Type of Transport
Identify the Transport Mechanisms

Cat | Name | Type |
A | Phagocytosis | cell engulfing a solid |
B | Pinocytosis | cell taking up fluid |
C | Receptor-mediated endocytosis | receptor-mediated engulfing |


- Classification:
- Based on energy use.
Active Transport:
Active Transport | • Against the concentration gradient | ㅤ |
↳ Primary | • Uses ATP directly • "ATP pump" | ㅤ |
ㅤ | ↳ Na+/K+-ATPase pump | • Pumps 3 Na+ out, 2 K+ in. |
ㅤ | ↳ Calcium ATPase | • Pumps Ca2+ for muscle relaxation to inside SR |
ㅤ | ↳ K+/H+ ATPase | • Secretes H+ ions • takes in K+ in parietal cell |
ㅤ | ↳ P-glycoprotein pump transporter | • ATP-binding cassette |
↳ Secondary | • Uses energy indirectly • Using gradient of other substance | ㅤ |
ㅤ | ↳ Symporter (same direction) | • Sodium Glucose cotransporter -1 • Sodium Iodide symporter • Sodium Amino acid cotransporter • Sodium Bicarbonate cotransporter |
ㅤ | ↳ Antiporter (opposite directions) | • Sodium calcium exchanger (NCX) • Sodium H' antiporter |
Based on direction | ㅤ | ㅤ |
Uniport | One substance is transported | ㅤ |
Symport | Two substances → same direction | ㅤ |
Antiport | Two substances → opposite directions | ㅤ |




Carrier Protein vs. Channel Protein:

ㅤ | Carrier Protein | Channel Protein |
Required for | • Facilitated diffusion • Active transport | • Simple diffusion |
Action | • Binds & • Changes shape during transport | • Pore or opening • Transport substances |
Saturation Property | • Present ↳ when all carriers are occupied | • Absent |
Passive Transport:
1. Osmosis
2. Diffusion
Simple Diffusion vs Facilitated Diffusion

ㅤ | Mechanism | Examples |
Passive Transport | ㅤ | ㅤ |
1. Simple diffusion | • Down concentration gradient | ㅤ |
↳ Non Selective | • Without any protein | CO2, O2, urea, Lipid-soluble molecules |
↳ Selective | • Ion channel proteins ↳ Inherent membrane properties • Channel protein → • already present in membranes | Sodium channel, Potassium channel |
2. Facilitated Diffusion | • Down concentration gradient | ㅤ |
ㅤ | • Requires a carrier protein • Not inherent property of membrane • Does not require energy Examples: | Protein in carried to membrane |
ㅤ | ↳ GLUT transporters | Insulin mediated |
ㅤ | ↳ ENaC | Mineralocorticoid |
ㅤ | ↳ Aquaporin 2 channels | Vasopressin |
3. Non-ionic diffusion | • Transport of weak acids or weak bases | ㅤ |



Transport Process MCQ Example

- Context: Diagram showing three transporters (X, Y, Z).
- Transporter X:
- Action: Pumps Sodium out (against gradient), Potassium in (against gradient).
- Identified as: Primary active transporter (specifically, Sodium potassium ATP pump).
- Transporter Y:
- Action: Moves Sodium along its gradient (high to low), Calcium against its gradient (low to high).
- Identified as: Antiporter, Secondary active transporter. (Uses energy from sodium movement. Example: Sodium calcium exchanger (NCX)).
- Transporter Z:
- Structure: Has a pore/opening.
- Action: Transports Chloride ions in both directions. No change in shape.
- Identified as: Simple diffusion (via a channel).
Glucose Reabsorption Mechanism

SGLTs and GLUTs
Glucose Transporters
Glucose Transporters | Apical side | Basolateral side | ㅤ |
Intestine | SGLT 1 | GLUT 2 | ㅤ |
Glucose Transporters | Luminal Membrane | Basolateral Membrane | Reabsorption % in kidney |
PCT | SGLT 2 | GLUT 2 | 90% |
PST | SGLT 1 | GLUT 1 | 10% |
Fructose uptake | Apical side | Basolateral side | ㅤ |
Intestine | GLUT 5 | GLUT 2 | ㅤ |
Mechanism | SGLT • Secondary active transport • co-transports Na⁺ and glucose | GLUT • Facilitated diffusion | ㅤ |
- Note: 100% reabsorption occurs in proximal tubules.
- Insulin dependent → GLUT4 → Skeletal muscle → SGLT3 is also seen
SGLT1 Transport Mechanism

- Location: Apical side of enterocytes
- Na⁺-K⁺ ATPase pump (basolateral side):
- pumps 3 Na⁺ out of enterocyte
- maintains low intracellular Na⁺.
- Due to this gradient:
- Na⁺ enters cell from lumen
- high → low concentration
- Energy released from Na⁺ influx is utilized
- to transport glucose into cell
- against its gradient.
Transporter | Type |
SGLT1 | • Intestine > PST |
SGLT2 | • PCT mainly |
SGLT3 | • Skeletal muscle • Glucose sensor in Small Intestine |
GLUT1 | • PST • Endothelial cell in BBB • RBCs, Placentas Where glucose is primarily needed ↳ Brain, RBC, Placenta, PST |
GLUT2 | • Enterocytes • Hepatocytes • Beta cells of pancreas • PCT cells Absorption and regulation |
GLUT3 | • Neuronal membrane (CNS) • RBCs, Placentas • Maximum affinity for glucose uptake |
GLUT4 | Most important insulin responsive GLUT • Skeletal Muscles • Cardiac Muscles • Adipose Tissues |
GLUT 5 | • Astrocytes (CNS) • Fructose transporter ↳ Seminal vesicle. |
GLUT 11 | • Also transports fructose |
GLUT 12 | • Also insulin responsive |
- Fructose
- GLUT → 5, 11
- Basolateral → GLUT 1, 2
- Brain
- GLUT → 1 (BBB), 3 (Neuronal membrane), 5 (Astrocystes)
- GLUT 4 → Insulin
- Remember exercise → Heart muscle, skeletal muscle, surrounding adipose

Revise Epilepsy
Epilepsy | Characteristic EEG |
GTCS | DOC • Phenytoin, Valproate |
Absence / Petit mal | • Spike & wave (dome) pattern • 3 Hz spikes DOC • Ethosuximide, Valproate • Absent? → Ethuvo ? (Ethosuximide) |
Infantile spasms | • Hypsarrhythmia Age • < 1 years DOC • without tuberous sclerosis: ACTH, Prednisolone • with tuberous sclerosis: Vigabatrin |
Juvenile myoclonic Epilepsy (Janz) | • 4–6 Hz polyspikes & slow wave discharge • JME → JANZ S → 4-5 letters → 4 - 6 Hz polyspikes, slow Age • 10 - 19 years DOC • Valproate |
Lennox Gastaut syndrome | • Slow (<3 Hz) spike wave complex • LGS → < 3Hz spike complex DOC • Valproate, Lamotrigine |
Hepatic encephalopathy | • Triphasic wave {- wave → +ve wave → - wave} |
1. SSPE → 8 years age 2. HIE 3 3. Comatose → (drug/severe hypothermia) | • Burst suppression |
Prion disease (Kuru) | • Periodic sharp wave complexes Age • 35 years |
HSV encephalitis | • Periodic lateralized epileptiform discharge • Affects temporal lobes • DOC: IV Acylovir • HSV → His Wife → Like temples (Period late) |
SSLC / SCENE Genes
SCN/SLC | Disease | Features |
SLC6A19 | Hartnup’s Disease (Chr 5) 6 days Hearty trip | • Defect of tryptophan transporter • Cutaneous photosensitivity (m/c symptom) • Obermeyer test → indoxyl in urine Accumulation of tryptophan in intestine → bacterial decomposition → indoxyl compounds → Indoles absorbed → excreted in urine as indoxyl sulfate→ bluish discoloration of diaper |
SLC2A1 | GLUT 1 defect SSLC → 2 times → bcz brain hypoglycemia | ↓ CSF glucose → seizures ↳ Rx: Pure ketogenic diet |
SCN1A | Dravet syndrome ↳ defective Nav1.1 Na channel ↳ ⛔ GABA | Seizures ↳ DOC: Valproate |
SCN5A (Loss of function) | Brugada syndrome ↳ defective Cardiac Na channel 1 Dragon drank 5 Bru | Brutal (Brugada) scene (SCN5A) guy like me (pseudo RBB) → drinking soda (Na channelopathy) → sudden seizure and death () Broad P wave → Long PQ seg → raised J point → coved ST → T inversion |
SCNN1B/G genes | Liddle Syndrome ↳ Defect: ENaC channel | • AD inheritance • Hypertension + Pseudoaldosteronism • Hypokalemic metabolic alkalosis |
Anti GM1 Antibody | Guillain Barre Syndrome (AIDP) | • Albumino-cytological dissociation • Earliest sign: Distal areflexia. • Bladder and bowel spared. • Bilateral ascending symmetrical flaccid paralysis. • Brighton Criteria for GBS |
Anti GQ1 Antibody. | Miller Fisher Fish vangan Que nikkanam | Triad • Ophthalmoplegia (3rd nerve palsy). • Areflexia. • Ataxia. |
anti P/Q antibody | Lambert Eaton Syndrome Eat 3, 4 Amino acid (3,4 aminopyridine) → gain strength → ↑↑ response | • Pre-junctional ↓↓ release of Ach at NMJ • Oat cell cancer lung → Paraneoplastic • Repetitive nerve stimulation test: ↳ Incremental response Treatment: • DOC: 3,4 aminopyridine • Pyridostigmine |
Insulin independent glucose transporter is present in all of the following except?
- Brain
- Adipose tissue
- RBC
- Pancreas
- Adipose tissue
ANS
Important Information:
- Heart prefers FA in adults
- due to continuous energy demands.
- Fetal heart and failing heart
- Rely on glucose (via GLUT-4).

Identify the Transporter and Transport Mechanism Involved

- Sodium Potassium ATPase.
- Primary active transport.
Epithelial cell junctions



- TAD GH
- CADherins (A → Adherans, D → Desmosomes)
- Cholera toxin (zonula occludens) receptor - GM1 Gangliosidosis

Junctions | Notes | ㅤ |
Tight junction - Zona occludens | • Apical margin • Paracellular movements • Prevents leakage between cells • Maintains cell polarity • Components: Claudins, occludins • Mnemonic: Tight clouds | ㅤ |
ㅤ | ↳ Watery diarrhea / Rice gruel diarrhea | ㅤ |
ㅤ | ↳ Claudin-16 mutation | Familial hypomagnesemia hypercalciuria |
Zona adherens | • Attached to actin • Contain Cadherin • Loss of E-cadherin promotes metastasis | ㅤ |
Desmosome (Macula Adherens / Spot Desmosome) | • “Spot weld” • Attached to intermediate filaments to neighboring cells | ㅤ |
ㅤ | ↳ Ab to Desmoglein 3 +/- Desmoglein 1 | Pemphigus vulgaris |
ㅤ | ↳ Ab to Desmoglein 1 | Pemphigus Foliaceus |
ㅤ | ↳ DEFECT IN DESMOSOMES • NAXOS syndrome • PLAKOGLOBIN gene mutation | Arrythmogenic Right Ventricular Cardiomyopathy |
Gap junction | • Contain Connexons • Enable electrical coupling • Responsible for functional syncytium • Gapil keri kona (connexin) adikkuka | ㅤ |
Hemidesmosome | • Basal surface of epithelial cells • Attached to intermediate filaments to basal lamina • Contain Integrins | ㅤ |
ㅤ | ↳ Abs | Bullous pemphigoid |
Connexin mutations
Connexin mutations | Conditions |
Connexin-32 | Charcot Marie Tooth disease |
Connexin-40 | Idiopathic atrial fibrillation |
CDH gene (E-cadherin):
- Chromosome 16
- "Glue" for cell-to-cell connection.
Loss/mutation
- Mnemonic: Kadich (CDH) → Breastlum Vyarilum
- "Golu" tumors/Kadicha tumors
- Diffuse Gastric Cancer
- Lobular Carcinoma Breast
- Indian File/Single File Pattern
- Mnemonic: File (Indian file) of Breast Ca patients
- Claudin low → EMT positive breast cancer
Lauren's Classification | Intestinal Lauren's Classification | Diffuse Lauren's Classification |
Epidemiological | Environmental | Familial |
Pathology | Gastric atrophy, intestinal metaplasia | Blood Group A |
Sex | m > F | F > M |
Age | ↑ Incidence with ↑Age | Younger age |
Morphology | Gland formation Round glands | Poorly differentiated |
Cell Type | ㅤ | • Gross: Linitis plastica ("leather bottle appearance"). • Microscopy: Signet ring cells. |
Genetics | APC gene mutations, Microsatellite instability p53, p16 inactivation | Loss of E-cadherin (↓ E-cadherin) p53, p16 inactivation |
Invasion | Hematogenous spread | Transmural/Lymphatic spread |

- Krukenberg tumor
- Stomach > Breast/ Colon
- Signet Ring Cells
- Retrograde lymphatic spread
NOTE: Miscellaneous one liners

