1/49
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced |
---|
No study sessions yet.
Glycolysis
2 pyruvate + 2NADH + 2ATP
Krebs cycle
Pyruvate (w O2) + 2NADH + 2ATP
ETC
uses 2ADP from krebs + 34 ATP = 38ATP
NADH from krebs activates what
ETC w 2ADP
If there is hypoxia …
Cellular metabolism has to recycle thru glycolysis ( NO O2 )
Positive of anaerobic glycolysis
2ATP, temp stop gap solution
Con of anaerobic glycolysis
2ATP is not enough, pyruvate accumulates
too much pyruvate can cause
Acidosis
Normal body pH
7.35-7.45
w/out atp
Na & K pump cannot maintain normal electrical cell mem status (turning it positive)
Sodium goes
Out
Glucose
Most important substance to create ATP
RMP is normally
Negative
Vitamins
“Support staff” for metabolic pathway
If intake of glucose is greater than cellular energy needs
Insulin directs excess glucose to be stores
glycogen
Excess glucose
Glycogenesis
Creation of glycogen
Regulatory processes
Insulin, glucose entering cells, glycogenesis
Counterregulatory hormones
Trigged by low blood glucose ( didn’t eat )
Epinephrine is from the
adrenal medulla
Cortisol is from the
Adrenal cortex
GH is from the
Pituitary
Glucagon is from the
Pancreas
Another word for stress hormones
Glucagon
Glycogenolysis
Uses Glucagon to convert stored glycogen to glucose
What converts glycogen to glucose
Glucagon
Glucaneogenesis
Use of any other substances besides carbohydrates
Gluconeogenesis breaks down
Fats and proteins
Ketones
Breakdown products of fats and proteins, offer some energy
Cons of Ketones
Are an acid so can cause acidosis
Can’t be used by the brain
The brain only uses what for energy
GLUCOSE
Normal counterregulatory processes
Glycogenolysis & glucogenesis
Glycogen storage diseases
Abnormalities in glycogenesis or glycogenolysis
McArdles disease
Autosomal recessive disease where normal ability to breakdown muscle glycogen is diminished
Type 1 diabetes mellitus
Glycogenesis extreme, NO insulin so glucose stays in blood cannot go in cell, HIGH blood glucose
Why are type 1 diabetics thin
The body uses sustained gluconeogenesis (fats and proteins) as its main energy pathway
Insulin
Gets glucose into cell
Hyperketonemia can be manifested by
High serum ketones
Ketoacidosis
Ketonuria
Acetone breath
Hyperketonemia causes
Low blood pH
Vitamins important to Maximize creation of ATP
Niacin
Thiamine
Riboflavin
Iron
Alcoholics have a high risk for
Vitamin deficiencies
Anemia
Less than normal numbers of RBCs, iron deficiency
Beriberi
Thiamine (B1) deficiency
thiamine B1
Important in functioning of neurological cells (brain tissue)
Thiamine deficiency issues
Wernicke Koraakoff syndrome
Parathesia
Wernicke Korsakoff syndrome
Memory loss, ataxia (staggering gait), eye movement issues
Parasthesia
Numbness and tingling usually in legs ( also seen in B12 deficiency)
Drug that interferes with vitamin absorption
Cyanide
Cyanide MOA
Inhibits cytochrome oxidase
cytochrome oxidase
Important to make enough ATP