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  1. Article ; Online: Effect of Grape Seed Procyanidins Combined with Allicin on Lipid Levels in Hyperlipidemic Rats.

    Sun, Liu-Qing / Zhu, Chao-Feng / He, Jiang-Qin

    Studies in health technology and informatics

    2023  Volume 308, Page(s) 130–136

    Abstract: Objectives: To study the effects of grape seed proanthocyanidins (GSP) combined with allicin on serum lipids level and vascular damage in a rat model of hyperlipidemia.: Materials and methods: SD rats(male, 170-220 gn= 40) were randomized into five ... ...

    Abstract Objectives: To study the effects of grape seed proanthocyanidins (GSP) combined with allicin on serum lipids level and vascular damage in a rat model of hyperlipidemia.
    Materials and methods: SD rats(male, 170-220 gn= 40) were randomized into five groups (n = 8/group): modelhigh fat and cholesterol diet; controlnormal diet; model+low-dose (GSP+allicin )(GSP 45mg/kg, allicin 30mg/kg, orally); model+high-dose (GSP+allicin) (GSP180mg/kg, allicin 90mg/kg, orally) and positive control (model+simvastatin (4 mg/kg)). Normal control group was fed conventionally, and remaining four groups were fed high cholesterol and fat food to replicate the high fat model. After 9 weeks, the normal control group continued to receive regular feeding, while the other groups continued to receive high-fat feeding. At the same time, model and normal control groups were given equal volume of physiological saline by gavage, and the other treatment groups began to receive corresponding drugs by gavage once a day. After 4 weeks, serum levels of total cholesterol (TC), triglyceride (TG), low density lipoprotein cholesterol (LDL-C) as well as high-density lipoprotein cholesterol (HDL-C) in rats were determined. And the body weight of rat, total antioxidant capacity (T-AOC), superoxide dismutase (SOD) and malondialdehyde (MDA)in serum were identified. The level of endothelin-1(ET-1) was quantitative analysis by ELISA assay.
    Results: In comparison to normal controls, the model group displayed a marked rise in body weight, an increment in serum concentrations of LDL-C, TG and TC, as well as a decline in HDL (P<0.01), demonstrating successful model replication; All doses of GSP in combination with allicin resulted in a reduction in TG, LDL-C, and TC and an enhancement in HDL-C in contrast to the model control (all P<0.05). High-dose (GSP+allicin ) decreased MDA, and increased T-AOC and SOD activity(all P<0.01). All doses of GSP combined with allicin decreased ET-1 (all P<0.05). In addition, the protective effect of GSP combined with allicin was dose-dependent.
    Conclusions: Studies have shown that GSP combined with allicin can significantly improve blood lipids in hyperlipidemic rats, and this mechanism may be related to antioxidants and reduced endothelial damage.
    MeSH term(s) Rats ; Male ; Animals ; Vitis ; Rats, Sprague-Dawley ; Proanthocyanidins/pharmacology ; Proanthocyanidins/therapeutic use ; Cholesterol, LDL/therapeutic use ; Lipids ; Hyperlipidemias/drug therapy ; Triglycerides/therapeutic use ; Antioxidants/pharmacology ; Antioxidants/therapeutic use ; Cholesterol/therapeutic use ; Superoxide Dismutase/therapeutic use ; Cholesterol, HDL/therapeutic use ; Body Weight ; Seeds
    Chemical Substances allicin (3C39BY17Y6) ; Proanthocyanidins ; Cholesterol, LDL ; Lipids ; Triglycerides ; Antioxidants ; Cholesterol (97C5T2UQ7J) ; Superoxide Dismutase (EC 1.15.1.1) ; Cholesterol, HDL
    Language English
    Publishing date 2023-11-26
    Publishing country Netherlands
    Document type Journal Article
    ISSN 1879-8365
    ISSN (online) 1879-8365
    DOI 10.3233/SHTI230833
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Limb-girdle muscular dystrophy due to GMPPB mutations: A case report and comprehensive literature review.

    Sun, LiuQing / Shen, DingGuo / Xiong, Ting / Zhou, Zhibin / Lu, Xianghui / Cui, Fang

    Bosnian journal of basic medical sciences

    2020  Volume 20, Issue 2, Page(s) 275–280

    Abstract: Mutations in the guanosine diphosphate mannose (GDP-mannose) pyrophosphorylase B (GMPPB) gene are rare. To date, 72 cases with GMPPB gene mutations have been reported. Herein, we reported a case of a 29-year-old Chinese male presenting with limb-girdle ... ...

    Abstract Mutations in the guanosine diphosphate mannose (GDP-mannose) pyrophosphorylase B (GMPPB) gene are rare. To date, 72 cases with GMPPB gene mutations have been reported. Herein, we reported a case of a 29-year-old Chinese male presenting with limb-girdle muscular dystrophy (LGMD) who was found to have two heterozygous GMPPB mutations. The patient had a progressive limb weakness for 19 years. His parents and elder brother were healthy. On examination he had a waddling gait and absent tendon reflexes in all four limbs. Electromyography showed myogenic damage. Muscle magnetic resonance imaging (MRI) showed fatty degeneration in the bilateral medial thigh muscles. High-throughput gene panel sequencing revealed that the patient carried compound heterozygous mutations in the GMPPB gene, c.553C>T (p.R185C, maternal inheritance) and c.346C>T (p.P116S, paternal inheritance). This case provides additional information regarding the phenotypic spectrum of GMPPB mutations in the Chinese population.
    MeSH term(s) Adult ; China ; Humans ; Male ; Muscular Dystrophies, Limb-Girdle/diagnosis ; Muscular Dystrophies, Limb-Girdle/genetics ; Mutation/genetics ; Nucleotidyltransferases/genetics
    Chemical Substances Nucleotidyltransferases (EC 2.7.7.-) ; mannose 1-phosphate guanylyltransferase (EC 2.7.7.13)
    Language English
    Publishing date 2020-05-01
    Publishing country Bosnia and Herzegovina
    Document type Case Reports ; Journal Article ; Review
    ZDB-ID 2240029-1
    ISSN 1840-4812 ; 1512-8601
    ISSN (online) 1840-4812
    ISSN 1512-8601
    DOI 10.17305/bjbms.2019.3992
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Genetic mutation analysis of hereditary spastic paraplegia: A retrospective study.

    Cui, Fang / Sun, LiuQing / Qiao, Jie / Li, JianYong / Li, Mao / Chen, SiYu / Sun, Bo / Huang, XuSheng

    Medicine

    2020  Volume 99, Issue 23, Page(s) e20193

    Abstract: Hereditary spastic paraplegias are heterogeneous disorders with diversified clinical manifestations, and genetic testing is important for the diagnosis and typing of hereditary spastic paraplegias.Gene panel sequencing containing 55 hereditary spastic ... ...

    Abstract Hereditary spastic paraplegias are heterogeneous disorders with diversified clinical manifestations, and genetic testing is important for the diagnosis and typing of hereditary spastic paraplegias.Gene panel sequencing containing 55 hereditary spastic paraplegias-related genes was performed to screen the pathogenic genes for hereditary spastic paraplegias. Sanger sequencing was adopted to validate if the family member carried the same pathogenic gene as the proband.Fifteen out of 53 patients carried mutation(s) in the screened hereditary spastic paraplegias-related genes. Among the 23 identified mutations, only one mutation had been previously reported as a pathogenic mutation. In the pedigree of case 6, the proband, his mother and uncle all carried the same novel deletion mutation (c.1459delA) at SPAST gene. Based on the pedigree, the disease was inherited in an AD pattern. In the pedigree of case 53, the family disease may be in an X-linked recessive inheritance pattern. The proband (case 53) carried two novel mutations in ALT1 gene and L1CAM gene (c.2511C>A), respectively. The L1CAM gene is the causative gene for the SPG1 X-linked recessive-hereditary spastic paraplegias.Our data confirm the genetic heterogeneity of hereditary spastic paraplegias, and SPG4/SPAST were the most frequent forms. The pathogenicity of the novel mutations is worth to be further investigated.
    MeSH term(s) DNA Mutational Analysis ; Female ; Humans ; Male ; Pedigree ; Retrospective Studies ; Sequence Deletion ; Spastic Paraplegia, Hereditary/genetics
    Language English
    Publishing date 2020-06-05
    Publishing country United States
    Document type Journal Article ; Observational Study
    ZDB-ID 80184-7
    ISSN 1536-5964 ; 0025-7974
    ISSN (online) 1536-5964
    ISSN 0025-7974
    DOI 10.1097/MD.0000000000020193
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Acute cholecystitis immediately after radical gastrectomy

    Xiao-Sun Liu, Qing Zhang, Jie Zhong, Kan-Kai Zhu, Yun-Chuan Mu, Ji-Ren Yu

    World Journal of Gastroenterology, Vol 16, Iss 21, Pp 2702-

    A report of three cases

    2010  Volume 2704

    Abstract: Acute cholecystitis is not a common complication of gastrectomy. Its clinical presentations and management strategies in old patients have not been well described in available literature. This report describes the clinical features, management strategies, ...

    Abstract Acute cholecystitis is not a common complication of gastrectomy. Its clinical presentations and management strategies in old patients have not been well described in available literature. This report describes the clinical features, management strategies, and treatment outcome of acute cholecystitis immediately after gastrectomy. Acute cholecystitis immediately after gastrectomy in old patients has different clinical presentations, such as fever and high plasma C-reaction protein level. Abdominal computed tomography (CT) scan and ultrasonography showed acute cholecystitis in our cases, which was treated with antibiotics and ultrasound-guided percutaneous transhepatic gallbladder drainage (PTGD). The results indicate that abdominal CT scan and ultrasonography can effectively diagnose acute cholecystitis after gastrectomy, which can be effectively treated with antibiotics and PTGD.
    Keywords Cholecystitis ; Ultrasonography ; Postoperative complication ; Gastrectomy ; Diseases of the digestive system. Gastroenterology ; RC799-869 ; Specialties of internal medicine ; RC581-951 ; Internal medicine ; RC31-1245 ; Medicine ; R ; DOAJ:Gastroenterology ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Subject code 610
    Language English
    Publishing date 2010-06-01T00:00:00Z
    Publisher Baishideng Publishing Group Co. Limited
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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