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1.
Asian-Australas J Anim Sci ; 31(11): 1795-1806, 2018 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-29642669

RESUMO

OBJECTIVE: The study was designed to establish choline deficiency model (CDM) in broilers for evaluating efficacy of polyherbal formulation (PHF) in comparison with synthetic choline chloride (SCC). METHODS: A total of 2,550 one-day-old Cobb 430 broiler chicks were randomly assigned to different groups in three experiments. In experiment 1, G1 and G2 served as normal controls and were fed a basal diet with 100% soybean meal (SBM) as a major protein source supplemented with and without SCC, respectively. In G3, G4, G5, and G6 groups, SBM was replaced at 25%, 50%, 75%, and 100% by soy protein isolate (SPI) to induce a graded level of choline deficiency. In experiment 2, PHF (500 and 1,000 g/ton) in comparison with SCC (1,000 g/ton) were evaluated. In experiment 3, dose-response of PHF (200, 400, and 500 g/ton) with SCC (400 g/ton) was determined. RESULTS: Replacement of SBM by SPI produced a linear decrease in body weight gain (BWG) with a poor feed conversion ratio (FCR). 25% SBM replacement by SPI yielded an optimum negative impact on BWG and FCR; hence, it is considered for further studies. In experiment 2, PHF (500 and 1,000 g/ton) and SCC (1,000 g/ton) showed a similar performance in BWG, FCR and relative liver weight. In experiment 3, PHF produced an optimum efficacy at 400 g/ton and was comparable to SCC in the restoration of serum aspartate aminotransferase activity, abdominal fat, breast muscle lipid content and liver histopathological abnormalities. CONCLUSION: Replacement of SBM by SPI caused choline deficiency characterised by worsening of BWG, FCR, elevation in liver enzymes and histopathological changes indicating fatty liver. CDM was found valid for evaluating SCC and PHF. It is concluded that PHF has the potential to mimic biological activities of SCC through the restoration of negative effects caused by CDM.

2.
Mol Cell Biochem ; 396(1-2): 281-93, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25073953

RESUMO

The Wnt and Notch1 signaling pathways play major roles in intestinal development and tumorigenesis. Sub-cellular localization of ß-catenin has been implicated in colorectal carcinogenesis. However, the ß-catenin and Notch intracellular domain (NICD) interaction has to be addressed. Immunohistochemistries of ß-catenin, NICD, and dual immunofluorescence of ß-catenin and NICD were analyzed in colorectal tissues and HT29 cell line. Moreover, real-time PCR analysis of CyclinD1, Hes1 and MUC2 was done in HT29 cells upon N-[N-(3, 5-difluorophenacetyl)-L-alanyl]-S-phenylglycine t-butyl ester (DAPT) treatment. Dual staining emphasized the strong interaction of ß-catenin and NICD in adenoma and adenocarcinoma than in normal tissues. Hes1 transcript levels were decreased 1.5- and 7.1-fold in 12.5 and 25 µM DAPT-treated HT29 cells. CyclinD1 transcript levels decreased 1.2- and 1.6-fold, and MUC2 transcript level increased 4.3- and 7.5-fold in 12.5 and 25 µM DAPT-treated HT29 cells. The results of this study showed that the sub-cellular localization of ß-catenin converges with NICD inducing proliferation through the activation of CyclinD1 and Hes1. Moreover, the inhibition of Notch1 signaling by DAPT leads to the arrest of cell proliferation and induces apoptosis leading to the upregulation of MUC2, a secretory cell lineage marker.


Assuntos
Neoplasias do Colo/metabolismo , Neoplasias do Colo/patologia , Ciclina D1/metabolismo , Receptor Notch1/metabolismo , beta Catenina/metabolismo , Adenocarcinoma/metabolismo , Adenocarcinoma/patologia , Adenoma/metabolismo , Adenoma/patologia , Fatores de Transcrição Hélice-Alça-Hélice Básicos/genética , Proliferação de Células , Neoplasias do Colo/genética , Neoplasias Colorretais/genética , Neoplasias Colorretais/metabolismo , Neoplasias Colorretais/patologia , Ciclina D1/genética , Dipeptídeos/farmacologia , Relação Dose-Resposta a Droga , Regulação Neoplásica da Expressão Gênica , Células HT29/efeitos dos fármacos , Células HT29/metabolismo , Proteínas de Homeodomínio/genética , Humanos , Mucina-2/genética , Mucina-2/metabolismo , Estrutura Terciária de Proteína , Valores de Referência , Transdução de Sinais , Fatores de Transcrição HES-1
3.
Mol Biol Rep ; 40(5): 3537-47, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23269621

RESUMO

The role of Notch signalling in congenital cardiovascular disease is evident by the identification of human mutations in several Notch signalling components, which also indicates the importance of activated Notch pathway in cardiovascular biology. Therefore, the aim of the present study is to investigate the expression pattern of the components of Notch signalling molecules and their role in mice embryonic heart and vascular development. Group A: normal control pregnant mice, group B: pregnant mice were injected with DMSO, group C: DAPT were subcutaneously injected to pregnant mice. The morphological and molecular changes of trabeculation-defective phenotype were analysed using histological, scanning electron microscope, immunoblot, immunolocalization and reverse transcriptase-PCR. E15.5 DAPT-treated mice revealed that there was a major reduction in the formation of septal walls between the ventricular chambers compared with normal control pregnant mice. VEGF expression was found in the DAPT treated and wild-type embryonic artery, whereas notch target genes GATA4, Hey1 expression were not found in the DAPT treated mice embryo. The role of Notch in ventricular development is supported by the trabeculation-defective phenotype seen in standard and endocardial-specific inhibition of Notch targets. The present study reveals the significant role of Notch signalling during the formation of ventricular septum and proper development of endothelial cell lineage and its precursor in mice cardiogenesis.


Assuntos
Sistema Cardiovascular/metabolismo , Receptores Notch/metabolismo , Transdução de Sinais , Animais , Artérias/metabolismo , Artérias/patologia , Artérias/ultraestrutura , Fatores de Transcrição Hélice-Alça-Hélice Básicos/genética , Fatores de Transcrição Hélice-Alça-Hélice Básicos/metabolismo , Sistema Cardiovascular/embriologia , Feminino , Fator de Transcrição GATA4/genética , Fator de Transcrição GATA4/metabolismo , Perfilação da Expressão Gênica , Regulação da Expressão Gênica no Desenvolvimento , Comunicação Interventricular/embriologia , Comunicação Interventricular/genética , Comunicação Interventricular/metabolismo , Comunicação Interventricular/patologia , Masculino , Camundongos , Gravidez , Proteínas Repressoras/genética , Proteínas Repressoras/metabolismo
4.
J Exp Zool B Mol Dev Evol ; 318(7): 572-85, 2012 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-22807097

RESUMO

Vitellogenin (VTG) synthesis in the hepatopancreas and ovary is negatively regulated by vitellogenesis-inhibiting hormone (VIH) produced in the neurosecretory cell of X-organ/sinus gland complex of the eyestalks of penaeid shrimp. Eyestalk ablation is used commercially to induce ovarian maturation in shrimps which leads to an eventual loss of the spawner. The aim of the present study was to understand the molecular mechanism of VIH regulation in ovarian development and its inhibition of VTG gene expression by using a MEK-specific inhibitor (U0126). The real-time quantitative PCR results showed VTG mRNA level was progressively increased in the ovary and hepatopancreas of unilateral eyestalk-ablated and inhibitor-treated shrimps. Western blot analysis also showed that phosphoMEK was detected only in the unilateral eyestalk-ablated and control shrimp, whereas phospho-MEK was not detected in inhibitor-treated shrimp. DAX-1, SF-1, and StAR expression correlated with changes in VIH mRNA and altered phospho-ERK levels. This is consistent with the hypothesis that suppression of DAX-1 results in SF-1-mediated StAR protein upregulation of estradiol that is implicated in vitellogenesis. This is the first report that demonstrates the molecular mechanism of VIH suppression via MEK pathway to induce ovarian maturation in female Penaeus monodon by molecular signal intervention, a less-invasive method than traditional eyestalk ablation.


Assuntos
Proteínas de Transporte/metabolismo , Inibidores Enzimáticos/farmacologia , Regulação da Expressão Gênica no Desenvolvimento/efeitos dos fármacos , Hormônios de Invertebrado/metabolismo , Ovário/crescimento & desenvolvimento , Penaeidae/crescimento & desenvolvimento , Maturidade Sexual/fisiologia , Vitelogeninas/metabolismo , Análise de Variância , Animais , Northern Blotting , Western Blotting , Butadienos , Cromatografia Líquida de Alta Pressão , Receptor Nuclear Órfão DAX-1/metabolismo , Primers do DNA/genética , Feminino , Regulação da Expressão Gênica no Desenvolvimento/genética , Hepatopâncreas/metabolismo , Técnicas Histológicas , Nitrilas , Ovário/metabolismo , Fosfoproteínas/metabolismo , Reação em Cadeia da Polimerase em Tempo Real , Maturidade Sexual/efeitos dos fármacos , Fator Esteroidogênico 1/metabolismo
5.
Pharmacognosy Res ; 10(1): 1-8, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29568180

RESUMO

BACKGROUND: The range of thermoneutral zone of chickens is narrow, and they become easily susceptible to environmental stress, a common and major concern for poultry causing a production loss. OBJECTIVE: The present study was designed to comparatively evaluate anti-stress activity of Phytocee™ and Vitamin C in chickens reared under heat stress. MATERIALS AND METHODS: A total of 600-day-old chicks of Cobb 400 were randomly assigned to 4 groups with 6 replicates comprising 25 birds each (n = 150). G1 served as a normal control (NC) and supplemented with Vitamin C at 100 g/ton of feed. G2 served as a heat stress control (HSC), subjected to heat stress (34°C-36°C) without Vitamin C supplementation. G3 and G4 served as positive control and treatment group (TC), subjected to heat stress and supplemented with Vitamin C and Phytocee™ at 100 g/ton of feed, respectively. The impact on zootechnical parameters and cloacal temperature was assessed at regular intervals, and blood was collected at the end of the experiment for evaluation of stress parameters, namely heterophil lymphocyte ratio (H:L ratio) and serum corticosterone. RESULTS: Exposure of chickens to heat stress caused a significant decrease in body weight, worsening of feed conversion ratio, higher mortality, and poor production efficiency. Moreover, serum corticosterone level, H:L ratio, and cloacal temperature were significantly increased in HSC as compared to NC. However, supplementation of Phytocee™ in feed significantly ameliorated the negative impact of heat stress in broiler birds. CONCLUSION: The supplementation of Phytocee™ demonstrated an anti-stress effect in chickens through restoration of serum corticosterone level, H:L ratio, and thermoregulatory mechanism. SUMMARY: Combating heat stress remains a challenge for the broiler industry in the tropics and subtropics, which is even aggravated by the changing climatic conditionsThe present study was designed to evaluate the anti-stressor activity of Phytocee™, a polyherbal formulation containing Emblica officinalis, Ocimum sanctum, and Withania somnifera in broiler using heat stress model in comparison with Vitamin CPhytocee™ demonstrated an anti-stress effect in the current study by ameliorating the negative effects of heat stress on zootechnical parameters, serum corticosterone, heterophil lymphocyte ratio, and cloacal temperature of broilers through modulating the hypothalamic-pituitary-adrenal axis and thermoregulatory mechanismHence, Phytocee™ could be recommended in broilers and livestock animals for modulating and combating adverse effects of heat stress and thereby reducing the economic losses incurred by farmers. Abbreviations Used: HPA axis: Hypothalamic pituitary adrenal axis.

6.
Cardiovasc Pathol ; 22(4): 257-63, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23273785

RESUMO

INTRODUCTION: The origin of heart-forming cells and their roles in organ development have fascinated biologists for over a century. C-X-C chemokine receptor type 4 plays a crucial role during embryonic development and in maintaining the stem cell niche and homing. The aim of the present was to study the expression pattern of resident cardiac stem cell markers and their homing factor in neonatal, postnatal, and adult mouse heart. METHODS: Cardiac stem cell protein expression was analyzed using immunofluorescence, immunohistochemistry, and Western blotting. The messenger ribonucleic acid expression of cardiac stem cell markers c-kit, stem cell antigen-1, and homing factor C-X-C chemokine receptor type 4 was quantitatively analyzed using quantitative polymerase chain reaction. Data were analyzed using Student's t test and two-way analysis using SPSS software. RESULTS: Stem cell antigen-1- and c-kit-positive cell populations were heterogeneously distributed in the adult and postnatal hearts but scattered in the neonatal heart. The expression of c-kit showed a significant difference between right and left atrium, though it was higher compared to ventricles. The homing factor C-X-C chemokine receptor type 4 expression was higher in the neonatal heart than in the postnatal heart but was not detectable in the adult heart. CONCLUSIONS: The present study reveals the distribution of cardiac stem cells in the different compartments of the heart and significant reduction in their number in adult heart. Cardiac stem cells are higher in the atrium than in the ventricle, suggesting the atria as the source of cardiac stem cell.


Assuntos
Antígenos Ly/metabolismo , Quimiotaxia , Proteínas de Membrana/metabolismo , Miocárdio/metabolismo , Proteínas Proto-Oncogênicas c-kit/metabolismo , Receptores CXCR4/metabolismo , Células-Tronco/metabolismo , Fatores Etários , Envelhecimento/metabolismo , Animais , Animais Recém-Nascidos , Biomarcadores/metabolismo , Western Blotting , Imunofluorescência , Átrios do Coração/citologia , Átrios do Coração/metabolismo , Ventrículos do Coração/citologia , Ventrículos do Coração/metabolismo , Imuno-Histoquímica , Masculino , Camundongos , Miocárdio/citologia , Reação em Cadeia da Polimerase em Tempo Real , Receptores CXCR4/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa
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