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CARBOHYDRATE MOLECULES ARE COMPOSED
C, H, AND O IN THE RATIO OF 1:2:1
If a carbohydrate consists of just one sugar molecule
It is a monosaccharide(Glucose)
Two linked monosaccharide form a
Disaccharide
A polymer of many monosaccharides is a
Polysaccharide
GLUCOSE(C6H12O6)
THE MOST COMMON MONOSACCHARIDE IN LIVING ORGANISMS
POLYSACCHARIDES
CHAINS OF SIMPLE SUGARS
Both Starch and Glycogen are polymers of glucose molecules
Starch
An energy storage molecule in plants, formed in roots and seeds
Glycogen
An energy storage molecule in animals, found in the liver and muscles
GLYCOPROTEINS
Conjugated proteins with oligosaccharide attached
Membrane proteins, antibodies, hormones, coagulation factors, and hemoglobin
Number of carbohydrate residues can be from 1-70% of the weight of the total glycoprotein
Glucose
The primary circulating sugar in the blood and the major energy source of the body – used to produce ATP
Gluconeogenesis
The formation of new glucose from non-carbohydrate sources (protein or fat) to store energy
Glycolysis
The breakdown of glucose (to produce energy)
Glycogen
The main form of carbohydrate storage primarily in the liver and muscle tissue; readily converted to glucose to satisfy its energy needs – facilitated by hormone
glucagon
Glycogenesis
Formation/synthesis of glycogen from glucose (to store energy) – facilitated by action of insulin
Glycogenolysis
Breakdown of glycogen to glucose (to produce energy)
Glycolysis
Cells require energy
Glycogenesis
With glucose excess
Glycogenolysis
When plasma(serum) glucose falls
Gluconeogenesis
In prolonged starvation
GLYCOLYSIS
GLU-6-PHOSPHATE A CENTRAL INTERMEDIATE GLUCOSE-6-PHOSPHATASE IS NECESSARY ENZYME
Glu=Glu-6-P=2 Pyruvate=2 Lactate
GLYCOGENOLYSIS
BREAKDOWN OF GLYCOGEN AND FORMATION OF GLU-6-PFORMATION OF GLU-6
Glycogen(In muscle/liver)=Glu-1-P=Glu-6-P
Controlled by glucagon( When low blood sugar) and epinephrine (Flight or fight)
GLYCOGENESIS
GLYCOGEN SYNTHESIS FROMSYNTHESIS FROM GLUCOSE
When glucose intake exceeds immediate needs
Facilitated by insulin and high blood glucose levels
Enzyme responsible is hexokinase (In Liver)
GLUCONEOGENESIS
THE PROCESS OF FORMING NEW GLUCOSE FROM NON-CARBOHYDRATE MOLECULES
AMINO ACIDS
•GLYCEROL(FROM FATS)
PROTECTS THE BODY, ESPECIALLY THE BRAIN, FROM THE DAMAGING EFFECTS OF HYPOGLYCEMIA BY ENSURING ATP SYNTHESIS CAN CONTINUE
Decrease blood glucose
Insulin
Increase blood glucose
Glucagon
Epinephrine
Cortisol
Growth Hormone
ACTH
Thyroxine
Somatostatin inhibit secretion
Of BOTH insulin and glucagon and different times. Indirect effect on blood glucose levels.
INSULIN
Body’s hypoglycemic agent
Secreted by the beta cell of islets of Langerhans in pancreas
Promote cellular uptake of glucose
Suppresses hepatic glucose production
Target organs: Liver, skeletal muscle, and adipose tissue
INSULIN
Secretion is stimulated by glucose, amino acids, pancreatic and GI hormones and
some medications.
Release is inhibited by hypoglycemia, somatostatin (which inhibits growth hormone),
and various drugs
Are the main signals in a feedback loop
Glucose and Insulin
ADVERSE EFFECTS OF INSULININSULI
HYPOGLYCEMIA UNAWARENESS
LIPODYSTROPHY
DAWN PHENOMENA—Poor blood glucose management at nights leads to waking up feeling sick and hypoglycemic
SOMOGYI EFFECT
COUNTER-REGULATORY HORMONES
OPPOSE ACTION OF INSULIN BY RAISING GLUCOSE LEVELS
GLUCAGON
Secreted by alpha cells of pancreas
Stimulates production of glucose in the liver
Secretion regulated by plasma glucose concertation
Stress, exercise and amino acids induce glucagon exercise
Insulin inhibits glucagon release and biosynthesis
EPINEPHRINE
Stimulates glycogenolysis
Inhibits: glucose movement into tissue & insulin secretion
Key role in glucose counter-regulation when glucagon secretion is impaired (in Type 1diabetes).
Physical or emotional stress increases secretion
GROWTH HORMONE
Produced by anterior pituitary gland
Stimulates gluconeogenesis
Enhances lipolysis (Breakdown of fats)
Opposes insulin stimulated glucose uptake
CORTISOL
SECRETED BY THE ADRENAL CORTEX IN RESPONSE TO ACTH
STIMULATES GLYCOGENOLYSIS AND GLUCONEOGENESIS
HYPOGLYCEMIA
Low blood sugar
Serum (Plasma) glucose level
Falls below 50 mg/dL
Glucagon is released when
Plasma glucose is < 70 mg / dL to inhibit insulin
Epinephrine, cortisol, and growth hormone
Released from adrenal gland to increase glucose metabolism and inhibit insulin
Age of onset of hypoglycemia
Is a convenient way to classify the disorder
Whipple’s Triad
Symptoms of hypoglycemia
Low plasma glucose at time of symptoms
Alleviation of symptoms with glucose
ingestion
HYPOGLYCEMIA IN NEWBORNS/ INFANTS
BLOOD GLUCOSE CONCENTRATION MUCH LOWER THAN ADULTS (35 MG/ML AVERAGE)
OFTEN IF MOTHER HAS DIABETES (ANY TYPE) THE INFANT IS BORN WITH
HYPOGLYCEMIA
FASTING HYPOGLYCHYPOGLYCEMIA IN ADULTS
Decreases rate of glucose production OR increased rate of glucose metabolism.
Symptoms usually arise around 55mg/mL (plasma glucose)
Brain function starts to go at less than 50mg/mL
72 hour fast often done to diagnose
HYPOGLYCEMIA AND DIABETES
Occurs very frequently in diabetic patients(Both type 1 and type 2)
Often occurs 1-2 times per week in type 1 diabetic patients
Counter Regulatory Mechanisms become impaired in diabetics (Glucagon and epinephrine secretion)
Often unaware of the condition until severe symptoms arise
GLYCOGEN STORAGE DISEASES
Enzyme deficiencies affecting glycogen storage
Most common and severe: von Gierke’s disease----Deficient in Glucose-6-phosphatase
Glycogen accumulates in liver(can’t be converted to glucose)
Liver transplant needed
GALACTOSEMIA
Galactose-1, Phosphate Uridyl-Transferase deficiency
Enzyme that converts galactose to glucose, patients can not change either galactose or lactose into glucose
Hypoglycemia an issue (Special needs)
LACTASE DEFICIENCY
GI deficient in lactase
Sensitive to dairy(Lactose Intolerant)
Most people self diagnose
Actual Diagnosis of Lactase Deficiency
Give Lactose and measure breath hydrogen levels ( Will see increase in hydrogen if intolerant).