Academic literature on the topic 'STZ diabetic rats'
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Journal articles on the topic "STZ diabetic rats"
Fernandes, Ana Angélica Henrique, Ethel Lourenzi Barbosa Novelli, Ary Fernandes Junior, and Cristiano Machado Galhardi. "Effect of naringerin on biochemical parameters in the streptozotocin-induced diabetic rats." Brazilian Archives of Biology and Technology 52, no. 1 (February 2009): 51–59. http://dx.doi.org/10.1590/s1516-89132009000100007.
Full textYusuksawad, Mariem, and Narongsak Chaiyabutr. "The beneficial effect of long-term supplementation of vitamin C on renal mitochondrial disturbances in streptozotocin-induced diabetic rats." Asian Biomedicine 5, no. 2 (April 1, 2011): 277–82. http://dx.doi.org/10.5372/1905-7415.0502.038.
Full textYanardag, R., O. Ozsoy-Sacan, S. Bolkent, H. Orak, and O. Karabulut-Bulan. "Protective effects of metformin treatment on the liver injury of streptozotocin-diabetic rats." Human & Experimental Toxicology 24, no. 3 (March 2005): 129–35. http://dx.doi.org/10.1191/0960327104ht507oa.
Full textCheng, Daye, Bin Liang, and Yunhui Li. "Antihyperglycemic Effect ofGinkgo bilobaExtract in Streptozotocin-Induced Diabetes in Rats." BioMed Research International 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/162724.
Full textTsai, Cheng-Chia, Kung-Shing Lee, Sheng-Hsien Chen, Li-Jen Chen, Keng-Fan Liu, and Juei-Tang Cheng. "Decrease of PPARδin Type-1-Like Diabetic Rat for Higher Mortality after Spinal Cord Injury." PPAR Research 2014 (2014): 1–7. http://dx.doi.org/10.1155/2014/456386.
Full textCassis, L. A. "Downregulation of the renin-angiotensin system in streptozotocin-diabetic rats." American Journal of Physiology-Endocrinology and Metabolism 262, no. 1 (January 1, 1992): E105—E109. http://dx.doi.org/10.1152/ajpendo.1992.262.1.e105.
Full textYamamoto, Tetsushi, Hiroko Otake, Noriko Hiramatsu, Naoki Yamamoto, Atsushi Taga, and Noriaki Nagai. "A Proteomic Approach for Understanding the Mechanisms of Delayed Corneal Wound Healing in Diabetic Keratopathy Using Diabetic Model Rat." International Journal of Molecular Sciences 19, no. 11 (November 18, 2018): 3635. http://dx.doi.org/10.3390/ijms19113635.
Full textMartínez, Isabel M., Inmaculada Morales, Guadalupe García-Pino, José E. Campillo, and María A. Tormo. "Experimental Type 2 Diabetes Induces Enzymatic Changes in Isolated Rat Enterocytes." Experimental Diabesity Research 4, no. 2 (2003): 119–23. http://dx.doi.org/10.1155/edr.2003.119.
Full textEl Barky, Amira Ragab, Samy A. Hussein, Abeer A. Alm-Eldeen, yehia A. Hafez, and Tarek M. Mohammed. "Saponin ameliorate diabetes in STZ-diabetic rats." Delta Journal of Science 38, no. 2 (December 1, 2017): 177–82. http://dx.doi.org/10.21608/djs.2017.139442.
Full textElBatsh, Maha Mohamed. "Antidepressant-like effect of simvastatin in diabetic rats." Canadian Journal of Physiology and Pharmacology 93, no. 8 (August 2015): 649–56. http://dx.doi.org/10.1139/cjpp-2014-0560.
Full textDissertations / Theses on the topic "STZ diabetic rats"
Thompson, Katherine Hirsch. "Effect of dietary manganese and vitamin E deficiencies on tissue antioxidant status in STZ-diabetic rats." Thesis, University of British Columbia, 1991. http://hdl.handle.net/2429/32171.
Full textLand and Food Systems, Faculty of
Graduate
Fullarton, Agneta Carol. "An investigation into the recovery of function after different types of injury and repair of peripheral nerve : a comparison between non-diabetic and STZ diabetic rats." Thesis, University of Edinburgh, 1995. http://hdl.handle.net/1842/20514.
Full textXiang, Hong. "Effects of myo-inositol and, or triiodothyronine (T₃) treatment on cardiac dysfunction and elevated myocardial lipid levels in STZ-diabetic rats." Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/26675.
Full textPharmaceutical Sciences, Faculty of
Graduate
Lemos, Virgínia Carvalho. "Evaluation of the effect of A. unedo L. extracts on blood indices and microelements status in high-fat STZ-induced diabetic rats." Master's thesis, Universidade de Aveiro, 2015. http://hdl.handle.net/10773/15469.
Full textThe strawberry tree (Arbutus unedo L.) is an endemic shrub, which grows in the Mediterranean region. In Portugal, it can be found through all the country but mostly in the south. The fruit is used to produce hams and jellies and firewater, reason why the fruit’s chemical composition is relatively well known, when compared to the leaves. Until now, there are only a few studies concerning the leaves’ chemical composition and the existing mainly focus on their phenolic content. This plant has long been used in folk medicine to treat a vast amount of illnesses like gastrointestinal disorders, gastritis, dermatologic and urological problems, kidney problems and cardiovascular diseases. However, very few studies in vivo have been performed about these medicinal properties until now. Diabetes is a pandemic disease that affects millions of people. There are only two studies about A. unedo root’s aqueous extract antidiabetic properties. This study evaluated the anti-diabetic effect of strawberry tree (Arbutus unedo L.) fruit and leaf aqueous extracts in streptozotocin (STZ) induced diabetic rats fed with a high-fat diet. Firstly the optimal parameters to obtain the fruit aqueous extract were established. After that, the leaves and fruits aqueous extracts were characterized in terms of total phenolic content (TPC). Leaf aqueous extracts presented a higher TPC concentration than the fruit aqueous extract. Male Wistar rats were injected with STZ, after a 2 week feeding with high-fat diet in order to induce non-insulin dependent type 2 diabetes. After confirmation of the rats’ diabetic state, the animals were fed with Arbutus unedo L. fruit aqueous extract or leaf aqueous extract added to the high-fat diet for 4 weeks. The extracts were given in the following doses: 1.25g /kg b.w./day for leaf extract and 0.5g /kg b.w./day for fruit extract. After the animals were sacrificed analyses were perform for blood indices, haematological indices, mineral tissular status and gene expression. Arbutus unedo L. fruit extract presented a tendency to lower blood glucose levels. More beneficial effects were seen for this extract in terms of regulating TNF-α gene expression in muscular tissue. Some effects in zinc renal homeostasis were also shown, although they were not very significant. The leaf extract, appeared to be more efficient in regulating insulin levels and improving HOMA-IR index. It also presented a tendency towards lowering blood glucose levels. Both extracts proved to efficiently improve insulin sensitivity (leaf extract in a larger extent). In this study, there were also some good preliminary results, as the groups supplemented with this extracts showed a tendency in decreasing serum creatinine and/or phosphatase concentration, improving the Red Cell Distribution Width measured with standard deviation (RDW-SD) and lymphocytes concentration. Positive antidiabetic and anti-inflammatory aspects were found for both aqueous extracts. The results obtained confirm the mid-therapeutically effects of A. unedo as the plant’s material effectively improved insulin sensitivity (HOMA-IR index) although failed to significantly modulate glucose metabolism. This study was the first in vivo trial on a type 2 diabetes animal model that evaluated the antidiabetic potential of Arbutus unedo L. fruits and leaves aqueous extracts.
O medronheiro (Arbutus unedo L.) é um arbusto endémico que cresce em toda a região Mediterrânica. Em Portugal, pode ser encontrado em todo o território continental, principalmente na zona sul do país. O fruto é utilizado na produção de compotas, marmeladas e aguardente, pelo que a composição química deste é relativamente bem conhecido quando comparado com as folhas. Actualmente, existem poucos estudos sobre a composição química das folhas, sendo que a maioria visa apenas o seu conteúdo em compostos fenólicos. Esta planta tem sido utilizada na medicina popular para tratar diversas doenças tais como distúrbios gastrointestinais, gastrite, problemas dermatológico, urológicos, renais e cardiovasculares. No entanto, até ao momento existem poucos estudos in vivo que atestem estas propriedades medicinais, o que justifica a realização deste tipo de ensaios. No caso da diabetes, que afecta milhões de pessoas em todo o mundo, existem apenas dois estudos sobre as propriedades antidiabéticas do extrato aquoso das raízes de A. unedo. O presente trabalho de mestrado avaliou o potencial antidiabético dos extractos aquosos das folhas e frutos do medronheiro. O estudo foi efectuado em ratos diabéticos (diabetes induzida por Estreptozotocina - STZ) alimentados com uma ração rica em gordura. Primeiramente foram optimizados os parâmetros de extracção para a obtenção do extrato aquosos do fruto. De seguida os extratos aquosos de folhas e frutos foram caracterizados em termos de teor em fenóis totais. O extrato aquoso das folhas apresentou uma maior concentração de fenóis totais do que o extrato aquoso do fruto. Ratos Wistar do sexo masculino foram injectados com STZ após serem alimentados durante 2 semanas com uma dieta rica em gordura. Desta forma induziu-se diabetes tipo 2, não dependente de insulina. Após a confirmação da condição diabética dos ratos, a dieta rica em gordura continuou a ser administrada aos animais. No entanto, as dietas foram suplementadas com extrato aquoso ou do fruto ou das folhas de Arbutus unedo L., num tratamento com a duração de 4 semanas. Os extratos foram administrados nas seguintes doses: 1.25g /kg peso corporal/dia no caso do extrato da folhas 0.5g /kg peso corporal/dia no caso do extrato do fruto. Efectuaram-se análises a parâmetros do sangue, hematológicos, à homeostasia mineral dos tecidos e à expressão de determinados genes após os animais serem sacrificados. O extrato do fruto apresentou uma tendência a regular os níveis de glucose no sangue. Outros efeitos benéficos foram atribuídos a este extrato, nomeadamente ao nível da regulação da expressão do gene de TNF-α a nível muscular. Este extrato também apresentou alguns efeitos ao nível da regulação da homeostase renal de zinco, embora não muito significativos. O extrato da folha provou ser mais eficiente a regular os níveis de insulina, a melhorar a resistência à insulina (HOMA-IR). Também apresentou uma tendência a regular os níveis de glucose no sangue. Ambos os extratos aumentaram de forma eficiente a sensibilidade à insulina (embora o extrato da folha o tenha feito de forma mais pronunciada). Obtiveram-se ainda bons resultados preliminares, uma vez que estes extratos demostraram que ocorreu uma tendência em termos de diminuição da concentração de creatinina e/ou fosfatase, de aumento do valor do parâmetro de Amplitude de Distribuição dos Eritrócitos medido como Desvio Padrão (RDW-SD), de aumento da concentração de linfócitos e diminuíram. Para ambos os extratos foram detectados efeitos antidiabéticos e anti-inflamatórios. Os resultados obtidos confirmam que A. unedo apresenta alguns efeitos terapêuticos, embora ligeiros. Os extratos desta planta melhoraram significativamente a sensibilidade à insulina mas não conseguiram regular significativamente o metabolismo da glucose. Este estudo foi o primeiro, num modelo animal de diabetes tipo 2 que avaliou o potencial antidiabético dos extratos aquosos dos frutos e folhas de Arbutus unedo L.
Cameron-Smith, David, and edu au jillj@deakin edu au mikewood@deakin edu au wildol@deakin edu au kimg@deakin. "THE INTERACTION OF DIETARY FIBRE, CARBOHYDRATE METABOLISM AND DIABETES IN THE RAT." Deakin University. School of Health and Behavioral Sciences, 1994. http://tux.lib.deakin.edu.au./adt-VDU/public/adt-VDU20040622.171657.
Full textSinzato, Yuri Karen. "Análise morfológica e imunológica das placentas de ratas com diabete de intensidade moderada /." Botucatu, 2009. http://hdl.handle.net/11449/106385.
Full textBanca: Marilza Vieira Cunha Rudge
Banca: Estela Maris Andrade Forell Bevillacqua
Banca: Renée Laufer Amorim
Banca: Teresa Cristina França Sartori
Resumo: Avaliar os efeitos do diabete moderado nos parâmetros reprodutivos maternos e no desenvolvimento placentário-fetal em ratas Wistar. Metodologia: No dia do nascimento, 147 ratas Wistar foram distribuídas aleatoriamente em dois grupos experimentais: Grupo não-diabético (Controle, n=45) - recebeu o veículo; Grupo diabético (STZ, n=102) - recebeu 100 mg streptozotocin/kg. Na fase adulta, as ratas foram acasaladas e, no dia 0 de prenhez, foram incluídas ratas controle que apresentassem glicemia abaixo de 120 mg/dL e, para o grupo diabete moderado, glicemia entre 120 e 300 mg/dL. Em diferentes momentos da prenhez, glicemia e peso corpóreo foram verificados. No 21º dia de prenhez, as ratas foram anestesiadas para coleta de sangue para dosagem de insulina e, em seguida, foi realizada laparotomia para retirada e pesagem dos fetos e placentas. Os dados maternos e fetais foram analisados por Twoway ANOVA seguida do Teste t. Os recém-nascidos (RN) foram classificados em pequenos, adequados e grandes para idade de prenhez e as comparações entre os grupos foram realizadas segundo o Teste de Qui-quadrado. As ratas STZ apresentaram glicemias maiores nos dias 0 e 14 de prenhez, menor número médio de fetos vivos, implantações e de corpos lúteos, aumento nas taxas de perdas embrionárias pós-implantação, no peso placentário e na proporção de RN pequenos (PIP) e grandes (GIP) para idade de prenhez, redução de RN AIP e inalteração nas concentrações de insulina. Portanto, o diabete de intensidade moderada alterou a glicemia materna no início da prenhez, que deflagrou alterações no organismo materno e/ou no desenvolvimento inicial do embrião, afetando sua implantação e futuro desenvolvimento placentário e fetal.
Abstract: To evaluate the mild diabetes effects on the maternal reproductive outcome and placental-fetal development in female Wistar rats. Methodology: At the birth day, 147 female rats were randomly distributed in two experimental groups: 1) Non-diabetic Group (Control, n=45) - received the vehicle; 2) Diabetic Group (STZ, n=102) - received 100 mg streptozotocin/kg. At the adult phase, the female rats were mated and, at the day 0 of pregnancy, they were included in the control group when presented glycemia below 120 mg/dL and, in the group STZ when showed glycemia between 120 and 300 mg/dL. In different moments of the pregnancy, glycemia and body weight were verified. At day 21 of pregnancy, the rats were anaesthetized to collect blood samples for insulin determination and, soon afterwards, the laparotomy was carried out to withdraw and weigh the fetuses and placentas. The maternal and fetal dates were analyzed by Two-way ANOVA followed by t Test. The newborns (NB) were classified in small, appropriate and large for gestational age and the comparisons between the groups were accomplished according to Qui-square Test. Rats STZ presented higher glycemia at days 0 and 14 of pregnancy, lower numbers of alive fetuses; implantations and corpora lutea; increased rate of embryonic losses, placental weight and proportion of small NB (SGA) and large (LGA); reduced rate of AGA NB and unaltered insulin concentrations. Therefore, the mild diabetes altered the maternal glycemia in the early pregnancy, which caused changes in the maternal organism and/or in the early development of the embryo, impairing its implantation and future placental and fetal development.
Doutor
Sinzato, Yuri Karen [UNESP]. "Análise morfológica e imunológica das placentas de ratas com diabete de intensidade moderada." Universidade Estadual Paulista (UNESP), 2009. http://hdl.handle.net/11449/106385.
Full textCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
Avaliar os efeitos do diabete moderado nos parâmetros reprodutivos maternos e no desenvolvimento placentário-fetal em ratas Wistar. Metodologia: No dia do nascimento, 147 ratas Wistar foram distribuídas aleatoriamente em dois grupos experimentais: Grupo não-diabético (Controle, n=45) - recebeu o veículo; Grupo diabético (STZ, n=102) - recebeu 100 mg streptozotocin/kg. Na fase adulta, as ratas foram acasaladas e, no dia 0 de prenhez, foram incluídas ratas controle que apresentassem glicemia abaixo de 120 mg/dL e, para o grupo diabete moderado, glicemia entre 120 e 300 mg/dL. Em diferentes momentos da prenhez, glicemia e peso corpóreo foram verificados. No 21º dia de prenhez, as ratas foram anestesiadas para coleta de sangue para dosagem de insulina e, em seguida, foi realizada laparotomia para retirada e pesagem dos fetos e placentas. Os dados maternos e fetais foram analisados por Twoway ANOVA seguida do Teste t. Os recém-nascidos (RN) foram classificados em pequenos, adequados e grandes para idade de prenhez e as comparações entre os grupos foram realizadas segundo o Teste de Qui-quadrado. As ratas STZ apresentaram glicemias maiores nos dias 0 e 14 de prenhez, menor número médio de fetos vivos, implantações e de corpos lúteos, aumento nas taxas de perdas embrionárias pós-implantação, no peso placentário e na proporção de RN pequenos (PIP) e grandes (GIP) para idade de prenhez, redução de RN AIP e inalteração nas concentrações de insulina. Portanto, o diabete de intensidade moderada alterou a glicemia materna no início da prenhez, que deflagrou alterações no organismo materno e/ou no desenvolvimento inicial do embrião, afetando sua implantação e futuro desenvolvimento placentário e fetal.
To evaluate the mild diabetes effects on the maternal reproductive outcome and placental-fetal development in female Wistar rats. Methodology: At the birth day, 147 female rats were randomly distributed in two experimental groups: 1) Non-diabetic Group (Control, n=45) - received the vehicle; 2) Diabetic Group (STZ, n=102) - received 100 mg streptozotocin/kg. At the adult phase, the female rats were mated and, at the day 0 of pregnancy, they were included in the control group when presented glycemia below 120 mg/dL and, in the group STZ when showed glycemia between 120 and 300 mg/dL. In different moments of the pregnancy, glycemia and body weight were verified. At day 21 of pregnancy, the rats were anaesthetized to collect blood samples for insulin determination and, soon afterwards, the laparotomy was carried out to withdraw and weigh the fetuses and placentas. The maternal and fetal dates were analyzed by Two-way ANOVA followed by t Test. The newborns (NB) were classified in small, appropriate and large for gestational age and the comparisons between the groups were accomplished according to Qui-square Test. Rats STZ presented higher glycemia at days 0 and 14 of pregnancy, lower numbers of alive fetuses; implantations and corpora lutea; increased rate of embryonic losses, placental weight and proportion of small NB (SGA) and large (LGA); reduced rate of AGA NB and unaltered insulin concentrations. Therefore, the mild diabetes altered the maternal glycemia in the early pregnancy, which caused changes in the maternal organism and/or in the early development of the embryo, impairing its implantation and future placental and fetal development.
Yi-Hui and 顏翊橞. "Anti-diabetic effects of mulberry leaf extract on STZ-induced diabetic rats." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/r768x3.
Full text中山醫學大學
營養學研究所
100
Diabetes Melitus (DM) is one of the most popular chronic diseases in the world. Poor glycemic control is a known major factor that leads to diabetic complications and is attributed to increased oxidative stress. According to previous studies, Morus alba leaves and its extract (ME) possesses hypoglycemic effect with 1-deoxynojirimycin (1-DNJ) as a functional compound. However, the mechanisms underlying which ME and 1-DNJ lowering blood glucose level remain to be clarified. It is also not known how ME and 1-DNJ affect the development of DM nephropathy. The aim of this study is to investigate the antidiabetic effect of ME and 1-DNJ including their effect on the development of diabetic nephropathy and the related mechanisms. Male Wistar rats were injected with streptozotocin (65 mg/kg BW, i.v.) to induce DM. Control rats were injected with citrate buffer solution. 7 days after induction, the DM rats were assigned randomly to six groups and were treated with 1, 3, 10, 30 mg/kg BW of ME, 30 mg/kg BW of DNJ or vehicle (d.d. H2O; 2 ml/kg BW) for a week. Normal control rats also received vehicle. OGTT was carried out at 7 or 11 days and ITT was carried out at 11 days after induction. At 14 days after induction, rats were killed with CO2 and organ/tissue samples collected for various biochemical analyses and the determination of oxidative stress and renal function. On the DM rats all doses of ME and 1-DNJ significantly ameliorated fasting blood glucose and AUC of glucose during OGTT period chronically and ME also showed such effect acutely. All doses of ME and 1-DNJ significantly increased peripheral and pancreatic levels of insulin and improved HOMA-IR in DM rats. Ten and 30 mg/kg of ME improved insulin-induced lowering of blood glucose level in DM rats. In the other hand, all doses of ME and 1-DNJ significantly reversed increased TBARS of the pancreas, kidneys, livers, muscles and peripheral blood in DM as well as decreased GRd activity of the pancreas and kidneys in DM. In addition, 1-DNJ significantly reversed lowered GPx and GRd activity of the livers and muscles in DM. ME at 30 mg/kg significantly reversed lowered GPx activity of the muscle, at 10 to 30 mg/kg significantly reversed lowered GRd activity of the kidneys, at 1 mg/kg significantly reversed lowered GRd activity of of the livers, at 3 to 30 mg/kg significantly reversed lowered GRd activity of the muscles. All ME doses and 1-DNJ significantly decreased NO content of the pancreas, kidneys, livers,and muscles in DM. The indices of renal function, including BUN, CCR, and GFR were all ameliorated by all doses of ME and 1-DNJ. In addition, 30 mg/kg of ME and 1-DNJ improved glomerular morphology of the kidneys and lowered blood pressure in DM. In conclusion, ME and 1-DNJ improved insulin secretion and insulin sensitivity and attenuated the development of diabetic nephropathy. The antidiabetic effects of ME and 1-DNJ is at least partly due to the amelioration of the increased oxidative stress in DM.
Yao, Jun. "Effects of vanadium compounds on diabetes induced changes in STZ-diabetic rats." Thesis, 1996. http://hdl.handle.net/2429/4473.
Full textChen, Tai-You, and 陳泰佑. "Effects of Cordyceps sinensis on Blood Glucose in STZ-induced Diabetic Rats." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/89246554680918450648.
Full text國立中興大學
獸醫學系暨研究所
101
In recent years, researches indicate diabetes implicated in metabolic syndrome. There are sulfonylurea, bioguanides, alpha-glucosidase inhibitor, thiazolidinediones, insulin, dipeptidyl peptidase-4 inhibitors and so on in diabetic drugs which have their indication and a lot of side effects. Therefore, many researchers develop drugs or extraction for natural products to improve metabolic syndrome and control diabetes, and moreover can reach prevention. Cordyceps has a large amount of biological ingredients which increase numbers of transporter proteins and stablelize concentration of blood glucose. Therefore, we found Cordyceps extract could prevent hyperglycemia in STZ-induced diabetic rats.
Books on the topic "STZ diabetic rats"
Akirav, Eitan Moshe. Leptin restoration in streptozotocin (STZ)-diabetic rats. Ottawa: National Library of Canada, 2002.
Find full textMontes, Danitza Eustolia Goche. Effects of restraint stress on hypothalamic-pituitary-adrenal activity in STZ-diabetic rats. 2005.
Find full textBook chapters on the topic "STZ diabetic rats"
Shintaku, H., M. Imanishi, M. Okumura, S. Fujii, E. Kawai, S. Genba, K. Takahashi, Y. Sawada, and T. Yamano. "The Effect of Tetrahydrobiopterin (BH4) on Diabetic Nephropathy in Streptozotocin (STZ) Induced Diabetic Rats." In Chemistry and Biology of Pteridines and Folates, 355–58. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/978-1-4615-0945-5_59.
Full textKaruppannan, P., K. Saravanan, and P. Premalatha. "Antidiabetic Activity of Ventilago maderaspatana Leaf Extracts on STZ Induced Diabetic Rats." In Drug Development for Cancer and Diabetes, 283–92. Includes bibliographical references and index.: Apple Academic Press, 2020. http://dx.doi.org/10.1201/9780429330490-24.
Full textElavarasi, S., G. Revathi, K. Saravanan, and Horne Iona Averal. "Antidiabetic and Antihyperlipidemic Activities of Cyathea nilgiriensis (Holttum) on STZ Induced Diabetic Rats." In Drug Development for Cancer and Diabetes, 233–48. Includes bibliographical references and index.: Apple Academic Press, 2020. http://dx.doi.org/10.1201/9780429330490-20.
Full textJaffar, S. K., S. M. Khasim, and M. S. K. Prasad. "Protective Effect of Mimusops elengi L. on Renal and Hepatic Markers in STZ-Induced Diabetic Rats." In Medicinal Plants: Biodiversity, Sustainable Utilization and Conservation, 509–20. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-1636-8_28.
Full textValdivielso, José M., Angel Montero, Karen A. Munger, and Kamal F. Badr. "Inhibition of 5-lo Activating Protein (Flap) Activity Decreases Proteinuria in Streptozotocin(Stz)-induced Diabetic Rats." In Advances in Experimental Medicine and Biology, 79–83. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/978-1-4615-0193-0_13.
Full textPoucheret, Patrick, René Gross, Anne Cadène, Michelle Mantéguetti, Jean-Jacques Serrano, Gérard Ribes, and Gérard Cros. "Long-term correction of STZ-diabetic rats after short-term i.p. VOSO4 treatment: Persistence of insulin secreting capacities assessed by isolated pancreas studies." In Vanadium Compounds: Biochemical and Therapeutic Applications, 197–204. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4613-1251-2_26.
Full textJasmine, R., and A. Sherlin Rosita. "Regeneration of Beta Cells by Inhibition of pro-Apoptotic Proteins through Phytocompound in STZ Induced Diabetic Albino Wistar Rats: In Vivo and In Silico Approach." In Structure and Health Effects of Natural Products on Diabetes Mellitus, 219–34. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-8791-7_12.
Full textUmrani, Dhananjay N., Dipali N. Bodiwala, and Ramesh K. Goyal. "Effect of sarpogrelate on altered STZ-diabetes induced cardiovascular responses to 5-hydroxytryptamine in rats." In Biochemistry of Diabetes and Atherosclerosis, 53–57. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4419-9236-9_7.
Full textSerradas, P., M. Dolz, M. Giroix, D. Bailbe, C. Cuzin-Tourrel, M. Kergoat, B. Portha, and J. Movassat. "Neonatally Streptozotocin- Induced (n-STZ) Diabetic Rats." In Animal Models of Diabetes, Second Edition, 223–50. CRC Press, 2007. http://dx.doi.org/10.1201/9781420009453.ch10.
Full textJatziry Hernández-Esparza, Manjury, Claudia Guadalupe Flores-Ledesma, Rocío Montoya-Pérez, Elizabeth Calderón-Cortés, Alfredo Saavedra-Molina, Alain Raimundo Rodríguez-Orozco, and Christian Cortés-Rojo. "Thiol Reduction and Cardiolipin Improve Complex I Activity and Free Radical Production in Liver Mitochondria of Streptozotocin-Induced Diabetic Rats." In Antioxidants [Working Title]. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.95112.
Full textConference papers on the topic "STZ diabetic rats"
Öztürk, Melek. "Dipeptidyl peptidase-4 inhibition causes liver regeneration in neonatal STZ-diabetic rats." In 15th International Congress of Histochemistry and Cytochemistry. Istanbul: LookUs Scientific, 2017. http://dx.doi.org/10.5505/2017ichc.pp-75.
Full textSarkodie, J., C. Asare, P. Debrah, and E. Oppong Bekoe. "Taraxacum officinale leaves aqueous extract-mediated glucose lowering effect in STZ-induced diabetic rats." In GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608450.
Full textTunçdemi̇r, Matem. "Investigation of the quercetin effect on apoptosis in diabetic nephropathy model rats induced by STZ." In 15th International Congress of Histochemistry and Cytochemistry. Istanbul: LookUs Scientific, 2017. http://dx.doi.org/10.5505/2017ichc.pp-20.
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