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1.
Turk J Gastroenterol ; 32(1): 97-105, 2021 01.
Article in English | MEDLINE | ID: mdl-33893772

ABSTRACT

BACKGROUND: Bile acid metabolism is a contributing factor that promotes cholelithiasis. Recent studies have suggested novel roles of leptin in the formation of gallbladder stones (GS); however, no evidence confirmed the function of leptin in the formation of primary intrahepatic bile duct stones (PIBDS) . In the current study, the liver tissues of patients with GS and PIBDS were collected to check the mRNA and protein expression levels of BSEP. METHODS: L02 cells stimulated with leptin were served for the expression of OB-Rb, AMPKα2, and BSEP by quantitative-polymerase chain reaction (q-PCR), Western blot, and immunohistochemistry, respectively. RESULTS: The results showed that the level of serum leptin was higher in the GS group than in the control and PIBDS groups. Compared with the control group, the expression levels of OB-Rb, p-AMPKa2, and BSEP decreased significantly in the GS and PIBDS groups. In vitro, compared with the control cells, the protein levels of OB-Rb, p-AMPKa2, and BSEP increased in the L02 cells cultured with leptin. However, these enhancements disappeared when the cells were co-cultured with leptin plus Compound C. CONCLUSION: The present results suggest that cholelithiasis, especially the formation of PIBDS, was connected with leptin, which could regulate bile acid metabolism through the OB-Rb/AMPKa2/BSEP signaling pathway.


Subject(s)
AMP-Activated Protein Kinases , ATP Binding Cassette Transporter, Subfamily B, Member 11 , Bile Acids and Salts , Cholelithiasis , Leptin , Receptors, Leptin , AMP-Activated Protein Kinases/biosynthesis , ATP Binding Cassette Transporter, Subfamily B, Member 11/biosynthesis , Adult , Aged , Bile Acids and Salts/blood , Bile Acids and Salts/metabolism , Bile Ducts, Intrahepatic/metabolism , Cell Line , Cholelithiasis/blood , Cholelithiasis/etiology , Cholelithiasis/metabolism , Cross-Sectional Studies , Energy Metabolism , Female , Gallstones/blood , Gallstones/metabolism , Hepatocytes/metabolism , Humans , Leptin/blood , Leptin/metabolism , Liver/metabolism , Male , Middle Aged , RNA, Messenger , Receptors, Leptin/metabolism , Signal Transduction
2.
Hepatogastroenterology ; 62(139): 723-6, 2015 May.
Article in English | MEDLINE | ID: mdl-26897961

ABSTRACT

BACKGROUND/AIMS: Islet cell tumours (ICTs) are uncommon tumours in clinical practice. Surgical resection is the treatment of choice for ICTs, but localisation of these lesions can be challenging. The aim of this study was to analyse the clinical diagnosis and treatment for ICTs. METHODOLOGY: Thirty-one patients with ICTs who were diagnosed and who underwent surgical treatment in the affiliate hospital of Luzhou Medical College from 1 January 2000 to 31 July 2013 were enrolled. The clinical data of these patients were retrospectively reviewed. RESULTS: Among 31 patients (6 males, 25 females), 15 cases (48.39%) had non-functional ICTs and 16 (51.61%) cases were insulinoma: The mean age of patients with non-functional ICTs was 42.73 ± 12.34 years and of those with insulinoma was 48.88 ± 13 years. Non-functional ICTs had a non-specific presentation. Insulinoma makes different clinical presentations mostly with symptoms of hypoglycaemia. CONCLUSIONS: Preoperative and/or intra-operative localisation is needed for ICTs; CT scan or MRI is used routinely as the first choice. If the lesion is very small, DSA is also good for localisation before operation. IOUS is a reliable technique in exactly localising insulinoma. ICTs are considered to be cured with successful surgical removal.


Subject(s)
Adenoma, Islet Cell/diagnosis , Adenoma, Islet Cell/surgery , Diagnostic Imaging/methods , Insulinoma/diagnosis , Insulinoma/surgery , Pancreatectomy , Pancreatic Neoplasms/diagnosis , Pancreatic Neoplasms/surgery , Adenoma, Islet Cell/pathology , Adult , Aged , Angiography, Digital Subtraction , China , Female , Humans , Insulinoma/pathology , Magnetic Resonance Imaging , Male , Middle Aged , Multimodal Imaging , Pancreatectomy/adverse effects , Pancreatic Neoplasms/pathology , Predictive Value of Tests , Reproducibility of Results , Retrospective Studies , Tomography, X-Ray Computed , Treatment Outcome , Tumor Burden , Young Adult
3.
Hepatogastroenterology ; 62(139): 773-6, 2015 May.
Article in English | MEDLINE | ID: mdl-26897971

ABSTRACT

BACKGROUND/AIMS: Islet cell tumours (ICTs) are uncommon tumours in clinical practice. Surgical resection is the treatment of choice for ICTs, but localisation of these lesions can be challenging. The aim of this study was to analyse the clinical diagnosis and treatment for ICTs. METHODS: Thirty-one patients with ICTs who were diagnosed and who underwent surgical treatment in the affiliate hospital of Luzhou Medical College from 1 January 2000 to 31 July 2013 were enrolled. The clinical data of these patients were retrospectively reviewed. RESULTS: Among 31 patients (6 males, 25 females), 15 cases (48.39%) had non-functional ICTs and 16 (51.61%) cases were insulinoma. The mean age of patients with non-functional ICTs was 42.73 ± 12.34 years and of those with insulinoma was 48.88 ± 13 years. Non-functional ICTs had a non-specific presentation. Insulinoma makes different clinical presentations mostly with symptoms of hypoglycaemia. CONCLUSIONS: Preoperative and/or intra-operative localisation is needed for ICTs; CT scan or MRI is used routinely as the first choice. If the lesion is very small, DSA is also good for localisation before operation. IOUS is a reliable technique in exactly localising insulinoma. ICTs are considered to be cured with successful surgical removal.


Subject(s)
Adenoma, Islet Cell/diagnosis , Adenoma, Islet Cell/surgery , Diagnostic Imaging/methods , Insulinoma/diagnosis , Insulinoma/surgery , Pancreatectomy , Pancreatic Neoplasms/diagnosis , Pancreatic Neoplasms/surgery , Adenoma, Islet Cell/pathology , Adult , Angiography, Digital Subtraction , China , Female , Humans , Insulinoma/pathology , Magnetic Resonance Imaging , Male , Middle Aged , Multimodal Imaging , Pancreatectomy/adverse effects , Pancreatic Neoplasms/pathology , Predictive Value of Tests , Reproducibility of Results , Retrospective Studies , Tomography, X-Ray Computed , Treatment Outcome , Tumor Burden
4.
Hepatobiliary Pancreat Dis Int ; 7(1): 65-9, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18234641

ABSTRACT

BACKGROUND: A significant relationship exists among food intake and nutritional status and cholelithiasis, including gallstone and hepatolithiasis. Leptin is associated with obesity. This study was to investigate the differences in serum leptin levels in patients with gallstone and hepatolithiasis and to evaluate the relationships among leptin, cholecystokinin (CCK), lipid and lipoprotein concentrations. METHODS: Body mass index (BMI), serum leptin, CCK, insulin, lipid and lipoprotein concentrations, and liver function were measured in 382 patients with gallstone (GS group), 83 patients with hepatolithiasis (HS group) and 30 healthy controls (control group). The values of these indices were compared among the groups. In each group, Pearson's product-moment correlation coefficient among these indices were evaluated. RESULTS: There were notable differences in serum leptin, CCK, total cholesterol, total triglycerides, apolipoprotein-a (APO-a), globulin, direct reacting bilirubin, and BMI between the GS and HS groups (P<0.05). Positive correlations between serum leptin and BMI, CCK, total cholesterol, gamma-glutamyl transpeptidase (GGT), aminotransferase, and insulin were found in the GS group (P<0.05). Positive correlations were observed between serum leptin and CCK, bilirubin, aminotransferase, GGT, in the HS group (P<0.05), but negative correlations between serum leptin and albumin or APO-a (P<0.05). CONCLUSIONS: Leptin participates in modulating lipid metabolism. There are notable differences in leptin, serum lipid, and CCK between patients with gallstone and those with hepatolithiasis. The role of leptin in the pathophysiological course of cholelithiasis needs further investigation.


Subject(s)
Cholecystokinin/blood , Cholelithiasis/blood , Gallstones/blood , Leptin/blood , Lipoproteins/blood , Adult , Aged , Apolipoproteins A/blood , Bile Ducts, Intrahepatic , Bilirubin/blood , Cholesterol/blood , Female , Globulins/metabolism , Humans , Lipid Metabolism , Male , Middle Aged , Triglycerides/blood
5.
Hepatobiliary Pancreat Dis Int ; 3(1): 144-8, 2004 Feb.
Article in English | MEDLINE | ID: mdl-14969859

ABSTRACT

BACKGROUND: Type 1 diabets is an autoimmune disease caused by the destruction of pancreatic beta-cell with an increased incidence worldwide in the closing decades of the 20th century. This study was to investigate the effects of human umbilical cord serum (UCS) on the proliferation and function of human fetal islet-like cell clusters (ICCs) in vitro. METHODS: Eight fresh pancreatic glands obtained after induction of labor with water bag were mildly exposed to collagenase V, and the digested cells were cultured in a RPMI-1640 medium plus 10% pooled UCS or fetal calf serum (FCS) to permit cells attachment and outgrowth of ICCs. RESULTS: In 8 consecutively explanted glands, development and proliferation of ICCs were observed. In the presence of FCS, the outgrowth of ICC took place on the top of a fibroblast monocellular layer. UCS affected less growth of fibroblasts and increased the formation of ICCs about four-fold compared with explants from the same glands maintained in FCS. In both UCS and FCS, the insulin content of the medium was variable to a certain extent and progressively declined from day 2 to day 6. Dithizone-stained ICCs in UCS suggested that most cell clusters were islet cells (beta-cells), and the purity of islets was estimated 80%-90%. The ultrastructure of the cultured cells showed a large number of granule-containing cells, most of which were identified as beta-cells. CONCLUSION: We conclude that in comparison with explants with FCS, the yield of ICCs and purification of islet cells are markedly increased by UCS and may facilitate the proliferation of pancreatic beta-cells intended for islet transplantation.


Subject(s)
Cell Division/physiology , Fetal Blood , Insulin/metabolism , Islets of Langerhans/embryology , Animals , Cattle , Cell Division/drug effects , Cells, Cultured , Fetus , Humans , Insulin/analysis , Insulin Secretion , Islets of Langerhans/metabolism , Islets of Langerhans Transplantation , Microscopy, Electron , Pancreas/cytology , Pancreas/diagnostic imaging , Pancreas/embryology , Probability , Ultrasonography
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