Dietary Energy Restriction in Mice Reduces Hepatic Expression of Glucose-Regulated Protein 78 (BiP) and 94 mRNA

The influence of life span-prolonging dietary energy restriction on hepatic expression of glucose-regulated protein 78 and 94 (GRP78 and GRP94) RNA was investigated in female C3B10RF1 mice. Mice were either fed ad libitum or fed diets reduced 20 or 40% in energy but containing approximately equivale...

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Veröffentlicht in:The Journal of nutrition 1990-11, Vol.120 (11), p.1412-1417
Hauptverfasser: Spindler, Stephen R., Crew, Mark D., Mote, Patricia L., Grizzle, Judith M., Walford, Roy L.
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container_end_page 1417
container_issue 11
container_start_page 1412
container_title The Journal of nutrition
container_volume 120
creator Spindler, Stephen R.
Crew, Mark D.
Mote, Patricia L.
Grizzle, Judith M.
Walford, Roy L.
description The influence of life span-prolonging dietary energy restriction on hepatic expression of glucose-regulated protein 78 and 94 (GRP78 and GRP94) RNA was investigated in female C3B10RF1 mice. Mice were either fed ad libitum or fed diets reduced 20 or 40% in energy but containing approximately equivalent amounts of protein, fats, vitamins and minerals. Aging produced no changes in GRP mRNA. However, GRP78 and GRP94 mRNA levels were reduced ∼ 50 and 40%, respectively, by 40% energy restriction. This level of energy restriction produced a 43% reduction in the mean plasma glucose levels of young and old mice. The changes in GRP mRNA expression appear to be specific, because the levels of these RNAs were normalized to the level of polyadenylated RNA, and no changes were detected in the levels of a number of other mRNAs. Although extreme glucose deprivation increases GRP mRNA levels in cultured cell lines, physiologically relevant reductions in blood glucose had the opposite effect in the liver, in vivo. The regulatory pathway responsible for these effects is not known. GRP mRNA levels are elevated by agents that increase the level of malfolded proteins in the endoplasmic reticulum. Thus, energy restriction may act to reduce malfolded proteins in the endoplasmic reticulum of hepatic cells.
doi_str_mv 10.1093/jn/120.11.1412
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Mice were either fed ad libitum or fed diets reduced 20 or 40% in energy but containing approximately equivalent amounts of protein, fats, vitamins and minerals. Aging produced no changes in GRP mRNA. However, GRP78 and GRP94 mRNA levels were reduced ∼ 50 and 40%, respectively, by 40% energy restriction. This level of energy restriction produced a 43% reduction in the mean plasma glucose levels of young and old mice. The changes in GRP mRNA expression appear to be specific, because the levels of these RNAs were normalized to the level of polyadenylated RNA, and no changes were detected in the levels of a number of other mRNAs. Although extreme glucose deprivation increases GRP mRNA levels in cultured cell lines, physiologically relevant reductions in blood glucose had the opposite effect in the liver, in vivo. The regulatory pathway responsible for these effects is not known. GRP mRNA levels are elevated by agents that increase the level of malfolded proteins in the endoplasmic reticulum. Thus, energy restriction may act to reduce malfolded proteins in the endoplasmic reticulum of hepatic cells.</description><subject>Aging - metabolism</subject><subject>Animals</subject><subject>ARN MENSAJERO</subject><subject>ARN MESSAGER</subject><subject>Biological and medical sciences</subject><subject>Carrier Proteins - genetics</subject><subject>Diet</subject><subject>DIETA</subject><subject>ENERGIA</subject><subject>ENERGIE</subject><subject>Energy Intake</subject><subject>energy restriction</subject><subject>Female</subject><subject>FOIE</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation</subject><subject>GLUCOSA</subject><subject>GLUCOSE</subject><subject>Glucose - administration &amp; dosage</subject><subject>Glucose - metabolism</subject><subject>glucose-regulated protein</subject><subject>GRP mRNA</subject><subject>Heat-Shock Proteins</subject><subject>HIGADO</subject><subject>HSP70 Heat-Shock Proteins</subject><subject>liver</subject><subject>Liver - metabolism</subject><subject>Liver. Bile. 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Psychology</topic><topic>Gene Expression Regulation</topic><topic>GLUCOSA</topic><topic>GLUCOSE</topic><topic>Glucose - administration &amp; dosage</topic><topic>Glucose - metabolism</topic><topic>glucose-regulated protein</topic><topic>GRP mRNA</topic><topic>Heat-Shock Proteins</topic><topic>HIGADO</topic><topic>HSP70 Heat-Shock Proteins</topic><topic>liver</topic><topic>Liver - metabolism</topic><topic>Liver. Bile. 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Mice were either fed ad libitum or fed diets reduced 20 or 40% in energy but containing approximately equivalent amounts of protein, fats, vitamins and minerals. Aging produced no changes in GRP mRNA. However, GRP78 and GRP94 mRNA levels were reduced ∼ 50 and 40%, respectively, by 40% energy restriction. This level of energy restriction produced a 43% reduction in the mean plasma glucose levels of young and old mice. The changes in GRP mRNA expression appear to be specific, because the levels of these RNAs were normalized to the level of polyadenylated RNA, and no changes were detected in the levels of a number of other mRNAs. Although extreme glucose deprivation increases GRP mRNA levels in cultured cell lines, physiologically relevant reductions in blood glucose had the opposite effect in the liver, in vivo. The regulatory pathway responsible for these effects is not known. 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subjects Aging - metabolism
Animals
ARN MENSAJERO
ARN MESSAGER
Biological and medical sciences
Carrier Proteins - genetics
Diet
DIETA
ENERGIA
ENERGIE
Energy Intake
energy restriction
Female
FOIE
Fundamental and applied biological sciences. Psychology
Gene Expression Regulation
GLUCOSA
GLUCOSE
Glucose - administration & dosage
Glucose - metabolism
glucose-regulated protein
GRP mRNA
Heat-Shock Proteins
HIGADO
HSP70 Heat-Shock Proteins
liver
Liver - metabolism
Liver. Bile. Biliary tracts
Membrane Proteins - genetics
Mice
Molecular Chaperones
mouse
PROTEINAS
PROTEINE
RATON
REGIME ALIMENTAIRE
RNA, Messenger - analysis
SOURIS
Vertebrates: digestive system
title Dietary Energy Restriction in Mice Reduces Hepatic Expression of Glucose-Regulated Protein 78 (BiP) and 94 mRNA
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