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1995 Fiscal Year Final Research Report Summary

Studies of glucose meetabolism in cats.

Research Project

Project/Area Number 06660414
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field Applied veterinary science
Research InstitutionNippon Veterinary Animal Science University

Principal Investigator

WASHIZU Tsukimi  Nippon Veterinary Animal Science University, Vet.Anim.Sci.Assis.Prof., 獣医畜産学部, 講師 (20191736)

Co-Investigator(Kenkyū-buntansha) ISHIDA Takuo  Nippon Veterinary Animal Science University, Vet.Anim.Sci.Assoc.Prof., 獣医畜産学部, 助教授 (30143506)
ARAI Toshiro  Nippon Veterinary Animal Science University, Vet.Anim.Sci.Assis.Prof., 獣医畜産学部, 講師 (70184257)
Project Period (FY) 1994 – 1995
Keywordsprimary culture / hepatocytes / cats / glucose metabolism / glucose transport
Research Abstract

Glucose transport activity and its metabolism of the liver were studied using cultured feline hepatocyes.
Feline hepatocytes were isolated by collagenase perfusion and cultured in Williams medium E with 10% FCS,10^<-7> M insulin, 10^<-7> M dexamethasone, 5000 KIU/I aprotinin in collagen-coated dishes under 37゚C in a humid atmosphere of 5% CO_2 in air. The metabolic functions of the cultured feline hepatocytes were evaluated by urea formation, gluconeogenesis and albumin synthesis. The viability of the isolated hepatocvtes was 80.3-87.5% and the yield was 5.1-18.9*10^6 cells/g liver. The hepatocytes became firmly attached to the dishes within 4h after the culture started, spreaded within 24h, formed confluent monolayr within 3 days, and were maintained at least for 7 days. The metabolic functions were well preserved at least for 5 days. Therefore, this primary cultured feline hepatocytes were recognized as a useful in vitro system for several biochemical studies.
Additionaly, we investigated the activities of cytosol enzymes for the glucose metabolism of the feline hepatocytes during culure. The activities of hexokinase, pyruvate kinase, glucose 6-phosphate dehydrogenase, and lactate dehydrogenase were measured as glycolytic enzymes. The activities of these enzymes were well preserved for 7 days.
Also, we studied the sinusoidal lymphocytes isolated by collagenase perfusion. Many of the lymphocytes obtained from both the perfusates and the digested liver were large granular cymphocytes.

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Published: 1997-03-04  

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