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1.
Public Health ; 226: 248-254, 2024 Jan.
Article En | MEDLINE | ID: mdl-38091813

OBJECTIVES: Carotid intima-media thickness (CIMT) is a noninvasive marker of atherosclerosis, a typical pathologic process underlying cardiovascular diseases (CVDs). It is essential to explore the relationships between weight loss and the reduction of CIMT. STUDY DESIGN: This was an updated systematic review and meta-analysis. METHODS: A systematic literature search was conducted to collect relevant clinical trials. The pooled results of meta-analyses were assessed by weighted mean difference (WMD) and the corresponding 95 % confidence interval (95% CI). RESULTS: Thirty-three articles involving 2273 participants were collected in this meta-analysis. Among all participants with obesity, the pooled mean of weight loss was -23.26 kg (95% CI: -27.71 to -18.81), and the pooled mean change of CIMT was -0.06 mm (95% CI: -0.08 to -0.04). Compared with Non-surgical interventions, Surgical ones could lead to much higher weight loss (Pbetween groups < 0.001). A more significant CIMT reduction was identified among Surgical intervention patients than among Non-surgical intervention participants (Pbetween groups < 0.001). CONCLUSIONS: Effective interventions, especially Surgical interventions, could reduce the weight of patients with obesity, followed by the decline of CIMT, which might further disturb atherosclerosis progression and lower CVD risk.


Atherosclerosis , Cardiovascular Diseases , Humans , Risk Factors , Carotid Intima-Media Thickness , Obesity/complications , Weight Loss
2.
Eur Rev Med Pharmacol Sci ; 24(24): 12938-12947, 2020 12.
Article En | MEDLINE | ID: mdl-33378044

OBJECTIVE: Abnormal lipid metabolism plays a role that cannot be ignored in articular cartilage bone marrow lesions, synovial inflammation, and the destruction of chondrocytes (CHs). Ceramide is one of the key constructions of membrane lipid bilayers, which is an intracellular lipid mediator regulating varieties of cellular behaviors. The purpose of this study was to explore the role of ceramide and its inhibitor in the development of the CHs degeneration. PATIENTS AND METHODS: CHs were isolated from the cartilage collecting from the osteoarthritis (OA) patients, and oleic acid/palmitic (O/P) acid was used to induce CHs lipid disordered. Then, myriocin was used to inhibit the accumulation of ceramide. After that, the apoptosis, cell viability, glucose uptake, oxidative stress, and the chondrogenic gene expression were tested to evaluate the degenerated degree of CHs. RESULTS: Results revealed that O/P induced CH apoptosis, ceramide accumulation, a higher level of oxidative stress, IL-1ß and MMP-13, but it also decreased the collagen-Ⅱ and SOX-9 expressions and affected the glucose uptake of CHs. After the stimulation of myriocin, the side effects induced by O/P was partly reversed. CONCLUSIONS: O/P induces the accumulation of ceramide and the degeneration of CHs, and myriocin can reject the harmful effect caused by O/P via the suppression of ceramide.


Ceramides/antagonists & inhibitors , Chondrocytes/drug effects , Fatty Acids, Monounsaturated/pharmacology , Oleic Acid/antagonists & inhibitors , Palmitates/antagonists & inhibitors , Adult , Aged , Cartilage, Articular/metabolism , Cartilage, Articular/pathology , Ceramides/metabolism , Chondrocytes/metabolism , Female , Humans , Male , Middle Aged , Oleic Acid/pharmacology , Osteoarthritis/metabolism , Osteoarthritis/pathology , Palmitates/pharmacology
3.
Eur Rev Med Pharmacol Sci ; 24(12): 6908-6918, 2020 06.
Article En | MEDLINE | ID: mdl-32633384

OBJECTIVE: Acute lung injury (ALI) is the most common organ damage in sepsis and sepsis-induced ALI is a clinically extremely dangerous disease. Therefore, it is essential to find an effective way to treat ALI. We hope to provide a new target for the treatment of clinical ALI by studying the effect of GDF11 on LPS-induced ALI. MATERIALS AND METHODS: C57BL/6 male mice and lipopolysaccharide (LPS) were used to induce mouse ALI. Recombinant GDF11 protein was used to treat mice to detect the effect of GDF11 on mouse ALI. In addition, BEAS-2B cells were used to further validate the effects of GDF11 on inflammation and apoptosis of alveolar epithelial cells. RESULTS: Recombinant GDF11 protein significantly reduced the expression of inflammatory factors and apoptosis-related pathways in mouse lung tissues. Overexpression of GDF11 in BEAS-2B cells also significantly attenuated the levels of inflammation and apoptosis in the cells. In addition, GDF11 can reduce the activity of TLR2/HMGB1/NF-κB signaling pathway, which is an important mechanism for GDF11 to play a role in lung protection. CONCLUSIONS: GDF11 can exert lung protection effects by inhibiting the TLR2/HMGB1/NF-κB signaling pathway and reduce the level of inflammation and apoptosis of the lung.


Acute Lung Injury/metabolism , Apoptosis , Bone Morphogenetic Proteins/metabolism , Growth Differentiation Factors/metabolism , Inflammation/metabolism , Acute Lung Injury/chemically induced , Acute Lung Injury/pathology , Animals , Apoptosis/drug effects , Bone Morphogenetic Proteins/genetics , Cells, Cultured , Disease Models, Animal , Growth Differentiation Factors/genetics , HMGB1 Protein/metabolism , Humans , Inflammation/chemically induced , Inflammation/pathology , Injections, Intravenous , Lipopolysaccharides/administration & dosage , Male , Mice , Mice, Inbred C57BL , NF-kappa B/metabolism , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Signal Transduction , Toll-Like Receptor 2/metabolism
4.
Genet Mol Res ; 15(1)2016 Feb 22.
Article En | MEDLINE | ID: mdl-26909998

We conducted a case-control study to assess the role of two IL10 gene polymorphisms (rs1800896 and rs1800872) in susceptibility to liver cirrhosis, and their association with chronic hepatitis B in a Chinese population. A case-control study was designed to investigate the association between functional polymorphisms of IL10 (rs1800896 and rs1800872) and the development of liver cirrhosis. Between March 2012 and March 2014, we recruited 241 patients with liver cirrhosis and 254 controls from Xianyang Central Hospital. Genotyping of IL10 rs1800896 and rs1800872 polymorphisms was carried out using the polymerase chain reaction coupled with restriction fragment length polymorphism. Using multivariate logistic regression analysis, we found that individuals with the AA genotype of IL10 rs1800896 showed an increased risk of liver cirrhosis compared with those with the GG genotype in a codominant model (OR = 2.01, 95%CI = 1.10-3.65). In dominant and recessive models, we found that the IL10 rs1800896 polymorphism was correlated with the development of liver cirrhosis (for the dominant model, OR = 1.46, 95%CI = 1.01-2.13; for the recessive model, OR = 1.72, 95%CI = 1.01-3.02). In summary, our study suggests that the IL10 rs1800896 polymorphism is associated with the development of liver cirrhosis.


Hepatitis B, Chronic/genetics , Interleukin-10/genetics , Liver Cirrhosis/genetics , Case-Control Studies , Female , Genetic Predisposition to Disease/genetics , Genotype , Humans , Male , Middle Aged
5.
Zhonghua Wai Ke Za Zhi ; 32(1): 49-50, 1994 Jan.
Article Zh | MEDLINE | ID: mdl-8045205

12 cases of enterogenous cysts were treated from 1985 to 1992, and its pathology, definition, clinical manifestation and treatment were discussed. A variety of terms has been used for this entity but enterogenous cyst is more suitable. The clinical manifestation varies with different location. Complications are the most common cause bringing a patient to the hospital. The key point for radical therapy is removal of entire cystic wall. One case was cured by intracystic injection of formalin.


Cysts/surgery , Intestinal Diseases/surgery , Adult , Child , Child, Preschool , Female , Humans , Infant , Intestines/abnormalities , Male , Retroperitoneal Space/surgery , Spinal Canal/surgery
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