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1.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 39(12): 1410-1414, 2022 Dec 10.
Article in Chinese | MEDLINE | ID: mdl-36453970

ABSTRACT

OBJECTIVE: To delineate a small supernumerary marker chromosome (sSMC) derived from chromosome 9 with combined cytogenetic and molecular methods. METHODS: For a pregnant woman with fetal ultrasound revealing left ventricular punctate hyperechoic echo, and a high risk for monosomy or partial deletion of chromosome 8, chromosome 9 trisomy, monosomy or partial deletion of chromosome 11 by non-invasive prenatal testing, and an abnormal MOM value revealed by mid-term serum screening, amniocentesis was performed for G banded chromosomal analysis and single nucleotide polymorphism array (SNP-array) assay. Peripheral blood samples of the woman and her spouse were also collected for the above tests. In addition, the woman was further subjected to C banding karyotyping analysis and fluorescence in situ hybridization (FISH) assay. RESULTS: The G-banded karyotype of the pregnant women was 47,XX,+mar[20]/46,XX[80], whilst C-banding analysis showed a deep stain in the middle of the sSMC (suggestive of centromeric region) and light stain at both ends (suggestive of euchromatism). FISH combined with DAPI banding analysis using 9pter/9qter probes revealed a karyotype of 47,XX,+mar.ish i(9)(9p10)(9p++)[2]/46,XX[18], whilst SNP-array has revealed a 68.1 Mb duplication in the 9p24.3q13 region. A database search has suggested the duplication to be likely pathogenic. No abnormality was found in her fetus and spouse by karyotyping and SNP-array analysis. CONCLUSION: Through combined cytogenetic and molecular genetic analysis, a sSMC derived from chromosome 9 was delineated, which has enabled genetic counseling for the couple.


Subject(s)
Chromosomes, Human, Pair 9 , Genetic Testing , Female , Humans , Pregnancy , Biomarkers , Chromosomes, Human, Pair 9/genetics , In Situ Hybridization, Fluorescence , Monosomy
2.
Brain Res Bull ; 142: 338-343, 2018 09.
Article in English | MEDLINE | ID: mdl-30172737

ABSTRACT

OBJECTIVES: The aim of this study was to investigate the expression of the mammalian Mg2+ transporter solute carrier family 41, member 1 (SLC41A1) in the striatum (STR) of a 6-hydroxydopamine (6-OHDA)-induced rat model, and its response to magnesium before the degenerative process commenced. MATERIALS AND METHODS: A unilateral parkinsonian rat model was induced by injection of 6-OHDA into the right medial forebrain bundle. Some rats received MgSO4 (90 mg/kg/day, intraperitoneal injection) for 7 or 14 days starting from the day following the 6-OHDA injection. The extent of dopamine depletion was determined by assessing the numbers of tyrosine hydroxylase (TH)-immunoreactive neurons in the substantia nigra pars compacta (SNc) and the apomorphine (APO)-induced rotational behavior. The mRNA and protein expression of SLC41A1 in STR were evaluated by real-time RT-PCR and western blotting respectively. RESULTS: APO-induced rotations increased significantly in the 6-OHDA lesioned rats compared with the controls, with MgSO4 administration significantly improving the behavior. The numbers of TH-immunoreactive neurons in SNc were significantly lower in the lesioned side than in the unlesioned side. Administration of MgSO4 for 14 days partly ameliorated the loss of TH-positive neurons. The mRNA and protein expressions of SLC41A1 in the lesioned STR were lower in the 6-OHDA lesioned rats than in the controls at both 7 and 14 days post-lesion induction. MgSO4 supplementation partly reversed the mRNA and protein expressions of SLC41A1. CONCLUSION: The regulation of SLC41A1 expression is responsive to magnesium in a 6-OHDA-induced rat model, wherein 6-OHDA may alter magnesium transport in the brain.


Subject(s)
Cation Transport Proteins/metabolism , Corpus Striatum/metabolism , Parkinsonian Disorders/metabolism , Animals , Antiparkinson Agents/pharmacology , Apomorphine/pharmacology , Corpus Striatum/drug effects , Dopamine Agonists/pharmacology , Dopaminergic Neurons/drug effects , Dopaminergic Neurons/metabolism , Gene Expression , Magnesium/metabolism , Magnesium Sulfate/pharmacology , Male , Movement/drug effects , Oxidopamine , Parkinsonian Disorders/drug therapy , RNA, Messenger/metabolism , Rats, Sprague-Dawley , Tyrosine 3-Monooxygenase/metabolism
3.
Biol Pharm Bull ; 26(7): 911-9, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12843610

ABSTRACT

Using a validated high-performance liquid chromatographic (HPLC) method, the pharmacokinetics of multi-constituents in Huangqin-Tang decoction were simultaneously studied both in the compound prescription and in each single herb decoction. At different intervals (0, 1, 2, 4, 8, 12, 24, 36, 48 h) after oral administration of the Huangqin-Tang decoction or a single herb decoction at a dose of 10 g x kg(-1), the concentrations of the constituents and their metabolites: baicalin (BG), wogonoside (WG), oroxylin-A-glucuronide (OG), baicalein (B), wogonin (W), oroxylin-A (O), paeoniflorin (PF), paeonimetabolin-I (PM-I), liquiritin (LG), liquiritigenin (L), glycyrrhizic acid (GL) and glycyrrhetinic acid (GA), were detected in the rat plasma. A new metabolite-3,5,7,2',6'-penta hydroxy flavone (visidulin I, VD-I) was found in rat plasma after oral administration of Huangqin-Tang or a single herb Huangqin decoction, and the quality was identified by HPLC and LC/MS. The pharmacokinetic parameters of the constituents and metabolites in the compound prescription and single herb decoctions were compared. All concentration-time curves corresponded to the one-compartment model. The constituents of BG, WG, OG, VD-I and LG had higher C(max) and AUC(0-lim) in the compound prescription than in the single herb decoction, and WG had significant difference. The constituents of PF, W and O only had a higher AUC(0-lim) in the compound prescription, and O had a significant difference. It was concluded, in brief, that there were obvious differences in the pharmacokinetic parameters of most constituents (especially constituent WG) between the compound prescription and single herb decoction. The constituents in the compound prescription had delayed absorption and elimination, a longer residence time in the body, and higher C(max) and AUC(0-lim), than those in the single herb decoction. Therefore, they were more efficient and durable, making them promising to exerting pharmacological effects in vivo.


Subject(s)
Drugs, Chinese Herbal/analysis , Drugs, Chinese Herbal/pharmacokinetics , Animals , Chromatography, High Pressure Liquid/methods , Male , Rats , Rats, Wistar
4.
Zhongguo Zhong Yao Za Zhi ; 28(3): 243-6, 2003 Mar.
Article in Chinese | MEDLINE | ID: mdl-15015311

ABSTRACT

OBJECTIVE: To compare the antibacterial effects of Huangqin-Tang with its metabolites produced by intestinal flora. METHOD: The antibacterial tests in vitro and in vivo were performed by agar dilution method and lethal protection of animal respectively. RESULT: Huangqin-Tang and its metabolites had antibacterial action on bacteria in vitro, however the antibacterial activity of metabolites of Huangqin-Tang on Salmomella, Dysentery bacillus and Proteus in vitro was stronger than Huangqin-Tang. The metabolites of Huangqin-Tang had protective effect on the animals infected by Staphylococcus aureus and Escherichia coli respectively from death, but Huangqin-Tang had no lethal protection action. CONCLUSION: The antibacterial effects of metabolites of Huangqin-Tang in vitro and in vivo are stronger than that of Huangqin-Tang, which shows that intestinal flora play a very important role in antibacterial effects of Huangqin-Tang.


Subject(s)
Anti-Bacterial Agents/pharmacology , Drugs, Chinese Herbal/pharmacology , Intestines/microbiology , Salmonella/drug effects , Staphylococcal Infections/drug therapy , Animals , Anti-Bacterial Agents/therapeutic use , Drugs, Chinese Herbal/therapeutic use , Escherichia coli Infections/drug therapy , Feces/microbiology , Male , Mice , Phytotherapy , Plants, Medicinal/chemistry , Proteus/drug effects , Shigella dysenteriae/drug effects
5.
Zhongguo Zhong Yao Za Zhi ; 28(9): 842-4, 2003 Sep.
Article in Chinese | MEDLINE | ID: mdl-15015378

ABSTRACT

OBJECTIVE: To compare the protective activity of liver injury induced by D-galactosamine (GalN) between Huangqin-Tang and their metabolites by human intestinal bacteria(HIB). METHOD: The liver injuries in conventional and pseudo-germfree mice were induced by GalN. After oral administration of Huangqin-Tang and their metabolites mixtures by HIB, the serum transaminase (ALT and AST) activities were detected. RESULT: In conventional mice, large and medium doses (20 and 10 g.kg-1) of Huangqin-Tang decoction significantly reduced the increase of serum ALT activity after 18 h GalN treatment. In pseudo-germfree mice, metabolites significantly reduced the ALT levels. However, Huangqing-Tang didn't affect the ALT levels in this kind of mice. To all of the animals, AST levels remained the same after oral Huangqin-tang or their metabolites. CONCLUSION: The metabolism by intestinal bacteria plays a role in pharmacological effects of constituents of Chinese herbal medicine. The metabolites of the constituents by intestinal bacteria were the real active components in vivo.


Subject(s)
Drugs, Chinese Herbal/pharmacology , Intestines/microbiology , Liver Diseases/metabolism , Protective Agents/pharmacology , Administration, Oral , Alanine Transaminase/blood , Animals , Aspartate Aminotransferases/blood , Bacteria/metabolism , Chemical and Drug Induced Liver Injury , Drugs, Chinese Herbal/isolation & purification , Drugs, Chinese Herbal/metabolism , Galactosamine , Male , Mice , Plants, Medicinal/chemistry , Protective Agents/metabolism
6.
Biol Pharm Bull ; 25(5): 558-63, 2002 May.
Article in English | MEDLINE | ID: mdl-12033492

ABSTRACT

In the course of studies on the metabolism of active components of Huangqin-Tang by human intestinal flora (HIF), Huangqin-Tang and all individual herbs in the decoctions were incubated with a human fecal suspension separately. By using a high-performance liquid chromatographic (HPLC) method which was previously established in our laboratory, the metabolites in both the compound prescription and all the single herb decoctions were identified and determined both qualitatively and quantitatively. We found that the constituents of Huangqin-Tang, incluing baicalin (baicalein 7-glucuronide; BG), wogonoside (wogoninoglucuronide; WG), oroxylin-A-glucuronide (OG) from Scutellariae Radix, paeoniflorin (PF) from Paeoniae Radix, liquiritin (liquiritigenin 4'-O-glucoside; LG), isoliquirtin (isoliquiritigenin 4-glucoside; ILG) and glycyrrhizic acid (GL) from Glycyhhizea Radix, were converted to their metabolites baicalein (B), wogonin (W), oroxylin-A (O), paeonimetabolin-I (PM-I), liquiritigenin (L), isoliquiritigenin (IL) and glycyrrhetinic acid (GA) by HIF. The contents of the metabolites in Huangqin-Tang and in each single herb decoction increased significantly after incubation with intestinal flora. Comparing with single herb decoctions, the transformation of BG, WG, OG, LG and ILG in the compound prescription was promoted, however, that of PF and GL was inhibited. All the results suggested that the glycosides of many medicinal herbs could be converted to aglycones by HIF, and the metabolism of most glycosides was improved in the compound prescription.


Subject(s)
Bacteria/metabolism , Drugs, Chinese Herbal/chemistry , Intestines/microbiology , Area Under Curve , Chromatography, High Pressure Liquid , Drug Stability , Feces/microbiology , Humans , Plants, Medicinal/chemistry
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