Anti-Obesity Drugs

Anti-Obesity Drugs

Anti-Obesity Drugs Aaron Cheatham Fat is just what we thought The cause of excess subcutaneous and visceral fat deposition in an individual is the cumulative effect of an imbalance between the energy of ingested food and that expended in the course of daily activities Essentially, the deposition of fat is an adaptive physiologic process of energy storage that became maladaptive when technological advances altered the balance between the availability of food and the bodys expenditure of energy. Historical Roots

Fat as a natural mechanism for storing food reserves The ability to store surplus fat from the least possible amount of food intake may have made the difference between life and death Evolutionary advantage Fat was culturally pleasing well into the first decades of the 20 th century Paintings, literature, politically The Venus of

Willendorf 25,000 BC President William Taft(18571930) At 511, 243 at graduation 320 pounds when he became secretary of war 340 pounds when he was in the White House

body mass index of more than 45 Taking Notice The health consequences of obesity began to be noted in the medical literature in the eighteenth century Throughout most of the nineteenth century and well into the early twentieth century, medical opinion held that carrying an extra 20 to 50 pounds of excess flesh was healthy It provided a reserve of vitality that would keep a person from being run down by a long lasting illness

Being thin was unhealthy and advice was geared towards how to gain weight First Alarm The first alarm against excess weight was sounded by the insurance industry By the 1930s, the medical profession made a total about face on the desirability of excess flesh and accepted excess fat as a health problem Psychiatrists capitalize by convincing people that obesity is a psychological malfunction, soon realized false

It was not until 1960s that the study of obesity was in full swing and it was at this time that fat became an organ with its own hormones, receptors, genetics, and cellular biology rather than the passive store of energy Advances Agricultural Revolutions good but bad Thermodynamics Nutritional balance Energy Conversion

Gastric physiology Alphonse Quetelets body mass index (BMI), is now used for the classification of overweight status. Classification Obesity is a medical condition in which excess body fat has accumulated to the extent that it may have an adverse effect on health. It is defined by body mass index (BMI) and further evaluated in terms of fat distribution via the waisthip ratio and total cardiovascular risk factors.

BMI is closely related to both percentage body fat and total body fat. Classification Metric: BMI = kilograms / meters2 US customary and imperial: BMI = lb * 703 / in2 BMI Classification < 18.5

underweight 18.524.9 normal weight 25.029.9 overweight 30.034.9 class I obesity 35.039.9 class II obesity 40.0

class III obesity Great Example!!!! Height: 58 Weight: 159 BMI: 23 Great Body weight! Effects on health cardiovascular diseases, diabetes mellitus type 2

obstructive sleep apnea certain types of cancer osteoarthritis Health Effects - Mortality Obesity is one of the leading preventable causes of death worldwide mortality risk is lowest at:

BMI of 2025 kg/m2 in non-smokers 2427 kg/m2 in current smokers BMI above 32 has been associated with a doubled mortality rate among women over a 16-year period On average, obesity reduces life expectancy by six to seven years Health Effects Morbidity Health consequences fall into two broad categories:

Those attributable to the effects of increased fat mass: Osteoarthritis(Compression) Obstructive sleep apnea(Soft Tissue) Social stigmatization Those due to the increased number of fat cells:

Diabetes(resistin hormone) Cancer(inflammation, cell communication) cardiovascular disease(Hypertension) non-alcoholic fatty liver disease(fat build-up Survival paradox A High BMI can be beneficial Heart disease Cardiac bypass surgery People lose weight to an unhealthy point maybe because of more intense treatment Causes Diet bad food

Sedentary Lifestyle Not enough exercise Genetics FTO gene(fat mass), perhaps inheritance of leptin resistance Medical and psychiatric illness Hypothyroidism, Cushing's syndrome, Eating disorders

Social determinants Poor equals fat Pathophysiology Leptin This field of study was relatively unexplored until leptin was discovered in 1994 plays a key role in regulating energy intake and energy expenditure, including appetite and metabolism. It is one of the most important adipose derived hormones Leptin circulates at levels proportional to body fat. It enters the central nervous system (CNS) in proportion to its plasma concentration. Its receptors are found in brain neurons involved in regulating energy intake and expenditure.

It controls food intake and energy expenditure by acting on receptors in the mediobasal hypothalamus[ Pathophysiology Adipose Tissue Brain Leptin Neurop eptide

Y anadami de CCK a-MSH PYY336 ghrelin Stomach Pathophysiology Leptin acts on receptors in the hypothalamus of the brain where it inhibits appetite by

: counteracting the effects of neuropeptide Y counteracting the effects of anandamide and CCK promoting the synthesis of -MSH and PYY 3-36 The absence of leptin (or its receptor) leads to uncontrolled food intake and resulting obesity. Pathophysiology Long-Term inhibition Neuropeptide Y: a potent feeding stimulant secreted by cells in the gut and in the hypothalamus

Anandamide: Stimulant secreted by the hypothalamus Melanocyte-stimulating hormone(a-MSH): appetite suppressant produced in pituitary gland Short term Cholecystokinin(CCK): Family of hormones responsible for digestion of fats Peptide YY(PYY3-36): Protein responsible for suppression of hunger Ghrelinis: a hormone produced mainly by P/D1 cells lining the fundus of the human stomach stimulates hunger. Ghrelin levels increase before meals and decrease after meals. It is considered the counterpart of the hormone leptin.

Pathophysiology Adipose Tissue Brain Leptin Neurop eptide Y anadami de CCK

a-MSH PYY336 ghrelin Stomach Pathophysiology Leptin and ghrelin are considered to be complementary in their influence on appetite, with ghrelin produced by the stomach modulating short-term appetitive control (i.e. to eat when the stomach is empty and to stop when the stomach is stretched). Leptin is produced by adipose tissue to signal fat storage reserves in the body, and mediates long-term appetitive controls

(i.e. to eat more when fat storages are low and less when fat storages are high). Studies show that the lower leptin levels promote uncontrolled fat storage. So why not just give a pill containing leptin? Leptin Deficient? Studies show that Obese individuals actually have very high levels of Leptin but their body seems to be Leptin resistant.

Perhaps reason for inheritance So what now? Sibutramine(meridia) Originally developed as an antidepressant but was not effective. was found to reduce body weight and appetite and increase satiety. Pharmacodynamics Sibutramine is a neurotransmitter reuptake inhibitor that reduces the reuptake of serotonin (by 53%), norepinephrine (by 54%), and dopamine (by 16%), thereby increasing the levels of these substances in synaptic clefts and helping enhance satiety.

()-dimethyl-1-[1-(4- chlorophenyl cyclobutyl]-N,N,3-trimethylbutan1-amine Sibutramine Pharmacokinetics Sibutramine is well absorbed from the GI tract (77%), but undergoes considerable first-pass metabolism, reducing its bioavailability. The drug itself reaches its peak plasma level after 1 hour and has also a half-life of 1 hour. Sibutramine is metabolized by cytochrome P450 in liver into two pharmacologically-active primary and secondary amines(M1 and M2) with half-lives of 14 and 16 hours Peak plasma concentrations of active metabolites 1 and 2 are reached after three to four hours The following metabolic pathway mainly results in two inactive conjugated and hydroxylated metabolites Sibutramine

Side effects dry mouth, paradoxically increased appetite, nausea, strange taste in the mouth, upset stomach, constipation, trouble sleeping, dizziness, drowsiness, menstrual cramps/pain, headache, flushing, or joint/muscle pain. The main side effect was an increase in blood pressure resulting in heart attacks and strokes Resulted in withdrawn from American market Orlistat(Xenical) The only FDA approved anti-obesity drug

Orlistat is the saturated derivative of lipstatin, a potent natural inhibitor of pancreatic lipases. Reduces blood pressure Reduces likely hood of type 2 diabetes by 40% Orlistat Orlistat works by inhibiting gastric and pancreatic lipases, the enzymes that break down triglycerides in the intestine When lipase activity is blocked, triglycerides from the diet are not hydrolyzed into absorbable free fatty acids, and are excreted undigested instead At the standard prescription dose of 120 mg three times

daily before meals, orlistat prevents approximately 30% of dietary fat from being absorbed Orlistat Side effects Diarrhea, Abdominal pain Some cases of liver failure Treatment The main treatment for obesity consists of dieting and physical exercise.

The most effective treatment for obesity is bariatric surgery. Surgery for severe obesity is associated with long-term weight loss and decreased overall mortality. Future Rather than stopping caloric intake there is starting the be a focus on speeding up metabolic process and bodies willingness to burn energy. With that, leptin and how it regulates other peptides involved in energy homeostasis Recognition of the importance of the hypothalamus in the regulation of energy homeostasis has led to the targeting of neuropeptides and their receptors in this

region for weight loss therapies. Also some fat gene isolations Readings http://jcem.endojournals.org/cgi/content/full/89/6/2616 Pharmacological Approaches to Weight Reduction: Therapeutic Targets Judith Korner and Louis J. Aronne Department of Medicine, Columbia University College of Physicians and Surgeons (J.K.), New York, New York 10032; and Weill Medical College of Cornell University, Comprehensive Weight Control Program (L.J.A.), New York, New York 10021 http://www.clinicaladvances.com/article_pdfs/gh-article-20

0711-redinger.pdf The Pathophysiology of Obesity and Its Clinical Manifestations Richard N. Redinger, MD Department MedicineUniversity of Louisville 530 South Jackson Street, 3rd floor Louisville, KY 40292 Questions 1. 2. 3. 4. 5. 6. 7.

Which industry gave first alarm about Obesity? What is also known as the The Quetelet Index and what is it used for? What life long complication is most associated with obesity? Name five health effects of excess weight. What hormone is most responsible for appetite? Why is it not as simple as giving obese people more Leptin to regulate their weight. Name two obesity drugs?

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