1.The clinical analysis of biliary pancreatitis.
Jong Myeong LEE ; Bong Oak YOO ; Eul Sam CHUNG
Journal of the Korean Surgical Society 1991;40(3):321-332
No abstract available.
Pancreatitis*
2.High glucose and palmitate increases bone morphogenic protein 4 expression in human endothelial cells.
Oak Kee HONG ; Soon Jib YOO ; Jang Won SON ; Mee Kyoung KIM ; Ki Hyun BAEK ; Ki Ho SONG ; Bong Yun CHA ; Hanjoong JO ; Hyuk Sang KWON
The Korean Journal of Physiology and Pharmacology 2016;20(2):169-175
Here, we investigated whether hyperglycemia and/or free fatty acids (palmitate, PAL) aff ect the expression level of bone morphogenic protein 4 (BMP4), a proatherogenic marker, in endothelial cells and the potential role of BMP4 in diabetic vascular complications. To measure BMP4 expression, human umbilical vein endothelial cells (HUVECs) were exposed to high glucose concentrations and/or PAL for 24 or 72 h, and the effects of these treatments on the expression levels of adhesion molecules and reactive oxygen species (ROS) were examined. BMP4 loss-of-function status was achieved via transfection of a BMP4-specific siRNA. High glucose levels increased BMP4 expression in HUVECs in a dose-dependent manner. PAL potentiated such expression. The levels of adhesion molecules and ROS production increased upon treatment with high glucose and/or PAL, but this eff ect was negated when BMP4 was knocked down via siRNA. Signaling of BMP4, a proinflammatory and pro-atherogenic cytokine marker, was increased by hyperglycemia and PAL. BMP4 induced the expression of infl ammatory adhesion molecules and ROS production. Our work suggests that BMP4 plays a role in atherogenesis induced by high glucose levels and/or PAL.
Atherosclerosis
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Diabetes Mellitus
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Diabetic Angiopathies
;
Endothelial Cells*
;
Fatty Acids, Nonesterified
;
Glucose*
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Human Umbilical Vein Endothelial Cells
;
Humans*
;
Hyperglycemia
;
Reactive Oxygen Species
;
RNA, Small Interfering
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Transfection
3.Chronic Alcohol Consumption Results in Greater Damage to the Pancreas Than to the Liver in the Rats.
Seong Su LEE ; Oak Kee HONG ; Anes JU ; Myung Jun KIM ; Bong Jo KIM ; Sung Rae KIM ; Won Ho KIM ; Nam Han CHO ; Moo Il KANG ; Sung Koo KANG ; Dai Jin KIM ; Soon Jib YOO
The Korean Journal of Physiology and Pharmacology 2015;19(4):309-318
Alcohol consumption increases the risk of type 2 diabetes. However, its effects on prediabetes or early diabetes have not been studied. We investigated endoplasmic reticulum (ER) stress in the pancreas and liver resulting from chronic alcohol consumption in the prediabetes and early stages of diabetes. We separated Otsuka Long-Evans Tokushima Fatty (OLETF) rats, a type-2 diabetic animal model, into two groups based on diabetic stage: prediabetes and early diabetes were defined as occurrence between the ages of 11 to 16 weeks and 17 to 22 weeks, respectively. The experimental group received an ethanol-containing liquid diet for 6 weeks. An intraperitoneal glucose tolerance test was conducted after 16 and 22 weeks for the prediabetic and early diabetes groups, respectively. There were no significant differences in body weight between the control and ethanol groups. Fasting and 120-min glucose levels were lower and higher, respectively, in the ethanol group than in the control group. In prediabetes rats, alcohol induced significant expression of ER stress markers in the pancreas; however, alcohol did not affect the liver. In early diabetes rats, alcohol significantly increased most ER stress-marker levels in both the pancreas and liver. These results indicate that chronic alcohol consumption increased the risk of diabetes in prediabetic and early diabetic OLETF rats; the pancreas was more susceptible to damage than was the liver in the early diabetic stages, and the adaptive and proapoptotic pathway of ER stress may play key roles in the development and progression of diabetes affected by chronic alcohol ingestion.
Alcohol Drinking*
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Animals
;
Body Weight
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Diet
;
Eating
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Endoplasmic Reticulum
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Endoplasmic Reticulum Stress
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Ethanol
;
Fasting
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Glucose
;
Glucose Tolerance Test
;
Liver*
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Models, Animal
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Pancreas*
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Prediabetic State
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Rats*
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Rats, Inbred OLETF