2.Mechanisms of Motility Change on Trinitrobenzenesulfonic Acid-Induced Colonic Inflammation in Mice.
Gab Jin CHEON ; Yuan CUI ; Dong Soo YEON ; Seong Chun KWON ; Byong Gon PARK
The Korean Journal of Physiology and Pharmacology 2012;16(6):437-446
Ulcerative colitis is an inflammatory bowel disease (IBD) characterized by recurrent episodes of colonic inflammation and tissue degeneration in human or animal models. The contractile force generated by the smooth muscle is significantly attenuated, resulting in altered motility leading to diarrhea or constipation in IBD. The aim of this study is to clarify the altered contractility of circular and longitudinal smooth muscle layers in proximal colon of trinitrobenzen sulfonic acid (TNBS)-induced colitis mouse. Colitis was induced by direct injection of TNBS (120 mg/kg, 50% ethanol) in proximal colon of ICR mouse using a 30 G needle anesthetized with ketamin (50 mg/kg), whereas animals in the control group were injected of 50% ethanol alone. In TNBS-induced colitis, the wall of the proximal colon is diffusely thickened with loss of haustration, and showed mucosal and mucular edema with inflammatory infiltration. The colonic inflammation is significantly induced the reduction of colonic contractile activity including spontaneous contractile activity, depolarization-induced contractility, and muscarinic acetylcholine receptor-mediated contractile response in circular muscle layer compared to the longitudinal muscle layer. The inward rectification of currents, especially, important to Ca2+ and Na+ influx-induced depolarization and contraction, was markedly reduced in the TNBS-induced colitis compared to the control. The muscarinic acetylcholine-mediated contractile responses were significantly attenuated in the circular and longitudinal smooth muscle strips induced by the reduction of membrane expression of canonical transient receptor potential (TRPC) channel isoforms from the proximal colon of the TNBS-induced colitis mouse than the control.
Acetylcholine
;
Animals
;
Colitis
;
Colitis, Ulcerative
;
Colon
;
Constipation
;
Contracts
;
Diarrhea
;
Edema
;
Ethanol
;
Humans
;
Inflammation
;
Inflammatory Bowel Diseases
;
Membranes
;
Mice
;
Mice, Inbred ICR
;
Models, Animal
;
Muscle, Smooth
;
Muscles
;
Needles
;
Protein Isoforms
3.A Case of Henoch - Shoenlein Purpura with Duodenal Involvement.
Byung Sup CHO ; Je Woong MOON ; Kyung Chul SHIN ; Ho Jung KIM ; Kyu Tae KIM ; Jae Gon AN ; Byong Chul LEE ; Ha Yung JUN ; In Whoan LEE ; Hak Jung KWON ; Hyang Ju LEE ; Suk Il JANG ; Dae Seob CHOI ; Jong Suk KIM
Korean Journal of Gastrointestinal Endoscopy 1996;16(4):639-643
Henoch-Shonlein(H-S) purpura, or anaphylactoid purpura is a hypersensitivity vasculitis characterized by palpable purpura usually on buttock and low extremities; arthralgia mostly polyarhtralgia in the absence of frank arthritis; gastraintestinal involvement with colicky abdominal pain, nausea, vomiting, diarrhea, constipation and bleeding; and renal involvement, manifested chiefly by hematuria and proteinuria. Gastrointestinal involvement is seen in 70 percent of pediatric patients and one third of adult patients. Any portion of the gastrointestinal tract distal to the esophagus maybe involved, but most frequently affected sites are jejunum and ileum. We report one case of H-S purpura with duodenal involvement observed in 16, male patient.
Abdominal Pain
;
Adult
;
Arthralgia
;
Arthritis
;
Buttocks
;
Constipation
;
Diarrhea
;
Esophagus
;
Extremities
;
Gastrointestinal Tract
;
Hematuria
;
Hemorrhage
;
Humans
;
Ileum
;
Jejunum
;
Male
;
Nausea
;
Proteinuria
;
Purpura*
;
Purpura, Schoenlein-Henoch
;
Vasculitis, Leukocytoclastic, Cutaneous
;
Vomiting
4.Near-Infrared Fluorescence Imaging Using a Protease-Specific Probe for the Detection of Colon Tumors.
Soon Man YOON ; Seung Jae MYUNG ; Byong Duk YE ; In Wha KIM ; Nam Gon LEE ; Yeon Mi RYU ; Kyeongsoon PARK ; Kwangmeyung KIM ; Ick Chan KWON ; Young Soo PARK ; Chan Sik PARK ; Dae Hyuk MOON ; Do Hoon KIM ; Mi Young DO ; Jeong Sik BYEON ; Suk Kyun YANG ; Jin Ho KIM
Gut and Liver 2010;4(4):488-497
BACKGROUND/AIMS: Early tumor detection is crucial for the prevention of colon cancer. Near-infrared fluorescence (NIRF) imaging using a target-activatable probe may permit earlier disease detection. Matrix metalloproteinases (MMPs) participate in tumorigenesis and tumor growth. The aim of this study was to determine whether NIRF imaging using an MMP-activatable probe can detect colon tumors at early stages. METHODS: We utilized two murine colon cancer models: a sporadic colon cancer model induced by azoxymethane (AOM), and a colitis-associated cancer model induced by a combination of AOM and dextran sodium sulfate (DSS). Colonic lesions were analyzed by histologic examination, Western blotting, immunohistochemical staining, and NIRF imaging using an MMP-activatable probe. RESULTS: Multiple variable-sized tumors developed in both models and progressed from adenomas to adenocarcinomas over time. At the early stage of the AOM/DSS model, diffuse inflammation was observed within the tumors. MMP expression increased progressively through normal, inflammation, adenoma, and adenocarcionoma stages. NIRF signal intensities were strongly correlated with each tumor stage from adenoma to adenocarcinoma. NIRF imaging also distinguished tumors from inflamed mucosa. CONCLUSIONS: NIRF imaging using a protease-activatable probe may be a useful tool for early tumor detection. This approach could translate to improve the endoscopic detection of colon tumors, especially in patients with inflammatory bowel disease.
Adenocarcinoma
;
Adenoma
;
Azoxymethane
;
Blotting, Western
;
Cell Transformation, Neoplastic
;
Colon
;
Colonic Neoplasms
;
Dextrans
;
Fluorescence
;
Humans
;
Inflammation
;
Inflammatory Bowel Diseases
;
Matrix Metalloproteinases
;
Optical Imaging
;
Sodium
;
Sulfates