Problems: Module 1
Write your answer first, then open the solution. Assignment key items show the points the grader awards; chart problems use the course figures; variants change the numbers or flip the premise; check-yourself items answer the end-of-module review questions.
Assignment key¶
Solution to Exercise 1
Regulated variable (2): concentration of extracellular fluid. “Dehydration” is half credit, because it is the idea but not a variable. (slide 37)
Sensing (2): too-concentrated extracellular fluid draws water out of the cell, which makes it shrivel. The shriveling is how the cell senses the stimulus.
Integration (4): the message does not travel (2 pts). Locally, the physical shriveling pulls open mechanically gated ion channels. Stimulus strength sets the degree of shriveling, and whether enough channels open is the integration and error signal (2 pts).
Efferent pathway (2): release of vasopressin, a chemical messenger circulating through the body.
Effector (2): the kidneys.
Correction (2): vasopressin tells the kidneys to stop getting rid of extra water, preventing further water loss. The key says not to go deeper, since kidneys have not been covered.
Solution to Exercise 2
Stimulus (3): platelets first contacting the exposed collagen. Vaguer answers like “a ruptured vessel” get partial credit.
Response (3): adhered platelets are activated by existing thrombin and start producing more thrombin.
Amplification (3): more thrombin activates more platelets, which produce more thrombin, which activates more platelets, and so on.
Cutoff (1): remove either the input (platelet contact with exposed collagen) or the amplifier (thrombin). Either answer is accepted. (slide 7)
Solution to Exercise 3
Phospholipid (3): phosphate head, hydrophilic. Fatty acid tails, hydrophobic. (slide 14)
Bilayer (2): tails face inward toward each other, heads face the watery environment on both sides. It forms because each end points toward the environment it has highest affinity for.
Permeability (4): hydrophobic molecules cross easily because they share the nonpolar, fat-soluble character of the membrane core. Hydrophilic molecules cannot, because they have the opposite character to that core. (slides 24, 26)
Paclitaxel (3): a sphere of a single layer of phospholipids, heads out and tails in, with the drug surrounded by hydrophobic tails. The key calls this a micelle and accepts either the term or the description.
Insulin (3): a bilayer envelope, so heads face both outward toward the blood and inward toward the drug, surrounding a hydrophilic payload with hydrophilic heads. The key’s term is liposome or bilayer vesicle.
Solution to Exercise 4
Ion | Outside (mEq/L) | Inside (mEq/L) | Diffusion |
|---|---|---|---|
Na+ | 135–145 | 10–15 | Into cell |
K+ | 3.5–5 | 120–140 | Out of cell |
Cl− | 95–105 | 4–10 | Into cell |
HCO3− | 22–28 | 10–12 | Into cell |
One point per blank. Any value inside the range scores. (slide 23)
Solution to Exercise 5
Alpha: exchanger. Na+ moves down its gradient, H+ up. “Secondary active transport” is justified because the Na+ gradient it runs on was created by the Na+-K+ pump, which is active transport. (slide 28)
Gamma: channel. No energy input, only dissipation of an existing gradient. The outward arrow matches K+'s outward gradient, so it is moving down it. (slide 27)
Beta: cotransporter. Na+ and HCO3− both move down their gradients.
Delta: cotransporter. Na+ down, K+ up, Cl− down. This is the NKCC.
Why the lecture’s “just follow Na+” works (4): all gradients actually sum as one vector, but the Na+ gradient is so large it dominates the sum. So if the Na+ gradient weakens, the net driving force weakens and transport of the other ions falls, even though direction does not change.
Epsilon: pump, both ions moving against their gradients. It needs ATP because neither solute moves down its gradient, so there is no existing gradient energy to exploit. (slide 29)
Solution to Exercise 6
Normal range is 280–310 mOsm/kg, so 308 is iso-osmotic. (slides 33–34)
0.45% is half as concentrated, so 4.5 g NaCl in 1 kg water. The rationale is worth 2 of the 3 points.
Red cell (4): water moves into the cell, because osmosis moves water from the less concentrated to the more concentrated compartment. The cell swells and, left unchecked, bursts. Since structure dictates function, it cannot deliver oxygen properly. (slides 34–37)
Solution to Exercise 7
Threat (3): the new osmotic gradient between cell interior and plasma drives water into red cells, triggering widespread hemolysis. Losing that many red cells removes oxygen-carrying capacity, and organs start shutting down.
Why they can’t compensate (3): the cell’s major solutes, hemoglobin and the cations Na+, K+ and Ca2+, cannot pass through the membrane, so the cell cannot shrink the gradient by exporting them.
Chart analysis¶
Solution to Exercise 8
Trial 1: 2.5/262 = 0.0095 %/s. Trial 2: 2.5/79 = 0.0316. Trial 3: 2.5/111 = 0.0225. Trial 4: 1.0/61 = 0.0164.
1 vs 2 isolates solute size. The small solute diffuses about 3.3× faster because molecular weight sits in the denominator of the rate expression.
2 vs 3 isolates temperature. Cooling slows molecular movement, so the rate drops by about 29%.
2 vs 4 isolates gradient. The smaller gradient reached equilibrium sooner because less change was needed, but the rate fell by about half because gradient magnitude drives the rate. (Lecture 1D)
Variant¶
Solution to Exercise 9
Solution to Exercise 10
Solution to Exercise 11
Time fell, from 79 s to 61 s, because equilibrium sat at 1% rather than 2.5%, so there was less concentration change to accomplish. The rate, change divided by time, fell from 0.0316 to 0.0164 %/s, because gradient magnitude sits in the numerator of the diffusion expression and directly drives the rate.
Solution to Exercise 12
Solution to Exercise 13
Hyper-osmotic. Water leaves the cell and it shrivels: crenation.
Solution to Exercise 14
Glucose is covalent and does not dissociate, so n = 1. At 277.5 it sits just below the 280–310 range: slightly hypo-osmotic. The trap is multiplying by 2.
Solution to Exercise 15
Solution to Exercise 16
Regulated variable: body temperature. Perturbation: hot day. Sensors: thermoreceptors in skin, brain, muscles, liver. Afferent: sensory nerves. Integrating center and set point: preoptic anterior hypothalamus. Error signal out along efferent motor nerves. Effectors: skin blood vessels dilate (convective and radiative heat loss) and sweat glands sweat (evaporative). (slide 6)
Solution to Exercise 17
Stimulus: the baby’s head presses on the cervix. Response: cervical stretch releases oxytocin, which drives stronger uterine contractions. Amplification: stronger contractions press the head harder, releasing more oxytocin. Cutoff: delivery removes the pressure. (slide 7)
Solution to Exercise 18
(a) Countertransporter. Na+ in down its gradient, Ca2+ out up its gradient. Secondary active: the Na+ gradient was built by the Na+-K+ pump.
(b) Cotransporter. Na+ in down its gradient drives glucose in.
(c) Pump (ATPase). Ca2+ moved up its gradient into the SR using ATP.
(d) Channel for water. Osmosis supplies the driving force. (slides 27–29, 32)
Check yourself¶
Solution to Exercise 19
Regulated variable on a seesaw → perturbation → sensor → afferent pathway → integrating center compares with the set point → error signal → efferent pathway → effector. Body temperature: thermoreceptors in skin, brain, muscle, liver → afferent sensory nerves → preoptic anterior hypothalamus (center and set point) → efferent motor nerves → skin vessels dilate and sweat glands sweat. (M1 slides 5–6)
Solution to Exercise 20
Negative feedback removes its own stimulus: as the variable returns to normal the error signal shrinks, so the loop shuts itself off. Positive feedback intensifies its stimulus, so nothing inside the loop stops it. Left running it drives the variable dangerously far from normal, which is why an outside event such as delivery of the baby has to end it. (M1 slide 7)
Solution to Exercise 21
Hydrophilic phosphate heads face the watery fluid on both sides and the hydrophobic fatty acid tails face each other, forming a lipid core. Water and anything that dissolves in water cannot cross that core, so the two watery compartments cannot mix. (M1 slide 14)
Solution to Exercise 22
Mostly C–H bonds with few oxygens and even sharing: nonpolar, crosses unaided by simple diffusion. Covalent with uneven sharing (O–H, many oxygens) and regional partial charges: polar, needs a carrier. Lost or gained electrons and a net charge: ionic, needs a channel. Polar and ionic solutes are both hydrophilic and cannot cross the lipid core. (M1 slides 18–20)
Solution to Exercise 23
Raise the rate: concentration gradient, surface area, temperature, membrane permeability. Lower it: membrane thickness, solute molecular weight, density of the medium. Electrical forces and distance also matter outside the expression. (M1 slide 24)
Solution to Exercise 24
Equilibrium sits halfway, so a 2% gradient only needs a 1% change against 2.5% for a 5% gradient. Less change takes less time (61 s against 79 s). The rate, change divided by time, still fell (0.0164 against 0.0316 %/s) because gradient magnitude drives the rate. (Lecture 1D)
Solution to Exercise 25
Ligand-gated ion channel, G protein-coupled receptor, catalytic receptor, and intracellular receptor. The intracellular receptor is not in the membrane because its ligands are hydrophobic: they cross the membrane on their own and bind inside, then act on gene expression. (M1 slide 16)
Solution to Exercise 26
No ATP is used. Solute A runs down its own gradient and the energy stored in that gradient pushes the “revolving door,” carrying B along even when B moves up its gradient. The transporter only spends an existing gradient, so it counts as passive (the key calls it secondary active, since a pump built the Na+ gradient elsewhere). (M1 slide 28)
Solution to Exercise 27
They are equal, so they pull water equally. NaCl dissociates into two particles; glucose, covalently bonded, stays as one. (M1 slide 33)
Solution to Exercise 28
ECF ends at 4,060 ÷ 276.8 = 14.67 L, ICF at 29.33 L. Right after infusion the ECF held 16 L, so 1.33 L moves into the cells. Assume 1 kg water = 1 L and that no solute crosses. (M1 slide 34)
Solution to Exercise 29
320 mOsm is more concentrated than the cell (about 290), so water leaves the cell. The cell shrivels like a raisin: crenation. Its changed shape impairs its function. (M1 slide 37)
Solution to Exercise 30
Concentrated extracellular fluid pulls water out of the neuron, which shrivels. The shriveling physically pulls open mechanically gated ion channels. Ions flow, the membrane potential changes, and the neuron fires, signaling vasopressin release and thirst. Dilute fluid swells the cell, the channels close, and the signals stop. (M1 slide 37)