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1.
Cell ; 175(7): 1756-1768.e17, 2018 12 13.
Artículo en Inglés | MEDLINE | ID: mdl-30550785

RESUMEN

Irisin is secreted by muscle, increases with exercise, and mediates certain favorable effects of physical activity. In particular, irisin has been shown to have beneficial effects in adipose tissues, brain, and bone. However, the skeletal response to exercise is less clear, and the receptor for irisin has not been identified. Here we show that irisin binds to proteins of the αV class of integrins, and biophysical studies identify interacting surfaces between irisin and αV/ß5 integrin. Chemical inhibition of the αV integrins blocks signaling and function by irisin in osteocytes and fat cells. Irisin increases both osteocytic survival and production of sclerostin, a local modulator of bone remodeling. Genetic ablation of FNDC5 (or irisin) completely blocks osteocytic osteolysis induced by ovariectomy, preventing bone loss and supporting an important role of irisin in skeletal remodeling. Identification of the irisin receptor should greatly facilitate our understanding of irisin's function in exercise and human health.


Asunto(s)
Adipocitos/metabolismo , Tejido Adiposo/metabolismo , Remodelación Ósea , Fibronectinas/metabolismo , Integrina alfaV/metabolismo , Osteocitos/metabolismo , Osteólisis/metabolismo , Adipocitos/patología , Animales , Línea Celular Tumoral , Femenino , Fibronectinas/genética , Células HEK293 , Humanos , Integrina alfaV/genética , Ratones , Osteocitos/patología , Osteólisis/genética
3.
Cell ; 157(6): 1279-1291, 2014 Jun 05.
Artículo en Inglés | MEDLINE | ID: mdl-24906147

RESUMEN

Exercise training benefits many organ systems and offers protection against metabolic disorders such as obesity and diabetes. Using the recently identified isoform of PGC1-α (PGC1-α4) as a discovery tool, we report the identification of meteorin-like (Metrnl), a circulating factor that is induced in muscle after exercise and in adipose tissue upon cold exposure. Increasing circulating levels of Metrnl stimulates energy expenditure and improves glucose tolerance and the expression of genes associated with beige fat thermogenesis and anti-inflammatory cytokines. Metrnl stimulates an eosinophil-dependent increase in IL-4 expression and promotes alternative activation of adipose tissue macrophages, which are required for the increased expression of the thermogenic and anti-inflammatory gene programs in fat. Importantly, blocking Metrnl actions in vivo significantly attenuates chronic cold-exposure-induced alternative macrophage activation and thermogenic gene responses. Thus, Metrnl links host-adaptive responses to the regulation of energy homeostasis and tissue inflammation and has therapeutic potential for metabolic and inflammatory diseases.


Asunto(s)
Tejido Adiposo Pardo/metabolismo , Factores de Crecimiento Nervioso/metabolismo , Animales , Glucosa/metabolismo , Interleucina-13/metabolismo , Interleucina-4/metabolismo , Hígado/metabolismo , Macrófagos/metabolismo , Ratones , Ratones Transgénicos , Músculo Esquelético/metabolismo , Factores de Crecimiento Nervioso/genética , Coactivador 1-alfa del Receptor Activado por Proliferadores de Peroxisomas gamma , Termogénesis , Factores de Transcripción/genética
4.
Cell ; 155(7): 1624-38, 2013 Dec 19.
Artículo en Inglés | MEDLINE | ID: mdl-24360282

RESUMEN

Ever since eukaryotes subsumed the bacterial ancestor of mitochondria, the nuclear and mitochondrial genomes have had to closely coordinate their activities, as each encode different subunits of the oxidative phosphorylation (OXPHOS) system. Mitochondrial dysfunction is a hallmark of aging, but its causes are debated. We show that, during aging, there is a specific loss of mitochondrial, but not nuclear, encoded OXPHOS subunits. We trace the cause to an alternate PGC-1α/ß-independent pathway of nuclear-mitochondrial communication that is induced by a decline in nuclear NAD(+) and the accumulation of HIF-1α under normoxic conditions, with parallels to Warburg reprogramming. Deleting SIRT1 accelerates this process, whereas raising NAD(+) levels in old mice restores mitochondrial function to that of a young mouse in a SIRT1-dependent manner. Thus, a pseudohypoxic state that disrupts PGC-1α/ß-independent nuclear-mitochondrial communication contributes to the decline in mitochondrial function with age, a process that is apparently reversible.


Asunto(s)
Envejecimiento/patología , Núcleo Celular/metabolismo , Mitocondrias/metabolismo , NAD/metabolismo , Fosforilación Oxidativa , Proteínas Quinasas Activadas por AMP/metabolismo , Animales , Subunidad alfa del Factor 1 Inducible por Hipoxia/metabolismo , Ratones , Músculo Esquelético/metabolismo , Coactivador 1-alfa del Receptor Activado por Proliferadores de Peroxisomas gamma , Especies Reactivas de Oxígeno/metabolismo , Sirtuina 1/metabolismo , Factores de Transcripción/metabolismo
5.
Proc Natl Acad Sci U S A ; 119(36): e2204835119, 2022 09 06.
Artículo en Inglés | MEDLINE | ID: mdl-36044549

RESUMEN

Physical activity provides clinical benefit in Parkinson's disease (PD). Irisin is an exercise-induced polypeptide secreted by skeletal muscle that crosses the blood-brain barrier and mediates certain effects of exercise. Here, we show that irisin prevents pathologic α-synuclein (α-syn)-induced neurodegeneration in the α-syn preformed fibril (PFF) mouse model of sporadic PD. Intravenous delivery of irisin via viral vectors following the stereotaxic intrastriatal injection of α-syn PFF cause a reduction in the formation of pathologic α-syn and prevented the loss of dopamine neurons and lowering of striatal dopamine. Irisin also substantially reduced the α-syn PFF-induced motor deficits as assessed behaviorally by the pole and grip strength test. Recombinant sustained irisin treatment of primary cortical neurons attenuated α-syn PFF toxicity by reducing the formation of phosphorylated serine 129 of α-syn and neuronal cell death. Tandem mass spectrometry and biochemical analysis revealed that irisin reduced pathologic α-syn by enhancing endolysosomal degradation of pathologic α-syn. Our findings highlight the potential for therapeutic disease modification of irisin in PD.


Asunto(s)
Cuerpo Estriado , Fibronectinas , Enfermedad de Parkinson , alfa-Sinucleína , Animales , Cuerpo Estriado/metabolismo , Modelos Animales de Enfermedad , Neuronas Dopaminérgicas/metabolismo , Fibronectinas/administración & dosificación , Fibronectinas/genética , Fibronectinas/metabolismo , Ratones , Enfermedad de Parkinson/metabolismo , Enfermedad de Parkinson/terapia , alfa-Sinucleína/genética , alfa-Sinucleína/metabolismo
6.
Proc Natl Acad Sci U S A ; 111(44): 15756-61, 2014 Nov 04.
Artículo en Inglés | MEDLINE | ID: mdl-25336758

RESUMEN

Peroxisome proliferator-activated receptor gamma coactivator 1-alpha 4 (PGC-1α4) is a protein isoform derived by alternative splicing of the PGC1α mRNA and has been shown to promote muscle hypertrophy. We show here that G protein-coupled receptor 56 (GPR56) is a transcriptional target of PGC-1α4 and is induced in humans by resistance exercise. Furthermore, the anabolic effects of PGC-1α4 in cultured murine muscle cells are dependent on GPR56 signaling, because knockdown of GPR56 attenuates PGC-1α4-induced muscle hypertrophy in vitro. Forced expression of GPR56 results in myotube hypertrophy through the expression of insulin-like growth factor 1, which is dependent on Gα12/13 signaling. A murine model of overload-induced muscle hypertrophy is associated with increased expression of both GPR56 and its ligand collagen type III, whereas genetic ablation of GPR56 expression attenuates overload-induced muscle hypertrophy and associated anabolic signaling. These data illustrate a signaling pathway through GPR56 which regulates muscle hypertrophy associated with resistance/loading-type exercise.


Asunto(s)
Regulación de la Expresión Génica/fisiología , Fibras Musculares Esqueléticas/metabolismo , Proteínas Musculares/metabolismo , Condicionamiento Físico Animal , Receptores Acoplados a Proteínas G/biosíntesis , Transducción de Señal/fisiología , Animales , Colágeno Tipo III/biosíntesis , Hipertrofia/metabolismo , Factor I del Crecimiento Similar a la Insulina/biosíntesis , Masculino , Ratones , Coactivador 1-alfa del Receptor Activado por Proliferadores de Peroxisomas gamma , Factores de Transcripción/metabolismo
7.
Am J Physiol Endocrinol Metab ; 306(2): E157-67, 2014 Jan 15.
Artículo en Inglés | MEDLINE | ID: mdl-24280126

RESUMEN

Diabetes risk increases significantly with age and correlates with lower oxidative capacity in muscle. Decreased expression of peroxisome proliferator-activated receptor-γ coactivator-1α (Pgc-1α) and target gene pathways involved in mitochondrial oxidative phosphorylation are associated with muscle insulin resistance, but a causative role has not been established. We sought to determine whether a decline in Pgc-1α and oxidative gene expression occurs during aging and potentiates the development of age-associated insulin resistance. Muscle-specific Pgc-1α knockout (MKO) mice and wild-type littermate controls were aged for 2 yr. Genetic signatures of skeletal muscle (microarray and mRNA expression) and metabolic profiles (glucose homeostasis, mitochondrial metabolism, body composition, lipids, and indirect calorimetry) of mice were compared at 3, 12, and 24 mo of age. Microarray and gene set enrichment analysis highlighted decreased function of the electron transport chain as characteristic of both aging muscle and loss of Pgc-1α expression. Despite significant reductions in oxidative gene expression and succinate dehydrogenase activity, young mice lacking Pgc-1α in muscle had lower fasting glucose and insulin. Consistent with loss of oxidative capacity during aging, Pgc-1α and Pgc-1ß expression were reduced in aged wild-type mouse muscle. Interestingly, the combination of age and loss of muscle Pgc-1α expression impaired glucose tolerance and led to increased fat mass, insulin resistance, and inflammatory markers in white adipose and liver tissues. Therefore, loss of Pgc-1α expression and decreased mitochondrial oxidative capacity contribute to worsening glucose tolerance and chronic systemic inflammation associated with aging.


Asunto(s)
Envejecimiento/fisiología , Intolerancia a la Glucosa/genética , Inflamación/genética , Músculo Esquelético/metabolismo , Factores de Transcripción/genética , Animales , Eliminación de Gen , Perfilación de la Expresión Génica , Intolerancia a la Glucosa/metabolismo , Inflamación/metabolismo , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Análisis por Micromatrices , Mitocondrias Musculares/metabolismo , Músculo Esquelético/patología , Fosforilación Oxidativa , Coactivador 1-alfa del Receptor Activado por Proliferadores de Peroxisomas gamma
8.
J Immunol ; 186(5): 3066-75, 2011 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-21263075

RESUMEN

Complement activation represents a crucial innate defense mechanism to invading microorganisms, but there is an eminent lack of understanding of the separate contribution of the different complement activation pathways to the host response during sepsis. We therefore investigated different innate host immune responses during cecal ligation and puncture (CLP)-induced sepsis in mice lacking either the alternative (fD(-/-)) or classical (C1q(-/-)) complement activation pathway. Both knockout mice strains showed a significantly reduced survival and increased organ dysfunction when compared with control mice. Surprisingly, fD(-/-) mice demonstrated a compensated bacterial clearance capacity as control mice at 6 h post CLP, whereas C1q(-/-) mice were already overwhelmed by bacterial growth at this time point. Interestingly, at 24 h after CLP, fD(-/-) mice failed to clear bacteria in a way comparable to control mice. However, both knockout mice strains showed compromised C3 cleavage during sepsis. Investigating potential causes for this discrepancy, we were able to demonstrate that despite normal bacterial clearance capacity early during the onset of sepsis, fD(-/-) mice displayed increased inflammatory cytokine generation and neutrophil recruitment into lungs and blood when compared with both control- and C1q(-/-) mice, indicating a potential loss of control over these immune responses. Further in vitro experiments revealed a strongly increased Nf-κB activation capacity in isolated neutrophils from fD(-/-) mice, supporting this hypothesis. Our results provide evidence for the new concept that the alternative complement activation pathway exerts a distinctly different contribution to the innate host response during sepsis when compared with the classical pathway.


Asunto(s)
Activación de Complemento/inmunología , Vía Alternativa del Complemento/inmunología , Vía Clásica del Complemento/inmunología , Choque Séptico/inmunología , Animales , Carga Bacteriana/inmunología , Ciego , Activación de Complemento/genética , Complemento C1q/deficiencia , Complemento C1q/genética , Factor D del Complemento/deficiencia , Factor D del Complemento/genética , Vía Alternativa del Complemento/genética , Vía Clásica del Complemento/genética , Inmunidad Innata/genética , Riñón/inmunología , Riñón/microbiología , Riñón/fisiopatología , Ligadura , Hígado/inmunología , Hígado/microbiología , Hígado/fisiopatología , Pulmón/inmunología , Pulmón/microbiología , Pulmón/fisiopatología , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Punciones , Choque Séptico/genética , Choque Séptico/mortalidad , Análisis de Supervivencia
9.
Neuron ; 111(22): 3619-3633.e8, 2023 11 15.
Artículo en Inglés | MEDLINE | ID: mdl-37689059

RESUMEN

A pathological hallmark of Alzheimer's disease (AD) is the deposition of amyloid-ß (Aß) protein in the brain. Physical exercise has been shown to reduce Aß burden in various AD mouse models, but the underlying mechanisms have not been elucidated. Irisin, an exercise-induced hormone, is the secreted form of fibronectin type-III-domain-containing 5 (FNDC5). Here, using a three-dimensional (3D) cell culture model of AD, we show that irisin significantly reduces Aß pathology by increasing astrocytic release of the Aß-degrading enzyme neprilysin (NEP). This is mediated by downregulation of ERK-STAT3 signaling. Finally, we show that integrin αV/ß5 acts as the irisin receptor on astrocytes required for irisin-induced release of astrocytic NEP, leading to clearance of Aß. Our findings reveal for the first time a cellular and molecular mechanism by which exercise-induced irisin attenuates Aß pathology, suggesting a new target pathway for therapies aimed at the prevention and treatment of AD.


Asunto(s)
Enfermedad de Alzheimer , Neprilisina , Ratones , Animales , Neprilisina/genética , Neprilisina/metabolismo , Fibronectinas/metabolismo , Regulación hacia Abajo , Astrocitos/metabolismo , Péptidos beta-Amiloides/metabolismo , Enfermedad de Alzheimer/metabolismo , Encéfalo/metabolismo
10.
Am J Physiol Endocrinol Metab ; 302(1): E108-16, 2012 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-21952038

RESUMEN

Epidemiological studies have indicated that obesity is associated with a higher risk for certain cancers caused by elevated levels of adipocyte-derived hormones. Leptin, one such hormone produced by adipocytes, is a major regulator of metabolism and has also been shown to modulate immunity. However, its role in regulating human natural killer (NK) cell functions is largely unknown. Here, we show that the leptin receptor (Ob-R) is expressed on 5% of NK cells isolated from blood donors, as measured with flow cytometry, and expression of the signal-transducing long form of the leptin receptor Ob-Rb was confirmed with quantitative PCR. The Ob-R+ subpopulation displayed a lower expression of CD16, a cell surface receptor mediating antibody-dependent activation. Short-term stimulation with leptin increased IFNγ secretion, CD69 activation marker expression, and cytotoxic lysis of tumor cells; this was mediated by an improved conjugate forming between NK cells and tumor cells as well as higher expression of tumor necrosis factor-related apoptosis-inducing ligand. On the contrary, long-term incubation with leptin significantly impaired these NK cell immune functions and decreased cell proliferation. In addition, phosphorylation of Jak-2 after leptin stimulation was reduced in peripheral mononuclear blood cells from obese humans compared with normal-weight controls. NK cells represent an immune cell population that is crucial for an effective antitumor response. Here, we show that long-term exposure to leptin, similarly to the situation in obese individuals with elevated serum leptin levels, significantly impairs integral parts of NK cell immune functions, possibly linking leptin to increased cancer susceptibility in obesity.


Asunto(s)
Citofagocitosis , Células Asesinas Naturales/inmunología , Leptina/metabolismo , Obesidad/inmunología , Receptores de Leptina/metabolismo , Células 3T3-L1 , Adipocitos/inmunología , Adipocitos/metabolismo , Animales , Apoptosis , Línea Celular Tumoral , Proliferación Celular , Células Cultivadas , Regulación de la Expresión Génica , Humanos , Interferón gamma/sangre , Interferón gamma/metabolismo , Células Asesinas Naturales/metabolismo , Leptina/sangre , Leptina/genética , Ratones , Neoplasias/complicaciones , Neoplasias/inmunología , Obesidad/sangre , Obesidad/complicaciones , Obesidad/metabolismo , Isoformas de Proteínas/química , Isoformas de Proteínas/genética , Isoformas de Proteínas/metabolismo , ARN Mensajero/metabolismo , Receptores de IgG/metabolismo , Receptores de Leptina/química , Receptores de Leptina/genética , Proteínas Recombinantes/metabolismo , Transducción de Señal , Ligando Inductor de Apoptosis Relacionado con TNF/metabolismo
11.
Commun Biol ; 5(1): 656, 2022 07 04.
Artículo en Inglés | MEDLINE | ID: mdl-35787681

RESUMEN

Both exercise-induced molecular mechanisms and physiological cardiac remodeling have been previously studied on a whole heart level. However, the regional microstructural tissue effects of these molecular mechanisms in the heart have yet to be spatially linked and further elucidated. We show in exercised mice that the expression of CITED4, a transcriptional co-regulator necessary for cardioprotection, is regionally heterogenous in the heart with preferential significant increases in the lateral wall compared with sedentary mice. Concordantly in this same region, the heart's local microstructural tissue helicity is also selectively increased in exercised mice. Quantification of CITED4 expression and microstructural tissue helicity reveals a significant correlation across both sedentary and exercise mouse cohorts. Furthermore, genetic deletion of CITED4 in the heart prohibits regional exercise-induced microstructural helicity remodeling. Taken together, CITED4 expression is necessary for exercise-induced regional remodeling of the heart's microstructural helicity revealing how a key molecular regulator of cardiac remodeling manifests into downstream local tissue-level changes.


Asunto(s)
Corazón , Factores de Transcripción/metabolismo , Remodelación Ventricular , Animales , Eliminación de Gen , Ratones
12.
J Neurosci Methods ; 358: 109179, 2021 07 01.
Artículo en Inglés | MEDLINE | ID: mdl-33819558

RESUMEN

BACKGROUND: Middle cerebral artery occlusion (MCAO) with 1 -h ischemia followed by reperfusion is a widely used stroke model in rodents that has significant limitations such as high mortality and severe neurological deficit hampering comprehensive neurobehavioral evaluation. The goal of this study was to establish a mouse model of 30-minute MCAO followed by 48 h of reperfusion and compare it with 1 -h MCAO followed by 24 h of reperfusion. NEW METHOD: Here we propose a modified MCAO model that is favorable for both neurobehavioral and infarct volume evaluation. The model includes shorter ischemic time (30 min) of MCAO followed by 48 h of reperfusion and use of standardized intraoperative partial and total reperfusion, which allows for the detailed evaluation of initial and total reperfusion by means of the monitoring of CBF by LDF. RESULTS AND COMPARISON WITH EXISTING METHOD: Intraoperative CBF parameters and infarct volume (1-h MCAO at 24 h: 69 ±â€¯9; 30-minute MCAO at 48 h: 65 ±â€¯14 mm3) did not significantly differ between groups. Neurological deficit was less severe in 30-minute MCAO group where mice also had significantly longer ambulatory distance and time, lower resting time, and higher vertical count on the OPF. The latency to fall in the rotarod test was significantly higher in 30-minute MCAO group. The mortality was higher after 1 -h MCAO. CONCLUSIONS: 30-minute MCAO followed by 48 h of reperfusion causes intraoperative ischemia, reperfusion and infarct volume comparable with 1 -h MCAO followed by 24 h of reperfusion but results in lower mortality with milder neurological deficit allowing for more extensive neurobehavioral evaluation.


Asunto(s)
Isquemia Encefálica , Accidente Cerebrovascular , Animales , Circulación Cerebrovascular , Modelos Animales de Enfermedad , Infarto de la Arteria Cerebral Media , Ratones , Reperfusión
13.
Front Aging Neurosci ; 13: 756537, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34992525

RESUMEN

Clinical and basic research suggests that exercise is a safe behavioral intervention and is effective for improving cognitive function in cerebrovascular diseases, including subcortical ischemic vascular dementia (SIVD). However, most of the basic research uses young animals to assess the effects of exercise, although SIVD is an age-related disease. In this study, therefore, we used middle-aged mice to examine how treadmill exercise changes the cognitive function of SIVD mice. As a mouse model of SIVD, prolonged cerebral hypoperfusion was induced in 8-month-old male C57BL/6J mice by bilateral common carotid artery stenosis. A week later, the mice were randomly divided into two groups: a group that received 6-week treadmill exercise and a sedentary group for observation. After subjecting the mice to multiple behavioral tests (Y-maze, novel object recognition, and Morris water maze tests), the treadmill exercise training was shown to only be effective in ameliorating cognitive decline in the Y-maze test. We previously demonstrated that the same regimen of treadmill exercise was effective in young hypoperfused-SIVD mice for all three cognitive tests. Therefore, our study may indicate that treadmill exercise during cerebral hypoperfusion has only limited effects on cognitive function in aging populations.

14.
Nat Metab ; 3(8): 1058-1070, 2021 08.
Artículo en Inglés | MEDLINE | ID: mdl-34417591

RESUMEN

Identifying secreted mediators that drive the cognitive benefits of exercise holds great promise for the treatment of cognitive decline in ageing or Alzheimer's disease (AD). Here, we show that irisin, the cleaved and circulating form of the exercise-induced membrane protein FNDC5, is sufficient to confer the benefits of exercise on cognitive function. Genetic deletion of Fndc5/irisin (global Fndc5 knock-out (KO) mice; F5KO) impairs cognitive function in exercise, ageing and AD. Diminished pattern separation in F5KO mice can be rescued by delivering irisin directly into the dentate gyrus, suggesting that irisin is the active moiety. In F5KO mice, adult-born neurons in the dentate gyrus are morphologically, transcriptionally and functionally abnormal. Importantly, elevation of circulating irisin levels by peripheral delivery of irisin via adeno-associated viral overexpression in the liver results in enrichment of central irisin and is sufficient to improve both the cognitive deficit and neuropathology in AD mouse models. Irisin is a crucial regulator of the cognitive benefits of exercise and is a potential therapeutic agent for treating cognitive disorders including AD.


Asunto(s)
Cognición , Fibronectinas/metabolismo , Hormonas/metabolismo , Condicionamiento Físico Animal , Animales , Conducta Animal , Trastornos del Conocimiento/etiología , Trastornos del Conocimiento/metabolismo , Trastornos del Conocimiento/psicología , Modelos Animales de Enfermedad , Fibronectinas/genética , Eliminación de Gen , Expresión Génica , Ratones , Ratones Noqueados , Fenotipo
15.
Brain Plast ; 5(2): 147-159, 2020 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-33282678

RESUMEN

BACKGROUND: Despite considerable research on exercise-induced neuroplasticity in the brain, a major ongoing challenge in translating findings from animal studies to humans is that clinical and preclinical settings employ very different techniques. OBJECTIVE: Here we aim to bridge this divide by using diffusion tensor imaging MRI (DTI), an advanced imaging technique commonly applied in human studies, in a longitudinal exercise study with mice. METHODS: Wild-type mice were exercised using voluntary free-wheel running, and MRI scans were at baseline and after four weeks and nine weeks of running. RESULTS: Both hippocampal volume and fractional anisotropy, a surrogate for microstructural directionality, significantly increased with exercise. In addition, exercise levels correlated with effect size. Histological analysis showed more PDGFRα+ oligodendrocyte precursor cells in the corpus callosum of running mice. CONCLUSIONS: These results provide compelling in vivo support for the concept that similar adaptive changes occur in the brains of mice and humans in response to exercise.

16.
Transl Stroke Res ; 11(3): 496-502, 2020 06.
Artículo en Inglés | MEDLINE | ID: mdl-31606888

RESUMEN

Clinical evidence suggests that patients with subcortical ischemic vascular dementia (SIVD) perform better at cognitive tests after exercise. However, the underlying mechanism for this effect is largely unknown. Here, we examined how treadmill exercise changes the cognitive function and white matter cellular pathology in a mouse model of SIVD. Prolonged cerebral hypoperfusion was induced in 2-month-old male C57BL/6J mice by bilateral common carotid artery stenosis. A week later, the mice were randomly divided into a group that received 6-week treadmill exercise and a sedentary group for observation. In multiple behavioral tests (Y-maze, novel object recognition, and Morris water maze tests), the treadmill exercise training was shown to ameliorate cognitive decline in the hypoperfused SIVD mice. In addition, immunohistological analyses confirmed that there was a larger population of oligodendrocyte precursor cells in the subventricular zone of exercised versus sedentary mice. Although further investigations are needed to confirm a causal link between these findings, our study establishes a model and cellular foundation for investigating the mechanisms through which exercise preserves cognitive function in SIVD.


Asunto(s)
Disfunción Cognitiva/patología , Disfunción Cognitiva/prevención & control , Demencia Vascular/patología , Células Precursoras de Oligodendrocitos/patología , Condicionamiento Físico Animal/psicología , Sustancia Blanca/patología , Animales , Disfunción Cognitiva/etiología , Demencia Vascular/complicaciones , Modelos Animales de Enfermedad , Masculino , Ratones Endogámicos C57BL
17.
Nutr Cancer ; 61(4): 484-91, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19838920

RESUMEN

Breast cancer continues to be a major cause of cancer deaths in women. Estrogen, which is also produced by the adipose tissue, is held responsible for the elevated risk of breast cancer in obese women. However, the adipose tissue secrets hormones and adipokines such as leptin and IGF-I and these substances could also contribute to an increased breast cancer risk for obese women. In this study, the impact of obesity on cell proliferation was investigated. The carcinogen 7, 12, dimethylbenz[a]anthracene (DMBA) was administered to normal weight and diet-induced obese female Sprague-Dawley rats. Cell proliferation was evaluated by immunohistological staining of BrdU-incorporation. In the mammary glands and inguinal lymphatic nodes of the obese rats, cell proliferation was significantly increased, indicating a significant influence of obesity on breast cancer. Effects of leptin, estrogen, and IGF-I on the proliferation of MCF-7 cells in vitro were assessed using an MTT assay. Cell culture experiments demonstrated a mitogenic role of these three mediators on cell proliferation. Our data demonstrate a stimulative effect of substances produced by the adipose tissue on breast cancer. Body weight specific cell proliferation suggests that obesity-related adipokines and mediators enhance cell proliferation and increase the risk for breast cancer.


Asunto(s)
Proliferación Celular , Estradiol/metabolismo , Factor I del Crecimiento Similar a la Insulina/metabolismo , Leptina/metabolismo , Neoplasias Mamarias Experimentales/patología , Obesidad/patología , 9,10-Dimetil-1,2-benzantraceno , Adenocarcinoma/patología , Análisis de Varianza , Animales , Peso Corporal , Neoplasias de la Mama/patología , Carcinógenos , Línea Celular Tumoral , Grasas de la Dieta/administración & dosificación , Modelos Animales de Enfermedad , Estradiol/administración & dosificación , Femenino , Ingle , Humanos , Inmunohistoquímica , Factor I del Crecimiento Similar a la Insulina/administración & dosificación , Leptina/administración & dosificación , Ganglios Linfáticos/metabolismo , Ganglios Linfáticos/patología , Metástasis Linfática , Neoplasias Mamarias Experimentales/inducido químicamente , Obesidad/metabolismo , Distribución Aleatoria , Ratas , Ratas Sprague-Dawley , Factores de Tiempo
18.
Prog Cardiovasc Dis ; 62(2): 172-178, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-30844383

RESUMEN

The beneficial effects of exercise on the brain are well known. However, the underlying molecular mechanisms are much less well understood. Interestingly, myokines, hormones secreted by muscle in response to exercise, gained attention as such beneficial mediators. In this review, we will focus on FNDC5 and its secreted form, the newly discovered myokine "irisin". We will discuss their role in the beneficial effects of exercise and its potential application in neurodegenerative disorders.


Asunto(s)
Encéfalo/metabolismo , Ejercicio Físico/fisiología , Fibronectinas , Enfermedades Neurodegenerativas , Cognición/fisiología , Fibronectinas/sangre , Fibronectinas/metabolismo , Humanos , Músculo Esquelético/metabolismo , Enfermedades Neurodegenerativas/metabolismo , Enfermedades Neurodegenerativas/prevención & control , Neuroprotección/fisiología
19.
Prog Cardiovasc Dis ; 62(2): 94-101, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-30802460

RESUMEN

To date there is no cure available for dementia, and the field calls for novel therapeutic targets. A rapidly growing body of literature suggests that regular endurance training and high cardiorespiratory fitness attenuate cognitive impairment and reduce dementia risk. Such benefits have recently been linked to systemic neurotrophic factors induced by exercise. These circulating biomolecules may cross the blood-brain barrier and potentially protect against neurodegenerative disorders such as Alzheimer's disease. Identifying exercise-induced systemic neurotrophic factors with beneficial effects on the brain may lead to novel molecular targets for maintaining cognitive function and preventing neurodegeneration. Here we review the recent literature on potential systemic mediators of neuroprotection induced by exercise. We focus on the body of translational research in the field, integrating knowledge from the molecular level, animal models, clinical and epidemiological studies. Taken together, the current literature provides initial evidence that exercise-induced, blood-borne biomolecules, such as BDNF and FNDC5/irisin, may be powerful agents mediating the benefits of exercise on cognitive function and may form the basis for new therapeutic strategies to better prevent and treat dementia.


Asunto(s)
Capacidad Cardiovascular/psicología , Demencia , Entrenamiento Aeróbico/métodos , Factores de Crecimiento Nervioso/fisiología , Neuroprotección/fisiología , Cognición/fisiología , Demencia/fisiopatología , Demencia/prevención & control , Ejercicio Físico/fisiología , Ejercicio Físico/psicología , Humanos
20.
Arthroscopy ; 23(8): 852-61, 2007 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-17681207

RESUMEN

PURPOSE: The objective of this study was to quantify the effect of different loading axes and of a valgus opening wedge high tibial osteotomy (HTO) on tibiofemoral cartilage pressure. METHODS: Six human knee specimens were tested with a load of 1000N in extension in a materials testing machine using a specially designed fixture. Pressure in the medial and lateral joint compartment was recorded using pressure-sensitive films. Different loading alignments (varus, straight, and valgus) were simulated. A medial opening wedge HTO was performed adjusting the loading axis to slight valgus. The first measurement was performed with intact medial collateral ligament (MCL). Then the MCL was dissected gradually and the cartilage pressure again analyzed. RESULTS: There was a significant correlation of the load distribution with the position of the loading axis. The medial compartment was predominantly loaded in the varus setting. The more lateral the loading line intersected the knee, the more pressure was redistributed laterally. The opening wedge HTO without the MCL release resulted in a significant increase of the pressure medially (P = .002). Only after a complete release of the MCL was a significant decrease of pressure medially observed after opening wedge HTO (P = .003). CONCLUSIONS: The position of the loading axis in the frontal plane has a strong effect on the tibiofemoral cartilage pressure distribution of the knee. The medial compartment is predominantly loaded in a varus knee; a neutral mechanical axis slightly loads the lateral more than the medial compartment. In valgus alignment, the main load runs through the lateral compartment. CLINICAL RELEVANCE: A medial opening wedge HTO maintains high medial compartment pressure despite the fact that the loading axis has been shifted into valgus. Only after complete release of the distal fibers of the MCL does the opening wedge HTO produce a decompression of the medial joint compartment.


Asunto(s)
Cartílago Articular/fisiopatología , Descompresión Quirúrgica/métodos , Articulación de la Rodilla/fisiopatología , Articulación de la Rodilla/cirugía , Ligamento Colateral Medial de la Rodilla/cirugía , Osteotomía/métodos , Tibia/cirugía , Anciano , Fenómenos Biomecánicos , Cadáver , Humanos , Masculino , Persona de Mediana Edad , Presión , Soporte de Peso
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