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Postulated Mechanisms of Insulin Postulated Mechanisms of Insulin Resistance Resistance PTP-1B PTP-1B Mass & Activity Mass & Activity Impaired Phosphorylation of Impaired Phosphorylation of Insulin Receptor, IRS-1 Insulin Receptor, IRS-1 PI-3 Kinase Activity PI-3 Kinase Activity Attenuated Insulin Signaling Attenuated Insulin Signaling Reduced Phosphorylation of ApoB or Reduced Phosphorylation of ApoB or an apoB-chaperone an apoB-chaperone Enhanced Stability and Accelerated Enhanced Stability and Accelerated Assembly of ApoB Assembly of ApoB Overproduction of VLDL Overproduction of VLDL ER-60 MTP

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Postulated Mechanisms of Insulin ResistancePostulated Mechanisms of Insulin Resistance

PTP-1BPTP-1B Mass & Activity Mass & Activity

Impaired Phosphorylation ofImpaired Phosphorylation ofInsulin Receptor, IRS-1Insulin Receptor, IRS-1

PI-3 Kinase ActivityPI-3 Kinase Activity

Attenuated Insulin SignalingAttenuated Insulin Signaling

Reduced Phosphorylation of ApoB or Reduced Phosphorylation of ApoB or an apoB-chaperonean apoB-chaperone

Enhanced Stability and Accelerated Assembly of ApoBEnhanced Stability and Accelerated Assembly of ApoB

Overproduction of VLDLOverproduction of VLDL

ER-60MTP

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Intestine

Contribution of the Intestinal LipoproteinsContribution of the Intestinal Lipoproteinsto Metabolic Dyslipidemia in Insulin Resistanceto Metabolic Dyslipidemia in Insulin Resistance

Liver

ApoB48

ApoB100

Intestinal Lipoprotein Metabolism

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Dietary Dietary

CholesterolCholesterol

Dietary Dietary

FatFat

LuminalLuminal

TriglycerideTriglyceride

LipasesLipases

Bile AcidsBile Acids

Fatty AcidsFatty Acids

Mocellar CholesterolMocellar Cholesterol

Fatty AcidsFatty Acids

CholrdyrtolCholrdyrtol

ApoB48 + TG + CEApoB48 + TG + CE

TGTG

CMCM

ABCA1ABCA1

ABCG5ABCG5

ABCG8ABCG8

Fatty Acid TransportersFatty Acid Transporters

Intestinal Epithelial CellIntestinal Epithelial Cell

(Intake)(Intake)

(Uptake)(Uptake)

(Chylomicron (Chylomicron

Assembly)Assembly)

(Cholesterol (Cholesterol

Excretion)Excretion)

Intestinal Lipid Absorption

(Trigleride (Trigleride

Synthesis)Synthesis)

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Hypothesis III:Fasting and postprandial hyperlipidemia in insulin resistant states may be attributable in part to intestinal oversecretion of apoB-48 containing lipoproteins

Experimental Approach:•Dietary induction of an insulin resistant state in

the hamster by high fructose feeding

• Isolation of adult viable villi from Syrian hamster small intestine.

• -In Vivo Studies to assess production rate of intestinal (apoB48-containing) lipoproteins

• -Ex Vivo Studies to assess intestinal apoB48 lipoprotein synthesis and secretion, mechanisms of chylomicron assembly, role of de novo lipogenesis in intestinal lipoprotein secretion in the fasting and postprandial states