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1.
PLoS Biol ; 18(3): e3000688, 2020 03.
Artículo en Inglés | MEDLINE | ID: mdl-32218572

RESUMEN

Obesity leads to multiple health problems, including diabetes, fatty liver, and even cancer. Here, we report that urolithin A (UA), a gut-microflora-derived metabolite of pomegranate ellagitannins (ETs), prevents diet-induced obesity and metabolic dysfunctions in mice without causing adverse effects. UA treatment increases energy expenditure (EE) by enhancing thermogenesis in brown adipose tissue (BAT) and inducing browning of white adipose tissue (WAT). Mechanistically, UA-mediated increased thermogenesis is caused by an elevation of triiodothyronine (T3) levels in BAT and inguinal fat depots. This is also confirmed in UA-treated white and brown adipocytes. Consistent with this mechanism, UA loses its beneficial effects on activation of BAT, browning of white fat, body weight control, and glucose homeostasis when thyroid hormone (TH) production is blocked by its inhibitor, propylthiouracil (PTU). Conversely, administration of exogenous tetraiodothyronine (T4) to PTU-treated mice restores UA-induced activation of BAT and browning of white fat and its preventive role on high-fat diet (HFD)-induced weight gain. Together, these results suggest that UA is a potent antiobesity agent with potential for human clinical applications.


Asunto(s)
Tejido Adiposo Pardo/metabolismo , Fármacos Antiobesidad/uso terapéutico , Cumarinas/uso terapéutico , Obesidad/prevención & control , Adipocitos Marrones/efectos de los fármacos , Adipocitos Marrones/metabolismo , Adipocitos Blancos/efectos de los fármacos , Adipocitos Blancos/metabolismo , Tejido Adiposo Blanco/metabolismo , Animales , Dieta Alta en Grasa/efectos adversos , Metabolismo Energético/efectos de los fármacos , Hígado Graso/prevención & control , Intolerancia a la Glucosa/prevención & control , Resistencia a la Insulina , Reacción de Maillard , Masculino , Ratones , Ratones Endogámicos C57BL , Ratones Obesos , Obesidad/metabolismo , Propiltiouracilo/toxicidad , Termogénesis , Triyodotironina/antagonistas & inhibidores , Triyodotironina/metabolismo , Aumento de Peso/efectos de los fármacos
2.
Gerontology ; 69(3): 301-311, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-36273450

RESUMEN

INTRODUCTION: Gait variability is associated with frailty, dementia, and falls. Studies on the association of physiological and cognitive factors with gait variability have seldom included middle-aged adults, even though these adults already experienced loss of muscular strength and postural stability. This study aimed a) to examine and compare the trend of gait variability in men and women, across the adult age spectrum, and b) to identify and compare the contributions of physiological and cognitive factors to gait variability. METHODS: This was a population-based cross-sectional study at a single center. A random sample of 507 community-dwelling, well-functioning adults aged 21-90 years were studied. Cognition was measured using the Repeatable Battery for the Assessment of Neuropsychological Status. Physiological factors examined included visual contrast sensitivity (VCS), postural sway, hand reaction time, handgrip strength (HGS), knee extensor strength, and gait variability (coefficient of variation [CoV]). Multivariable regression models were used to examine the association between physiological and cognitive performance with gait CoV. RESULTS: Women walked with greater stride width CoV (p < 0.01) and double support time (DST) CoV (p < 0.01) than men. The stride width (p = 0.01) and DST variability (p = 0.03) were significantly higher in older men as compared to men in younger age-groups. Gait speed accounted for most of the gait CoV variances and attenuated the effects of physiological performance and/or attention cognition on most gait variability, except for CoV of DST and stride width. Adults with better VCS (ß = -0.19), faster hand reaction (ß = 0.12), and greater HGS (ß = -0.15) had lower variability in step length. CONCLUSION: The trends of stride width CoV and DST CoV across adult age spectrum were different between men and women. Greater stride width variability was partly attributed to greater HGS, possibly to better control lateral stability during walking. Physiological factors outweigh cognition in regulating most of the gait CoV in this study. They are modifiable and potential targets for healthy aging program.


Asunto(s)
Marcha , Fuerza de la Mano , Masculino , Humanos , Femenino , Persona de Mediana Edad , Anciano , Estudios Transversales , Marcha/fisiología , Caminata/fisiología , Cognición/fisiología
3.
J Biochem Mol Toxicol ; 36(9): e23120, 2022 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-35670589

RESUMEN

Bisphenol A (BPA), as a widely used plasticizer, is easily absorbed by animals and humans. It has certain toxic effects on various tissues, including liver, heart, kidney, testis, and ovary. The toxic effects of BPA on animal reproduction have aroused widespread concern, but its regulatory mechanism and antidote in female animals estrus cycle remain unclear. In this study, the results displayed that BPA destroyed the normal estrus cycle of mice through decreasing the levels of progesterone and estradiol. Furthermore, BPA significantly increased the levels of oxidative stress, autophagy, and apoptosis in ovaries and granulosa cells. Interestingly, we found that the natural antioxidant resveratrol rescued estrus disorder and impaired estradiol secretion, reduced the abnormal reactive oxygen species accumulation, autophagy, and apoptosis in BPA exposed ovarian tissues. Moreover, transmission electron microscopy showed that resveratrol reduced BPA-induced autophagic vesicles formation and flow cytometry showed that resveratrol inhibited the increase of apoptotic cells induced by BPA on granulosa cells. Therefore, the supplement of resveratrol could restore BPA-induced estrus disorder by protecting ovarian granulosa cells. Overall, resveratrol is a potential drug to alleviate BPA-induced estrous cycle disorders and ovarian damage.


Asunto(s)
Antioxidantes , Progesterona , Animales , Antídotos , Antioxidantes/metabolismo , Antioxidantes/farmacología , Apoptosis , Autofagia , Compuestos de Bencidrilo/toxicidad , Estradiol/farmacología , Estro , Femenino , Humanos , Masculino , Ratones , Estrés Oxidativo , Fenoles , Plastificantes/farmacología , Progesterona/farmacología , Especies Reactivas de Oxígeno , Resveratrol/farmacología
4.
Gerontology ; 67(4): 457-466, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33752216

RESUMEN

BACKGROUND: Studies indicate that physiological and cognitive aging are causally related and functionally interdependent. However, the relative contribution of physiological factors and cognition to dual-task costs (DTC) of gait parameters has not been well studied. In this cross-sectional study, we examined the trajectory of DTC of gait parameters across the adult age spectrum for both sexes and identified the contributions of physical and cognitive performance to DTC of gait. METHODS: A total of 492 community-dwelling adults, aged 21-90 years, were randomly recruited into the study. Participants were divided into 7 age groups, with 10-year age range for each group. Demographic data, height, body mass, education level, and information on comorbidities were recorded. Cognition was measured using the Repeatable Battery for the Assessment of Neuropsychological Status. Physical performance included visual contrast sensitivity, postural sway, hand reaction time, handgrip strength, knee extensor strength, and single-task and dual-task gait assessments. Stepwise multivariable regression was used to examine the association between physical and cognitive performance with DTC of gait parameters. RESULTS: Women were found to have significantly higher DTC of gait speed (p = 0.01), cadence (p < 0.01), and double support time (p < 0.01) than men. However, significant aging effect on DTC of gait speed (p = 0.01), step length (p = 0.01), and double support time (p = 0.01) was observed in men but not in women. Immediate memory was the primary determinant for the DTC of gait speed (ß = -0.25, p < 0.01), step length (ß = -0.22, p < 0.01), and cadence (ß = -0.15, p = 0.03) in men. Besides immediate memory, postural sway (ß = -0.13, p = 0.03) and hand reaction (ß = 0.14, p = 0.02) were also significantly associated with DTC of step length and cadence, respectively, in women. CONCLUSION: There were sex differences in the amplitude and trajectories of DTC of gait parameters. The DTC increased with age in men but not in women. Immediate memory was the primary determinant of DTC of gait parameters in men while immediate memory, postural sway, and reaction time were associated with DTC of gait in women. Future studies should investigate the clinical implications of the sex differences in the DTC with fall risks.


Asunto(s)
Marcha , Fuerza de la Mano , Adulto , Anciano , Anciano de 80 o más Años , Cognición , Estudios Transversales , Femenino , Humanos , Masculino , Persona de Mediana Edad , Velocidad al Caminar
5.
Int J Mol Sci ; 18(11)2017 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-29140299

RESUMEN

Suitable intramuscular fat (IMF) content improves porcine meat quality. The vital genes regulating IMF deposition are necessary for the selection and breeding of an IMF trait. However, the effect and mechanism of PDGFRα on IMF deposition are still unclear. Here, PDGFRα is moderately expressed in porcine longissimus dorsi muscle (LD), whereas it highly expressed in white adipose tissue (WAT). Moreover, PDGFRα-positive cells were located in the gaps of LD fibers which there were IMF adipocytes. Compared with 180-day-old and lean-type pigs, the levels of PDGFRα were much higher in one-day-old and fat-type pigs. Meanwhile the levels of PDGFRα gradually decreased during IMF preadipocyte differentiation. Furthermore, PDGFRα promoted adipogenic differentiation through activating Erk signaling pathway. Based on PDGFRα upstream regulation analysis, we found that the knockdown of FoxO1 repressed lipogenesis by downregulating PDGFRα, and miR-34a inhibited adipogenesis through targeting PDGFRα. Collectively, PDGFRα is a positive regulator of IMF deposition. Therefore, we suggest that PDGFRα is a possible target to improve meat quality.


Asunto(s)
Adipocitos/metabolismo , Adipogénesis/genética , Factores de Transcripción Forkhead/metabolismo , Sistema de Señalización de MAP Quinasas , MicroARNs/metabolismo , Músculos/citología , Receptor alfa de Factor de Crecimiento Derivado de Plaquetas/metabolismo , Adiposidad , Animales , Diferenciación Celular/genética , Perfilación de la Expresión Génica , Regulación de la Expresión Génica , Técnicas de Silenciamiento del Gen , Lipogénesis , MicroARNs/genética , Receptor alfa de Factor de Crecimiento Derivado de Plaquetas/genética , Sus scrofa , Factores de Tiempo
6.
Int J Mol Sci ; 18(10)2017 Oct 06.
Artículo en Inglés | MEDLINE | ID: mdl-28984821

RESUMEN

Intramuscular fat (IMF) content affects the tenderness, juiciness, and flavor of pork. An increasing number of studies are focusing on the functions of microRNAs (miRs) during porcine intramuscular preadipocyte development. Previous studies have proved that miR-425-5p was enriched in porcine skeletal muscles and played important roles in multiple physiological processes; however, its functions during intramuscular adipogenesis remain unclear. To explore the role of miR-425-5p in porcine intramuscular adipogenesis, miR-425-5p agomir and inhibitor were used to perform miR-425-5p overexpression and knockdown in intramuscular preadipocytes, respectively. Our results showed that the agomir of miR-425-5p dramatically inhibited intramuscular adipogenic differentiation and downregulated the expression levels of adipogenic marker genes PPARγ, FABP4, and FASN, whereas its inhibitor promoted adipogenesis. Interestingly, the agomir repressed proliferation of porcine intramuscular preadipocytes by downregulation of cyclin B and cyclin E. Furthermore, we demonstrated that miR-425-5p inhibited adipogenesis via targeting and repressing the translation of KLF13. Taken together, our findings identified that miR-425-5p is a novel inhibitor of porcine intramuscular adipogenesis possibly through targeting KLF13 and subsequently downregulating PPARγ.


Asunto(s)
Adipogénesis/fisiología , Adipocitos/metabolismo , Adipogénesis/genética , Animales , Diferenciación Celular/genética , Diferenciación Celular/fisiología , Proliferación Celular/genética , Proliferación Celular/fisiología , Acido Graso Sintasa Tipo I/genética , Acido Graso Sintasa Tipo I/metabolismo , Proteínas de Unión a Ácidos Grasos/genética , Proteínas de Unión a Ácidos Grasos/metabolismo , MicroARNs/genética , PPAR gamma/genética , PPAR gamma/metabolismo , Porcinos
7.
Cell Biol Int ; 39(5): 554-62, 2015 May.
Artículo en Inglés | MEDLINE | ID: mdl-25639984

RESUMEN

C1q/tumor necrosis factor-related protein 6 (CTRP6), an adipose-tissue secretory factor, plays an important role in inflammatory reaction and carcinogenesis. However, the biological function of CTRP6 in adipogenesis remains unclear. In this study, we examined the effects of CTRP6 knockdown on lipogenesis of 3T3-L1 adipocytes. The results showed that after 3T3-L1 adipocytes transfected with anti-CTRP6 small interfering RNA (siRNA), not only levels of secreted CTRP6 protein in the culture medium but also the expression level of the CTRP6 protein in the 3T3-L1 adipocytes was significantly reduced (P < 0.01). In addition, the number of lipid droplets in the adipocytes was reduced, as well as the OD values reflecting the fat content being significantly decreased (P < 0.01). Meanwhile the levels of adipogenic markers, including peroxisome proliferator activated receptor γ (PPARγ), CCAAT/enhancer-binding protein α (C/EBPα), CCAAT/enhancer-binding protein ß (C/EBPß) and adipocyte fatty acid-binding protein 4 (aP2), were decreased after treatment with anti-CTRP6 siRNA, whereas the expression of adipose triglyceride lipase (ATGL) and triacylglycerol hydrolase (TGH) were increased. Furthermore, after transfection, activity of phosphorylated Erk1/2 (p-Erk1/2) was inhibited in the early stage of differentiation, but in terminal differentiation of adipocytes, its activity was activated. Taken together, the results indicate that knockdown of CTRP6 can inhibit adipogenesis of 3T3-L1 adipocytes through lipogenic marker genes and Erk1/2 signaling pathway.


Asunto(s)
Adipogénesis/genética , Adipoquinas/genética , Lipólisis/genética , Sistema de Señalización de MAP Quinasas/genética , Factores de Necrosis Tumoral/genética , Células 3T3-L1 , Adipocitos/efectos de los fármacos , Adipocitos/fisiología , Adipogénesis/efectos de los fármacos , Adipoquinas/antagonistas & inhibidores , Adipoquinas/metabolismo , Animales , Biomarcadores/metabolismo , Regulación hacia Abajo/efectos de los fármacos , Regulación hacia Abajo/genética , Técnicas de Silenciamiento del Gen , Lipólisis/efectos de los fármacos , Sistema de Señalización de MAP Quinasas/efectos de los fármacos , Ratones , Ratones Endogámicos C57BL , ARN Interferente Pequeño/farmacología , Inhibidores del Factor de Necrosis Tumoral
8.
J Pharmacol Sci ; 127(1): 75-82, 2015 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-25704022

RESUMEN

3,3'-Diindolylmethane (DIM), a major acid-condensation product or metabolite of indole-3-carbinol which is found in cruciferous vegetables, has been shown to have anticancer, anti-inflammatory, and multiple immune stimulating effects. However, its function in bone metabolism is poorly understood. This study evaluated the effect of DIM on bone mass in mice under physiological and pathological conditions. Eight-week-old female mice received injections of a vehicle or 0.1mg/g of DIM, twice a week for four weeks. We found that DIM treatment significantly increased bone mass as assessed by dual-energy X-ray absorptiometry (DEXA) and micro-computed tomography (µCT). Further, Bone histomorphometric analyses showed that this treatment significantly reduced bone resorption parameters, but did not increase bone formation parameters. Furthermore, we use ovariectomized (OVX)-induced osteoporotic mouse model, and explore function of DIM in skeletal pathological processes. Bone phenotype analyses revealed that the administration of DIM in this study effectively prevented OVX-induced bone loss resulting from increased bone resorption. Our results demonstrated that DIM increased bone mass by suppressing osteoclastic bone resorption in bone metabolism under both physiological and pathological conditions. Accordingly, DIM may be of value in the treatment and the possible prevention of bone diseases characterized by bone loss, such as postmenopausal osteoporosis.


Asunto(s)
Densidad Ósea/efectos de los fármacos , Resorción Ósea/prevención & control , Indoles/farmacología , Indoles/uso terapéutico , Osteoporosis Posmenopáusica/tratamiento farmacológico , Animales , Densidad Ósea/fisiología , Huesos/anatomía & histología , Huesos/efectos de los fármacos , Huesos/fisiología , Femenino , Humanos , Ratones , Osteoclastos/efectos de los fármacos , Osteogénesis/efectos de los fármacos , Osteogénesis/fisiología , Osteoporosis Posmenopáusica/fisiopatología , Ovariectomía
9.
Exp Cell Res ; 319(5): 670-83, 2013 Mar 10.
Artículo en Inglés | MEDLINE | ID: mdl-23313858

RESUMEN

Adipose tissue is an important energy reservoir, and its over-development results in obesity in humans or body fat over-deposition in livestock. Loss of preadipocytes through apoptosis has been proposed as an alternative way to reduce adipose tissue mass. At present, the effect and regulatory mechanism of Sirt1 and camptothecin on porcine preadipocyte apoptosis are still largely unknown. Here, we evaluated whether Sirt1 had any role in the basal cellular and camptothecin-induced conditions in porcine preadipocytes. Flow cytometric analysis shows that viable cells decrease as well as early apoptotic and late apoptotic cells increase after knockdown of Sirt1 in porcine preadipocytes. Camptothecin induces porcine preadipocyte apoptosis in a dose-dependent manner, assessed with the Hoechst staining and western blot analysis. Interestingly, silencing of Sirt1 significantly enhances sensitivity of porcine preadipocytes to camptothecin, which may be due to upregulation of p53, acetylated p53, Bax, cleaved caspase-3 and downregulation of Bcl-2. On the contrary, under the Sirt1 overexpression condition viable cells' number significantly increases when challenging with camptothecin, and the protein levels of cleaved caspase-3, p53, acetylated p53 and Bax are downregulated. We also find that hyperacetylated p53 is the major effect of Sirt1 knockdown by overexpression of a mutated p53, whereas Sirt1 overexpression prevents camptothecin-induced apoptosis through p53 deacetylation in preadipocytes. Furthermore, repressing preadipocyte apoptosis of Sirt1 is mediated by direct interaction with cleaved caspase-3 using immunoprecipitation and inhibition of caspase-3 transcriptional activity using luciferase reporter assays.


Asunto(s)
Adipocitos/efectos de los fármacos , Antineoplásicos Fitogénicos/farmacología , Apoptosis/efectos de los fármacos , Camptotecina/farmacología , Caspasa 3/metabolismo , Sirtuina 1/metabolismo , Acetilación , Adipocitos/citología , Adipocitos/metabolismo , Animales , Western Blotting , Sinergismo Farmacológico , Citometría de Flujo , Lentivirus/genética , Luciferasas/metabolismo , ARN Interferente Pequeño/genética , Transducción de Señal/efectos de los fármacos , Sirtuina 1/antagonistas & inhibidores , Sirtuina 1/genética , Porcinos , Proteína p53 Supresora de Tumor/metabolismo
10.
Zygote ; 22(2): 175-81, 2014 May.
Artículo en Inglés | MEDLINE | ID: mdl-23194694

RESUMEN

Low-density lipoproteins (LDL) is known to protect boar sperm during freezing-thawing, but little information is known about the effects of LDL extracted from different avian egg yolks on post-thaw boar semen quality. The purpose of this study was to compare and analyze the effects of LDL at various concentrations and different species on boar sperm quality after freezing-thawing. LDL extracted from the yolk of hen egg, duck egg, quail egg, pigeon egg or ostrich egg was added to the extender at the concentrations of 0.06, 0.07, 0.08, 0.09 and 0.1 g/ml, respectively, and their effects on frozen-thawed boar sperm quality were assessed. According to all measured parameters, the results showed that sperm motility, acrosome integrity and plasma membrane integrity were 43.20%, 52.57% and 48.13%, respectively, after being frozen-thawed with 0.09 g/ml LDL extracted from pigeon egg yolk. All these quality parameters were higher than that of other groups (P < 0.05). In conclusion, our results confirmed that LDL extracted from pigeon egg yolk had the best cryoprotective effects on frozen-thawed boar sperm among all of the groups supplemented with LDL from five kinds of avian egg in extender. The optimum concentration of LDL extracted from pigeon egg in boar semen freezing extender was 0.09 g/ml.


Asunto(s)
Acrosoma/efectos de los fármacos , Yema de Huevo/química , Lipoproteínas LDL/farmacología , Motilidad Espermática/efectos de los fármacos , Espermatozoides/citología , Espermatozoides/fisiología , Animales , Células Cultivadas , Criopreservación , Congelación , Masculino , Porcinos
11.
Asian-Australas J Anim Sci ; 27(9): 1254-62, 2014 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-25178368

RESUMEN

Lymphoid enhancer binding factor 1 (LEF-1) is a member of the T-cell specific factor (TCF) family, which plays a key role in the development of breast endothelial cells. Moreover, LEF-1 gene has been identified as a candidate gene for teat number trait. In the present study, we detected two novel mutations (NC_010450.3:g. 99514A>G, 119846C>T) by DNA sequencing and polymerase chain reaction-restriction fragment length polymorphism in exon 4 and intron 9 of LEF-1 in Guanzhong Black, Hanjiang Black, Bamei and Large White pigs. Furthermore, we analyzed the association between the genetic variations with teat number trait in these breeds. The 99514A>G mutation showed an extremely significant statistical relevance between different genotypes and teat number trait in Guanzhong (p<0.001) and Large White (p = 0.002), and significant relevance in Hanjiang (p = 0.017); the 119846C>T mutation suggested significant association in Guanzhong Black pigs (p = 0.042) and Large White pigs (p = 0.003). The individuals with "AG" or "GG" genotype displayed more teat numbers than those with "AA"; the individuals with "TC" or "CC" genotype showed more teat numbers than those with "TT". Our findings suggested that the 99514A>G and 119846C>T mutations of LEF-1 affected porcine teat number trait and could be used in breeding strategies to accelerate porcine teat number trait improvement of indigenous pigs breeds through molecular marker assisted selection.

12.
Org Lett ; 26(22): 4690-4694, 2024 Jun 07.
Artículo en Inglés | MEDLINE | ID: mdl-38804574

RESUMEN

Zn-mediated generation of alkoxyl radicals from N-alkoxyphthalimides emerged as an efficient approach for forming diverse and valuable alkyl radicals through ß-scission or a hydrogen atom transfer process. The alkyl radical species can be further trapped by α-trifluoromethyl alkenes to construct a series of gem-difluoroalkenes.

13.
J Cell Biochem ; 114(11): 2500-12, 2013 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-23749759

RESUMEN

PU.1 is an Ets family transcription factor involved in the myelo-lymphoid differentiation. We have previously demonstrated that PU.1 is also expressed in the adipocyte lineage. However, the expression levels of PU.1 mRNA and protein in preadipocytes do not match the levels in mature adipocytes. PU.1 mRNA level is higher in preadipocytes, whereas its protein is expressed in the adipocytes but not in the preadipocytes. The underlying mechanism remains elusive. Here, we find that miR-155 knockdown or overexpression has no effect on the levels of PU.1 mRNA and protein in preadipocytes or adipocytes. MiR-155 regulates adipogenesis not through PU.1, but via C/EBPß which is another target of miR-155. We also checked the expression levels of PU.1 mRNA and antisense long non-coding RNA (AS lncRNA). Interestingly, compared with the level of PU.1 mRNA, the level of PU.1 AS lncRNA is much higher in preadipocytes, whereas it is opposite in the adipocytes. We further discover that PU.1 AS lncRNA binds to its mRNA forming an mRNA/AS lncRNA compound. The knockdown of PU.1 AS by siRNA inhibits adipogenesis and promotes PU.1 protein expression in both preadipocytes and adipocytes. Furthermore, the repression of PU.1 AS decreases the expression and secretion of adiponectin. We also find that the effect of retroviral-mediated PU.1 AS knockdown on adipogenesis is consistent with that of PU.1 AS knockdown by siRNA. Taken together, our results suggest that PU.1 AS lncRNA promotes adipogenesis through preventing PU.1 mRNA translation via binding to PU.1 mRNA to form mRNA/AS lncRNA duplex in preadipocytes.


Asunto(s)
Adipogénesis/fisiología , Proteínas Proto-Oncogénicas/metabolismo , ARN Mensajero/genética , Transactivadores/metabolismo , Células 3T3-L1 , Adipogénesis/genética , Adiponectina/genética , Adiponectina/metabolismo , Animales , Western Blotting , Diferenciación Celular , Células Cultivadas , Masculino , Ratones , Ratones Endogámicos C57BL , MicroARNs/genética , Proteínas Proto-Oncogénicas/genética , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Transactivadores/genética
14.
Mol Biol Rep ; 40(1): 129-39, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23065251

RESUMEN

The effects of Sirt1 gene and resveratrol on porcine preadipocyte apoptosis have not been characterized. Here, we investigated the apoptotic effects of Sirt1 and resveratrol on porcine preadipocytes, finding that resveratrol-induced preadipocyte apoptosis and up-regulated protein levels of Sirt1. Intriguingly, Sirt1 knockdown by RNAi also resulted in preadipocyte apoptosis. Combining resveratrol treatment and Sirt1 knockdown has an additive effect to promote porcine preadipocyte death. We found that resveratrol treatment alone dose-dependently increased caspase-3 cleavage, as well as the levels of Bax, p53 and acetylated-p53. Interestingly, the ratio of acetylated-p53 over p53 was declined owing to deacetylation by increased Sirt1 expression. Down-regulation of Sirt1 also elevated the cleavage of caspase-3 with a decrease of p53 acetylation. These data indicate that although resveratrol treatment up-regulates Sirt1 expression, it augments porcine preadipocyte apoptosis in a Sirt1-independent manner. The regulation of apoptosis by resveratrol and Sirt1 may provide a novel insight to control preadipocyte number through cellular apoptosis.


Asunto(s)
Antineoplásicos Fitogénicos/farmacología , Apoptosis/efectos de los fármacos , Apoptosis/genética , ARN Interferente Pequeño/genética , Transducción de Señal/efectos de los fármacos , Sirtuina 1/genética , Estilbenos/farmacología , Adipocitos , Animales , Caspasa 3/metabolismo , Células Cultivadas , Silenciador del Gen , Vectores Genéticos , Lentivirus/genética , ARN Interferente Pequeño/metabolismo , Resveratrol , Sirtuina 1/metabolismo , Porcinos
15.
Clin Interv Aging ; 15: 1753-1765, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-33061327

RESUMEN

BACKGROUND: Age-related slowing of gait has been reported to start as early as the fifth decade and accelerate beyond the seventh decade of life. A single cut-off for slow gait may not be appropriate for men and women of different ages. We aimed to report reference values for gait speed and spatiotemporal gait parameters of adult age groups in a South East Asian population. METHODS: A total of 507 community-dwelling adults, aged 21-90 years were recruited into the study through random sampling, filling quotas of 20-40 participants in each sex and age group (10-year age groups between 21 and 60 years; 5-year age groups beyond age 60 years). Demographic data, height, weight and information on comorbidities were recorded. Habitual gait speed and spatiotemporal parameters were measured, and the average of three trials was recorded using the GAITRite system. RESULTS: Gait speed peaked in their 40s for both men and women, but the trajectories differed slightly across age groups. Although similar for men in their 50s and 60s, gait speed was significantly slower among those aged 71 years and older. For women beyond 50 years old, gait slowed with age. After adjusting for height, women were found to walk significantly faster and with a longer step length than men. Women also walked with a significantly narrower stride width and less external rotation of the feet. The lowest quintile for gait speed in our study cohort was 0.9m/s, below the recommended cut-off of 1.0m/s. CONCLUSION: We established the reference values as well as the quintiles for gait speed and spatiotemporal gait parameters across adult age groups in a multi-ethnic Asian population. This contributes to a valuable database for gait assessment and evaluation of preventive or rehabilitative programs.


Asunto(s)
Marcha/fisiología , Navegación Espacial/fisiología , Adulto , Factores de Edad , Envejecimiento , Asia Sudoriental , Pesos y Medidas Corporales , Comorbilidad , Femenino , Humanos , Vida Independiente , Masculino , Persona de Mediana Edad , Valores de Referencia , Factores Socioeconómicos , Velocidad al Caminar/fisiología , Adulto Joven
16.
Theriogenology ; 130: 146-156, 2019 May.
Artículo en Inglés | MEDLINE | ID: mdl-30897429

RESUMEN

ε-polylysine (ε-PL) has potent antibacterial effects and is often used in the food industry. However, no studies have clarified the antibacterial effects of ε-PL during storage of boar semen. In this study, boar semen samples were diluted with BTS buffer supplemented with different concentrations (0, 0.04, 0.08, 0.16, 0.32, 0.64, and 1.28 g/L) of ε-PL and different combinations of ε-PL plus gentamicin during liquid storage at 17 °C for 5 days. Bacterial concentrations, bacterial community compositions, sperm quality parameters, and in vitro fertilization (IVF) were evaluated in order to analyze the antibacterial effects of these parameters during boar semen preservation. The results indicated that the optimum concentration of ε-PL was 0.16 g/L, which significantly improved sperm quality parameters, including sperm motility, plasma membrane integrity, mitochondrial membrane potential, and acrosome integrity, and changed bacterial proliferation and composition (P < 0.05). Moreover, compared with the control group, IVF parameters in the treatment groups also significantly improved (P < 0.05), although there were no significant differences among treatment groups. Interestingly, the antibacterial effect of 0.16 g/L ε-PL in combination with 0.125 g/L gentamycin was similar to that of 0.25 g/L gentamicin alone. In conclusion, our results showed that 0.16 g/L ε-PL is promising for the replacement of gentamicin to improve sperm quality parameters, sperm capacitation, and IVF by reducing bacterial concentrations and disrupting bacterial community composition.


Asunto(s)
Antiinfecciosos/farmacología , Polilisina/farmacología , Preservación de Semen/veterinaria , Semen/microbiología , Porcinos , Animales , Relación Dosis-Respuesta a Droga , Masculino , Preservación de Semen/métodos , Manejo de Especímenes , Motilidad Espermática/efectos de los fármacos , Factores de Tiempo
17.
Meat Sci ; 147: 116-126, 2019 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-30219363

RESUMEN

Intramuscular fat (IMF) plays an important role in pork quality. However, differences in the adipogenic regulation of IMF content between pig longissimus thoracis (LT) and semitendinosus (ST) remain unclear. Here, we found that IMF content of 180-day-old pig LT was greater than that of pig ST. Furthermore, lipid accumulation was earlier and greater in LT intramuscular preadipocytes (L-IMA) than in ST intramuscular preadipocytes (S-IMA) during differentiation. Interestingly, glucose consumption was lower in L-IMA than in S-IMA. Moreover, monounsaturated fatty acid content was greater in L-IMA than in S-IMA, whereas polyunsaturated fatty acid content was lower. Levels of the expression of key adipogenic genes were higher in L-IMA than S-IMA. Compared with S-IMA, adipogenic signals were more activated in L-IMA after adipogenic induction. In conclusion, IMF deposition differences between pig LT and ST were due to different glucose consumption, fatty acid composition, expression of key adipogenic genes and level of activating adipogenic signals between S-IMA and L-IMA during adipogenesis.


Asunto(s)
Adipocitos/fisiología , Adipogénesis/fisiología , Músculo Esquelético/fisiología , Sus scrofa/fisiología , Adipogénesis/genética , Tejido Adiposo/metabolismo , Animales , Diferenciación Celular , Células Cultivadas , Ácidos Grasos/metabolismo , Perfilación de la Expresión Génica , Glucosa/metabolismo , Músculo Esquelético/citología , Carne Roja
18.
Yi Chuan ; 30(2): 185-9, 2008 Feb.
Artículo en Zh | MEDLINE | ID: mdl-18244924

RESUMEN

Total RNA was extracted from soleus muscle, gastrocnemius muscle and extensor digitorum longus in hind leg of the 6-month-old male Bamei, Landrace, and the crossbred pigs (LandracexBamei). The primers of pig FoxO1 were designed and synthesized according to its homologous sequences of human, chimpanzee and rat. The optimal reaction condition and system of PCR was sieved to clone pig FoxO1 gene. Subsequently, the differential expression of FoxO1 mRNA was investigated in different types of skeletal muscle from Bamei, Landrace, and the crossbred pigs by SQ RT-PCR. The expression level of beta-actin was determined as a loading control. The results showed that the expression level of FoxO1 was different in various economic pig breeds and skeletal muscle types. The expression of FoxO1 in skeletal muscle of Bamei and the crossbred pigs was significantly higher than that of Landrace (Plt;0.01). Moreover, the expression of FoxO1 was lowest in soleus muscle, which mainly contains typemuscle fiber, and most abundant in extensor digitorum longus, which mainly contains typeb muscle fiber. This suggests that FoxO1 expression level has the negative correlation with the con-tent of typemuscle fiber. Skeletal muscle development of different economic types of pig breeds may be closely related to the regulation of FoxO1 gene.


Asunto(s)
Quimera/genética , Factores de Transcripción Forkhead/genética , Regulación de la Expresión Génica , Músculo Esquelético/metabolismo , Porcinos/genética , Actinas/genética , Animales , Factores de Transcripción Forkhead/metabolismo , Masculino , Fibras Musculares Esqueléticas/metabolismo , Músculo Esquelético/citología , ARN Mensajero/genética , ARN Mensajero/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Porcinos/clasificación , Porcinos/metabolismo
19.
Yi Chuan Xue Bao ; 33(6): 515-24, 2006 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-16800382

RESUMEN

H-FABP(Heart fatty acid-binding protein), a member of FABP family, plays an essential role in long-chain fatty acid uptake and metabolic homeostasis. Its role in pig intramuscular fat content remains poorly understood, especially in local pig breeds in western China. In this study, the genetic variations of 5'-upstream region and the second intron in porcine H-FABP gene were investigated by PCR-RFLP in 256 pigs including Duroc, Large White, Landrace, Neijiang, Rongchang, Bamei pig, Hanjiang Black, Hanzhong White, and the wild ones. The effect of H-FABP gene on the IMF content was analyzed by the least square method. Lipid droplet morphology and content in adipocytes cultured from pigs with different H-FABP genotypes, were studied by oil red O staining and a triglyceride assay kit. Results showed a Hinf I -RFLP in these eight pig breeds and wild pigs, among which Large white, Bamei pig, Hanjiang Black, Hanzhong White, and wild pigs presented with low polymorphism while the other breeds had intermediate polymorphism. There was no Hae III or Msp I -RFLPs in the four Chinese local pig breeds tested, but Duroc, Landrace, Large White, Hanzhong White and wild pig had polymorphism. Landrace, Large White and wild pigs had low levels of Hae III- and Msp I -RFLP, whereas others had intermediate polymorphism. H-FABP genotypes significantly affected the IMF content (P<0.05). The IMF content ordered by H-FABP genotypes were HH>Hh>hh, DD

Asunto(s)
Adipocitos/fisiología , Cuerpo Adiposo/fisiología , Proteínas de Unión a Ácidos Grasos/genética , Polimorfismo Genético , Sus scrofa/genética , Animales , Cruzamiento , China , Proteínas de Unión a Ácidos Grasos/metabolismo , Frecuencia de los Genes , Genotipo , Sus scrofa/metabolismo , Sus scrofa/fisiología
20.
Yi Chuan ; 28(11): 1462-6, 2006 Nov.
Artículo en Zh | MEDLINE | ID: mdl-17098719

RESUMEN

Sirt1 (Sirtuin type 1), a member of the conserved sirtuin family, is a NAD+ -dependent histone deacetylase. It is intimately related to cell proliferation, differentiation, apoptosis, and metabolism. Its role in senescence and metabolism has recently come to light. Sirt1 promotes fat mobilization in white adipocytes by repressing PPARgamma and inhibits myoblast differentiation by down-regulating muscle gene expression. Therefore, Sirt1 is not only an important longevity factor, but also may play a key modulatory role in animal fat deposition and muscle development.


Asunto(s)
Adipocitos/citología , Adipocitos/metabolismo , Células Musculares/citología , Células Musculares/metabolismo , Sirtuinas/metabolismo , Animales , Diferenciación Celular , Senescencia Celular , Humanos , Movilización Lipídica , Sirtuinas/química
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