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The kidney is vulnerable to hypoxia-induced injury. One of the mechanisms underlying this phenomenon is cell apoptosis triggered by hypoxia-inducible factor-1-alpha (HIF-1α) activation. MicroRNA-210 (miR-210) is known to be induced by HIF-1α and can regulate various pathological processes, but its role in hypoxic kidney injury remains unclear. Here, in both kinds of rat systemic hypoxia and local kidney hypoxia models, we found miR-210 levels were upregulated significantly in injured kidney, especially in renal tubular cells. A similar increase was observed in hypoxia-treated human renal tubular HK-2 cells. We also verified that miR-210 can directly suppress HIF-1α expression by targeting the 3' untranslated region (UTR) of HIF-1α mRNA in HK-2 cells in severe hypoxia. Accordingly, miR-210 overexpression caused significant inhibition of the HIF-1α pathway and attenuated apoptosis caused by hypoxia, while miR-210 knockdown exerted the opposite effect. Taken together, our findings verify that miR-210 is involved in the molecular response in hypoxic kidney lesions in vivo and attenuates hypoxia-induced renal tubular cell apoptosis by targeting HIF-1α directly and suppressing HIF-1α pathway activation in vitro.
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Lesión Renal Aguda/genética , Subunidad alfa del Factor 1 Inducible por Hipoxia/genética , Hipoxia/genética , Riñón/citología , MicroARNs , Lesión Renal Aguda/metabolismo , Animales , Apoptosis , Línea Celular , Humanos , Hipoxia/metabolismo , Subunidad alfa del Factor 1 Inducible por Hipoxia/metabolismo , Riñón/metabolismo , Masculino , Ratas Sprague-DawleyRESUMEN
Glutathione S-transferases (GSTs) are multifunctional enzymes, and insect GSTs play a pivotal role in the metabolism of insecticides. Grapholita molesta is a worldwide pest that causes substantial economic losses to the fruit industry. However, it remains unclear how imidacloprid, a commonly used insecticide in orchards, is metabolized by G. molesta. In the present study, the synergist diethyl maleate (DEM), which inhibits the GST activity, exhibited a 22-fold synergistic ratio against imidacloprid. Two new GST genes, GmGSTD2 (OR096251) and GmGSTD3 (OR096252), were identified and successfully cloned, showing the highest expression in the Malpighian tubes. Knockdown of GmGSTD2 and GmGSTD3 by RNA interference, increased the mortality of G. molesta from 28% to 47% following imidacloprid treatment. Both recombinant GmGSTD2 and GmGSTD3 proteins exhibited 1-chloro-2,4-dinitrobenzene (CDNB) activity and could be inhibited by imidacloprid in vitro, with maximum inhibition was 60% for GmGSTD2 and 80% for GmGSTD3. These results suggested that GSTs participate in the metabolism of imidacloprid with GmGSTD2 and GmGSTD3 playing key roles in this process.
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Glutatión Transferasa , Insecticidas , Neonicotinoides , Nitrocompuestos , Neonicotinoides/metabolismo , Nitrocompuestos/metabolismo , Insecticidas/metabolismo , Glutatión Transferasa/metabolismo , Glutatión Transferasa/genética , Animales , Proteínas de Insectos/genética , Proteínas de Insectos/metabolismo , Imidazoles/metabolismoRESUMEN
Objectives: This research aimed to present a novel glasses-free distance random-dot stereotest system (GFDRDSS) using an eye-tracking method. Methods: A single-view autostereoscopic display applying a backlight control system combined with an eye-tracking method and the corresponding random-dot stereotest software were developed to create a GFDRDSS with a viewing distance of 5 m. The stereoacuity of 12 subjects with normal eye position was evaluated using the Randot Stereotest, Stereoscopic Test Charts vol. 3 (Yan's Charts), Distance Randot® Stereotest, and GFDRDSS. Results: The GFDRDSS could provide distinct and stable glasses-free stereoscopic perception even while the subject was moving their head. It could evaluate binocular disparities of 40-2,400 arcsec. Eleven subjects with normal near visual acuity had fine near stereovision (20-60 arcsec) using the Randot stereotest and Yan's Charts. Under refractive correction, 10 subjects had fine stereovision (≤60 arcsec) using the GFDRDSS at a distance of 5 m, and 9 had fine stereovision using the Distance Randot® Stereotest at 3 m. Other subjects described the 100 arcsec-level stereograms correctly. The results exhibited a concordance of stereoacuity within one degrade between the two distance stereotests. Conclusion: The proposed GFDRDSS can alternately project a couple of random-dot stereograms to the subjects' eyes and provide a glasses-free distance stereotest, which showed good concordance with the Distance Randot® Stereotest. More data are needed for statistical studies.
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Objective: To observe the effects of repeated horizontal -Gx acceleration exposure on cardiac structure in New Zealand rabbits. Methods: Twenty New Zealand rabbits were divided into 2 groups (n=10): control group and -Gx acceleration exposure group. The rabbits in -Gx acceleration exposure group were exposed to -3. 6 Gx with 2 s, at intervals of 5 min, repeated 20 times daily, with a total of 30 d; the control group didn't undergo the acceleration stress. After the last -Gx acceleration exposure, the animals were killed by intravenous injection of air, and two small pieces of myocardium were immediately dissected from the left ventricles for structure examination using optical microscope and transmission electron microscope. Results: There was no significant difference in the myocardial cell morphology and arrangement observed under the optical microscope between the -Gx acceleration exposure group and the control group; the myocardial fibers arranged in disorder, myocardial cell edema, nuclear membrane expansion, vascular endothelial basement membrane separation were observed in the -Gx acceleration exposure group under transmission electron microscope, compared with the control group. Conclusion: -Gx acceleration exposure can lead to ultrastructural damage in rabbit cardiac myocytes. It suggested that the more attention should be paid to the effect and protection of long-term horizontal -Gx acceleration exposure on the cardiac function of carrier fighter pilots.
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Aceleración , Miocardio/patología , Miocitos Cardíacos/patología , Animales , ConejosAsunto(s)
Angiotensina II/farmacología , Calcio/metabolismo , Células Endoteliales/fisiología , Potencial de la Membrana Mitocondrial/fisiología , Oxígeno/metabolismo , Hipoxia de la Célula/efectos de los fármacos , Hipoxia de la Célula/fisiología , Células Cultivadas , Células Endoteliales/efectos de los fármacos , Células Endoteliales/metabolismo , Humanos , Potencial de la Membrana Mitocondrial/efectos de los fármacosRESUMEN
OBJECTIVE: To investigate the correlation between atorvastatin inhibiting the expression level of matrix metalloproteinase 9 (MMP-9) and peroxisome proliferator activated receptor alpha (PPARalpha) signal channel in myocyte of aging rat. METHODS: Primary cultures of myocyte were got ten from aging rats. Myocyte were divided into control group, DMSO group, atorvastatin group, atorvastatin plus GW6471 group, which treated respectively by cell culture medium, DMSO, atorvastatin, atorvastatin plus GW6471. The expression of MMP-9 mRNA was evaluated by RT-PCR, and content of MMP-9 protein was detected by Western blot. RESULTS: (1) There was no difference between control group and DMSO group in level of MMP-9 mRNA and protein expression (P > 0.05); (2) The level of MMP-9 mRNA and MMP-9 protein expression in atorvastatin group were significantly lower than those in control group (P < 0.01); (3) Both level of MMP-9 mRNA and protein expression in atorvastatin plus GW6471 group were significantly higher than those in atorvastatin group (P < 0.05), but were still lower than those in control group (P < 0.05). CONCLUSION: Atorvastatin inhibit MMP-9 expression of aging myocytes by PPARalpha signal channel.
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Envejecimiento , Ácidos Heptanoicos/farmacología , Metaloproteinasa 9 de la Matriz/metabolismo , Células Musculares/efectos de los fármacos , Células Musculares/metabolismo , PPAR alfa/metabolismo , Pirroles/farmacología , Animales , Atorvastatina , Células Cultivadas , Oxazoles/farmacología , Ratas , Ratas Wistar , Transducción de Señal , Tirosina/análogos & derivados , Tirosina/farmacologíaRESUMEN
OBJECTIVE: To study EEG during simulated flight training, then to explore the situational character of mental fatigue of the pilots. METHODS: Fifty male pilots were randomly choice to be recorded their EEG including rest,flight and recovery phase. Then the band waves of EEG were analysed among the three phase. RESULTS: (1) During flight, the amplitude of alpha, beta, SMR, theta, gamma waves tended to increase. These changes seemed obviously in SMR, theta waves. (2) After flight, all the amplitude of the waves declined except for beta wave of the right lobe,and most of them were still higher than those before flight (P < 0.05); (3) The right brain showed a higher cerebration than the left, especially in theta wave. CONCLUSION: Mental fatigue is started during the flight training, and the right lobe has a severe mental fatigue than the left. After flight, mental fatigue showed a slow recovery.
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Medicina Aeroespacial , Electroencefalografía , Fatiga Mental/fisiopatología , Adulto , Humanos , Masculino , Educación y Entrenamiento FísicoRESUMEN
<p><b>OBJECTIVE</b>To obtain DNA aptamers with a highly specific affinity to HIV gp41 antigen using SELEX screening for detection of HIV.</p><p><b>METHODS</b>The specific DNA aptamers of HIV gp41 antigen were screened from the double-stranded DNA derived from the single-stranded DNA (ssDNA) library with agarose beads as the supportive medium and HIV gp41 antigen as the target molecule using SELEX technique and real-time quantitative PCR.</p><p><b>RESULTS</b>The secondary ssDNA library obtained after 6 rounds of screening was amplified by PCR to obtain dsDNA. The dsDNA was linked with pMD18-T vector, cloned and sequenced to obtain 4 aptamers of HIV gp41 antigen. The affinities of the 4 aptamers (K) all reached the nanomolar level. Among the 4 aptamers, the No.15 aptamer showed the strongest affinity. Specificity analysis of the aptamers revealed that all these 4 aptamers had specific affinity to HIV gp41 antigen with no affinity to other non-specific proteins.</p><p><b>CONCLUSION</b>We successfully obtained DNA aptamers with highly specific affinity to the HIV gp41 antigen from random single-stranded oligonucleotide library, and the obtained aptamers have the ability to antagonize HIV gp41 antigen.</p>
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Objective To explore the effects of gastric motility (GM) related hormones on the GM of uncomplicated obese binge eater, and to explore the effect of electroacupuncture on weight loss. MethodsThirty-two obese subjects with habit of immoderate eating and 20 healthy subjects with normal weight were enrolled. Venous blood samples were collected at 8:00p. m. after an overnight fast and collected again 30min after meal, then stored at -70oCerum ghrelin and GLP-1 were determined with ELISA method and motilin and leptin levels were determined by radioimmunoassay. 30min stimulation of electroacupuncture was performed daily on the obese persons for a week. On the eighth day, blood samples of the obese were collected again. Results Whether before or after meal, serum motilin and leptin levels were higher in obese group than in the control group (P0.05), and serum GLP-1 increased significantly in comparison with those before stimulation (P<0.01) in the obese group. ConclusionElectroacupuncture stimulation gives a certain therapeutic effect on loss of body weight in uncomplicated obese population with immoderate eating by affecting the endocrines related to GM.
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OBJECTIVE: In this study, we pretreated the mice ASMCs by dexamethasone (Dex) within 10 min, to test the peak of [Ca2+]i and phospho-PLCbeta (ser1105) in the cells by treated with Ach. METHODS: The peak of [Ca2+]i was measured by Fura-2/AM methods and the phospho-PLCbeta-ser1105 was by Western blot, and compared with dexamethasone pretreated groups. Glucocorticoid receptor antagonist RU486 and the protein synthesis inhibitor cycloheximide groups were settled in our study. RESULTS: Glucocorticoids (GCs) significantly decreased the resting values and peak of [Ca2+]i elevation and elevated the intracellular levels of phospho-PLCbeta (ser1105) in 10 min. Neither the RU486 nor cycloheximide could alter the inhibitory effects of glucocorticoids stated above. CONCLUSION: Our results demonstrate that glucocorticoids exert rapid inhibitory effects. The series of signal changes in this process that restrain the peak of [Ca2+]i may be responsible for the rapid nongenomic inhibitory effects of GCs by reducing the activity of PLC.
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Calcio/metabolismo , Glucocorticoides/farmacología , Músculo Liso/efectos de los fármacos , Músculo Liso/metabolismo , Fosfolipasa C beta/metabolismo , Animales , Células Cultivadas , Dexametasona/farmacología , Cobayas , Masculino , Mifepristona/farmacología , Ratas , Ratas Sprague-Dawley , Tráquea/citologíaRESUMEN
<p><b>BACKGROUND</b>Toll-like receptor-4 (TLR-4) is integrally involved in lipopolysaccharide (LPS) signaling and has a requisite role in the activation of nuclear factor-κB (NF-κB). The exact mechanisms that lend perfluorocarbon (PFC) liquids a cytoprotective effect have yet to be elucidated. Therefore we examined in an in vitro model the cytoprotective effect of PFC on LPS-stimulated alveolar epithelial cellls (AECs).</p><p><b>METHODS</b>AECs (A549 cells, human lung adenocarcinoma cell line) were divided into four groups: control, PFC, LPS and LPS + PFC (coculture group) groups. Intercellular adhesion molecule-1 (ICAM-1) was detected by ELISA, tumor necrosis factor-α (TNF-α) and interleukin-8 (IL-8) were detected by radioimmunological methods. The expression of TLR-4 mRNA and protein was detected by real time PCR and Western blotting, respectively. The activation of NF-κB was detected by Western blotting (proteins of I-κBa and NF-κB p65).</p><p><b>RESULTS</b>ICAM-1, TNF-α and IL-8 were significantly increased in LPS-stimulated AECs groups. The expression of TLR-4 mRNA and protein in LPS-stimulated groups was markedly increased. Meanwhile, NF-κB was activated as indicated by the significant degradation of IκB-α and the significant release of NF-κB P65 and its subsequent translocation into the nucleus. There were no significant effects of PFC alone on any of the factors studied while the coculture group showed significant downregulation of the secretion of ICAM-1, TNF-α and IL-8, the expression of TLR-4 mRNA and the activity of NF-κB.</p><p><b>CONCLUSIONS</b>Taken together, our results demonstrate that LPS can induce AEC-related inflammatory injury via the activation of TLR-4 and subsequent activation of NF-κB. PFC is able to protect AECs from LPS-induced inflammatory injury by blocking the initiation of the LPS signaling pathway, which is indicated by the significant decrease of TLR-4 expression and NF-κB activation.</p>
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Humanos , Western Blotting , Línea Celular Tumoral , Células Epiteliales , Alergia e Inmunología , Fluorocarburos , Farmacología , Inflamación , Alergia e Inmunología , Molécula 1 de Adhesión Intercelular , Genética , Metabolismo , Interleucina-8 , Genética , Metabolismo , Lipopolisacáridos , Farmacología , FN-kappa B , Genética , Metabolismo , Alveolos Pulmonares , Biología Celular , Reacción en Cadena en Tiempo Real de la Polimerasa , Receptor Toll-Like 4 , Genética , Metabolismo , Factor de Necrosis Tumoral alfa , Genética , MetabolismoRESUMEN
To investigate the chemical constituents of the roots of Aconitum taipaicum, silica gel column chromatography was used for the isolation and purification of compounds. A new norditerpenoid alkaloid, isodelelatine (1), along with five known alkaloids, atisine (2), delfissinol (3), liangshanine (4), hypaconitine (5) and delelatine (6) were isolated and identified. The structure of the new compound was elucidated on the basis of spectral data.
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Aconitina , Química , Aconitum , Química , Alcaloides , Química , Diterpenos , Química , Estructura Molecular , Raíces de Plantas , Química , Plantas Medicinales , QuímicaRESUMEN
<p><b>OBJECTIVE</b>To study the chemical constituents from Delphinium honanense var. piliteram.</p><p><b>METHOD</b>The constituents were isolated and purified with chromatographic methods, identified by NMR, MS and IR.</p><p><b>RESULT</b>Six compounds were isolated and elucidated as siwanine E (1), isoatisine (2), 12-epi-napelline (3), acontine (4), ajadelphinine (5) and beta-sitosterol (6).</p><p><b>CONCLUSION</b>Compounds 1-6 are all isolated from the plant for the first time.</p>
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Delphinium , Química , Medicamentos Herbarios Chinos , Química , Plantas Medicinales , QuímicaRESUMEN
<p><b>OBJECTIVE</b>To evaluate the effects of Qingre Liqi Granule (QLG) on clinical therapeutic efficacy, electrogastrogram (EGG) and gastric emptying in patients with functional dyspepsia (FD).</p><p><b>METHODS</b>Thirty-two FD patients of dyskinesis type enrolled were treated with QLG by oral taking for 6 days. Scoring on 8 kinds of symptoms, including abdominal distension, abdominal pain, morning gastric fullness, belching, regurgitation, nausea, vomiting, and anorexia, fasting EGG and the gastric emptying determination were performed using single photon emission computed tomography (SPECT) before and after treatment.</p><p><b>RESULTS</b>The total and individual scores of clinical symptoms, expect that of vomiting, significantly decreased after treatment (P < 0.05), and the percentage of patients with tachygastria and bradygastria significantly decreased (P<0.01) at the same time. EGG after treatment showed significantly elevated rates of normal slow wave dominant power, and nearly normalized dominant frequency. An increased gastric emptying rate at different phases after 75 min (P < 0.05), and significantly shortened gastric emptying half-time (P < 0.01) were shown meanwhile in gastric emptying detection. The improvement of symptom score and gastric emptying half-time showed significant positive linear correlation (r =0.8929, P < 0.01).</p><p><b>CONCLUSION</b>QLG can improve symptoms of FD patients by regulating the rhythm and power of gastric electro-wave, increasing gastric motility and enhancing gastric emptying function.</p>
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Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Método Doble Ciego , Medicamentos Herbarios Chinos , Usos Terapéuticos , Dispepsia , Quimioterapia , Electromiografía , Vaciamiento Gástrico , Complejo Mioeléctrico Migratorio , Fitoterapia , Resultado del TratamientoRESUMEN
<p><b>OBJECTIVE</b>To separate and identify the constituents from Clerodendron fragrans.</p><p><b>METHOD</b>The constituents were isolated and purified with chromatographic methods, identified by NMR, MS, IR.</p><p><b>RESULT</b>Beta-sitosterol (1), clerosterol (2), daucosterol (3), caffeic acid (4), kaempferol (5), 5,4'-dihydroxy-kaempferol-7-O-beta-rutinoside (6), acteoside (7) and leucoseceptoside A (8), were isolated and identified.</p><p><b>CONCLUSION</b>Compound 7 and 8 were identified for the first time from Clerodendron fragrans.</p>
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Clerodendrum , Química , Glucósidos , Química , Glicósidos , Química , Fenoles , Química , Hojas de la Planta , Química , Plantas Medicinales , Química , Sitoesteroles , QuímicaRESUMEN
<p><b>OBJECTIVE</b>To study the constituents from Clerodendrum bungei.</p><p><b>METHOD</b>The constituents were isolated and purified with chromatographic methods, and identified by NMR, MS and IR.</p><p><b>RESULT</b>Five compounds were isolated, beta-sitosterol (1), taraxerol (2), glochidone (3), glochidonol (4), glochidiol (5).</p><p><b>CONCLUSION</b>Compounds (3), (4) and (5) were isolated for the first time from C. bungei.</p>