Estudo dos efeitos inotrópicos e toxicológicos de extratos da Tithonia diversifolia (Hemsl.) A. Gray em mamíferos

Detalhes bibliográficos
Autor(a) principal: Lima, Adriana Karla de
Data de Publicação: 2013
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UFS
Texto Completo: https://ri.ufs.br/handle/riufs/3564
Resumo: Extracts from Tithonia diversifolia (TD) have been widely employed in Central and South America, Asia and Africa to help in the treatment of malaria, a disease to which millions of people are subjected in tropical countries. In spite of this, we were not able to find any scientific report dealing with their effects on the heart muscle functioning or describing their toxic effects. Such gaps are barriers for the TD derivatives to become a phytotherapic agent. Therefore, we have planned this study aiming to clarify the inotropic and toxicological effects of TD derivatives. Their effects on the muscle inotropism were investigated in isolated guinea pig atrium mounted in an organ chamber containing Tyrode solution oxygenated by carbogen mixture (5% CO2, 95% O2). The atria were stretched (1 gf) and stimulated at 2 Hz with suprathreshold electrical pulses. Their contractile forces were captured isommetrically and stored in computer to be analysed off line. The effect of AqF was determined after this fraction be added to the organ bath. The evaluation concerned to its effect on the L-type calcium current (ICa,L) was carried out in ventricular cardiomyocytes isolated according to the steps described by Shioya (2007). The intracellular calcium transients were also studied in these cells previously loaded with FLUO4-AM and monitored by confocal microscopy. The acute (ATx) and subacute (STx) toxicities of the crude extract of TD (CE) were evaluated in rats according to the steps proposed by OECD (2001a,b). Briefly: animals were separated by gender to create one control group and two treated groups. For the ATx study, the animals pertaining to the control group received orally only distilled water, whereas rats pertaining to the treated groups received, respectively, 2.5 g/kg and 5.0 g/kg of CE administered in a unique dose. The animals involved in the study were monitored for abnormal signals during 14 days. In the STx evaluation, the animals of the two treated groups received, respectively, 0.125 g/kg/day CE and 0.250 g/kg/day CE during 30 days. Animals were carefully observed for signals representing physiological and/or behavioral abnormalities. At the end of each toxicological protocol, the animals were anaesthetized for collecting blood and after that they were euthanized for the removal of organs. Our results showed that AqF depresses the atrial contractility in a dose-dependent fashion. However, concentrations greater than 2 g/l cause mechanical alternans , indicating that AqF can disturb the dynamics of the calcium release channels, which are present in the sarcoplasmic reticulum membrane. The effect of AqF on the L-type calcium current (ICa,L) was studied by recording how this fraction changes the inotropic effect produced by increasing concentrations of CaCl2. Our data showed that 2 g/l AqF increased the CaCl2 EC50 from 1.207 ± 0.139 to 2.846 ± 0.035 mM (n = 4, p < 0.05), suggesting that AqF is able to reduce ICa,L. Such conclusion was reinforced by testing the Bowditch phenomenon in atria incubated with 1.3 g/l AqF. In these experiments, AqF completely abolished the force overshoot , which is normally seen in the positive staircase Bowditch phenomenon. The depressant effect of AqF on the ICa,L was also supported by the decrease of intracellular fluorescence related to the subcellular calcium from 6.9 ± 0.4 (n = 53) to 5.3 ± 0.3 u.a. (n = 51; p < 0.05). In fact, direct measurements of ICa,L performed in patch clamped cardiomyocytes, confirmed the depressant effect of AqF on ICa,L. In these experiments, 80 g/ml of AqF reduced the density of ICa,L from 10.00 ± 1.22 to 7.80 ± 1.19 A/F (n = 4, p < 0.05). An expected consequence for the ICa,L reduction is the increase of the time required for the myocardial electrical wave to cross the atrioventricular node. Electrocardiograms from isolated guinea pig hearts confirmed the reduction of ICa,L because in the presence of AqF the heart presented a complete atrioventricular block (AVB). There was no involvement of potassium channels, neither the muscarinic nor the opioids receptors in the AqF myocardial depressant effect. We can conclude that the depressant effects of AqF in the myocardium contractility are due to a reduction of ICa,L. Studies concerned to the ATx and STx showed that the CE does not promote any signal of pain, abnormal behavior or mortality in the rats (DL50>5.0 g/kg). In STx, CE does not change water or food intakes, but in the animals treated with 0.250 g/kg/day a gain of weight occurred, suggesting water retention in the animal s body. Neutropenia, eosinopenia, lymphocytosis, and monocytosis were observed in treated animals during the ATx study. In animals pertaining to the STx study it was seen leucopenia, neutropenia, and monocytopenia. In ATx evaluation, the biochemical profile of the blood showed a reduction in the plasmatic urea but the aspartate and alanine aminotransferases, alkaline phosphatase, total and direct bilirubin, total protein, globulin, sodium, and uric acid increased. Similar results were found in the STx study, except for the urea that remained unchanged and for the glucose, creatinin, albumin, and potassium that presented an increase in their serum levels. These findings advise for precaution when TD derivatives were proposed as a therapeutic agent. We conclude that AqF reduces ICa,L leading to a negative inotropism and an AVB. The CE interferes with the hematopoietic system and promotes injuries for the liver and kidneys leading to a non-inflammatory tissue reaction.
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spelling Lima, Adriana Karla dehttp://lattes.cnpq.br/2934503756437998Garcia, Eduardo Antônio Condehttp://lattes.cnpq.br/45324318988337152017-09-26T12:07:06Z2017-09-26T12:07:06Z2013-06-14LIMA, Adriana Karla de. Study of inotropic and toxicologic effects produced by extracts obtained from Tithonia diversifolia (Hemsl.) A. Gray leaves in mammalians. 2013. 169 f. Tese (Doutorado em Ciências da Saúde) - Universidade Federal de Sergipe, Aracaju, 2013.https://ri.ufs.br/handle/riufs/3564Extracts from Tithonia diversifolia (TD) have been widely employed in Central and South America, Asia and Africa to help in the treatment of malaria, a disease to which millions of people are subjected in tropical countries. In spite of this, we were not able to find any scientific report dealing with their effects on the heart muscle functioning or describing their toxic effects. Such gaps are barriers for the TD derivatives to become a phytotherapic agent. Therefore, we have planned this study aiming to clarify the inotropic and toxicological effects of TD derivatives. Their effects on the muscle inotropism were investigated in isolated guinea pig atrium mounted in an organ chamber containing Tyrode solution oxygenated by carbogen mixture (5% CO2, 95% O2). The atria were stretched (1 gf) and stimulated at 2 Hz with suprathreshold electrical pulses. Their contractile forces were captured isommetrically and stored in computer to be analysed off line. The effect of AqF was determined after this fraction be added to the organ bath. The evaluation concerned to its effect on the L-type calcium current (ICa,L) was carried out in ventricular cardiomyocytes isolated according to the steps described by Shioya (2007). The intracellular calcium transients were also studied in these cells previously loaded with FLUO4-AM and monitored by confocal microscopy. The acute (ATx) and subacute (STx) toxicities of the crude extract of TD (CE) were evaluated in rats according to the steps proposed by OECD (2001a,b). Briefly: animals were separated by gender to create one control group and two treated groups. For the ATx study, the animals pertaining to the control group received orally only distilled water, whereas rats pertaining to the treated groups received, respectively, 2.5 g/kg and 5.0 g/kg of CE administered in a unique dose. The animals involved in the study were monitored for abnormal signals during 14 days. In the STx evaluation, the animals of the two treated groups received, respectively, 0.125 g/kg/day CE and 0.250 g/kg/day CE during 30 days. Animals were carefully observed for signals representing physiological and/or behavioral abnormalities. At the end of each toxicological protocol, the animals were anaesthetized for collecting blood and after that they were euthanized for the removal of organs. Our results showed that AqF depresses the atrial contractility in a dose-dependent fashion. However, concentrations greater than 2 g/l cause mechanical alternans , indicating that AqF can disturb the dynamics of the calcium release channels, which are present in the sarcoplasmic reticulum membrane. The effect of AqF on the L-type calcium current (ICa,L) was studied by recording how this fraction changes the inotropic effect produced by increasing concentrations of CaCl2. Our data showed that 2 g/l AqF increased the CaCl2 EC50 from 1.207 ± 0.139 to 2.846 ± 0.035 mM (n = 4, p < 0.05), suggesting that AqF is able to reduce ICa,L. Such conclusion was reinforced by testing the Bowditch phenomenon in atria incubated with 1.3 g/l AqF. In these experiments, AqF completely abolished the force overshoot , which is normally seen in the positive staircase Bowditch phenomenon. The depressant effect of AqF on the ICa,L was also supported by the decrease of intracellular fluorescence related to the subcellular calcium from 6.9 ± 0.4 (n = 53) to 5.3 ± 0.3 u.a. (n = 51; p < 0.05). In fact, direct measurements of ICa,L performed in patch clamped cardiomyocytes, confirmed the depressant effect of AqF on ICa,L. In these experiments, 80 g/ml of AqF reduced the density of ICa,L from 10.00 ± 1.22 to 7.80 ± 1.19 A/F (n = 4, p < 0.05). An expected consequence for the ICa,L reduction is the increase of the time required for the myocardial electrical wave to cross the atrioventricular node. Electrocardiograms from isolated guinea pig hearts confirmed the reduction of ICa,L because in the presence of AqF the heart presented a complete atrioventricular block (AVB). There was no involvement of potassium channels, neither the muscarinic nor the opioids receptors in the AqF myocardial depressant effect. We can conclude that the depressant effects of AqF in the myocardium contractility are due to a reduction of ICa,L. Studies concerned to the ATx and STx showed that the CE does not promote any signal of pain, abnormal behavior or mortality in the rats (DL50>5.0 g/kg). In STx, CE does not change water or food intakes, but in the animals treated with 0.250 g/kg/day a gain of weight occurred, suggesting water retention in the animal s body. Neutropenia, eosinopenia, lymphocytosis, and monocytosis were observed in treated animals during the ATx study. In animals pertaining to the STx study it was seen leucopenia, neutropenia, and monocytopenia. In ATx evaluation, the biochemical profile of the blood showed a reduction in the plasmatic urea but the aspartate and alanine aminotransferases, alkaline phosphatase, total and direct bilirubin, total protein, globulin, sodium, and uric acid increased. Similar results were found in the STx study, except for the urea that remained unchanged and for the glucose, creatinin, albumin, and potassium that presented an increase in their serum levels. These findings advise for precaution when TD derivatives were proposed as a therapeutic agent. We conclude that AqF reduces ICa,L leading to a negative inotropism and an AVB. The CE interferes with the hematopoietic system and promotes injuries for the liver and kidneys leading to a non-inflammatory tissue reaction.Extratos das folhas da Tithonia diversifolia (TD) têm sido empregados nas Américas do Sul e Central, Ásia e África como agentes antimaláricos entre outros usos. Seus possíveis efeitos sobre o coração e sua toxicidade, contudo, não estão relatados. Estas lacunas comprometem a expectativa de os derivados da planta virem a interessar à indústria de fitoterápicos e por esta razão, o presente trabalho visou complementar tais lacunas, trazendo para o conhecimento as propriedades inotrópicas e toxicológicas de derivados das folhas desta planta. Os estudos inotrópicos foram realizados com a fração aquosa (FAq) e em átrio esquerdo isolado de cobaia montado em cuba para órgão. Os átrios foram estirados a 1 gf e estimulados com pulsos de corrente supralimiares. A força atrial foi captada isometricamente e armazenada em computador. A ação da FAq foi avaliada adicionando-a ao banho. Para estudos com célula isolada, foram obtidos cardiomiócitos pela técnica de dissociação proposta por Shioya (2007). O efeito da FAq sobre a corrente de cálcio tipo L (ICa,L) foi estudado em cardiomiócitos ventriculares de rato e os de camundongo foram usados para estudar os transientes de cálcio subcelular, empregando-se, para isso, a sonda fluorescente Fluo4-AM. Os registros foram feitos com microscopia confocal de varredura a laser. A toxicidade aguda (TxA) e subaguda (TxS) do extrato bruto da TD (EB) foi avaliada em ratos de acordo com as regras da OECD. Resumidamente: os animais foram separados por gênero em grupos controle e tratados. Nos estudos de TxA, os animais do grupo controle receberam água destilada, enquanto que os dos grupos tratados receberam, p.o., 2,5 g/kg e 5,0 g/kg de EB. Os efeitos foram monitorados por 14 dias. Na avaliação referente à TxS, os grupos tratados receberam, p.o., durante 30 dias, 0,125 g/kg/dia ou 0,250 g/kg/dia de EB. Os animais foram observados para sinais de alterações fisiológicas e/ou comportamentais. Em seguida, foram anestesiados, o sangue coletado e depois eutanasiados para a histopatologia dos órgãos. Os resultados mostraram que a FAq deprime a contratilidade atrial e que concentrações acima de 2 g/l induzem o alternância mecânica, sugerindo que ela leva à disfunção dos canais liberadores de cálcio existentes no retículo sarcoplasmático. Para avaliar a ação da FAq sobre a ICa,L, foi estudada a sua ação sobre a curva concentração-efeito para o CaCl2. Neste estudo, a FAq produziu aumento da CE50 de 1,207 ± 0,139 mM para 2,846 ± 0,035 mM (n = 4, p < 0,05). A incubação do átrio com 1,3 g/l de FAq aboliu completamente o overshoot de força do fenômeno de Bowditch (n = 4, p < 0,05), indicando que ela reduz ICa,L. Esta hipótese foi igualmente suportada no fato de que a fração diminuiu a fluorescência para o cálcio subcelular de 6,9 ± 0,4 u.a. (n = 53) para 5,3 ± 0,3 u.a. (n = 51; p < 0,01) e também porque, quando empregada a 80 g/ml, ela reduziu a densidade da ICa,L de 10,00 ± 1,22 A/F para 7,80 ± 1,19 A/F (n = 4, p < 0,05). A FAq produziu bloqueio de condução no nódulo atrioventricular. O mecanismo de ação da FAq não envolveu receptores muscarínicos, opióides, nem canais para potássio, mas está baseado na diminuição da ICa,L. A avaliação da TxA e TxS mostrou que o EB é de baixa toxicidade pois sua DL50 foi maior do que 5,0 g/kg. O EB não alterou o consumo de água ou de comida, mas nos animais tratados com 0,250 g/kg/dia houve ganho de peso, sugerindo retenção hídrica, pois o peso dos órgãos não se modificou. Neutropenia, eosinofilopenia, linfocitose e monocitose foram observadas na TxA, mas na TxS ocorreu leucopenia, neutropenia e monocitopenia. A análise bioquímica na TxA mostrou redução da ureia plasmática, porém aumento da aspartato e da alanina aminotransferases, fosfatase alcalina, bilirrubinas total e direta, proteína total, globulina, sódio e ácido úrico. Resultados semelhantes foram encontrados nos estudos sobre a TxS, exceto para ureia, que se manteve constante e para glicose, creatinina, albumina e potássio, cujos níveis sanguíneos aumentaram. A histopatologia mostrou sinais de injúria hepática e renal. Concluimos que a FAq reduz a ICa,L como consequência ela é inotrópica negativa e induz BAV. Ela interfere com o sistema hematopoiético e promove lesão hepática e renal sem causar mortalidade e induz reação inflamatória tissular.application/pdfporUniversidade Federal de SergipePós-Graduação em Ciências da SaúdeUFSBRTithonia diversifoliaContratilidade miocárdicaPlantas medicinaisCanal de cálcio tipo LFluorescênciaToxicidadeFisiologiaTithonia diversifoliaMyocardium contractilityMedicinal plantsCalcium channels L- typeFluorescenceToxicityCNPQ::CIENCIAS DA SAUDE::FARMACIAEstudo dos efeitos inotrópicos e toxicológicos de extratos da Tithonia diversifolia (Hemsl.) A. Gray em mamíferosStudy of inotropic and toxicologic effects produced by extracts obtained from Tithonia diversifolia (Hemsl.) A. Gray leaves in mammaliansinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSinstname:Universidade Federal de Sergipe (UFS)instacron:UFSTEXTADRIANA_KARLA_LIMA.pdf.txtADRIANA_KARLA_LIMA.pdf.txtExtracted texttext/plain299987https://ri.ufs.br/jspui/bitstream/riufs/3564/2/ADRIANA_KARLA_LIMA.pdf.txt786435be3e162c7c3860ff1a7bb77311MD52THUMBNAILADRIANA_KARLA_LIMA.pdf.jpgADRIANA_KARLA_LIMA.pdf.jpgGenerated Thumbnailimage/jpeg1383https://ri.ufs.br/jspui/bitstream/riufs/3564/3/ADRIANA_KARLA_LIMA.pdf.jpg35af28e901de89d0d053e7334afdc9aeMD53ORIGINALADRIANA_KARLA_LIMA.pdfapplication/pdf3203294https://ri.ufs.br/jspui/bitstream/riufs/3564/1/ADRIANA_KARLA_LIMA.pdfd0c554694d5abb55770df5f7c8eb8fa6MD51riufs/35642018-02-20 19:53:17.712oai:ufs.br:riufs/3564Repositório InstitucionalPUBhttps://ri.ufs.br/oai/requestrepositorio@academico.ufs.bropendoar:2018-02-20T22:53:17Repositório Institucional da UFS - Universidade Federal de Sergipe (UFS)false
dc.title.por.fl_str_mv Estudo dos efeitos inotrópicos e toxicológicos de extratos da Tithonia diversifolia (Hemsl.) A. Gray em mamíferos
dc.title.alternative.eng.fl_str_mv Study of inotropic and toxicologic effects produced by extracts obtained from Tithonia diversifolia (Hemsl.) A. Gray leaves in mammalians
title Estudo dos efeitos inotrópicos e toxicológicos de extratos da Tithonia diversifolia (Hemsl.) A. Gray em mamíferos
spellingShingle Estudo dos efeitos inotrópicos e toxicológicos de extratos da Tithonia diversifolia (Hemsl.) A. Gray em mamíferos
Lima, Adriana Karla de
Tithonia diversifolia
Contratilidade miocárdica
Plantas medicinais
Canal de cálcio tipo L
Fluorescência
Toxicidade
Fisiologia
Tithonia diversifolia
Myocardium contractility
Medicinal plants
Calcium channels L- type
Fluorescence
Toxicity
CNPQ::CIENCIAS DA SAUDE::FARMACIA
title_short Estudo dos efeitos inotrópicos e toxicológicos de extratos da Tithonia diversifolia (Hemsl.) A. Gray em mamíferos
title_full Estudo dos efeitos inotrópicos e toxicológicos de extratos da Tithonia diversifolia (Hemsl.) A. Gray em mamíferos
title_fullStr Estudo dos efeitos inotrópicos e toxicológicos de extratos da Tithonia diversifolia (Hemsl.) A. Gray em mamíferos
title_full_unstemmed Estudo dos efeitos inotrópicos e toxicológicos de extratos da Tithonia diversifolia (Hemsl.) A. Gray em mamíferos
title_sort Estudo dos efeitos inotrópicos e toxicológicos de extratos da Tithonia diversifolia (Hemsl.) A. Gray em mamíferos
author Lima, Adriana Karla de
author_facet Lima, Adriana Karla de
author_role author
dc.contributor.author.fl_str_mv Lima, Adriana Karla de
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/2934503756437998
dc.contributor.advisor1.fl_str_mv Garcia, Eduardo Antônio Conde
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/4532431898833715
contributor_str_mv Garcia, Eduardo Antônio Conde
dc.subject.por.fl_str_mv Tithonia diversifolia
Contratilidade miocárdica
Plantas medicinais
Canal de cálcio tipo L
Fluorescência
Toxicidade
Fisiologia
topic Tithonia diversifolia
Contratilidade miocárdica
Plantas medicinais
Canal de cálcio tipo L
Fluorescência
Toxicidade
Fisiologia
Tithonia diversifolia
Myocardium contractility
Medicinal plants
Calcium channels L- type
Fluorescence
Toxicity
CNPQ::CIENCIAS DA SAUDE::FARMACIA
dc.subject.eng.fl_str_mv Tithonia diversifolia
Myocardium contractility
Medicinal plants
Calcium channels L- type
Fluorescence
Toxicity
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS DA SAUDE::FARMACIA
description Extracts from Tithonia diversifolia (TD) have been widely employed in Central and South America, Asia and Africa to help in the treatment of malaria, a disease to which millions of people are subjected in tropical countries. In spite of this, we were not able to find any scientific report dealing with their effects on the heart muscle functioning or describing their toxic effects. Such gaps are barriers for the TD derivatives to become a phytotherapic agent. Therefore, we have planned this study aiming to clarify the inotropic and toxicological effects of TD derivatives. Their effects on the muscle inotropism were investigated in isolated guinea pig atrium mounted in an organ chamber containing Tyrode solution oxygenated by carbogen mixture (5% CO2, 95% O2). The atria were stretched (1 gf) and stimulated at 2 Hz with suprathreshold electrical pulses. Their contractile forces were captured isommetrically and stored in computer to be analysed off line. The effect of AqF was determined after this fraction be added to the organ bath. The evaluation concerned to its effect on the L-type calcium current (ICa,L) was carried out in ventricular cardiomyocytes isolated according to the steps described by Shioya (2007). The intracellular calcium transients were also studied in these cells previously loaded with FLUO4-AM and monitored by confocal microscopy. The acute (ATx) and subacute (STx) toxicities of the crude extract of TD (CE) were evaluated in rats according to the steps proposed by OECD (2001a,b). Briefly: animals were separated by gender to create one control group and two treated groups. For the ATx study, the animals pertaining to the control group received orally only distilled water, whereas rats pertaining to the treated groups received, respectively, 2.5 g/kg and 5.0 g/kg of CE administered in a unique dose. The animals involved in the study were monitored for abnormal signals during 14 days. In the STx evaluation, the animals of the two treated groups received, respectively, 0.125 g/kg/day CE and 0.250 g/kg/day CE during 30 days. Animals were carefully observed for signals representing physiological and/or behavioral abnormalities. At the end of each toxicological protocol, the animals were anaesthetized for collecting blood and after that they were euthanized for the removal of organs. Our results showed that AqF depresses the atrial contractility in a dose-dependent fashion. However, concentrations greater than 2 g/l cause mechanical alternans , indicating that AqF can disturb the dynamics of the calcium release channels, which are present in the sarcoplasmic reticulum membrane. The effect of AqF on the L-type calcium current (ICa,L) was studied by recording how this fraction changes the inotropic effect produced by increasing concentrations of CaCl2. Our data showed that 2 g/l AqF increased the CaCl2 EC50 from 1.207 ± 0.139 to 2.846 ± 0.035 mM (n = 4, p < 0.05), suggesting that AqF is able to reduce ICa,L. Such conclusion was reinforced by testing the Bowditch phenomenon in atria incubated with 1.3 g/l AqF. In these experiments, AqF completely abolished the force overshoot , which is normally seen in the positive staircase Bowditch phenomenon. The depressant effect of AqF on the ICa,L was also supported by the decrease of intracellular fluorescence related to the subcellular calcium from 6.9 ± 0.4 (n = 53) to 5.3 ± 0.3 u.a. (n = 51; p < 0.05). In fact, direct measurements of ICa,L performed in patch clamped cardiomyocytes, confirmed the depressant effect of AqF on ICa,L. In these experiments, 80 g/ml of AqF reduced the density of ICa,L from 10.00 ± 1.22 to 7.80 ± 1.19 A/F (n = 4, p < 0.05). An expected consequence for the ICa,L reduction is the increase of the time required for the myocardial electrical wave to cross the atrioventricular node. Electrocardiograms from isolated guinea pig hearts confirmed the reduction of ICa,L because in the presence of AqF the heart presented a complete atrioventricular block (AVB). There was no involvement of potassium channels, neither the muscarinic nor the opioids receptors in the AqF myocardial depressant effect. We can conclude that the depressant effects of AqF in the myocardium contractility are due to a reduction of ICa,L. Studies concerned to the ATx and STx showed that the CE does not promote any signal of pain, abnormal behavior or mortality in the rats (DL50>5.0 g/kg). In STx, CE does not change water or food intakes, but in the animals treated with 0.250 g/kg/day a gain of weight occurred, suggesting water retention in the animal s body. Neutropenia, eosinopenia, lymphocytosis, and monocytosis were observed in treated animals during the ATx study. In animals pertaining to the STx study it was seen leucopenia, neutropenia, and monocytopenia. In ATx evaluation, the biochemical profile of the blood showed a reduction in the plasmatic urea but the aspartate and alanine aminotransferases, alkaline phosphatase, total and direct bilirubin, total protein, globulin, sodium, and uric acid increased. Similar results were found in the STx study, except for the urea that remained unchanged and for the glucose, creatinin, albumin, and potassium that presented an increase in their serum levels. These findings advise for precaution when TD derivatives were proposed as a therapeutic agent. We conclude that AqF reduces ICa,L leading to a negative inotropism and an AVB. The CE interferes with the hematopoietic system and promotes injuries for the liver and kidneys leading to a non-inflammatory tissue reaction.
publishDate 2013
dc.date.issued.fl_str_mv 2013-06-14
dc.date.accessioned.fl_str_mv 2017-09-26T12:07:06Z
dc.date.available.fl_str_mv 2017-09-26T12:07:06Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
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dc.identifier.citation.fl_str_mv LIMA, Adriana Karla de. Study of inotropic and toxicologic effects produced by extracts obtained from Tithonia diversifolia (Hemsl.) A. Gray leaves in mammalians. 2013. 169 f. Tese (Doutorado em Ciências da Saúde) - Universidade Federal de Sergipe, Aracaju, 2013.
dc.identifier.uri.fl_str_mv https://ri.ufs.br/handle/riufs/3564
identifier_str_mv LIMA, Adriana Karla de. Study of inotropic and toxicologic effects produced by extracts obtained from Tithonia diversifolia (Hemsl.) A. Gray leaves in mammalians. 2013. 169 f. Tese (Doutorado em Ciências da Saúde) - Universidade Federal de Sergipe, Aracaju, 2013.
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dc.publisher.none.fl_str_mv Universidade Federal de Sergipe
dc.publisher.program.fl_str_mv Pós-Graduação em Ciências da Saúde
dc.publisher.initials.fl_str_mv UFS
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d0c554694d5abb55770df5f7c8eb8fa6
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFS - Universidade Federal de Sergipe (UFS)
repository.mail.fl_str_mv repositorio@academico.ufs.br
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