Reaktion von Glycidaten mit o-Aminophenolen erhältlich. Alle Ringtransformationen verlaufen stereoselektiv, so daß enantiomerenreine Produkte erhalten werden. / Heterocycles with an a-hydroxycarbonyl moiety such as 3-hydroxy-[1,5]-benzothiazepin-4-ones or 3-hydroxychroman-4-ones are of interest because they are frequently encountered in pharmaceuticals (e.g. Diltiazem®) or natural products (e.g. flavonoids). Ring transformation of optically active oxirane carboxylic acid derivatives with ambident nucleophiles provide a useful synthetic method for such type of products. Depending on the position of attack on the oxirane ring by the nucleophile (a- or b-attack) two types of products with different ring sizes are formed. The mode of reaction depends on the type of binucleophile, the substituents at the oxirane, and the reaction conditions. 4-Hydroxypyrazolidin-3-ones are formed in the reaction of glycidates with hydrazines. Reaction of 1-amino-2-mercapto nucleophiles exclusively afforded [1,4]-thiazin-3-ones. Governed by the substituents at the oxirane on the reaction of glycidates with o-phenylendiamines result either in tetrahydroquinoxalin-2-ones or 3-hydroxy-[1,5]-benzodiazepin-2-ones. In the formation of tetrahydroquinoxalin-2-ones from asymmetrically substituted o-phenylendiamines, high stereoselectivity was observed. Epoxyamides, formed from glycidic acids and o-aminophenols, cyclize to [1,4]-benzoxazin-3-ones under basic conditions while 3-hydroxy-[1,5]-oxazepin-4-ones are formed in the presence of a Lewis acid. Reaction of oxirane carboxylic acid amides with o-lithiated phenol derivatives afforded epoxyketones that could be transformed to 2-alkyliden-coumaranones and 3-hydroxychroman-4-ones. Without the use of the carbonyl group [1,4]-benzoxazines are available in the reaction of glycidates with o-aminophenols. All ring transformations were highly stereoselective giving enantiomerically pure products.

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