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Regulation of Body Weight Regulation of body weight and set point theory. Leptin and body weight regulation. Melanocortin system: anorexigenic signaling. NPY and AGRP: orexigenic signaling. Putting it all together. Theories of Obesity
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Regulation of Body Weight Regulation of body weight and set point theory. Leptin and body weight regulation. Melanocortin system: anorexigenic signaling. NPY and AGRP: orexigenic signaling. Putting it all together.
Theories of Obesity • Can BW be regulated in the face of high or low caloric consumption (Jules Hirsch, early 1970’s)??? • Subjects • 100 healthy male volunteers with stable body weight for at least 6 months • three groups: thin, healthy weight, and overweight • confined to a sedentary life in a metabolic ward of a hospital • Design • food availability was systematically varied to promote: • a 10% BW gain • a 10% BW loss • measurements: • body weight, body mass index • food intake • feelings of hunger/satiety • mood
165 lbs + 10% 150 lbs - 10% 135 lbs “Fattening Phase” • forced to increase intake • hi fat diet • hi carbohydrate diet “Slimming Phase” • caloric restriction • low fat diet • low carbohydrate diet
165 lbs + 10% 150 lbs - 10% 135 lbs • Results – Following a 10% body weight loss • increase in appetite • food obsessions • felt sluggish • decrease in metabolic rate • When given free access to food, subjects • consumed larger meals • consumed more frequent meals • re-gained the weight lost during the “slimming phase”
165 lbs + 10% 150 lbs - 10% 135 lbs • Results – Following a 10% body weight gain • decrease in appetite • food aversions • bloating, gastrointestinal distress • increase in metabolic rate • When given free access to food, subjects • consumed smaller meals • consumed less frequent meals • chose foods that were low in fat content • lost the weight gained during the “fattening” phase
165 lbs + 10% 150 lbs - 10% 135 lbs • Conclusions • body weight is a regulated variable • transient behavioral changes • (i.e., over/under-eating) induces • behavioral (appetite) and physiological • (metabolic) changes that help to “defend” • a person’s body weight increased satiety signaling • The Big Question…. • Well, there are actually 2…. • How does the brain sense the body’s • level of adiposity stores? • If our body weights are regulated, how does • one become overweight/obese or maintain • a significant weight loss? increased orexigenic signaling
leptin leptin brain Factors that Regulate Body Weight • Leptin • protein product of the ob gene (also called OB protein) • synthesized in white adipose tissue • secreted in proportion to body adiposity • functions as a hormone • binds to leptin receptor (OB-R) in the brain • acts on multiple brain regions (ARC, VMH, DMH) • expression is sexually dimorphic
Melanocortin System • family of peptides cleaved from the proopiomelanoocortin (POMC) precursor • POMC neurons are expressed solely in the arcuate nucleus (ARC) • one product of POMC neurons is aMSH aMSH POMC protein • aMSH • alpha-melanocyte-stimulating hormone • synthesized within POMC neurons; secreted from the PVN • binds with melanocortin receptors in the PVN (MC4 receptor) • decreases food intake • release of aMSH is regulated by leptin • POMC neurons contain leptin receptors (OB-R) • melanocortin receptor knockout mice
NPY • neuropeptide Y • neurotransmitter; widespread expression in the brain • multiple biological actions • suppress reproductive function • causes smooth muscle to relax • decreases grooming behavior (in rats!) • anxiolytic effects • increases food intake • synthesized in the arcuate nucleus (ARC) • secreted from the paraventricular nucleus (PVN) in • response to a decline in energy stores • central administration of NPY • increases food intake • increases fat storage • decreases metabolic energy expenditure • increases body weight
AGRP • agouti-related protein • synthesized in the ARC (co-localized with NPY) • secreted in the PVN • endogenous antagonist of MC-4 receptor • stimulates food intake and weight gain • also regulated by leptin
Activation of the Melanocortin System Inhibits Food Intake Satiety Signal Decrease in Food Intake PVN MC4-R ARC
+ + Melanocortin System Is Modulated by Leptin Increased Satiety Signal Decrease in Food Intake PVN MC4-R OB-R Increased Leptin Secretion ARC
Melanocortin System Is Modulated by Leptin Decreased Satiety Signal Increase in Food Intake PVN - MC4-R OB-R + Decreased Leptin Secretion ARC
Orexigenic Signal Increase in Food Intake • AGRP • agouti-related protein • synthesized in the ARC (co-localized with NPY) • secreted in the PVN • endogenous antagonist of MC-4 receptor • stimulates food intake and weight gain • also regulated by leptin PVN ARC
Satiety Signal Decrease in Food Intake PVN + - ARC Dual Systems Function to Keep Body Weight Stable
How Does Leptin Regulate Body Adiposity? % body fat A)Healthy BW:Leptin secretion is stable and supports energy balance (FI = EE). B)Healthy BW:Decrease in leptin secretion signals a decrease in adipose stores and produces a positive energy balance (FI > EE). C)Healthy BW:Increase in leptin secretion signals an increase in adipose stores and produces a negative energy balance (FI < EE). D)Obese:Set point is elevated. Increase in leptin secretion fails to signal an increase in adipose stores and, thereby, fails to produce a negative energy balance (FI = EE). ** WHY ???
OVEREAT brain senses rise in plasma leptin 1) appetite is suppressed 2) metabolism increases Increased Leptin Secretion In an Individual with a Healthy Body Weight….
In an Overweight Individual…. OVEREAT brain senses rise in plasma leptin 1) appetite is not suppressed 2) metabolism doesn’t change Increased Leptin Secretion
In an Individual with a Healthy Body Weight…. Increased release of a-MSH Decreased release of AGRP Decreased release of NPY OVEREAT brain senses excessive calories 1) appetite is suppressed 2) metabolism increases Increased Leptin Secretion