presenters: huma younus faisal r. khan · 1.00 1.25 1.50 1.75 2.00 lean obese tlr2 protien in...
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THE SUPPRESSION OF TOLL LIKE RECEPTORS (TLR) BY INSULIN
Presenters:
Huma Younus Faisal R. Khan Mentor:
Paresh Dandona, M.B.B.S., Ph.D., F.R.C.P, F.A.C.P, F.A.C.C
Chief of Endocrinology, SUNY at Buffalo
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• Diabetes affects 25.8 million people of all ages
• 8.3 percent of the U.S. population
• DIAGNOSED 18.8 million people
• UNDIAGNOSED 7.0 million people
FAST FACTS … DIABETES MELLITUS
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CLINICAL QUESTION
• Type 2 Diabetes is caused by Insulin resistance at cellular level…
1. How does that happen (basic
mechanism) ?
2. What pathways are involved?
3. Is there a way to reverse it?
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1.Mechanism of Insulin Resistance ... Role of Innate Immune System
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BACKGROUND..
INNATE IMMUNE SYSTEM
• Consists of germline defense mechanisms that are directed against molecular components found only in microorganisms
• The cardinal signs of inflammation i.e. tumor, rubor, calor, and dolor are products of the innate immune response
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FUNCTIONS OF THE INNATE IMMUNE SYSTEM
• Detection of microorganisms and first-line defense against invasion and infection.
• Activation and instruction of adaptive
immune responses.
• Regulation of inflammation.
• Maintenance of “immunologic homeostasis” within the host.
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Three Main components: 1). Pathogen-Associated Molecular Patterns (PAMPs): Various molecules that activate the innate immune system. 2). Pattern Recognition Receptors(PRRs): Recognize PAMPs( LPS etc.) and initiate the inflammatory pathways. 3). Inflammatory cytokines.
COMPONENTS OF INNATE IMMUNE SYSTEM
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• A prototypical PAMP is bacterial endotoxin, or lipopolysaccharide (LPS), which is a component of the outer membrane of all gram-negative bacteria.
• Endotoxins contain Lipid A which interacts with the toll-like receptors (PRRs).
PATHOGEN-ASSOCIATED MOLECULAR PATTERNS (PAMPS)
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• Innate immune system recognizes microbes through PRRs also known as pathogen recognition receptors.
• Expressed constitutively on many types of innate immune cells and on the professional antigen presenting cells (macrophages, dendritic cells, monocytes, and B lymphocytes).
• Include TLRs, NLRs, RLRs.
Pattern Recognition Receptors (PRRs)
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• Structure.
• Distribution.
• Types.
TOLL LIKE RECEPTORS
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STRUCTURE OF TLRS All TLRs have:
• An extracellular ligand
recognition and binding domain.
• A single trans-membrane domain
• The cytoplasmic (signaling) domain is homologous to the interleukin-1 .
Variations in TLR ligands initiate specific immunological responses
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Toll like receptors (TLR) are located on macrophages, monocytes, neutrophils,
dendritic cells, mast cells, mucosal epithelial cells and endothelial cells, all of which are
the mediators of innate immunity.
CELLULAR DISTRIBUTION OF TLRS
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TYPES OF TOLL LIKE RECEPTORS
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• TLR2 is a cell surface receptor. • Recognizes certain lipid moieties
derived from bacteria such as bacterial lipoproteins and peptidoglycans.
• TLR2 might play a role in ischemia-reperfusion induced myocardial injury.
TLR 2
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• Similar to TLR 2 in distribution and activation.
• TLR4 has also been shown to play an important role in atherogenesis and diet-induced obesity and related insulin resistance
TLR 4
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TLR 7 & 9
• TLR7 and TLR9 are endosomic receptors, that recognizes single stranded viral RNA (ssRNA) and microbial DNA, respectively.
• Therefore, TLR7 and TLR9 modulate adaptive immune responses including autoimmunity against chromatin, e.g., in systemic lupus erythematosus (SLE)
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PATHWAYS INVOLVED AND ROLE OF TOLL LIKE RECEPTORS IN INFLAMMATORY CASCADE..
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• Activated by PAMPS.
• Cause transcriptional activation of genes encoding for pro-inflammatory cytokines, chemokines etc.
• Result in activation of antigen-specific adaptive immune response
ACTIVATION OF TLR SIGNALING
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TLR ORGANIZATION AND SIGNALING PATHWAYS
• IL-1 receptor associated kinases 1 and 4 (IRAK1, IRAK4).
• Tumor necrosis factor receptor associated factor 6. TRAF 6
• Transforming growth factor beta activated protein kinase 1 (TAK1) • Mitogen activated protein kinases (MAPKs).
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• All TLRs except TLR3 utilize myeloid differentiation
primary response protein 88 (MyD88).
• MyD88 adapter connects with various molecules including IRAK, TRAF6, TAK.
• This complex kinase cascade culminates in activation of broad array of genes influencing cell survival, activation, and proliferation through AP-1 and NF-kappa B
SIGNALING PATHWAYS
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• Plasma concentration of LPS is significantly increased in obese patients and is significantly related to plasma insulin concentration and HOMA-IR index of insulin resistance, showing a link between LPS concentration and insulin resistance.
• Human atherosclerotic plaques contain endothelial cells and macrophages expressing TLR1/2 and TLR4.
• High LPS concentrations can potentially lead to TLR activation and induction of inflammation leading to insulin resistance.
ROLL OF TLRS IN INFLAMMATION, ATHEROSCLEROSIS AND IR
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ROLL OF TLRS IN INFLAMMATION, ATHEROSCLEROSIS AND IR
• Although the physiological reason for the presence of these receptors is to recognize pathogens and to trigger immune mechanisms, their over stimulation or abnormal responses could easily mediate processes which could lead to chronic or auto-immune inflammation.
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3. WAYS TO REVERSE INFLAMMATION AND INSULIN
RESISTANCE
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EARLY 18TH CENTURY
• High doses of sodium salicylate (5.0–7.5 g/d) were first demonstrated to diminish glycosuria in diabetic patients having “the milder form of the disease,” presumably type 2 diabetes.
• 1876 Ebstein concluded that sodium salicylate could make the symptoms of diabetes mellitus totally disappear. (1, 3).
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HISTORICAL BACKGROUND
1957 Reid and colleagues found • Insulin-treated diabetic, given high-dose aspirin to
treat the arthritis no longer required daily insulin injections(4).
• Upon resolution of the joint symptoms, aspirin was discontinued, and a repeat glucose tolerance test was grossly abnormal.
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MORE RECENTLY
• Increased levels of markers and mediators of inflammation and acute-phase reactants such as fibrinogen, C-reactive protein (CRP), IL-6, plasminogen activator inhibitor-1 (PAI-1), sialic acid, and white cell count correlate with incident T2D.
• Adipose tissue–derived proinflammatory cytokines such as TNF-α could actually cause insulin resistance in experimental models.
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OTHER OBSERVATIONS
• TNF-α, IL-6, MCP-1 etc produced by adipose tissue as well as by mononuclear cells(MNC).
• So Adipose tissue and MNC are the key cells involved in producing the inflammatory cytokines and inducing insulin resistance….
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FACTORS AND MECHANISM OF OBESITY INDUCED DM2 --THE “INFLAMMATION HYPOTHESIS”
. Obesity-induced chronic inflammation is a key component in the pathogenesis of Insulin resistance. Pro-inflammatory cytokines can cause insulin resistance (IR) in adipose tissue, skeletal muscle and liver by inhibiting insulin signal transduction. Positive correlation between BMI and plasma TNFα concentrations. However, the exact mechanism is still poorly understood
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PATHWAYS… OVERVIEW
• Two major pathways
• JNK and IKKβ pathways, involving cytokines and TLRs.
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Stimuli that have been shown to activate these pathways during metabolic dysregulation include ligands for TNF-α, IL-1, Toll, or AGE receptors (TNFR, IL-1R, TLR, or RAGE, respectively). Obesity-induced IKKβ activation leads to NF-κB translocation and the increased expression of numerous markers and potential mediators of inflammation that can cause insulin resistance. Obesity-induced JNK activation promotes the phosphorylation of IRS-1 at serine sites that negatively regulate normal signaling through the insulin receptor/IRS-1 axis. Examples include serine-302 (pS302) and serine-307 (pS307).
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HYPOTHESIS
• First controlled trial to investigate the effect of insulin on the expression of TLR in the peripheral blood mononuclear cells (MNC) and adipose tissue of obese and Type 2 diabetes mellitus subjects.
• The central hypothesis of this application was that insulin will suppress the expression of TLR2, TLR4, TLR7 and TLR9 at the mRNA and protein levels in MNC and adipose tissue of obese and type 2 diabetic subjects.
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Thank You.. Please stay tuned for the second part of presentation…
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Clinical trial and results
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CHALLENGES
• What came first ? Obesity or Diabetes (chicken or egg)? • Prove that obesity induces resistance. • Why do Type 2 diabetics improve with insulin if they are
not deficient in it??? • Why do they require huge amounts of insulin?? • When should Insulin be started?? Should we wait for
their pancreas to totally fail before we do it? • Why Why Why………. Why did I even take this project!!
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STUDY DESIGN
Double blinded, cross-over and controlled prospective study.
A total of 60 subjects divided into 20 lean, 20
obese and 20 obese type 2 diabetic (DM) subjects were enrolled.
Fasting blood samples and fat biopsies were
collected from all subjects to compare basal TLR expression between the groups.
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EXPERIMENTAL METHOD
• Insulin/dextrose/potassium regimen at 3 different doses of insulin (2, 3.5 and 5 U/hr) were given to obese and diabetic subjects in the experimental arm followed by the control arm where 3 infusions with dextrose/potassium regimen only in quantities similar to those infused with each of the 3 insulin doses and a normal physiological saline infusion was given.
• Dextrose infusion rate was titrated to maintain blood
glucose concentration at target levels within 10mg of the baseline glucose concentration (usually 80-120 mg/dl).
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EXPERIMENTAL METHOD • Potassium Chloride was co-infused to prevent
hypokalemia and was monitored every 2 hourly during all insulin infusions.
• Blood samples (30 ml/time point for a total of 210 ml/visit) were drawn at Baseline, 2, 4, 8 and 14 hours following the start of the infusions.
• Fat biopsy samples were taken at three separate visits, for a total of six fat biopsies one in the fasting stage and one at 12 hours.
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INCLUSION CRITERIA
• Lean Group:1)Age: 20 to 65 years 2) Sex: male or female 3)Normal fasting plasma glucose (65-100 mg/dl), 4)Normal BMI (20-25).
• Obese Group:1)Age: 20 to 65 years 2) Sex: male or female 3)Normal fasting plasma glucose (65-100 mg/dl), 4)BMI> 30.
• DM Group: 1)Type 2 Diabetes Mellitus 2)Age: 20 to 65 years 3)Sex: male or female 4)BMI >30 5)Hba1c < 8% 6)If on statins, angiotensin converting enzyme inhibitor, angiotensin receptor blocker or low dose aspirin, should be on a stable dose for one month.
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EXCLUSION CRITERIA
• Pregnancy • Congestive heart failure. • Heart Rate <50 beats /minute , Sick Sinus
Syndrome , Second or third degree heart block. • Blood pressure <80 mm systolic or > 160/100
mmHg • Coronary event or procedure (myocardial
infarction, unstable angina, coronary artery bypass surgery or coronary angioplasty) in the previous three months 8)Hepatic disease (transaminase > 3 times normal)
• Renal impairment (serum creatinine > 1.5)
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EXCLUSION CRITERIA
• Participation in any other concurrent clinical trial • Potassium (K+) values <3.5 meq/l to > 5.5 meq/l) • Use of an investigational agent or therapeutic regimen
within 30 days of study • Type 2 diabetics on thiazolidinediones and/ or insulin • Subjects on steroids, NSAIDS or antioxidants • Patients taking exenatide or sitaglipin or loop diuretics. • Anemia (Hemoglobin level less than 12gm/dl in females
and 13gm/dl in males). • Any other life-threatening, non-cardiac disease.
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LABORATORY PROCEDURES
• MNC isolation by Ficoll-hypaque method. This method provides yields greater than 95% pure PMN and MNC suspensions.
• Quantification of TLRs (2, 4, 7 and 9) mRNA in MNC and adipose tissue by RT-PCR.
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RESULTS: 1
1. What came first….. 2. Prove obesity causes insulin resistance….
TLR expression in Obese as compared to lean subjects.
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TLR EXPRESSION IN ADIPOSE TISSUE FROM LEAN AND OBESE SUBJECTS
• Fat aspiration was performed lean BMI: 22.8±1.9 and obese BMI: 35.6±5.1 subjects following an overnight fast.
• The mRNA expression of TLR2, TLR4, TLR7 and TLR9 were measured by real time RT-PCR.
• There were no significant statistical differences in
baseline characteristics between the two groups.
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TRL2 TLR4 TLR7 TLR9
mR
NA
Exp
ress
ion
in A
dipo
se T
issu
e (A
rbitr
ary
Uni
ts)
0.00
0.25
0.50
0.75
1.00
1.25
1.50
1.75
2.00LEANOBESE
TL
R2
pro
tie
n in
Ad
ipo
se
Tis
su
e
(Arb
itra
ry U
nit
s)
0
20
40
60
80
100
120LEANOBESE
*
A B TLRs in adipose tissue from obese and lean subjects. A) TLR2, TLR4, TLR7 and TLR9 mRNA expression in Adipose tissue of obese and lean subjects. B) TLR-2 protein expression in adipose tissue from obese and lean subjects (n=8 vs. 8) *= P<0.05, t-test.
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RESULTS: 2
What happens to TLRs after a high fat high carbohydrate(HFHC) meal in lean subjects.
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EFFECT OF HIGH FAT HIGH CARBOHYDRATE (HFHC) MEAL ON TLR4 EXPRESSION AND PLASMA ENDOTOXIN
CONCENTRATIONS
• Four groups (10-12 each) of healthy lean subjects were given either 300 Calories of glucose, 300 Calories of dairy cream, 900 Calories HFHC meal or water to ingest following an overnight fast.
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Hours After Challenge0 1 2 3
80
90
100
110
120
130
140
150
160WaterGlucoseCreamMeal
*#
*#% C
hange in
TLR4 mR
NA Expre
ssion in
MNC* +$+$
Hours After Challenge0 1 2 3
% chang
e in TLR
4 protein
levels in
MNC
75
90
105
120
135
150
165
*#+$#
*#
WaterGlucoseCreamMeal
TLR4 mRNA (A) and protein (B) expression in MNC following glucose, cream and meal intake compared to water intake in normal healthy subjects. *= P<0.05 by RMANOVA compared to baseline following cream challenge; #= P<0.05 by two-way ANOVA comparing cream and water groups; += P<0.05 by RMANOVA compared to baseline following meal challenge and $=P<0.05 by two-way ANOVA comparing meal and water groups.
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HOURS0 1 2 3%
chan
ge in
Plasm
a End
otoxin
Conc
entra
tions
60
80
100
120
140
160
180
200
220WaterGlucoseCreamMeal
*#
*#
Percent change in Plasma Endotoxin concentrations following glucose, cream and meal intake compared to water intake in normal healthy subjects. *= P<0.05 by RMANOVA compared to baseline following cream challenge; #= P<0.05 by two-way ANOVA comparing cream and water groups
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INFERENCES
• There is an acute elevation of plasma endotoxin levels following a high fat and/or high carbohydrate (HFHC) meal.
• There is increased expression of TLR mRNA and proteins following HFHC meal.
• Since TLR are activated by endotoxins, elevated endotoxin levels can stimulate TLRs and initiate an inflammatory response.
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ANSWERS
1. No one knows what came first…but if you are overweight , Diabetes is certainly coming.
2. Obesity causes resistance by activating inflammation. Watch what you eat. It’s a good idea to cut the cream in your Double Double coffee.
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RESULTS: 3
1. Why do Type 2 diabetics improve with insulin if they are not deficient in it???
2. Why do they require huge amounts of insulin?? 3. When should Insulin be started?? Should we wait for
their pancreas to totally fail before we do it? Lets give Insulin and see !!!! Effect of Insulin on Toll Like Receptors in Obese and Diabetic groups
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Hours0 2 4 6
% Chan
ge in TL
R2 mRNA
Express
ion
60
80
100
120
140
160
InsulinDextroseSaline
*# *
Hours0 2 4 6
% Chan
ge in TL
R4 mRNA
Express
ion
40
60
80
100
120
140 InsulinDextroseSaline
*# *#
Figure 1: TLRs mRNA expression by RT-PCR following insulin, dextrose or saline infusion in DM subjects. A) TLR2, B) TLR4 mRNA expression in MNC of DM subjects following 2unit/hour insulin infusion compared to dextrose infusion control. *= P<0.05, RMANOVA compared to baseline and # P<0.05, 2-way RMANOVA compared to control groups.
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Hours0 2 4 6
% Chan
ge in TL
R7 mRNA
Express
ion
40
60
80
100
120
140 InsulinDextroseSaline
*# *#
Hours0 2 4 6
% Chan
ge in TL
R9 mRNA
Express
ion
40
60
80
100
120
140 InsulinDextroseSaline
*# *#
Figure 2: TLRs mRNA expression by RT-PCR following insulin, dextrose or saline infusion in DM subjects. A) TLR7 and B) TLR9 mRNA expression in MNC of DM subjects following 2unit/hour insulin infusion compared to dextrose infusion control. *= P<0.05, RMANOVA compared to baseline and # P<0.05, 2-way RMANOVA compared to control groups.
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Hours following Infusion0 2 4 8 14 16
Chan
ge in
TLR4
mRNA
Expre
ssion
in M
NC (%
)
70
80
90
100
110
120 DextroseInsulinSaline
*#
*#
Effect of Low Dose Insulin infusion on TLR4 mRNA in MNC in Obese subjects
* P < 0.05 by One Way RM ANOVA # P < 0.05 by Two Way RM ANOVA
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Hours following Infusion0 2 4 8 14 16
Chan
ge in
TLR4
Prote
in Ex
press
ion in
MNC
(%)
60
70
80
90
100
110
120 DextroseInsulin
*#
Effect of Low Dose Insulin infusion on TLR4 protein in MNC in Obese subjects
* P < 0.05 by One Way RM ANOVA # P < 0.05 by Two Way RM ANOVA
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INFERENCES
• Insulin suppresses the mRNA expression of TLR2, 4, 7 and 9 from MNC within 2 hours of the commencement of insulin infusion with a maximum fall at 4 hours.
.
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INSULIN AS INSULIN SENSITIZER
• It is hypothesized that through its anti-inflammatory effects insulin possibly acts as a self sensitizer.
• This can be explained on the basis of the fact that insulin signaling and serine kinase inflammatory pathway intersect at IRS (Insulin receptor signaling) molecule level.
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Figure: Insulin-receptor signaling interfaces with inflammatory signaling at the level of insulin-receptor substrates through activation of serine kinases. These kinases respond to both lipids and cytokines. Both IRS-1 and IRS-2 contain a number of serine residues (indicated by white stars) that are targeted by various kinases, which have been more extensively mapped for IRS-1 (ref. 50). All of the molecules listed that regulate insulin action in response to inflammatory signals converge on IRS-1.
Common target
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Hours following Infusion0 2 4 8 14 16
Change
in P38 P
rotein in
MNC (%
)
60
70
80
90
100
110
120
130 DextroseInsulinSaline
*
Effect of Low Dose Insulin infusion on p38 protein in MNC in Obese (Upper) and T2DM(Lower) subjects.
Hours following Infusion0 2 4 8 14 16
Change
in P38 P
rotein in
MNC (%
)
70
80
90
100
110
120DextroseInsulinSaline
*#
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Effect of Low Dose Insulin infusion on PTP-1B protein in MNC in Obese and T2DM subjects
Hours following Infusion0 2 4 8 14 16Cha
nge in P
TP-1B Pr
otein in
MNC (%
)
60
70
80
90
100
110
120
130 DextroseInsulinSaline
*# *
Hours following Infusion0 2 4 8 14 16Cha
nge in P
TP-1B Pr
otein in
MNC (%
)
60
70
80
90
100
110
120
130 DextroseInsulinSaline
*# *
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Effect of Low Dose Insulin infusion on JNK-1 protein in MNC in Obese and T2DM subjects
Hours following Infusion0 2 4 8 14 16
Change
in JNK-
1 Protei
n in MN
C (%)
60
70
80
90
100
110
120
130DextroseInsulinSaline
*#
Hours following Infusion0 2 4 8 14 16
Change in
JNK-1 Pr
otein in M
NC (%)
60
70
80
90
100
110
120
130 DextroseInsulinSaline
*# *#
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Hours following Infusion0 2 4 8 14 16
Change
in PKC-
βIImRN
A Expres
sion in M
NC (%)
70
80
90
100
110
120 DextroseInsulinSaline
*# *#
PKC-β II mRNA- Adipose tissue Insulin Dextrose Saline
% Chan
ge
0
20
40
60
80
100
120 0hr14 hr
*#
Effect of Low Dose Insulin infusion on PKC-β ΙΙ mRNA in Adipose Tissue and MNC in Obese subjects
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IKK-β mRNA- Adipose tissue Insulin Dextrose Saline
% C
hang
e
0
20
40
60
80
100
120 0hr14 hr
*#
Effect of Low Dose Insulin infusion on IKK-β mRNA in Adipose Tissue in Obese subjects
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WHAT DOES ALL THIS FANCY DATA TRANSLATE INTO ???? ANSWERS
1. Why do Type 2 diabetics improve with insulin if they are not deficient in it???
2. Why do they require huge amounts of insulin?? • Insulin has the power to overcome the serine
kinase induced inflammatory and insulin resistance cascade probably by competitive activation of IRS.
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3. When should Insulin be started?? Should we wait for their pancreas to totally fail before we do it? • Early insulin administration in Obese with
metabolic syndrome and type 2 diabetes patients may overcome the resistance and provide better glycemic control than oral hypoglycemics alone.
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REFERENCES
1. Ebstein W. Zur therapie des Diabetes mellitus, insbesondere über die Anwendung des salicylsauren Natron bei demselben. Berliner Klinische Wochenschrift. 1876;13:337–340.
2. Williamson R.T. On the treatment of glycosuria and diabetes mellitus with sodium salicylate. Br. Med. J. 1901;1:760–762.
3. Shoelson S. Invited comment on W. Ebstein: on the therapy of diabetes mellitus, in particular on the application of sodium salicylate. J. Mol. Med. 2002;80:618–619.[PubMed]
4. Reid J., Macdougall A.I., Andrews M.M. On the efficacy of salicylate in treating diabetes mellitus. Br. Med. J. 1957;2:1071–1074. [PMC free article][PubMed]
5. Hecht A., Goldner M.G. Reappraisal of the hypoglycemic action of acetylsalicylate. Metabolism. 1959;8:418–428.[PubMed]
6. Gilgore S.G. The influence of salicylate on hyperglycemia. Diabetes. 1960;9:392–393.
7. Baron S.H. Salicylates as hypoglycemic agents. Diabetes Care. 1982;5:64–71.[PubMed]
8. Yuan M., et al. Reversal of obesity- and diet-induced insulin resistance with salicylates or targeted disruption ofIkkβ. . Science. 2001;293:1673–1677.[PubMed]
9. Hundal R.S., et al. Mechanism by which high-dose aspirin improves glucose metabolism in type 2 diabetes. J. Clin. Invest. 2002;109:1321–1326. doi: 10.1172/JCI200214955. [PMC free article][PubMed] [Cross Ref]
10. Shoelson S.E., Lee J., Yuan M. Inflammation and the IKKβ/IκB/NF-κB axis in obesity- and diet-induced insulin resistance. Int. J. Obes. Relat. Metab. Disord. 2003;27(Suppl. 3):S49–S52.[PubMed]
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THANK YOU FOR YOUR TIME…