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1997 Fiscal Year Final Research Report Summary

OPTIMUM POTASSIUM CONCENTRATION OF THE PULMONARY PRESERVATION SOLUTION FOR CULTURED PULMONARY ENDOTHELIAL AND SMOOTH MUSCLE CELLS

Research Project

Project/Area Number 08671538
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Thoracic surgery
Research InstitutionOsaka University (1997)
Wakayama Medical University (1996)

Principal Investigator

MIYOSHI Shinichiro  Osaka University Medical School, Associate Professor, 医学部, 助教授 (00190827)

Co-Investigator(Kenkyū-buntansha) BESSHO Toshiya  Wakayama Medical College, Assistant Professor, 第一外科, 助手 (60254538)
Project Period (FY) 1996 – 1997
Keywordslung transplantation / lung preservation solution / human pulmonary artery endothelial cell / human pulmonary artery smooth muscle cell / optimal potasssium concentration / MTT assay
Research Abstract

The optimal potassium concentration of lung preservation solution has not been investigated systematically. The purpose of this study was to evaluate the effect of solutions with different potassium concentration on cultured pulmonary artery endothelial and smooth muscle cells.
A low potassium dextran solution with 4 mmol/L K+(LPD), a moderate potassium dextran solution with 60 mmoI/L K+(MPD) and a high potassium dextran solution with 100 mmol/L K (HPD) were used for preservation.
The viability of those cells stored in each solution at 10゚C was determined by MTT assay. MTT assay absorbance values for cultured pulmonary artery endothelial cells after 24 hours of cold storage were 0.147 * 0.011(mean*standard error) in LIP, 0.125*0.013 in MPD, and 0.189 * 0.039 in HPD (P<0.05 : HPD vs LPD and MPD). MTT assay absorbance values f* cultured pulmonary artery smooth muscle cells after 24 hours of cold storage were 0.028 * 0.003 in LPD, 0.042*0.008 in MPD, and 0.053*0.008 in HPD (PK<O.05 : HPD vs LPD and MPD).
From our results , we conclude that HPD is superior to LPD or MPD in 24-hour cold preservation of pulmonary artery endothelial and smooth muscle cells.

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Published: 1999-12-08  

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