MBBS Physiology Short Answers
Based on GK Paul | Ganong's | Guyton & Hall
1. After-Depolarisation (After-Potentials)
Definition: After-potentials are the small voltage changes that follow the spike (main action potential) during membrane recovery.
Types of After-Potentials
| Type | Also Called | What Happens | Duration |
|---|
| Negative After-potential | Depolarizing after-potential | Membrane remains slightly depolarized after spike | Few ms |
| Positive After-potential | Hyperpolarizing after-potential | Membrane becomes MORE negative than resting (-ve to resting) | 40-100 ms |
Simple Flowchart
Resting Membrane Potential (-70 mV)
|
Stimulus applied
|
Depolarization → ACTION POTENTIAL (SPIKE) +30 mV
|
Repolarization begins (K⁺ efflux)
|
┌─────────────────────────────────────┐
│ NEGATIVE AFTER-POTENTIAL │
│ (membrane still slightly │
│ depolarized - Na⁺ channels still │
│ partially open) │
└─────────────────┬───────────────────┘
|
K⁺ channels remain open
→ EXCESS K⁺ leaves cell
|
┌─────────────────────────────────────┐
│ POSITIVE AFTER-POTENTIAL │
│ (membrane HYPERPOLARIZED │
│ below resting level -75 to -90mV) │
│ = RELATIVE REFRACTORY PERIOD │
└─────────────────────────────────────┘
|
Na/K ATPase pump restores
resting membrane potential
Refractory Periods (linked to After-Depolarisation)
ABSOLUTE REFRACTORY PERIOD
(during spike + negative after-potential)
→ Na⁺ channels INACTIVATED
→ NO new AP possible (even with strong stimulus)
→ ~1 ms in myelinated nerve
RELATIVE REFRACTORY PERIOD
(during positive after-potential / hyperpolarization)
→ K⁺ channels still open
→ New AP possible BUT needs STRONGER stimulus
→ 2-4 ms
Key point for exam: After a neuron fires, Na⁺ channel inactivation gates close; they only reopen once the membrane returns close to its resting potential. The maximum firing rate of a large myelinated fiber = ~1000 impulses/second.
2. Hypothalamus
Definition: The hypothalamus is the chief integrating center for homeostasis, located below the thalamus, forming the floor and lower walls of the third ventricle.
Simple Diagram of Hypothalamic Nuclei
HYPOTHALAMUS
─────────────────────────────────────
ANTERIOR MIDDLE POSTERIOR
(Parasympathetic) (Autonomic mix) (Sympathetic)
─────────────────────────────────────
• Preoptic • Dorsomedial • Mammillary
• Suprachiasmatic • Ventromedial • Posterior
• Supraoptic • Arcuate • Lateral
• Paraventricular • Tuberal
Mnemonic for Hypothalamic Functions: "HEAL + TRF"
| Function | Area |
|---|
| Hunger/satiety | Lateral (hunger) / Ventromedial (satiety) |
| Endocrine control | Tuberal - releasing hormones |
| Autonomic regulation | Posterior (SNS) / Anterior (PSNS) |
| Limbic/emotion | Mammillary bodies |
| Temperature | Anterior - heat loss / Posterior - heat conservation |
| Reproduction | Preoptic, arcuate |
| Fluids/osmoregulation | Supraoptic (ADH), Paraventricular (Oxytocin) |
Flowchart - Hypothalamus as Master Controller
HYPOTHALAMUS
|
┌────────────────┼─────────────────┐
| | |
PITUITARY AUTONOMIC LIMBIC SYSTEM
(via portal NERVOUS SYSTEM (emotion/memory)
vessels) |
| ┌────┴──────┐
Releasing SNS PSNS
hormones (posterior (anterior
(TRH, CRH, hypothal.) hypothal.)
GnRH etc.)
|
Anterior & Posterior
Pituitary hormones
(GH, TSH, FSH, LH,
ACTH, ADH, Oxytocin)
3. Sleep - Reflex & Neural Mechanisms ("Capillary of Sleep" = Sleep Centres)
Definition: Sleep is a state of unconsciousness from which a person CAN be aroused by sensory stimuli (distinguishes it from coma).
Two Types of Sleep - Quick Comparison
SLEEP
|
┌────┴──────┐
| |
NREM REM
(Non-REM) (Rapid Eye Movement)
(Slow Wave) (Paradoxical Sleep)
| |
75% of night 25% of night
Stages 1-4 Every ~90 min
Restful Dreaming
BP↓, RR↓, Brain active
BMR↓ 10-30% EEG like waking
Muscle ATONIA
Heart rate irregular
Neural Centres of Sleep (Sleep "Reflex" / Mechanism)
WAKEFULNESS
↑ (activated by)
Reticular Activating System (RAS)
- Midbrain & upper pons
- Positive feedback loop with cortex
|
| (fatigues after many hours)
↓
SLEEP PROMOTING CENTRES take over:
1. Raphe Nuclei (lower pons + medulla)
→ secrete SEROTONIN → induces sleep
2. Anterior Hypothalamus (suprachiasmatic area)
→ lesion here = intense wakefulness
3. Nucleus tractus solitarius (medulla)
→ visceral afferents help promote sleep
4. Thalamic diffuse nuclei
Sleep-Wake Cycle Flowchart
Waking Hours Pass
↓
Sleep factors accumulate
(Muramyl peptide, delta sleep-inducing peptide)
↓
Serotonin from Raphe Nuclei ↑
↓
RAS inhibited → NREM sleep begins
↓
Every 90 min: ACh neurons activate
↓
REM sleep (dreaming, rapid eye movements)
↓
Orexin (hypocretin) from hypothalamus
→ maintains wakefulness in morning
↓
Cycle repeats ~4-5 times per night
Note - SCN (Suprachiasmatic Nucleus): Master circadian clock in hypothalamus. Entrained by light via retinohypothalamic tract. Controls melatonin secretion from pineal gland at night.
4. Stick (Rod/Scotopic) Adaptation - "Dark Adaptation"
Definition: When a person moves from bright light to darkness, the retina gradually becomes more sensitive to dim light. This is called dark adaptation (stick = rod adaptation, as rods are the "sticks").
Simple Diagram - Dark Adaptation Curve
VISUAL
THRESHOLD
(log units)
High | ╲
| ╲ CONE branch
| ╲ (fast, 5-10 min)
| ╲___
| ╲
| ╲ ROD (STICK) branch
Low | ╲______________________
└────────────────────────────────→
5 10 20 30
TIME IN DARK (min)
Mechanism of Dark (Rod/Stick) Adaptation
In BRIGHT LIGHT:
Rhodopsin (in rods) → bleached by light
→ Retinal + Opsin (broken down)
→ Rods insensitive
Move to DARKNESS:
↓
Opsin + 11-cis-retinal (from Vitamin A)
↓ (takes ~20 minutes)
Rhodopsin REGENERATES
↓
Rods become progressively MORE SENSITIVE
↓
Visual threshold FALLS (can see dim light)
= DARK ADAPTATION
Two-Component Dark Adaptation
| Component | Time | Cells Involved |
|---|
| First (fast) drop in threshold | 0-5 min | Cones - adapt rapidly |
| Second (slow) major drop | 5-20+ min | Rods (Sticks) - rhodopsin regeneration |
Exam tip: Radiologists and pilots wear RED GOGGLES in bright rooms before entering dark areas - red light stimulates cones (colour vision preserved) but does NOT bleach rhodopsin in rods, so rods stay adapted to darkness.
Vitamin A deficiency → Night blindness (Nyctalopia): Cannot regenerate rhodopsin, so rods fail to dark-adapt.
5. Special Cases of Aphasia
Definition: Aphasia is an acquired disorder of language (speaking, understanding, reading, writing) due to brain lesion, usually in the dominant (left) hemisphere.
Language Areas - Simple Diagram
LEFT HEMISPHERE (lateral view)
┌─────────────────────────────────────┐
│ │
│ FRONTAL TEMPORAL │
│ LOBE LOBE │
│ │
│ [BROCA's AREA] [WERNICKE's AREA]│
│ (Area 44,45) (Area 22) │
│ Inferior frontal Superior temporal│
│ gyrus gyrus │
│ \ / │
│ \ ARCUATE / │
│ FASCICULUS │
│ (connects both) │
└─────────────────────────────────────┘
Types of Aphasia - Comparison Table
| Type | Fluency | Comprehension | Repetition | Location |
|---|
| Broca | Nonfluent (telegraphic) | INTACT | Impaired | Inferior frontal gyrus |
| Wernicke | Fluent (jargon) | IMPAIRED | Impaired | Superior temporal gyrus |
| Global | Nonfluent | IMPAIRED | Impaired | Large MCA territory |
| Conduction | Fluent | Intact | SEVERELY Impaired | Arcuate fasciculus |
| Transcortical Motor | Nonfluent | Intact | INTACT | Anterior to Broca |
| Transcortical Sensory | Fluent | Impaired | INTACT | Posterior to Wernicke |
| Anomic | Fluent | Intact | Intact | Angular gyrus |
Flowchart - Quick Identification of Aphasia Type
Is speech FLUENT?
|
┌──┴────────────┐
NO YES
| |
Is repetition Is comprehension
intact? intact?
| |
NO YES NO YES
| | | |
Broca Transcort. Wernicke Is repetition
Motor OR Global intact?
|
NO YES
| |
Conduction Anomic or
Transcort.
Sensory
Special/Important Cases
Broca Aphasia:
- Speech: Nonfluent, telegraphic ("wife...hospital...come")
- Comprehension: Preserved (follows commands)
- Lesion: Inferior frontal gyrus (Broca's area, L hemisphere)
- Associated: Right hemiparesis (motor strip nearby)
Wernicke Aphasia:
- Speech: Fluent but meaningless (jargon, neologisms)
- Comprehension: SEVERELY impaired (cannot follow commands)
- Lesion: Superior temporal gyrus
- Associated: No hemiparesis
Global Aphasia:
- All language functions severely impaired
- Lesion: Large left MCA territory (both Broca + Wernicke areas)
- Associated: Dense right hemiparesis + hemisensory loss + hemianopia
Conduction Aphasia:
- Striking defect: Repetition SEVERELY impaired out of proportion
- Fluent speech, intact comprehension
- Lesion: Arcuate fasciculus (disconnects Broca from Wernicke)
- Classic exam: Patient says "I like girls better" when asked to repeat "boy"
Sources: Ganong's Review of Medical Physiology (26th Ed), Guyton & Hall Textbook of Medical Physiology, Bradley & Daroff's Neurology in Clinical Practice - consistent with GK Paul Physiology for MBBS.