• 제목/요약/키워드: Renal excretion

검색결과 263건 처리시간 0.021초

담도계로 배설되지 않는 $^{99m}Tc-DISIDA$ 신티그램의 임상적 응용 (Clinical Application of $^{99m}Tc-DISIDA$ Scintigraphy with Nonvisualization of Biliary Excretion)

  • 문태용;김용기;김동수
    • 대한핵의학회지
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    • 제21권1호
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    • pp.25-32
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    • 1987
  • Authors analysed biochemical studies and scintigraphic findings of obstructive jaundice and nonobstructive jaundice in 44 cases of $^{99m}Tc-DISIDA$ scintigraphy with nonvisualization of biliary excretion till 120 min or 240 min after injection of $^{99m}Tc-DISIDA$. Causative diseases of $^{99m}Tc-DISIDA$ scintigraphy with nonvisualization of biliary excretion were in order to choledocholithiasis (25%), hepatitis (25%), cholangiocarcinoma (14%), cholangitis (14%) and pancreas head tumor (11%). In obstructive jaundice, statistically significant findings were elevated alkaline phosphatase above 300 IU/L on biochemical study and single lobe enlargement of the liver, irregular radioisotope uptake of the liver and concave indentation of the gall bladder fossa of the liver on scintigraphy. In nonobstructive jaundice, statistically significant findings were persistent renal excretion of $^{99m}Tc-DISIDA$ and more increased uptake density of the heart than the liver on scintigraphy.

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Feeding, excretion, survival, and histological alterations in zebrafish Danio rerio from single and combined exposure to microplastics and copper

  • Hyeon Jin Kim;So Ryung Shin;Jung Jun Park;Jung Sick Lee
    • 환경생물
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    • 제42권1호
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    • pp.1-14
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    • 2024
  • This study evaluated the risk of single and combined exposure to microplastics in zebrafish (Danio rerio) through biomarkers, such as survival rate, excretion rate, and histological alterations of organ systems. The experimental groups were the control(Cont.), single microplastics exposure group(MPs, 1.83%/fish total weight(g)), the copper group(Cu, 21.6 ㎍ L-1), and a group with combined exposure to MPs and copper (MPs*Cu). The experiment was conducted with individual exposure (7 days) for MP excretion rate analysis and group exposure (14 days) for biomarker analysis. The daily excretion rate of MPs tended to decrease in a time-dependent manner. The copper concentration in the body was not significantly different between single and combined copper exposure. The degeneration of mucous cells in the skin, capillary dilation of the gill lamella, increased intestinal mucous, hepatocyte hypertrophy, and the degeneration of glomeruli and renal tubules were observed in all exposure groups. These histological alterations showed the highest tendency in the MPs*Cu group. In this study, the changes in biomarkers were attributed to the single effect of copper or the combined effect of copper and MPs rather than being solely influenced by MPs.

Effect of Renal Ischemia in Tetraethylammonium Transport in Rabbit Renal Coritcal Slices

  • Joo, Woo-Sik;Nam, Yun-Jeong;Jung, Jin-Sup;Kim, Yong-Keun
    • The Korean Journal of Physiology
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    • 제25권2호
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    • pp.171-177
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    • 1991
  • This study was carried out to determine effect of acute renal ischemia on transport function of organic cation, tetraethylammonium (TEA), in rabbit kidney proximal tubule. Clamping of the renal artery for 30 and 60 min produced a polyuria which was accompanied by an increase in $Na^+$ excretion. The capacity of kidney cortical slices to accumulate TEA was increased after 30 and 60 min of ischemia. When blood flow was restored for 30 min after 30 and 60 min of ischemia, the augmented TEA uptake was recovered to the control values. Oxygen consumption of cortical slices was stimulated after 30 min of ischemia, whereas it was not altered by 60 min of ischemia. A 90-min ischemia produced a significant inhibition of TEA uptake and tissue oxygen consumption. These results suggest that the basolateral transport system for organic cation persists after ischemic periods of 60 min despite evidence that tubular reabsorptive mechanism of $Na^+$ and water is markedly impaired. This may indicate that the active secretory systems of proximal tubule are more resistant to ischemic injury than the reabsorptive systems.

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개에서 Gentamicin과 Ethylene glycol에 임상병리학적 진단 (Clinicopathological Diagnosis of Gentamicin and Ethylene glycol Induced Acute Renal Failure in Dogs)

  • 김지현;이영재;이경갑
    • 한국임상수의학회지
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    • 제17권2호
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    • pp.327-333
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    • 2000
  • The diagnostic method was, evaluated in experimentally induced acute renal failure in doges. Ten male dogs weighing from 5 to 10 kg were assigned to two groups(gentamicin & ethylene glycol treated group) al random. Gentamicin sulfate at 10 mg/kg of body weight, t.i.d., for 7 days and ethylene glycol at 3 ml/kg of body weight once used in a randomized complete block design with tee treatments in block. The samples(blood, urine) were collected before and 1,3,5,7,9 and l1th day after administration. The serum creatinine concentration and BUN(blood urea nitrogen) were sig- nificantly increased at the 7th day than before administration in gentamicin treated group (p<0.05), bolt there was significant increase at the 1st day than before administration in ethylene glycol treated group(p<0.05). The urine GGT(gramma glutamyl transpeptidase) and GGT/creatinine were significantly increased at the 1st (lay after administration in gentamicin treated group (p<0.05). But in ethylene glycol treated group, there was no significant changes. The value of FENa (fractional excretion of sodium) was significantly increased at the 3rd day after administration in gentamicin treated group and the 1 st day after administration in ethylene glycol treated group (p<0.05). These results suggest that FENa was a good parameter of renal function in dogs with acute renal failure.

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Familial Juvenile Hyperuricemic Nephropathy and Uromodulin Gene Mutation

  • Lee, Young-Ki;Lee, Dong Hun;Noh, Jung-Woo
    • Journal of Genetic Medicine
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    • 제10권1호
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    • pp.7-12
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    • 2013
  • Familial Juvenile hyperuricemic nephropathy (FJHN) is a rare autosomal dominant disorder, characterized by early onset of hyperuricemia, gout and progressive kidney disease. Hyperuricemia prior to renal impairment and decreased fractional excretion of uric acid are hallmarks of FJHN. Renal dysfunction gradually appears early in life and results in end-stage renal disease usually between the ages of 20 and 70 years. FJHN is mostly caused by mutations in the uromodulin gene located at 16p12. The course of FJHN is highly variable. Treatment includes management for hyperuricemia, gout and progressive kidney disease. Individuals with gout have been usually treated with allopurinol. But controversy exists as to whether uric acid lowering therapy prevents the progression of chronic kidney disease.

개에서 비뇨기계 질환의 진단영상 (Diagnostic Imaging of Urological Diseases in Dogs)

  • 장동우;정주현;장진회;정우조;원성준;이기창;최호정;이희천;윤화영
    • 한국임상수의학회지
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    • 제18권4호
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    • pp.459-464
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    • 2001
  • Excretory urography is a procedure where opacification of the kidneys, renal pelvic diverticula, ureters, and urinary bladder is a result of renal excretion of an intravenously administered iodinated contrast agent providing both anatomical and functional assessment. And ultrasonography is a non-invasive modality to evaluate the important anatomic information concerning the size, shape, and internal architecture of kidney even in the presence of impaired renal function or abdominal fluid. We describe four dogs with urological signs diagnosed with excretory urography and ultrasonography. Parients showed a variety of clinical signs including vomiting, hematuria, anorexia, abdominal pain, and abdominal distension. The hydronephrosis was diagnosed in case 1, 2, and 3 that had pelvic dilation, dilation of pelvic recesses, ureteral dilation. In case 3, proximal ureteral rupture was diagnosed with evidence of contrast media leakage was seen in proximal ureter. In case 4, the rupture of urinary bladder was diagnosed with leakage of contrast media through its ventral portion.

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소아 신장질환에서 요 β2-microglobulin검사의 분석 (Analysis of urine β2-microglobulin in pediatric renal disease)

  • 김동운;임인석
    • Clinical and Experimental Pediatrics
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    • 제50권4호
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    • pp.369-375
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    • 2007
  • 목 적 : 각 소아 신장 질환에서 요 ${\beta}_2$-M 검사 결과를 비교해 보고, 일차성 신증후군에서 ${\beta}_2$-M 수치와 스테로이드를 사용한 기간과의 상관관계를 확인하고, 신세뇨관 손상을 반영하는 요 ${\beta}_2$-M과 신기능의 보편적 지표인 BUN, Ccr을 비교하여 신기능의 지표로 ${\beta}_2$-M이 유용한 지를 보았다. 방 법 : 2003년 1월부터 2006년 1월까지 중앙대학교 용산병원에 내원하여 24시간 소변검사를 시행 받고 ${\beta}_2$-M 검사를 시행 받은 혈뇨, 부종, 단백뇨 등의 증상이 있는 0-4세 사이의 환아 102명의 신장질환자와 같은 연령대의 대조군 22명을 대상으로 하여 후향적인 자료분석을 하였다. 각 신장 질환을 구분하여 독립변수로 삼았다. 각 신장 질환의 요 ${\beta}_2$-M 검사치를 종속변수로 삼아 독립표본 T검정을 이용하여 통계적 차이를 검증하였다. 또한 일차성 신증후군에서 ${\beta}_2$-M 수치가 의미 있게 높았던 군(양성)과 낮은 군을 구분하여(기준=$150{\mu}g/g-Cr$), 소변에서 단백뇨가 호전되어 퇴원하기까지의 치료기간을 비교하였다. 결 과 : 신장 질환자 102명 중 신증후군이 52명(MCNS(n=45, $72{\pm}45{\mu}g/g-Cr$), MPGN(n=3, $154{\pm}415{\mu}g/g-Cr$), FSGS(n=4, 1$188{\pm}046{\mu}g/g-Cr$), APSGN은 6명($93{\pm}404{\mu}g/g-Cr$), IgA 신병증은 7명($3414{\pm}106{\mu}g/g-Cr$), 급성 신우신염은 9명($742{\pm}160{\mu}g/g-Cr$), 방광염은 16명($179{\pm}168{\mu}g/g-Cr$), 그리고 HSPN은 12명($109{\pm}898{\mu}g/g-Cr$)으로 신증후군 환자가 65%로 가장 많았다. 그 중 IgA 신병증 과 급성 신우신염이 다른 군과 비교하여 24시간 요 ${\beta}_2$-M이 유의하게 높았다(P<0.05). 일차성 신증후군환자의 ${\beta}_2$-M 검사상 높은 군이 낮은 군과 비교하여 유의하게 치료기간이 길었으나(P<0.05), 각 신장질환에서 신기능 지표인 Ccr과 BUN, Cr 등은 24시간 요 ${\beta}_2$-M 과 유의한 차이가 없었다(P>0.05). 결 론 : 각 신장 질환의 24시간 요 ${\beta}_2$-M 수치를 조사한 결과 IgA nephropathy와 급성신우염이 다른 신질환 군과 비교하여 24시간 요 ${\beta}_2$-M 값이 유의하게 높았다. ${\beta}_2$-M 수치는 전반적인 신기능의 지표와 조직병리소견의 예측인자로써는 부적합하나, 상부 하부 요로감염의 감별과 신증후군 환자의 치료기간을 예측하는 데는 유용해 보였다.

오가피(五加皮) 물추출물이 허혈-재관류로 유발된 급성 신부전에 미치는 영향 (Effect of Acanthopanacis cortex Water Extract on Renal Function in Ischemia/Reperfusion-lnduced Acute Renal Failure Rats)

  • 이안숙;강대길;김은주;양선녀;엄재연;안준석;이호섭
    • 동의생리병리학회지
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    • 제21권5호
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    • pp.1201-1209
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    • 2007
  • The present study was designed to examine whether water extract of Acanthopanacis cortex(AC) has an effect on renal functional parameters in association with the expression of aquaporin 2 (AQP-2) and heme oxygenase-1 (HO-1) in the ischemia/reperfusion induced acute renal failure (ARF) rats. Polyuria caused by down-regulation of renal AQP 2 in the ischemia-induced ARF rats was markedly restored by administration of AC (200 mg/kg, p.o.) with restoring expression of AQP 2 in the kidney. Administration of AC lowered the renal expression of HO-1, which was upregulated in rats with ischemia/reperfusion-induced ARF. The renal functional parameters including creatinine clearance, urinary sodium excretion, urinary osmolality, and solute-free reabsorption were also markedly restored in ischemia-ARF rats by administration of AC. Histological study also showed that renal damages in the ARF rats were abrogated by administration of AC. Taken together, the present data indicate that AC ameliorates renal defects in rats with ischemia/reperfusion-induced ARF.

Dopamine $D_2$ Receptor 차단제인 Raclopride의 신장작용 (Renal Action of Raclopride, a Dopamine $D_2$ Receptor Antagonist, in Dogs)

  • 고석태
    • 약학회지
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    • 제45권6호
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    • pp.683-693
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    • 2001
  • This study was attempted to investigate the effect of raclopride, a dopamine $D_2$ receptor antagonist, on renal function in dog. Raclopride (70-220$\mu\textrm{g}$/kg), when given intravenously, Produced antidiuresis along with the decrease in free water clearance ( $C_{H_2O}$), urinary excretion of sodium and potassium ( $E_{Na}$ , $E_{K}$), partially decreased osmolar clearance ( $C_{osm}$) and increased reabsorption rates of sodium and potassium in renal tubules ( $R_{Na}$ , $R_{K}$). Raclopride administered into a renal artery did not influence on renal function in small doses (10 and 30$\mu\textrm{g}$/kg), whereas exhibited the decrease of urine volume (Vol) and $C_{H_2O}$ both in experimental and control kidney in much dose (100$\mu\textrm{g}$/kg), at this time, the decreased rates of both Vol. and $C_{H_2O}$) were more prominent in control kidney rather than that elicited in experimental kidney, and then only via was decreased in control kidney but increased in experimental kidney. Raclopride administered via carotid artery (30-200$\mu\textrm{g}$/kg) did not influence at all on renal function. Antidiuretic action induced by raclopride given intravenously was not affected by renal denervation. Raclopride given into carotid artery was little effect on renal function without relation to renal denervation. Above results suggest that raclopride produces antidiuresis by potentiation of antidiuretic hormone (ADH) action in blood without increase of ADH secretion in posterior pituitary gland, it is not related to renal nerve function in dogs.ogs.s.

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신규 백금착물 항암제 KBP31705-C127, KBP30603-901의 Cisplatin 및 Carboplatin과의 약동력학적 동태 비교 (Comparisons in Pharmacokinetic Profiles of New Platinum Coordination Complexes, KBP31705-C127 and KBP30603-901 with Cisplatin and Carboplatin)

  • 정인숙;이주선;허수정;김진숙;진창배;김동현;김명배;박경수;손연수
    • Biomolecules & Therapeutics
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    • 제4권4호
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    • pp.349-353
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    • 1996
  • The present study examined pharmacokinetic profiles of KBP31705-Cl27 and KBP30603-901, new platinum coordination complexes synthesized as anticancer candidates, in comparison with two well-known platinum-containing anticancer agents, cisplatin and carboplatin in rats. Under sodium pentobarbital anesthesia of male Sprague-Dawley rats, urinary bladder, and femoral artery and vein were catheterized for urine collection, blood sampling and drug injection, respectively Following i.v. administration of cisplatin (2 mg/kg), KBP31705-C127 (2 mg/kg), carboplatin (20 mg/kg) or KBP30603-901 (20 mg/kg), blood samples were collected at 2, 4, 6, 8, 10, 15, 20, 30, 45, 60 and 120 minutes. Urine samples were collected at 1-hr interval for 4 hr. Platinum concentrations in plasma and urine were measured using an inductively coupled plasmamass spectrometer. The plasma concentration-time curves were biphasic for all drugs during the time period studied. Compared with cisplatin, KBP31705-C127 showed similar decay patters in the alpha- and betaphases with slightly lower plasma concentrations. Urinary platinum excretion for cisplatin and KBP31705-C 127 was 56 and 52% of the administered dose in 4 hr, respectively. With regard to carboplatin and KBP 30603-901, a similar decay pattern was also observed in the alpha-phase. The half life of KBP30603-901 in the beta-phase, however, was much longer than that of carboplatin, which was consistent with the urinary excretion results that 46 and 59% of the administered dose were excreted in the urine in 4hr, respectively. The results suggest that platinum coordination complexes are primarily excreted via the renal route and KBP30603-901 can elicit longer duration of action due to slower renal excretion compared to carboplatin.

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