The Circulatory System – Cambridge IGCSE/A‑Level Biology
Learning Objective
State the functions of tissue fluid and describe how tissue fluid is formed in a capillary network.
1. Overview of the Human Circulatory System
- Double circulation: the heart pumps blood through two separate circuits – the systemic circuit and the pulmonary circuit – before the blood returns to the heart.
- Systemic circuit:
- Oxygen‑rich blood leaves the left ventricle via the aorta.
- It is distributed to all body tissues.
- De‑oxygenated blood returns to the right atrium through the superior and inferior venae cavae.
- Pulmonary circuit:
- Oxygen‑poor blood leaves the right ventricle through the pulmonary artery.
- It passes through the lung capillaries where gas exchange occurs.
- Oxygen‑rich blood returns to the left atrium via the pulmonary veins.
- Major vessel types: arteries → arterioles → capillaries → venules → veins.
2. Structure & Function of Blood Vessels
| Vessel Type | Wall Structure (key layers) | Physiological Role |
|---|
| Elastic arteries (e.g., aorta) | Thick tunica media rich in elastic fibres; inner tunica intima | Absorb the high‑pressure pulse from the heart and maintain continuous flow (Windkessel effect). |
| Muscular arteries (e.g., femoral artery) | Thick tunica media with abundant smooth muscle | Regulate blood flow to organs by vasoconstriction and vasodilation. |
| Arterioles | Thin tunica media, few elastic fibres | Principal site of resistance; control arterial blood pressure and distribution of blood to capillary beds. |
| Capillaries | Single layer of endothelial cells (≤10 µm) supported by a basement membrane | Site of exchange of gases, nutrients, wastes and formation of tissue fluid. |
| Venules | Thin walls, small amount of smooth muscle | Collect blood from capillaries; begin the low‑pressure return to the heart. |
| Veins (large) | Thin tunica media, thick tunica externa with valves | Capacitance (reservoir) vessels; store up to 70 % of total blood volume and ensure unidirectional flow back to the heart. |
3. Blood‑Pressure Regulation
- Arteriolar tone – the main determinant of total peripheral resistance; controlled by sympathetic nerves and circulating hormones.
- Baroreceptor reflex – stretch receptors in the carotid sinus and aortic arch send signals to the medulla; an increase in arterial pressure triggers parasympathetic activation (↓ heart rate) and sympathetic inhibition (vasodilation).
- Renin–angiotensin–aldosterone system (RAAS) – low renal perfusion → renin release → angiotensin II formation → vasoconstriction and aldosterone‑mediated sodium/water retention, raising blood volume and pressure.
- Antidiuretic hormone (ADH) – released from the posterior pituitary when plasma osmolality rises; increases water re‑absorption in the kidneys, expanding blood volume.
4. Practical Tip – Recognising Vessels and Blood Cells in Slides
- Arteries: thick, elastic walls; lumen relatively small; internal elastic lamina visible.
- Veins: thin walls, larger lumen, valves (triangular “flaps”).
- Capillaries: barely visible; appear as a fine branching network.
- Red blood cells (RBCs): biconcave discs, ~7 µm diameter, no nucleus.
- Leukocytes (required for the syllabus):
- Neutrophils – multilobed nucleus, fine granules; primary phagocytes.
- Lymphocytes – large, round nucleus, scant cytoplasm; adaptive immunity.
- Monocytes – large nucleus, abundant cytoplasm; become macrophages in tissues.
- Eosinophils – bilobed nucleus, large orange‑red granules; combat parasites and modulate allergic responses.
5. Blood Composition & the Role of Water
- Plasma (≈55 % of blood volume) – ~90 % water; the solvent for:
- Ions (Na⁺, K⁺, Ca²⁺, Cl⁻, HCO₃⁻)
- Hormones (insulin, adrenaline, ADH, etc.)
- Metabolites (glucose, urea, amino acids)
- Plasma proteins:
- Albumin – maintains colloid (oncotic) pressure.
- Globulins – transport of lipids, metal ions; immune functions.
- Fibrinogen – clot formation.
- Water’s high specific heat and solvent properties allow:
- Efficient transport of heat (temperature regulation).
- Dissolution and distribution of metabolic substances throughout the body.
6. Functions of Tissue Fluid (Interstitial Fluid)
- Provides a medium for the exchange of O₂, CO₂, nutrients, and metabolic wastes between capillary blood and body cells.
- Maintains a stable extracellular environment (homeostasis) essential for cellular metabolism.
- Acts as a transport pathway for hormones, enzymes and immune cells to their sites of action.
- Serves as a reservoir for plasma proteins; excess fluid that cannot re‑enter the capillary is collected by lymphatic capillaries and returned to the circulation.
7. Formation of Tissue Fluid in a Capillary Network
Fluid movement across the capillary wall is governed by Starling’s forces – the balance between hydrostatic and oncotic pressures.
| Location along capillary | Dominant Process | Key Forces (typical values) |
|---|
| Arterial end | Filtration of plasma into the interstitial space | - Capillary hydrostatic pressure, Pc ≈ 35 mmHg
- Interstitial hydrostatic pressure, Pi ≈ 0–2 mmHg
- Capillary oncotic pressure, πc ≈ 25 mmHg
- Interstitial oncotic pressure, πi ≈ 1 mmHg
- Net filtration pressure (NFP) = (Pc – Pi) – (πc – πi) ≈ (+35 – 0) – (25 – 1) = +11 mmHg → fluid leaves the capillary.
|
| Mid‑capillary | Equilibrium – little net movement | Forces are roughly balanced; NFP ≈ 0 mmHg. |
| Venous end | Reabsorption of fluid back into the capillary | - Capillary hydrostatic pressure falls to ≈ 15 mmHg
- πc remains ≈ 25 mmHg
- NFP = (15 – 0) – (25 – 1) = –9 mmHg → fluid enters the capillary.
|
Step‑by‑step formation of tissue fluid
- Blood enters the capillary at the arterial end; high Pc forces plasma (water + small solutes) out of the lumen.
- Filtration creates interstitial (tissue) fluid that bathes the cells.
- As blood progresses, resistance in the arteriolar‑capillary network lowers Pc.
- Reabsorption occurs at the venous end where πc exceeds the reduced Pc, pulling most of the filtered fluid back into the capillary.
- Any fluid that remains in the interstitial space is collected by lymphatic capillaries, becomes lymph, and is returned to the venous circulation via the thoracic duct.
8. Clinical Link – Edema
Disturbance of Starling forces leads to excess interstitial fluid (edema). Common causes examined in Cambridge papers:
- ↑Pc – e.g., heart failure or venous obstruction.
- ↓πc – e.g., hypo‑albuminaemia (liver disease, nephrotic syndrome).
- ↑πi – e.g., inflammation, increased capillary permeability.
- ↓ lymphatic drainage – e.g., filariasis.
9. Summary Flowchart (text description for diagram)
Draw a single capillary tube:
- Left (arterial) end – arrow outward labelled “Filtration (Pc > πc)”.
- Middle – label “Equilibrium (NFP ≈ 0)”.
- Right (venous) end – arrow inward labelled “Reabsorption (πc > Pc)”.
- Outside the capillary, show an arrow from the interstitial space to a lymphatic capillary labelled “Excess fluid → lymph → venous circulation”.
Key Points to Remember for the Exam
- Hydrostatic pressure pushes fluid out of capillaries; oncotic pressure (mainly albumin) pulls fluid in.
- Typical pressures: Pc 35 mmHg (arterial) → 15 mmHg (venous); πc ≈ 25 mmHg; Pi ≈ 0–2 mmHg; πi ≈ 1 mmHg.
- Net filtration occurs at the arterial end, net reabsorption at the venous end; the balance creates tissue fluid.
- Functions of tissue fluid tie directly to the three main roles of the circulatory system: transport, regulation and protection.
- Edema results when filtration exceeds reabsorption or lymphatic return is impaired.
- Know the four leukocyte types (neutrophil, lymphocyte, monocyte, eosinophil) and one distinguishing feature of each.
- Remember that veins act as capacitance vessels, storing a large proportion of the blood volume.