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1.
J Phys Ther Sci ; 28(6): 1669-72, 2016 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-27390391

RESUMO

[Purpose] The effect of duration of smartphone use on neck and shoulder muscle fatigue and pain was investigated in adults with forward head posture. [Subjects and Methods] Thirty-four adults with forward head posture were classified into groups by duration of smartphone use: 11 used a smartphone for 10 minutes each (group 1), 12 for 20 minutes each (group 2), and 11 for 30 minutes each (group 3). Fatigue cervical erector spinae and upper trapezius muscles was measured by electromyography, and pain before and after the experiment was evaluated using Visual Analog Scale (VAS) scores. [Results] There was a significant difference in the degree of fatigue in the left upper trapezius muscles in group 2 and left cervical erector spinae and bilateral upper trapeziuses group 3. There was a significant difference in fatigue in the left upper trapezius in groups 1 and 3. The VAS showed significant differences in all groups before and after the experiment and between groups 1 and 3. [Conclusion] Pain and fatigue worsened with longer smartphone use. This study provided data on the proper duration of smartphone use. Correct posture and breaks of at least 20 minutes are recommend when using smartphones.

2.
Biol Pharm Bull ; 27(7): 1106-11, 2004 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15256749

RESUMO

Yomogin is an active compound isolated from Artemisia princep, a traditional Oriental medicinal herb, which has been shown to inhibit tumor cell proliferation. In this study, we investigated the effects of yomogin on the cytotoxicity, induction of apoptosis, and putative pathways of its actions in human promyelocytic leukemia cells. Yomogin-treated HL-60 cells displayed several features of apoptosis, including DNA fragmentation, formation of DNA ladders in agarose gel electrophoresis, and externalization of annexin-V targeted phosphatidylserine residues. We observed that yomogin caused activation of caspase-8, caspase-9, and caspase-3. A general caspase inhibitor (z-VAD-fmk), caspase-8 inhibitor (z-IETD-fmk) and caspase-3 inhibitor (z-DEVD-fmk), almost completely suppressed the yomogin-induced DNA fragmentation. We further demonstrated that yomogin induced Bid cleavage, mitochondrial translocation of Bax from the cytosol, and cytochrome c release from mitochondria in a caspase-8-dependent manner. Taken together, our data indicate that yomogin is a potent inducer of apoptosis and facilitates its activity via caspase-8 activation, Bid cleavage, Bax translocation to mitochondria, and subsequent release of cytochrome c into the cytoplasm, providing a potential mechanism for the anticancer activity of yomogin.


Assuntos
Apoptose/efeitos dos fármacos , Sesquiterpenos/farmacologia , Apoptose/fisiologia , Artemisia , Proliferação de Células/efeitos dos fármacos , Células HL-60 , Humanos , Extratos Vegetais/química , Extratos Vegetais/isolamento & purificação , Extratos Vegetais/farmacologia , Sesquiterpenos/química , Sesquiterpenos/isolamento & purificação , Sesquiterpenos de Eudesmano
3.
J Ethnopharmacol ; 91(1): 1-6, 2004 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-15036459

RESUMO

Mucopolysaccharide (YMP) of yam (Dioscorea batatas Decne) was tested for immunomodulatory activity in vitro. We examined the effect of YMP on the viability, cell-mediated cytotoxicity and IFN-gamma secretion of splenic lymphocytes. The cytotoxic activity of mouse splenocyte against leukemia cell was increased in the presence of YMP (10 microg/ml). However, YMP (10 microg/ml) did not affect the viability of splenocytes. The production of IFN-gamma was significantly increased in the YMP treated splenocytes, suggesting that YMP may induce cell-mediated immune responses. The effects of YMP on phagocytic activity were studied in relation to uptaking capacity and lysosomal phosphatase activity of the mouse peritoneal macrophages in vitro. YMP (50 microg/ml) was found to increase uptaking capacity and lysosomal phosphatase activity of peritoneal macrophages. In addition, YMP (10-100 microg/ml) significantly increased the viability of peritoneal macrophages (P<0.05). The data obtained demonstrate that the YMP may be used as sources of immunoactive polysaccharides.


Assuntos
Glicosaminoglicanos/imunologia , Interferon gama/biossíntese , Leucemia/imunologia , Macrófagos Peritoneais/imunologia , Extratos Vegetais/imunologia , Baço/imunologia , Animais , Sobrevivência Celular/efeitos dos fármacos , Células Cultivadas , Dioscorea , Ensaio de Imunoadsorção Enzimática , Glicosaminoglicanos/isolamento & purificação , Glicosaminoglicanos/farmacologia , Macrófagos Peritoneais/metabolismo , Camundongos , Camundongos Endogâmicos BALB C , Baço/metabolismo
4.
Phytother Res ; 17(6): 627-32, 2003 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12820230

RESUMO

Recent evidence suggests that high concentrations of tumor necrosis factor-alpha (TNF-alpha) and nitric oxide (NO) are thought to increase the apoptosis in osteoblasts and bone resorption and may have important roles in the regulation of osteoblast and osteoclast metabolism, especially in rheumatoid arthritis. The present study was performed to investigate the effect of soybean ethanol extract on the scavenging properties using DPPH and the TNF-alpha and NO production of osteoblastic MC3T3-E1 cells. The soy extract and its fractions according to polarity displayed a strong free radical scavenger activity at 0.01 approximately 0.1g/L, except for aquous fraction which had no significant effect on the function of MC3T3-E1 cells (p < 0.05). TNF-alpha secretion by MC3T3-E1 cells was reduced significantly when stimulated with soy extract (0.05 g/L). Nitrite accumulation in culture medium and apoptosis of MC3T3-E1 cells were induced by the addition of 10(-10) M TNF-alpha, and inhibited by the simultaneous addition of soy extract (0.05g/L).


Assuntos
Sequestradores de Radicais Livres/farmacologia , Glycine max , Osteoblastos/efeitos dos fármacos , Estresse Oxidativo/efeitos dos fármacos , Fitoterapia , Extratos Vegetais/farmacologia , Fosfatase Alcalina/efeitos dos fármacos , Apoptose/efeitos dos fármacos , Artrite Reumatoide/tratamento farmacológico , Compostos de Bifenilo , Sequestradores de Radicais Livres/administração & dosagem , Sequestradores de Radicais Livres/uso terapêutico , Humanos , Óxido Nítrico/metabolismo , Picratos , Extratos Vegetais/administração & dosagem , Extratos Vegetais/uso terapêutico , Fator de Necrose Tumoral alfa/metabolismo
5.
Arch Pharm Res ; 25(6): 820-3, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12510832

RESUMO

The diethylether fraction from the leaves extract of Ligularia fischeri var. spiciformis (Compositae) was subjected to silica gel column chromatography and yielded three new terpenoids named spiciformisin a (1), spiciformisin b (3), and monocyclosqualene (2). Acyclic diterpenes, spiciformisin a and -b, were established as 3,7,11,15-tetramethyl-1,3(20)-hexadecadiene and 3,7,11,15-tetramethyl-1,3,6,10,14-hexadecapentaene (IUPAC), respectively. A monocyclic triterpene, monocyclosqualene, were determined as [3,8,12,16,16-pentamethyl-(3,7,11,15-hexadecatetraenyl)]-3,3,5-trimethyl-1-cyclohexene. The structures were determined on the basis of NMR and MS analysis. Spiciformicin b showed potent cytotoxicity (IC50, <9.7 microg/ml against HL-60) in contrast to no cytotoxicity (IC50, >200 microg/ml against HL-60 cells) of spiciformicin a with a cis-conjugated dienyl diexomethylene.


Assuntos
Asteraceae/toxicidade , Diterpenos/química , Diterpenos/toxicidade , Esqualeno/análogos & derivados , Esqualeno/química , Esqualeno/toxicidade , Diterpenos/isolamento & purificação , Células HL-60 , Humanos , Estrutura Molecular , Extratos Vegetais/química , Extratos Vegetais/isolamento & purificação , Extratos Vegetais/toxicidade , Folhas de Planta , Plantas Medicinais/química , Plantas Medicinais/toxicidade , Esqualeno/isolamento & purificação , Células U937
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