πŸ”¬ Physiology Β· Cell Physiology

Memory tricks for how cells actually work

Cell physiology is the foundation of everything β€” action potentials, membrane transport, osmosis, and cell signaling underpin every organ system. Master these concepts and the rest of physiology becomes much clearer.

πŸ”¬ Cell Physiology

Memory Tricks

Proven Mnemonics & Acronyms β€” fast to learn, hard to forget.

Membrane Transport
PACE β€” Passive Β· Active Β· Co-transport Β· Endocytosis
Four categories of membrane transport β€” no energy vs energy required
How substances cross cell membranes β€” four transport mechanisms
Passive transport moves substances DOWN their concentration gradient β€” no ATP required. Includes simple diffusion (gases, lipids), facilitated diffusion (glucose via GLUT transporters), and osmosis (water via aquaporins). Active transport moves substances AGAINST their gradient β€” requires ATP. Primary active transport uses ATP directly (Na+/K+ ATPase). Secondary active transport uses the gradient created by primary transport (sodium-glucose cotransporter). Endocytosis brings large particles IN; exocytosis sends them OUT.
Simple diffusion
O2, CO2, lipids β€” no protein needed, moves with gradient.
Facilitated
Glucose, ions β€” channel or carrier protein, still with gradient.
Active transport
Against gradient β€” Na+/K+ ATPase pumps 3 Na+ out, 2 K+ in per ATP.
Endocytosis
Phagocytosis (solids), pinocytosis (liquids), receptor-mediated (specific).
Na+/K+ ATPase Pump
3 OUT Β· 2 IN β€” Three Na+ out, Two K+ in, One ATP used
The most important pump in cell physiology
The sodium-potassium pump β€” why it matters for every cell in the body
The Na+/K+ ATPase pump is the most important active transport protein in the body. For every ATP used: 3 sodium ions pumped OUT of the cell, 2 potassium ions pumped IN. This creates the electrochemical gradients essential for nerve impulses, muscle contraction, and nutrient absorption. The pump uses approximately 30% of the body's total ATP at rest. Cardiac glycosides (digoxin) inhibit this pump β€” increasing intracellular sodium β†’ more calcium β†’ stronger cardiac contractions.
3 Na+ OUT
Na+ higher outside cell β€” drives secondary active transport (glucose absorption).
2 K+ IN
K+ higher inside cell β€” essential for resting membrane potential.
1 ATP used
~30% of resting ATP consumption. Inhibited by ouabain and digoxin.
Net charge
3+ out, 2+ in = net -1 charge movement out β†’ contributes to resting potential.
Osmosis and Tonicity
Water follows salt β€” always moves toward higher solute concentration
Isotonic Β· Hypotonic Β· Hypertonic β€” cell behavior in each solution
Osmosis β€” which direction water moves and what happens to cells
Osmosis is the movement of water across a semipermeable membrane from low solute to high solute concentration. Isotonic solution (same concentration as cell): no net water movement β€” cell stays normal. Hypotonic solution (less solute than cell): water moves INTO cell β€” cell swells, may lyse. Hypertonic solution (more solute than cell): water moves OUT of cell β€” cell shrinks (crenation). Clinical: IV fluids must be chosen carefully β€” 0.9% NaCl is isotonic, D5W becomes hypotonic after glucose is metabolized.
Isotonic
0.9% NaCl, Lactated Ringer's β€” cell unchanged. Used for volume replacement.
Hypotonic
0.45% NaCl β€” water into cells. Used for dehydration with hypernatremia.
Hypertonic
3% NaCl β€” water out of cells. Used for severe hyponatremia or cerebral edema.
Osmolarity
Normal serum = 275–295 mOsm/kg. Calculated: 2Γ—Na + glucose/18 + BUN/2.8.
Action Potential Phases
DRRAP β€” Depolarization Β· Rising Β· Repolarization Β· After-hyperpolarization Β· Polarized (resting)
Five phases of the neuronal action potential
The action potential β€” how nerve cells fire electrical signals
Resting membrane potential: -70 mV (more negative inside β€” K+ leaks out, Na+ pumped out). Depolarization: stimulus opens voltage-gated Na+ channels β†’ Na+ rushes IN β†’ membrane potential rises to +30 mV. Repolarization: Na+ channels inactivate, K+ channels open β†’ K+ rushes OUT β†’ returns to -70 mV. After-hyperpolarization: K+ channels slow to close β†’ briefly more negative than resting (-80 mV). Absolute refractory period: cannot fire again regardless of stimulus strength.
Resting (-70 mV)
K+ leaks out, Na+ pumped out by Na+/K+ ATPase. Stable baseline.
Depolarization
Na+ channels open β†’ Na+ IN β†’ -70 to +30 mV. Threshold = -55 mV.
Repolarization
Na+ channels inactivate, K+ channels open β†’ K+ OUT β†’ back to -70 mV.
Absolute refractory
Na+ channels inactivated β€” no AP possible. Ensures unidirectional conduction.
Relative refractory
After-hyperpolarization β€” larger than normal stimulus can fire another AP.
Cell Signaling
GPCR β†’ cAMP β†’ PKA Β· RTK β†’ RAS β†’ MAPK
Two major intracellular signaling cascades
How hormones and signals get inside the cell β€” two main pathways
Water-soluble hormones cannot cross the lipid membrane β€” they bind surface receptors and use second messengers. GPCR pathway: ligand β†’ G-protein coupled receptor β†’ adenylyl cyclase β†’ cAMP β†’ protein kinase A β†’ cellular response. RTK pathway: growth factors β†’ receptor tyrosine kinase β†’ RAS β†’ MAPK cascade β†’ gene expression. Lipid-soluble hormones (steroids, thyroid hormones) cross the membrane directly and bind intracellular receptors β†’ bind DNA β†’ change gene expression directly.
GPCR
Epinephrine, glucagon, TSH β€” cAMP second messenger. Fast response.
RTK
Insulin, growth factors β€” phosphorylation cascade. Gene expression changes.
IP3/DAG pathway
Some GPCRs β†’ phospholipase C β†’ IP3 + DAG β†’ Ca2+ release + PKC activation.
Steroid hormones
Lipid-soluble β†’ cross membrane β†’ intracellular receptor β†’ DNA binding β†’ gene expression.
Diffusion Rate Factors
SAID β€” Surface area Β· Area thickness Β· Ion charge Β· Diffusion coefficient
Fick's Law β€” four factors that determine rate of diffusion
What determines how fast substances diffuse β€” Fick's Law simplified
Fick's Law states that diffusion rate is proportional to surface area Γ— concentration gradient Γ— diffusion coefficient, and inversely proportional to membrane thickness. Surface area: larger area = faster diffusion (alveoli have huge surface area for this reason). Membrane thickness: thicker membrane = slower diffusion. Concentration gradient: steeper gradient = faster diffusion. Molecular weight: smaller molecules diffuse faster. Lipid solubility: lipid-soluble molecules diffuse faster through membranes. CO2 diffuses 20Γ— faster than O2 across the alveolar membrane.
Surface area ↑
Faster diffusion β€” alveoli optimized with 70 mΒ² surface area.
Thickness ↑
Slower diffusion β€” pulmonary fibrosis thickens alveolar membrane β†’ hypoxia.
Gradient ↑
Faster diffusion β€” breathing 100% O2 increases gradient β†’ more O2 absorbed.
Molecular size ↓
Smaller = faster. H2O diffuses faster than glucose.
Resting Membrane Potential
-70 mV β€” Mostly K+ leak Β· Na+ pumped out Β· Negative proteins inside
Three factors that create the -70 mV resting potential
Why cells have a negative resting membrane potential
The resting membrane potential of -70 mV in neurons exists because: K+ channels are open at rest and K+ leaks OUT (following its concentration gradient), making the inside more negative. Na+/K+ ATPase continuously pumps Na+ out and K+ in. Large negatively charged proteins are trapped inside cells. K+ equilibrium potential is -90 mV, Na+ equilibrium potential is +60 mV β€” the resting potential of -70 mV sits between these, dominated by K+ permeability. Nernst equation calculates the equilibrium potential for a single ion.
K+ leak channels
Always open at rest β€” K+ flows out, making inside negative. Major contributor.
Na+/K+ pump
Maintains gradients. Also contributes -3 to -4 mV directly (electrogenic).
Anions inside
Large proteins with negative charges trapped inside β€” cannot cross membrane.
Threshold
-55 mV β€” depolarize to here and action potential fires automatically.
Cell Organelles and Function
MERGE β€” Mitochondria Β· ER Β· Ribosome Β· Golgi Β· lysosomal Enzymes
Five organelles every physiology student must know cold
Key organelles and their physiological roles
Mitochondria: powerhouse β€” ATP production via oxidative phosphorylation. Contains its own DNA. Endoplasmic reticulum: rough ER (ribosomes, protein synthesis), smooth ER (lipid synthesis, detoxification, Ca2+ storage). Ribosomes: protein synthesis β€” free ribosomes make cytoplasmic proteins, bound ribosomes make secretory and membrane proteins. Golgi apparatus: protein processing, sorting, and packaging. Lysosomes: contain hydrolytic enzymes β€” digest cellular debris and pathogens (pH 4.5).
Mitochondria
ATP via ETC. Own DNA β€” supports endosymbiotic theory. Ca2+ buffer.
Rough ER
Ribosomes on surface β€” proteins destined for secretion or membrane insertion.
Smooth ER
Lipid synthesis, steroid hormones, drug detox (liver), Ca2+ storage (muscle SR).
Golgi
Cis face receives, trans face ships. Glycosylation, sorting, vesicle budding.
Lysosomes
pH 4.5 β€” hydrolytic enzymes digest debris. Failure = lysosomal storage diseases.
ATP Production Pathways
2-2-34 β€” Glycolysis Β· Krebs Β· ETC
2 ATP from glycolysis Β· 2 ATP from Krebs Β· 34 ATP from ETC
How cells make ATP β€” three stages and their yields
Cellular respiration produces ~38 ATP per glucose molecule. Glycolysis (cytoplasm, no O2 needed): glucose β†’ 2 pyruvate + 2 ATP + 2 NADH. Krebs cycle (mitochondrial matrix): 2 acetyl-CoA β†’ 2 ATP + NADH + FADH2 carriers. Electron transport chain (inner mitochondrial membrane, requires O2): NADH and FADH2 β†’ ~34 ATP via oxidative phosphorylation. Without oxygen: anaerobic glycolysis only produces 2 ATP + lactic acid. Cyanide and carbon monoxide poison the ETC by blocking Complex IV.
Glycolysis
Cytoplasm. No O2. 2 ATP net. Glucose β†’ 2 pyruvate. Always available.
Krebs cycle
Mitochondrial matrix. 2 ATP + 8 NADH + 2 FADH2 per glucose. Requires O2.
ETC
Inner mitochondrial membrane. ~34 ATP. NADH β†’ 2.5 ATP, FADH2 β†’ 1.5 ATP.
Anaerobic
Glycolysis only β†’ 2 ATP + lactate. Muscle fatigue during intense exercise.