Efeitos de alendronato de sódio, sinvastatina, crisina e tintura de Camellia sinensis na osteoporose induzida por dexametasona em ratas

Detalhes bibliográficos
Autor(a) principal: Sequetto, Priscila Lima
Data de Publicação: 2008
Tipo de documento: Dissertação
Idioma: por
Título da fonte: LOCUS Repositório Institucional da UFV
Texto Completo: http://locus.ufv.br/handle/123456789/2405
Resumo: The present work had the objective to evaluate the influence of the sodium alendronate, simvastatin, flavononoid chrysin and the Camellia sinensis ticture used separately and in associated, in osteoporose induced for the administration of dexametasone (dose of 7mg/kg of weight), in rats of the Wistar ancestry (Rattus norvegicus albinus). The used dosages were: sodium alendronate dose 1 (0,20 mg), dose 2 (0,40 mg) and dose 3 (0,60 mg); simvastatin dose 1 (0,40 mg), dose 2 (0,70 mg) and dose 3 (1,0 mg); flavonoid dose 1 (35 mg), dose 2 (60 mg) and dose 3 (90 mg) and phytoterapic dose (0,01 mg), dose 2 (0,02 mg) and dose 3 (0,03 mg), treated once a day orally. After the osteoporosis induction period, the treatments were initiated. The animals were distributed in fourteen groups: G1 = Comercial ration (Control); G2 = Comercial ration + Dexametasone (Control with osteoporose); G3 = Comercial ration + Dexametasone + Biphosphonate dose 1; G4 = Comercial ration + Dexametasone + Biphosphonate dose 2; G5 = Comercial ration + Dexametasone + Biphosphonate dose 3; G6 = Comercial ration + Dexametasone + Biphosphonate dose 1 + simvastatin dose 1; G7 = Comercial ration + Dexametasone + Biphosphonate dose 2 + simvastatin dose 2; G8 = Comercial ration + Dexametasone + Biphosphonate dose 3 + simvastatin dose 3; G9 = Comercial ration + Dexametasone + Flavonoid dose 1; G10 = Comercial ration + Dexametasone + Flavonoid dose 2; G11 = Comercial ration + Dexametasone + Flavonoid dose 3; G12 = Comercial ration + Dexametasone + Phytoterapic dose 1; G13 = Comercial ration + Dexametasone + Phytoterapic dose 2; G14 = Comercial ration + Dexametasone + Phytoterapic dose 3. After 30 days from the start of the treatment, seven animals of each group had been euthanasieted by anesthetical overdosage of 180 mg/Kg de ketamin e 10 mg/Kg de xilasin, route to intraperitoneal. It has been collected of each animal, 5,0 mL of blood by cardiac punction, for the hematological analyses and biochemist quantification of the serum levels of calcium, phosphorus, glucose, fosfatase alkaline total, urea, creatinina, proteins, total cholesterol, tryacylglicerols, gamma GT and albumen. The results of the biochemists analyses of calcium, phosphorus, glucose, fosfatase alkaline total, urea, creatinina, proteins, total cholesterol, tryacylglicerols, gamma GT and albumen had not shown significant differences among the treated groups, being significant only in relation to the control animals (with osteoporosis). Also, it had not have significant differences in the dosages of the hematological parameters between the control group and the control group with osteoporosis, as well as, among them and the treated groups. The electronic microphotographs shows that there was an increase of the porosity in the bones of the control animals (with osteoporosis) and a reduction of these pores in the treated animals. This could also be observed through the evaluation of the bone histopatology, that it showed a recovery in the trabecular area on the treated animals when compared to the control with osteoporosis.
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spelling Sequetto, Priscila Limahttp://lattes.cnpq.br/2288558104248144Nagem, Tanus Jorgehttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4788999D3Carlo, Ricardo Junqueira Delhttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4788143A9Oliveira, Tânia Toledo dehttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4787758J2Oliveira, Maria Goreti de Almeidahttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4790894D6Pacheco, Sérgiohttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4783552Z6Pinto, Aloísio da Silvahttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4709052D42015-03-26T13:07:26Z2009-07-032015-03-26T13:07:26Z2008-03-25SEQUETTO, Priscila Lima. The effects of sodium alendronate, simvastatin, chrysin, and the Camellia sinensis ticture in osteoporosis induced for dexametasona in rats. 2008. 220 f. Dissertação (Mestrado em Bioquímica e Biologia molecular de plantas; Bioquímica e Biologia molecular animal) - Universidade Federal de Viçosa, Viçosa, 2008.http://locus.ufv.br/handle/123456789/2405The present work had the objective to evaluate the influence of the sodium alendronate, simvastatin, flavononoid chrysin and the Camellia sinensis ticture used separately and in associated, in osteoporose induced for the administration of dexametasone (dose of 7mg/kg of weight), in rats of the Wistar ancestry (Rattus norvegicus albinus). The used dosages were: sodium alendronate dose 1 (0,20 mg), dose 2 (0,40 mg) and dose 3 (0,60 mg); simvastatin dose 1 (0,40 mg), dose 2 (0,70 mg) and dose 3 (1,0 mg); flavonoid dose 1 (35 mg), dose 2 (60 mg) and dose 3 (90 mg) and phytoterapic dose (0,01 mg), dose 2 (0,02 mg) and dose 3 (0,03 mg), treated once a day orally. After the osteoporosis induction period, the treatments were initiated. The animals were distributed in fourteen groups: G1 = Comercial ration (Control); G2 = Comercial ration + Dexametasone (Control with osteoporose); G3 = Comercial ration + Dexametasone + Biphosphonate dose 1; G4 = Comercial ration + Dexametasone + Biphosphonate dose 2; G5 = Comercial ration + Dexametasone + Biphosphonate dose 3; G6 = Comercial ration + Dexametasone + Biphosphonate dose 1 + simvastatin dose 1; G7 = Comercial ration + Dexametasone + Biphosphonate dose 2 + simvastatin dose 2; G8 = Comercial ration + Dexametasone + Biphosphonate dose 3 + simvastatin dose 3; G9 = Comercial ration + Dexametasone + Flavonoid dose 1; G10 = Comercial ration + Dexametasone + Flavonoid dose 2; G11 = Comercial ration + Dexametasone + Flavonoid dose 3; G12 = Comercial ration + Dexametasone + Phytoterapic dose 1; G13 = Comercial ration + Dexametasone + Phytoterapic dose 2; G14 = Comercial ration + Dexametasone + Phytoterapic dose 3. After 30 days from the start of the treatment, seven animals of each group had been euthanasieted by anesthetical overdosage of 180 mg/Kg de ketamin e 10 mg/Kg de xilasin, route to intraperitoneal. It has been collected of each animal, 5,0 mL of blood by cardiac punction, for the hematological analyses and biochemist quantification of the serum levels of calcium, phosphorus, glucose, fosfatase alkaline total, urea, creatinina, proteins, total cholesterol, tryacylglicerols, gamma GT and albumen. The results of the biochemists analyses of calcium, phosphorus, glucose, fosfatase alkaline total, urea, creatinina, proteins, total cholesterol, tryacylglicerols, gamma GT and albumen had not shown significant differences among the treated groups, being significant only in relation to the control animals (with osteoporosis). Also, it had not have significant differences in the dosages of the hematological parameters between the control group and the control group with osteoporosis, as well as, among them and the treated groups. The electronic microphotographs shows that there was an increase of the porosity in the bones of the control animals (with osteoporosis) and a reduction of these pores in the treated animals. This could also be observed through the evaluation of the bone histopatology, that it showed a recovery in the trabecular area on the treated animals when compared to the control with osteoporosis.O presente trabalho teve como objetivo avaliar a influência do alendronato de sódio, sinvastatina, flavonóide crisina e tintura da planta Camellia sinensis usado isoladamente e em associação, na osteoporose induzida pela administração de dexametasona (dose de 7mg/kg de peso), em ratas da linhagem Wistar (Rattus norvegicus albinus). As dosagens foram: alendronato de sódio dose 1 (0,20 mg), dose 2 (0,40 mg) e dose 3 (0,60 mg); sinvastatina dose 1 (0,40 mg), dose 2 (0,70 mg) e dose 3 (1,0 mg); crisina dose 1 (35mg), dose 2 (60 mg) e dose 3 (90 mg) e extrato hidroalcoólico de Camellia sinensis dose 1(0,01 mg), dose 2 (0,02 mg) e dose 3 (0,03 mg), administradas diariamente por via oral. Após o período de indução da osteoporose, iniciaramse os tratamentos. Os animais foram distribuídos em quatorze grupos: G1 = Ração (Controle); G2 = Ração + Dexametasona (Controle com osteoporose); G3 = Ração + exametasona + Alendronato de sódio dose 1; G4 = Ração + Dexametasona + Alendronato de sódio dose 2; G5 = Ração + Dexametasona + Alendronato de sódio dose 3; G6 = Ração + Dexametasona + Alendronato de sódio dose 1 + Sinvastatina dose 1; G7 = Ração + Dexametasona + Alendronato de sódio dose 2 + Sinvastatina dose 2; G8 = Ração + Dexametasona + Alendronato de sódio dose 3 + Sinvastatina dose 3; G9 = Ração + Dexametasona + Crisina dose 1; G10 = Ração + Dexametasona + Crisina dose 2; G11 = Ração + Dexametasona + Crisina dose 3; G12 = Ração + Dexametasona + Extrato hidroalcoólico de Camellia sinensis dose 1; G13 = Ração + Dexametasona + Extrato hidroalcoólico de Camellia sinensis dose 2; G14 = Ração + Dexametasona + Extrato hidroalcoólico de Camellia sinensis dose 3. Após completar 30 dias, a partir da data de início do tratamento, os sete animais de cada grupo foram eutanasiados por sobredosagem anestésica, utilizando 180 mg/Kg de ketamina e 10 mg/Kg de xilasina, administrados por via intraperitoneal. Foram coletados, então, de cada animal, 5,0 mL de sangue por punção cardíaca, para realização das análises hematológicas e quantificação bioquímica dos níveis séricos de cálcio, fósforo, glicose, fosfatase alcalina total, uréia, creatinina, proteínas, colesterol total, triacilgliceróis, gama GT e albumina. Os resultados das análises bioquímicas quanto aos valores de cálcio, fósforo, glicose, fosfatase alcalina total, uréia, creatinina, proteínas, colesterol total, triacilgliceróis, gama GT e albumina mostraram diferenças estatisticamente significativas entre os grupos tratados e os animais doentes (controle com osteoporose). Também houve diferenças significativas nas dosagens dos parâmetros hematológicos, entretanto, para alguns parâmetros avaliados como: mielócitos, volume corpuscular médio, hemoglobina corpuscular média, concentração de hemoglobina corpuscular média e amplitude de distribuição do tamanho das hemácias, não foram observadas diferenças estatisticamente significativas entre o grupo controle com osteoporose e os outros grupos tratados. As microfotografias eletrônicas de varredura mostraram que houve um aumento da porosidade nos ossos dos animais doentes (controle com osteoporose) e uma diminuição destes poros nos animais tratados. Isto também pôde ser observado através da avaliação da histopatologia óssea, que mostrou uma recuperação no tamanho das trabéculas ósseas nos animais tratados quando comparados ao controle osteopórotico.Coordenação de Aperfeiçoamento de Pessoal de Nível Superiorapplication/pdfporUniversidade Federal de ViçosaMestrado em Bioquímica AgrícolaUFVBRBioquímica e Biologia molecular de plantas; Bioquímica e Biologia molecular animalOsteoporoseFlavonóidesDexametasonaCamellia sinensisOsteoporosisFlavononoidDexametasonaCamellia sinensisCNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA::BIOLOGIA MOLECULAREfeitos de alendronato de sódio, sinvastatina, crisina e tintura de Camellia sinensis na osteoporose induzida por dexametasona em ratasThe effects of sodium alendronate, simvastatin, chrysin, and the Camellia sinensis ticture in osteoporosis induced for dexametasona in ratsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:LOCUS Repositório Institucional da UFVinstname:Universidade Federal de Viçosa (UFV)instacron:UFVORIGINALtexto completo.pdfapplication/pdf8523514https://locus.ufv.br//bitstream/123456789/2405/1/texto%20completo.pdfe44f3546b04b5def90447922eef25c4fMD51TEXTtexto completo.pdf.txttexto completo.pdf.txtExtracted texttext/plain382955https://locus.ufv.br//bitstream/123456789/2405/2/texto%20completo.pdf.txt43e3a2073fac403ea1ee57e07352cc3cMD52THUMBNAILtexto completo.pdf.jpgtexto completo.pdf.jpgIM Thumbnailimage/jpeg3881https://locus.ufv.br//bitstream/123456789/2405/3/texto%20completo.pdf.jpg27605f237be6960540275c0c3adcad43MD53123456789/24052016-04-07 23:20:27.237oai:locus.ufv.br:123456789/2405Repositório InstitucionalPUBhttps://www.locus.ufv.br/oai/requestfabiojreis@ufv.bropendoar:21452016-04-08T02:20:27LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)false
dc.title.por.fl_str_mv Efeitos de alendronato de sódio, sinvastatina, crisina e tintura de Camellia sinensis na osteoporose induzida por dexametasona em ratas
dc.title.alternative.eng.fl_str_mv The effects of sodium alendronate, simvastatin, chrysin, and the Camellia sinensis ticture in osteoporosis induced for dexametasona in rats
title Efeitos de alendronato de sódio, sinvastatina, crisina e tintura de Camellia sinensis na osteoporose induzida por dexametasona em ratas
spellingShingle Efeitos de alendronato de sódio, sinvastatina, crisina e tintura de Camellia sinensis na osteoporose induzida por dexametasona em ratas
Sequetto, Priscila Lima
Osteoporose
Flavonóides
Dexametasona
Camellia sinensis
Osteoporosis
Flavononoid
Dexametasona
Camellia sinensis
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA::BIOLOGIA MOLECULAR
title_short Efeitos de alendronato de sódio, sinvastatina, crisina e tintura de Camellia sinensis na osteoporose induzida por dexametasona em ratas
title_full Efeitos de alendronato de sódio, sinvastatina, crisina e tintura de Camellia sinensis na osteoporose induzida por dexametasona em ratas
title_fullStr Efeitos de alendronato de sódio, sinvastatina, crisina e tintura de Camellia sinensis na osteoporose induzida por dexametasona em ratas
title_full_unstemmed Efeitos de alendronato de sódio, sinvastatina, crisina e tintura de Camellia sinensis na osteoporose induzida por dexametasona em ratas
title_sort Efeitos de alendronato de sódio, sinvastatina, crisina e tintura de Camellia sinensis na osteoporose induzida por dexametasona em ratas
author Sequetto, Priscila Lima
author_facet Sequetto, Priscila Lima
author_role author
dc.contributor.authorLattes.por.fl_str_mv http://lattes.cnpq.br/2288558104248144
dc.contributor.author.fl_str_mv Sequetto, Priscila Lima
dc.contributor.advisor-co1.fl_str_mv Nagem, Tanus Jorge
dc.contributor.advisor-co1Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4788999D3
dc.contributor.advisor-co2.fl_str_mv Carlo, Ricardo Junqueira Del
dc.contributor.advisor-co2Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4788143A9
dc.contributor.advisor1.fl_str_mv Oliveira, Tânia Toledo de
dc.contributor.advisor1Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4787758J2
dc.contributor.referee1.fl_str_mv Oliveira, Maria Goreti de Almeida
dc.contributor.referee1Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4790894D6
dc.contributor.referee2.fl_str_mv Pacheco, Sérgio
dc.contributor.referee2Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4783552Z6
dc.contributor.referee3.fl_str_mv Pinto, Aloísio da Silva
dc.contributor.referee3Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4709052D4
contributor_str_mv Nagem, Tanus Jorge
Carlo, Ricardo Junqueira Del
Oliveira, Tânia Toledo de
Oliveira, Maria Goreti de Almeida
Pacheco, Sérgio
Pinto, Aloísio da Silva
dc.subject.por.fl_str_mv Osteoporose
Flavonóides
Dexametasona
Camellia sinensis
topic Osteoporose
Flavonóides
Dexametasona
Camellia sinensis
Osteoporosis
Flavononoid
Dexametasona
Camellia sinensis
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA::BIOLOGIA MOLECULAR
dc.subject.eng.fl_str_mv Osteoporosis
Flavononoid
Dexametasona
Camellia sinensis
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA::BIOLOGIA MOLECULAR
description The present work had the objective to evaluate the influence of the sodium alendronate, simvastatin, flavononoid chrysin and the Camellia sinensis ticture used separately and in associated, in osteoporose induced for the administration of dexametasone (dose of 7mg/kg of weight), in rats of the Wistar ancestry (Rattus norvegicus albinus). The used dosages were: sodium alendronate dose 1 (0,20 mg), dose 2 (0,40 mg) and dose 3 (0,60 mg); simvastatin dose 1 (0,40 mg), dose 2 (0,70 mg) and dose 3 (1,0 mg); flavonoid dose 1 (35 mg), dose 2 (60 mg) and dose 3 (90 mg) and phytoterapic dose (0,01 mg), dose 2 (0,02 mg) and dose 3 (0,03 mg), treated once a day orally. After the osteoporosis induction period, the treatments were initiated. The animals were distributed in fourteen groups: G1 = Comercial ration (Control); G2 = Comercial ration + Dexametasone (Control with osteoporose); G3 = Comercial ration + Dexametasone + Biphosphonate dose 1; G4 = Comercial ration + Dexametasone + Biphosphonate dose 2; G5 = Comercial ration + Dexametasone + Biphosphonate dose 3; G6 = Comercial ration + Dexametasone + Biphosphonate dose 1 + simvastatin dose 1; G7 = Comercial ration + Dexametasone + Biphosphonate dose 2 + simvastatin dose 2; G8 = Comercial ration + Dexametasone + Biphosphonate dose 3 + simvastatin dose 3; G9 = Comercial ration + Dexametasone + Flavonoid dose 1; G10 = Comercial ration + Dexametasone + Flavonoid dose 2; G11 = Comercial ration + Dexametasone + Flavonoid dose 3; G12 = Comercial ration + Dexametasone + Phytoterapic dose 1; G13 = Comercial ration + Dexametasone + Phytoterapic dose 2; G14 = Comercial ration + Dexametasone + Phytoterapic dose 3. After 30 days from the start of the treatment, seven animals of each group had been euthanasieted by anesthetical overdosage of 180 mg/Kg de ketamin e 10 mg/Kg de xilasin, route to intraperitoneal. It has been collected of each animal, 5,0 mL of blood by cardiac punction, for the hematological analyses and biochemist quantification of the serum levels of calcium, phosphorus, glucose, fosfatase alkaline total, urea, creatinina, proteins, total cholesterol, tryacylglicerols, gamma GT and albumen. The results of the biochemists analyses of calcium, phosphorus, glucose, fosfatase alkaline total, urea, creatinina, proteins, total cholesterol, tryacylglicerols, gamma GT and albumen had not shown significant differences among the treated groups, being significant only in relation to the control animals (with osteoporosis). Also, it had not have significant differences in the dosages of the hematological parameters between the control group and the control group with osteoporosis, as well as, among them and the treated groups. The electronic microphotographs shows that there was an increase of the porosity in the bones of the control animals (with osteoporosis) and a reduction of these pores in the treated animals. This could also be observed through the evaluation of the bone histopatology, that it showed a recovery in the trabecular area on the treated animals when compared to the control with osteoporosis.
publishDate 2008
dc.date.issued.fl_str_mv 2008-03-25
dc.date.available.fl_str_mv 2009-07-03
2015-03-26T13:07:26Z
dc.date.accessioned.fl_str_mv 2015-03-26T13:07:26Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
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dc.identifier.citation.fl_str_mv SEQUETTO, Priscila Lima. The effects of sodium alendronate, simvastatin, chrysin, and the Camellia sinensis ticture in osteoporosis induced for dexametasona in rats. 2008. 220 f. Dissertação (Mestrado em Bioquímica e Biologia molecular de plantas; Bioquímica e Biologia molecular animal) - Universidade Federal de Viçosa, Viçosa, 2008.
dc.identifier.uri.fl_str_mv http://locus.ufv.br/handle/123456789/2405
identifier_str_mv SEQUETTO, Priscila Lima. The effects of sodium alendronate, simvastatin, chrysin, and the Camellia sinensis ticture in osteoporosis induced for dexametasona in rats. 2008. 220 f. Dissertação (Mestrado em Bioquímica e Biologia molecular de plantas; Bioquímica e Biologia molecular animal) - Universidade Federal de Viçosa, Viçosa, 2008.
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dc.publisher.initials.fl_str_mv UFV
dc.publisher.country.fl_str_mv BR
dc.publisher.department.fl_str_mv Bioquímica e Biologia molecular de plantas; Bioquímica e Biologia molecular animal
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