Carbodiedrates. Flashcards

1
Q

Define and explain carbohydrate structures and classifications

Monosaccharide

A

A basic sugar. Examples: Galactose, glucose.

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2
Q

Define and explain carbohydrate structures and classifications

Disaccharide

A

Two monosaccharides joined by a glycosidic linkage. Example: Lactose

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3
Q

Define and explain carbohydrate structures and classifications

Polysaccharide

A

More than 3 monosaccharides joined by glycosidic linkages. Example: Starch, glycogen

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4
Q

Explain the process of digestion and absorption of dietary carbohydrates

A

Polysaccharides: Starch or glycogen are broken down by alpha amylase into disacchardies, which are picked up by micro villi in the GI tracts and broken down into monosaccharides which are released into the blood

Monosaccharides: pass into the blood directly

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5
Q

Explain the main transport routes and uptake of carbohydrates

A

(a guess)
Glycogenesis: Glucose -> Glycogen in the liver and muscle
Glycogenolysis: Glycogen -> glucose
Gluconeogenesis: Non-CHO sources -> glucose (proteins, generally)
Glycolysis: glucose -> CO2+H2O+ATP

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6
Q

State the main physiologic functions of carbohydrates

A

Glucose: Primary energy source for the body
Glycogen: Liver storage form of glucose
fats: long term storage of energy

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7
Q

Explain the effect of hormones in regulation of blood glucose levels

A

Insulin: Increases glycogenesis and glycolysis: Glucose -> glycogen ->pyruvate -> acetyl-CoA

Glucagon: Increases glycogenlysis: glycogen ->glucose
Increases gluconeogenesis: fatty acids ->acetyl-CoA ->ketones, proteins ->amino acids

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8
Q

Discuss the maintenance of blood glucose levels in the “fed state” (parenteral)

A

Fed state:
Insulin from Pancreatic beta cells (islets of Langerhans) preproinsulin ->proinsulin -> insulin and C-peptide (a byproduct)
Promotes cellular uptake of glucose

insulin increased:
lipogenesis
protein synthesis
glycogenesis

Insulin decreased:
lipolysis
ketone formation
gluconeogenesis
glycogenolysis

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9
Q

Discuss the maintenance of blood glucose levels in the “fasting state”

A

glucagon from pancreatic alpha cells
liver converts glucagon into glucose, releases to the blood
muscle converts glucagon to glucose-6-PO4, remains inthe muscle cell

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10
Q

Explain the formation and significance of hemoglobin A1C

A

HbA is glycated making HbA1c. It serves as a more accurate read of glucose levels for diabetics, since glucose varies greatly.

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11
Q

Explain etiology, symptoms, and effects of hypergylcemia

Type1a:

A

Pancreatic beta cell destruction (autoimmune disorder) leading to absolute insulin deficiency
Must take insulin to survive
usually young, onset days to weeks
islet cell antibodies present

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12
Q

Explain etiology, symptoms, and effects of hypergylcemia

Type1b

A

Idiopathic

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13
Q

Explain etiology, symptoms, and effects of hypergylcemia

Type2:

A

Insulin resistance, and secretory defect in the beta cells
variable
highly associated with family history, >40 yo, obesity and lack of exercise.

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14
Q

Explain etiology, symptoms, and effects of hypergylcemia

Gestational:

A

pregnancy
frequent, but transitory
human placental lactogen
>= 140 mg/dl one hour after 50g glucose load

Any two of the following (100G):
fasting plasma glucose >=95mg/dl
>=180mg/dl after 1 hour
>=155mg/dl at 2 hours
>=140mg/dl at 3 hours

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15
Q

Explain the diagnostic criteria for

Type 1

A

Pancreatic beta cell destruction (autoimmune disorder) leading to absolute insulin deficiency
Must take insulin to survive
usually young, onset days to weeks
islet cell antibodies present

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16
Q

Explain the diagnostic criteria for

Type 2

A

Normal: Fasting plasma glucose (FPG) 70-99 mg/dl
Impaired: FPG 100-125 mg/dl
Provision diabetes: FPG >=126 mg/dl

17
Q

Explain the diagnostic criteria

GDM

A

> = 140 mg/dl one hour after 50g glucose load
Any two of the following (100G):
fasting plasma glucose >=95mg/dl
=180mg/dl after 1 hour
=155mg/dl at 2 hours
=140mg/dl at 3 hours

18
Q

Explain etiology, symptoms, effects and diagnostic criteria of hypogylcemia

A

cause: Insulin OD, drugs (sulfonylureas,antihistamines), alcoholism, galactosemia, glucogon storage disease

Symptoms: Headache, shaky, dizziness, hunger, sweating

Glucose alert: <=70mg/dl
clin. sig.: <54 mg/dl
severe: no specific value

19
Q

Discuss methodologies for carbohydrate determinations

A

Whole blood
plasma/serum: 10-15% higher than whole blood lvls
CSF: 40-70 mg/dl
Urine: <30mg/dl random, <500 mg/24 hr