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1.
Zhonghua Yi Xue Za Zhi ; 101(3): 205-211, 2021 Jan 19.
Artículo en Chino | MEDLINE | ID: mdl-33370867

RESUMEN

Objective: To observe the efficacy and safety of Kangbingdu granules (KBD) in the treatment of influenza. Methods: A multicenter, randomized, double-blind, double-dummy, and positive-drug parallel control trial was conducted in 27 Grade ⅢA hospitals in China and the subjects were randomly assigned to the KBD test group or the oseltamivir phosphate capsule control group at a ratio of 1∶1. 200 subjects were planned to be enrolled in each group. The experimental group was given KBD (18g each time, 3 times a day) and oseltamivir phosphate simulator orally, while the control group was given oseltamivir phosphate capsule (75 mg each time, twice a day) and KBD simulator orally for 5 days. The primary efficacy indicators included the remission time of major clinical symptoms and the time of complete defervescence. The secondary efficacy indicators included dosage of acetaminophen, the change of traditional Chinese medicine (TCM) syndrome score and the remission time of other important clinical symptoms. The efficacy of KBD in the test group and Oseltamivir phosphate control group were compared. Adverse events or adverse reactions were observed at the same time to evaluate the safety of KBD Granules. Results: A total of 393 subjects from 27 Grade ⅢA hospitals in China were enrolled. The experimental group included 195 subjects and 191 subjects (97.95%) completed the trial, While the control group included 198 subjects and 195 subjects (98.48%) completed the trial. There was no significant difference in the shedding rate and rejection rate between the two groups (P>0.05). In the Full Analysis Set (FAS), the mean age of the experimental group was (34.9±14.4) years old, with 83 males (42.78%). The mean age of the control group was (33.3±13.5) years old, with 78 males (39.59%). There were no statistically significant differences between the two groups in demographic data, physical examination, viral pathogen detection, total score of TCM syndromes and scores of each symptom at baseline (P>0.05). In the FAS, the remission time M (Q1, Q3) of major clinical symptoms was 3.0 (3.0, 4.0) days in the experimental group and 3.0 (3.0, 4.0) days in the control group, and the difference was not statistically significant (P>0.05). The time M (Q1, Q3) of complete defervescence was 34.0 (20.3, 49.0) hours in the experimental group and 36.5 (19.6, 48.8) hours in the control group, and the difference was not statistically significant (P>0.05). KBD granules had the same effect as Oseltamivir phosphate capsule (P>0.05) in terms of acetaminophen dosage, TCM syndrome effect and disappearance rate of most important clinical symptoms. Meanwhile, the disappearance rate of dizziness and chest distress on day 3 in the KBD granules group was better than that of oseltamivir phosphate capsule (P<0.05). Conclusion: KBD granules have the same efficacy as Oseltamivir Phosphate capsule in the treatment of influenza and the drug safety is good.


Asunto(s)
Antivirales , Gripe Humana , Preparaciones Farmacéuticas , Adulto , Antivirales/uso terapéutico , China , Método Doble Ciego , Humanos , Gripe Humana/tratamiento farmacológico , Masculino , Persona de Mediana Edad , Oseltamivir , Resultado del Tratamiento , Adulto Joven
2.
Phys Rev Lett ; 121(20): 207003, 2018 Nov 16.
Artículo en Inglés | MEDLINE | ID: mdl-30500229

RESUMEN

A general feature of unconventional superconductors is the existence of a superconducting dome in the phase diagram. Here we report a series of discrete superconducting phases in the simplest iron-based superconductor, FeSe thin flakes, by continuously tuning the carrier concentration through the intercalation of Li and Na ions with a solid ionic gating technique. Such discrete superconducting phases are robust against the substitution of 20% S for Se, but they are vulnerable to the substitution of 2% Cu for Fe, highlighting the importance of the iron site being intact. The superconducting phase diagram for FeSe derivatives is given, which is distinct from that of other unconventional superconductors.

3.
Zhonghua Er Ke Za Zhi ; 54(12): 927-930, 2016 Dec 02.
Artículo en Chino | MEDLINE | ID: mdl-27938594

RESUMEN

Objective: To investigate the incidence, clinical, biochemical and gene mutation characteristics of short chain acyl-coenzyme A dehydrogenase deficiency (SCADD). Method: From January, 2009 to October, 2015, a retrospective analysis of the urine organic acids and acyl-coenzyme A dehydrogenase (ACADS) gene mutation characteristics of patients diagnosed as SCADD by newborn screening using tandem mass spectrometry in Department of Genetics and Metabolism (Newborn screening Center of Zhejiang Province), Children's Hospital, Zhejiang University School of Medicine. Dietary guidance, life management and supplementation of L-carnitine were conducted, and growth and intelligence development were observed during follow-up among the SCADD patients. Result: A total of 1 430 024 neonates, seventeen cases were diagnosed with SCADD with an incidence of 1/84 117. All patients had no clinical symptoms, and intelligence and physical development were normal. Blood butylacyl-carnitine (C4) levels and the ratios increased, C4 0.713.14 µmol/L(reference value 0.03-0.48 µmol/L), C4/C2 0.07-0.23(reference value 0.01-0.04), C4/C3 0.65-2.04(reference value 0.05-0.39). Thirteen with increased urinary ethyl malonic acid (9.30-90.99 mg/g creatinine (reference value 0-6.20 mg/g creatinine )), one patient was accompanied by increased methyl succinic acid (12.33 mg/g creatinine(reference value 0-6.40 mg/g creatinine)), one subject with increased acetylglycine (3.52 mg/g creatinine(reference value 0-0.70 mg/g creatinine)). A total of 13 known mutations were detected in the ACADS gene, 1 homozygous mutation (c.1031A>G), the others are compound heterozygous mutations. One frameshift mutation (c.508_509delGC) and 12 missense mutations were detected. Common mutation were c. 1031A>G(35.3%), c. 164C>T(20.6%) and c. 991G>A(11.8%). SCADD in newborn screening program had no clinical symptoms and normal growth development after 8-42 months follow-up. Conclusion: Cases with SCADD had no clinical symptoms with an incidence of 1/84117. The c. 164C>T and c. 1031A>G may be the common mutations.


Asunto(s)
Acil-CoA Deshidrogenasa/deficiencia , Errores Innatos del Metabolismo de los Aminoácidos/genética , Errores Innatos del Metabolismo Lipídico/genética , Tamizaje Neonatal/métodos , Acil-CoA Deshidrogenasa/sangre , Acil-CoA Deshidrogenasa/genética , Errores Innatos del Metabolismo de los Aminoácidos/sangre , Errores Innatos del Metabolismo de los Aminoácidos/etnología , Carnitina/sangre , Niño , China/epidemiología , Homocigoto , Humanos , Incidencia , Recién Nacido , Errores Innatos del Metabolismo Lipídico/sangre , Errores Innatos del Metabolismo Lipídico/etnología , Masculino , Mutación , Estudios Retrospectivos , Espectrometría de Masas en Tándem
4.
Plant Dis ; 97(6): 848, 2013 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-30722622

RESUMEN

Snow lotus (Saussurea involucrata Kar. et Kir.) is a rare and beneficial traditional Chinese medicinal herb, growing in the mountains at heights of 4,000 to 4,300 m in the Tianshan and A'er Tai areas in China (2). Because of its very slow growth and exhaustive plant collection, the wild population has been listed as a protected plant by the Chinese government. In recent years, it has succeeded in artificial cultivation. Since 2010, severe powdery mildew infections were repeatedly observed on leaves of the plant of artificial cultivation in Urumqi, Xinjiang Autonomous Region of China. White superficial mycelia were present epiphyllously on both sides of the leaves as well as on young stems, forming a thin, irregular covering. Infections often cause leaf yellowing, reduced growth, and premature defoliation. On the basis of microscopic examination, the morphology of the fungus can be described as follows: Conidiophores emerged through leaf stomata, singly or branched, and form dimorphic conidia. Primary conidia are lanceolate with distinct apical points and 44 to 63 × 12 to 22 µm. Secondary conidia are ellipsoid to cylindrical and 41 to 59 × 12 to 20 µm. The germ tube has indistinct appressoria, is longer than conidia length, and arises from the subterminal region of conidia. These morphological features are typical of the anamorphic stage description of Leveillula taurica (Lév.) Arnaud (1). No ascomata were observed. Representative voucher specimens were deposited in the fungal herbarium of Xinjiang Agriculture University (HMACC 40731). To verify the identity of the fungus, the internal transcribed spacer (ITS) rDNA was amplified and sequenced, and the sequences were deposited as GenBank Accession No. KC292212. Comparison with sequences in the GenBank database revealed that the ITS sequence showed 99% homology with the sequence of L. taurica on Helianthus sp. (AB044378) and Gundelia tournefortii (AB667874). Thus, the pathogen was identified as L. taurica on the basis of the morphological characters and the ITS sequence. Pathogenicity was confirmed through inoculation by gently pressing diseased leaves onto leaves of healthy potted plants. Three inoculated plants were kept under a plastic humid chamber, whereas the same number of non-inoculated plants served as the control. The plants were placed under natural conditions (25 to 28°C) with 80 to 90% humidity. At 5 days after inoculation, typical symptoms of powdery mildew developed on the inoculated plants. No symptoms were seen on the control plants. To our knowledge, this is the first record of L. taurica on S. involucrata in the world. Because the plant is becoming widely cultivated in the Urumqi for use as a Chinese medicinal herb, the occurrence of powdery mildew poses a potential threat to the health of snow lotus. References: (1) U. Braun. A Monograph of the Erysiphales (Powdery Mildews). Nova Hedwigia Beiheft 89:1, 1987. (2) L. G. Fu. China Plant Red Data Book - Rare and Endangered Plants, vol 1. Chinese Science Press, Beijing, 1992.

5.
Brain Res Bull ; 55(2): 309-12, 2001 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-11470332

RESUMEN

Cretinism is a disease characterized by neurological defects associated with severe iodine deficiency. In a rat model of severe iodine deficiency, we investigated the distribution pattern of trace elements (iodine [I], selenium [Se], and bromine [Br] in brain tissue samples; potassium [K], calcium [Ca], manganese [Mn], iron [Fe], copper [Cu], zinc [Zn], rubidium [Rb], and lead [Pb] in erythrocytes) after supplementing the rats with I and/or Se. Neutron activation analysis, proton induced x-ray emission and x-ray fluorescence were used. The serum levels of total and free thyroxine (T4, FT4), and of total, free, and reverse triiodothyronine (T3, FT3, rT3, respectively) were assessed by radioimmunoassay. The results were statistically evaluated by one-way analysis of variance and bivariate correlation. The study indicated that the levels of T4, FT4, and rT3 increased in the serum of iodine-deficient rats supplemented with I or I + Se. In the same animals, we documented alterations of the content of Br in the brain, and of Zn, Mn, Cu, and Rb in erythrocytes, whereas the brain content of I and Se was unchanged. Thus, I and I + Se supplementation improves thyroid hormone metabolism but affects the content of selected trace elements in erythrocytes and of Br in the brain. The data stimulate further clarification of the role of trace elements in the central nervous system.


Asunto(s)
Encéfalo/metabolismo , Eritrocitos/metabolismo , Yodo/deficiencia , Yodo/farmacología , Selenio/farmacología , Hormonas Tiroideas/biosíntesis , Oligoelementos/sangre , Animales , Encéfalo/fisiopatología , Hipotiroidismo Congénito/metabolismo , Hipotiroidismo Congénito/fisiopatología , Modelos Animales de Enfermedad , Ratas , Ratas Wistar
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