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Cisplatin reabsorption from the ileal conduit ; a comparative study of blood concentration between inferior vena cava and portal vein in rat model

Research Project

Project/Area Number 12671570
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Urology
Research InstitutionFukuoka University

Principal Investigator

ARIYOSHI Asami  School of Medicine, Fukuoka University, Professor, 医学部, 教授 (00078768)

Co-Investigator(Kenkyū-buntansha) TOMITA Yoshihiro  School of Medicine, Fukuoka University, Instructor, 医学部, 助手 (60341434)
KANEGAE Shigehiro  School of Medicine, Fukuoka University, Instructor, 医学部, 助手 (10291840)
Project Period (FY) 2000 – 2001
Project Status Completed (Fiscal Year 2001)
Budget Amount *help
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 2001: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 2000: ¥1,600,000 (Direct Cost: ¥1,600,000)
KeywordsIleal conduit / Cisplatin / Inferior vena cava / Portal vein / Rat model
Research Abstract

1. LONG-TERM EXPERIMENTAL MODEL ; At first, we intended to make ten rat models of ileal conduit urinary diversion for a long-term experimental observation. Although 51 rats were operated, most of them died of bleeding due to self-injury of the urinary stom a with their teeth. So we altered our initial plan to a new experiment as shown below.
2. ACUTE EXPERIMENTAL MODEL ; Materials and Methods : Six male Wistar rats weighing 350〜500g were used for the ileal conduit model. A 10-cm ileal segment was attached to the bladder with a handmade connector and the distal end was opened on the abdomen to create a urinary stoma. The ileal segment was not connected to the bladder in 6 control rats. A bolus of cisplatin (1 mg/kg B. W.) was intravenously administered. After 20 minutes, blood sampling was done from both inferior vena cava (IVC) and portal vein (PV). Urine was collected for 20 minutes after the injection. Results : Body weight, urine volume, urinary concentration, excreted volume and excretion rate of cisplatin in urine showed no difference between the ileal conduit and the control (p=0.44, p=0.70, p=0.53, p=0.92, p=0.98). No difference was also observed in the blood cisplatin consentration between IVC and PV. But the cisplatin concentration ratio between PV and IVC (P/I ratio) was larger in the ideal conduit group (p=0.04) than that of the control group.
Discussion : Two possibilities are considered on the difference between cisplatin concentration of IVC and PV. One may be much water reabsorption from the ileal conduit. The other may be a shorter time of higher cisplatin concentration in urine than that in blood. This might result in less passive transport (reabsorption) of cisplatin from the ileal conduit. Further long-term experimental observation will be needed for pharmacological significance of cisplatin reabsorption from the intestine incorporated in the urinary tract.

Report

(3 results)
  • 2001 Annual Research Report   Final Research Report Summary
  • 2000 Annual Research Report

URL: 

Published: 2000-04-01   Modified: 2016-04-21  

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