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1.
J Chromatogr A ; 1674: 463134, 2022 Jul 05.
Artículo en Inglés | MEDLINE | ID: mdl-35598538

RESUMEN

An enzyme-assisted extraction and an ion pairing reversed phase chromatography (IP-RPC) coupled to inductively coupled plasma tandem mass spectrometry (ICP-MS/MS) method were established for the simultaneous analysis of five selenium species in rice: selenious acid (SeIV), selenic acid (SeVI), selenocystine (SeCys2), methylselenocysteine (SeMeCys) and selenomethionine (SeMet). Optimal extraction efficiencies were obtained by using 15 mg protease XIV, water bath temperature of 45°C, pH of 6.5 and incubation of six hours. The total extracted Se species account for 92.5-109.3 % of the total Se in rice. The instrumental limits of detection for five selenium species ranged from 0.04 to 0.12 ng Se g-1. Spike recovery experiments performed on rice samples were in the range of 96.1-102.9 % for all analytes except for SeCys2 (66.1-77.1 %). A consistency of Se elemental response was observed among Se species analyzed in this study as the ratio of linear equation slope ranged from 1.020 to 1.036 (SeIV as reference) in rice matrix. The developed compound-independent calibration method was applied to detect Se species in eleven rice samples from China. Both selenium-enriched rice and regular rice were predominated with SeMet, accounting for ∼89.4 % of total selenium.


Asunto(s)
Oryza , Compuestos de Selenio , Selenio , Calibración , Cromatografía Líquida de Alta Presión/métodos , Cromatografía de Fase Inversa , Oryza/química , Selenio/análisis , Compuestos de Selenio/análisis , Compuestos de Selenio/química , Selenometionina/análisis , Espectrometría de Masas en Tándem
2.
Chem Biodivers ; 18(12): e2100436, 2021 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-34664781

RESUMEN

Three undescribed hydroxycinnamic acid amide dimers 1-3 were isolated and identified from an extract of Goji berry. Their molecular structures were elucidated based on NMR, MS, and IR spectra analysis. Compounds 1-3 were hydroxycinnamic acid amide dimers, which possess a cyclic butane moiety formed by head-to-head connection. These compounds at 25 µM showed the disaggregation potency on the copper-mediated Aß1-42 aggregation ranging from 27.3±3.2 to 31.0±2.9 %. This study provides new information on the antiaging traditional usage of goji berry.


Asunto(s)
Enfermedad de Alzheimer/tratamiento farmacológico , Amidas/farmacología , Ácidos Cumáricos/farmacología , Lycium/química , Fármacos Neuroprotectores/farmacología , Extractos Vegetales/farmacología , Enfermedad de Alzheimer/metabolismo , Amidas/química , Amidas/aislamiento & purificación , Péptidos beta-Amiloides/antagonistas & inhibidores , Péptidos beta-Amiloides/metabolismo , Ácidos Cumáricos/química , Ácidos Cumáricos/aislamiento & purificación , Relación Dosis-Respuesta a Droga , Humanos , Conformación Molecular , Fármacos Neuroprotectores/química , Fármacos Neuroprotectores/aislamiento & purificación , Fragmentos de Péptidos/antagonistas & inhibidores , Fragmentos de Péptidos/metabolismo , Extractos Vegetales/química , Extractos Vegetales/aislamiento & purificación , Agregado de Proteínas/efectos de los fármacos
3.
Zhonghua Er Ke Za Zhi ; 51(1): 47-51, 2013 Jan.
Artículo en Chino | MEDLINE | ID: mdl-23527931

RESUMEN

OBJECTIVE: Periodic paralysis (PP) is one type of skeletal muscle channelopathies characterized by episodic attacks of weakness. It is usually classified into hyperkalemic periodic paralysis (HyperPP), hypokalemic periodic paralysis (HypoPP) and normokalemic periodic paralysis (NormoPP) based on the blood potassium levels. HypoPP is the most common type of these three and NormoPP is the rarest one. The aim of this study was to explore the clinical and genetic features of a Chinese family with normokalemic periodic paralysis (NormoKPP). METHOD: Clinical features of all patients in the family with NormoKPP were analyzed. Genomic DNA was extracted from peripheral blood leukocytes and amplified with PCR. We screened all 24 exons of SCN4A gene and then sequence analysis was performed in those who showed heteroduplex as compared with unaffected controls. RESULT: (1) Fifteen members of the family were clinically diagnosed NormoKPP, and their common features are: onset within infacy, episodic attacks of weakness, the blood potassium levels were within normal ranges, high sodium diet or large dosage of normal saline could attenuate the symptom. One muscle biopsy was performed and examination of light and electronic microscopy showed occasionally degenerating myofibers. (2) Gene of 12 patients were screened and confirmed mutations of SCN4A genes--c. 2111 T > C/p. Thr704Met. CONCLUSION: The study further defined the clinical features of patients with NormoKPP, and molecular genetic analysis found SCN4A gene c. 2111 T > C/p. Thr704Met point mutation contributed to the disease. In line with the autosomal dominant inheritance laws, this family can be diagnosed with periodic paralysis, and be provided with genetic counseling. And the study may also help the clinical diagnosis, guide treatment and genetic counseling of this rare disease in China.


Asunto(s)
Canalopatías/genética , Mutación , Canal de Sodio Activado por Voltaje NAV1.4/genética , Parálisis Periódicas Familiares/genética , Secuencia de Aminoácidos , Canalopatías/diagnóstico , Canalopatías/patología , Niño , Análisis Mutacional de ADN , Femenino , Humanos , Masculino , Músculo Esquelético/patología , Músculo Esquelético/fisiopatología , Parálisis Periódicas Familiares/diagnóstico , Parálisis Periódicas Familiares/patología , Linaje , Reacción en Cadena de la Polimerasa , Potasio/sangre
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