1.Pancreatic Enzyme Elevations in Korean Chronic Renal Failure Patients.
Sun Young LEE ; Kyu Taek LEE ; Tae Wook KANG ; Won MOON ; Sang Soo LEE ; Ji Young HWANG ; Jong Kyun LEE ; Seung Woon PAIK ; Jong Chul RHEE
The Korean Journal of Gastroenterology 2005;45(2):125-129
BACKGROUND/AIMS: Increased levels of pancreatic enzymes have been reported in patients with renal insufficiency even in the absence of pancreatic diseases. Here, we analyzed serum amylase and lipase levels in chronic renal failure patients according to the degree of azotemia and the treatment modality. METHODS: Serum amylase and lipase levels were reviewed in 95 patients on continuous ambulatory peritoneal dialysis, 105 patients on hemodialysis, 71 patients with renal transplantation, and 73 patients without treatment. Age and sex matched 344 normal healthy controls were selected among those who checked their serum amylase and lipase levels during the same study period. RESULTS: Mean value of amylase level in the patient group (93.7+/-76.5 U/L) was higher than healthy controls (63.8+/-21.4 U/L) (p<0.001) and lipase level in the patient group (212.3+/-195.0 U/L) was higher than healthy control (95.2+/-45.1 U/L) (p<0.001). There was no significant difference in amylase and lipase levels according to the treatment modality in the patient group. The correlations between creatinine clearance and amylase (r=-0.148, p=0.012) or lipase (r=-0.119, p=0.042) were found to be inverse only when the creatinine clearance falls below 50 mL/min. CONCLUSIONS: Serum amylase and lipase levels are about 1.5 times and 2.2 times higher in chronic renal failure patients than healthy controls regardless of treatment modality. The elevations of amylase and lipase levels are inversely correlated with creatinine clearance when it falls below 50 mL/min.
Adolescent
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Adult
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Aged
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Aged, 80 and over
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Amylases/*blood
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Creatinine/blood
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Female
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Humans
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Kidney Failure, Chronic/*enzymology/therapy
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Lipase/*blood
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Male
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Middle Aged
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Renal Replacement Therapy
2.MAPK p38 pathway may be involved in renal function improvement in chronic renal failure rats treated with Jianpi Qinghua decoction.
Xiao-Hong MA ; Yun ZOU ; Yue ZHANG ; Li-Qun HE
Journal of Zhejiang University. Medical sciences 2013;42(5):567-572
OBJECTIVETo investigate the involvement of MAPK p38 pathway in treatment of chronic renal failure with Jianpi Qinghua Decoction in rats.
METHODSForty SPF SD rats were divided into sham group (n=10),model group (n=10), Jianpi Qinghua group (n=10) and losartan group (n=10). Rat chronic renal failure was induced by 5/6 nephrectomy (Platt method) in model, Jianpi Qinghua and losartan groups, and rats in sham group received sham operation. Jianpi Qinghua decoction (3.9 g 200 g(-1)) or losartan (3.3 g 200 g(-1)) daily were administrated by gavage in Jianpi Qinghua and losartan groups for 60 days, respectively, Rats in sham and model groups were orally administered with saline of the same volume. The serum levels of creatinine and urea nitrogen were measured by biochemical method, the expression of MAPK p38 was detected by Western Blot,and renal pathological changes were observed with hematoxylin-eosin staining.
RESULTSCompared to model group,serum creatinine levels after 60d in Jianpi Qinghua and losartan groups were decreased significantly (42.67 ± 5.98 or 40.90 ± 5.07 compared with 60.90 ± 9.54, both P<0.01), the expression of MAPK p38 was significantly down-regulated (0.555 ± 0.004 or 0.587 ± 0.045 compared with 0.930 ± 0.265,both P<0.01) and serum urea nitrogen was also decreased (8.56 ± 0.75 or 7.97 ± 0.86 compared with 8.62 ± 0.62,both P<0.05). The renal pathology in the model group presented glomerular mesangial proliferation,hyperplasia of glomenrulus mesangial cells and interstitial inflammation. Those pathological changes were attenuated significantly in Jianpi Qinghua and losartan groups.
CONCLUSIONJianpi Qinghua Decoctions can improve the renal function and renal pathological changes in a rat with chronic renal failure, which may be associated with down-regulation of MAPK p38 immune inflammatory pathways.
Animals ; Blood Urea Nitrogen ; Creatinine ; blood ; Disease Models, Animal ; Drugs, Chinese Herbal ; therapeutic use ; Kidney Failure, Chronic ; drug therapy ; enzymology ; MAP Kinase Signaling System ; Male ; Rats ; Rats, Sprague-Dawley ; p38 Mitogen-Activated Protein Kinases ; metabolism
3.Erythropoietin does not affect nitric oxide system in rats with chronic renal failure.
Soo Wan KIM ; Jong Un LEE ; Dae Gill KANG ; Kwon JUNG ; Nam Ho KIM ; Soon Pal SUH ; Ki Chul CHOI ; Young Joon KANG
Journal of Korean Medical Science 2000;15(2):183-188
We investigated to see whether an altered role of nitric oxide (NO) system is involved in erythropoietin (EPO)-induced hypertension in chronic renal failure (CRF). Male Sprague-Dawley rats were five-sixths nephrectomized to induce CRF. Six weeks after the operation, EPO or vehicle was injected for another 6 weeks. Plasma and urine nitrite/nitrate (NOx) levels were determined. Expression of NO synthase (NOS) proteins in the aortae and kidneys were also determined. In addition, the isometric tension of isolated aorta in response to acetylcholine and nitroprusside was examined. Blood pressure progressively rose in CRF groups, the degree of which was augmented by EPO treatment. Plasma NOx levels did not differ among the groups, while urine NOx levels were lower in CRF groups. Endothelial NOS expression was lower in the kidney and aorta in CRF rats, which was not further affected by EPO-treatment. The inducible NOS expression in the kidney and aorta was not different among the groups. Acetylcholine and sodium nitroprusside caused dose-dependent relaxations of aortic rings, the degree of which was not altered by EPO-treatment. Taken together, EPO-treatment aggravates hypertension in CRF, but altered role of NO system may not be involved.
Acetylcholine/pharmacology
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Anemia/metabolism
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Anemia/etiology
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Anemia/drug therapy*
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Animal
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Aorta, Thoracic/physiology
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Body Weight
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Erythropoietin/pharmacology*
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Hypertension, Renal/metabolism
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Hypertension, Renal/drug therapy
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Isometric Contraction/drug effects
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Kidney/enzymology
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Kidney Failure, Chronic/metabolism*
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Kidney Failure, Chronic/complications
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Male
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Nitrates/urine
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Nitrates/blood
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Nitric Oxide/metabolism*
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Nitric-Oxide Synthase/metabolism
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Nitrites/urine
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Nitrites/blood
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Nitroprusside/pharmacology
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Rats
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Rats, Sprague-Dawley
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Vasoconstriction/drug effects
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Vasoconstrictor Agents/pharmacology
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Vasodilator Agents/pharmacology
4.Higher Prevalence of Klebsiella pneumoniae Extended-Spectrum beta-Lactamase in Patients on Renal Replacement Therapy.
Hyang Lim LEE ; Dong Hee WHANG ; Dong Won PARK ; Young Jin LEE ; Yeong Hoon KIM ; Ho Jun CHIN ; Suhnggown KIM ; Ho Seok KOO
Journal of Korean Medical Science 2013;28(8):1187-1193
The prevalence of antibiotic resistance is higher in patients undergoing renal replacement therapy (RRT) than in patients who did not undergo RRT. We investigated the presence of KP (Klebsiella pneumoniae) in patients who underwent RRT. All data were collected retrospectively by accessing patient medical records from 2004 to 2011 for the culture results of all patients who were positive for KP. We grouped the patients by the presence of extended-spectrum beta-lactamase (ESBL) into a KP ESBL(-) group (KP[-]) and a KP ESBL(+) group (KP[+]). In total, 292 patients (23.1%) were in the KP(+) group, and 974 patients (76.9%) were in the KP(-) group. A greater percentage of KP(+) was found in patients who underwent RRT (7.5%) than in patients who did not undergo RRT (3.2%) (OR, 2.479; 95% CI,1.412-4.352). A Cox's hazard proportional model analysis was performed, and for patients with pneumonia, the risk of KP(+) was 0.663 times higher in patients who had lower albumin levels, 2.796 times higher in patients who had an inserted Levin tube, and 4.551 times higher in patients who underwent RRT. In conclusion, RRT can be a risk factor for KP(+) in patients with pneumonia.
Adult
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Aged
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Aged, 80 and over
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Female
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Humans
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Kaplan-Meier Estimate
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Kidney Failure, Chronic/*microbiology/therapy
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Klebsiella Infections/*epidemiology/microbiology/mortality
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Klebsiella pneumoniae/*enzymology/isolation & purification
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Male
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Middle Aged
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Odds Ratio
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Pneumonia/diagnosis/*epidemiology/microbiology
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Prevalence
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Proportional Hazards Models
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Renal Replacement Therapy
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Retrospective Studies
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Risk Factors
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Serum Albumin/analysis
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beta-Lactamases/*metabolism