Lecture 12: Capillaries, Lymphatics, and Veins

Lecture 12: Capillaries, Lymphatics, and Veins

Lecture Objectives

  • Anatomy and Function of Capillaries

    • Understand the structure of capillaries.

    • Comprehend their role in nutrient, gas, and waste exchange.

  • Leaky Capillaries

    • Identify different levels of "leakiness" of various capillary types.

  • Fluid Regulation

    • Discuss the factors and forces regulating fluid leakage from capillaries.

  • Lymphatic System

    • Explain how the lymphatic system returns filtered fluid to the cardiovascular system.

  • Arteries vs. Veins

    • Differentiate the structural features of arteries and veins and their functions as pressure and volume reservoirs, respectively.

Capillaries: The Microcirculation

  • Primary Exchange Site

    • Responsible for the exchange of:

    • Gases

    • Nutrients

    • Water

    • Waste products

  • Capillary Density

    • Density is greatest in tissues with high oxygen consumption or exchange requirements:

    • High Density Examples:

      • Heart

      • Skeletal muscle

      • Glands

      • Brain

    • Low Density Examples:

      • Cartilage

      • Subcutaneous tissue

    • Not all capillaries are open at all times: only 20% of those in skeletal muscle are open at rest.

    • Regulation occurs through arterioles and metarterioles; sphincters are controlled locally by metabolites, not innervated.

Types of Capillaries

  • Tight Capillaries

    • Most common type.

    • Characterized by well-sealed junctions (10-15 nm wide).

    • Example: Blood-brain barrier containing tight junctions to prevent large molecules from leaking.

  • Fenestrated Capillaries

    • Contain fenestrations (membrane-lined holes) which range from 20-100 nm in diameter and can be closed by a diaphragm.

    • Found in:

    • Intestine

    • Glomerulus

    • Exocrine glands

  • Sinusoidal Capillaries

    • Have large gaps between cells (100-1000 µm wide).

    • Facilitate cell movements in and out of circulation.

    • Examples: Liver, bone marrow, spleen.

Mechanisms of Transcapillary Exchange

  • Transcapillary Exchange Mechanisms

    • Diffusion

    • Main route for gases, water, and small solutes.

    • Filtration

    • Occurs mainly at fenestrations.

    • Vesicular Transport

    • Bi-directional; includes:

      • Transcytosis of Macromolecules

      • Transendothelial Channels: a stack of fused endocytotic vesicles across endothelial cells.

Diffusion and Fick's Law

  • Gases

    • Exchange occurs via direct diffusion across the endothelial membrane.

  • Small Solutes

    • Allows diffusion through small pores and clefts.

  • Polar Molecules

    • Exhibit decreased permeability due to poor lipid solubility.

  • Large Molecules

    • Typically, no diffusion occurs for molecules larger than 60 kDa (e.g., albumin, which is 69 kDa).

  • Flux Equation: J=PA([solute]<em>out[solute]</em>in)J = - P \cdot A \cdot ([solute]<em>{out} - [solute]</em>{in})

    • Where:

      • JJ: Flux (quantity moved per unit time)

      • PP: Permeability coefficient

      • AA: Capillary surface area

Capillary Exchange: Starling Forces

  • Net Filtration Pressure

    • Calculated as follows:
      ΔP=P<em>capillaryP</em>interstitial\Delta P = P<em>{capillary} - P</em>{interstitial}

    • Typically, P<em>interstitialP<em>{interstitial} is approximately 0; thus ΔPP</em>c\Delta P \approx P</em>c, which is essentially the blood pressure.

  • Oncotic Pressure

    • Defined as colloid osmotic pressure with the difference:
      Δπ=π<em>capπ</em>interstitial\Delta \pi = \pi<em>{cap} - \pi</em>{interstitial}

  • Equation for Oncotic Pressure:
    π=σRT(C<em>iC</em>o)\pi = \sigma R T (C<em>i - C</em>o)

    • Where:

      • σ\sigma: Colloid reflection coefficient

  • Fluid Movement by Convection

    • The net filtration pressure can thus be represented as:
      Net Filtration Pressure=ΔPΔπ\text{Net Filtration Pressure} = \Delta P - \Delta \pi

  • Typical Values

    • Actual net filtration pressure is around 0.3 mmHg, resulting in 2-3 liters of fluid movement daily from blood to interstitial fluid (IF).

Pathological Conditions Affecting Capillary Dynamics

  • Increased Blood Volume

    • Causes a rise in plasma proteins, reducing colloid osmotic pressure and increasing fluid filtration.

  • Inflammation

    • Increases capillary leakiness and the number of open capillaries.

  • Other Disturbances

    • Can lead to:

    • Edema

    • Increased venous pressure

    • Factors related to pregnancy, capillary injury, burns, inflammation, dehydration, lymphatic obstruction.

Lymphatic System

  • Overview

    • Lymphatic capillaries have closed ends with valve-like inter-endothelial junctions instead of tight junctions, and fine filaments anchor them to surrounding tissues.

  • Lymphatic Flow Dynamics

    • Expansion Phase:

    • Hydrostatic pressure in capillaries >> lymphatic pressure; interendothelial valves allow interstitial fluid to enter lymphatics.

    • Compression Phase:

    • Tissue movement compresses lymphatics, causing lymphatic pressure >> hydrostatic pressure; valves close to force lymph downstream.

  • Lymphatic Flow

    • Approximately 2-3 liters per day.

    • Primarily unidirectional, aided by:

    • Increased interstitial pressure

    • Compression from skeletal muscle contractions

    • Myogenic tone of lymphatic smooth muscle (VSM) cells which contract due to stretch.

Pathology of the Lymphatic System

  • Elephantiasis

    • Characterized by extreme swelling, primarily in the lower body due to obstruction of lymph flow from:

    • Parasitic infections (e.g., filariasis)

    • Persistent exposure to alkaline soils (e.g. podoconiosis)

  • Consequences of Lymph Node Removal

    • Such as post-mastectomy for breast cancer, which can lead to lymphedema in the arm and other nearby regions.

Veins and Their Characteristics

  • Structure of Veins

    • Composed of three layers:

    • Tunica Intima: Endothelial cells

    • Tunica Media: VSM cells

    • Tunica Adventitia: Connective tissue with fewer elastin fibers compared to arteries.

  • Valves in Veins

    • Present to ensure unidirectional flow of blood back to the heart.

  • Compliance and Capacitance

    • Veins exhibit high compliance, allowing for significant volume changes with little change in pressure.

    • Venous pooling occurs as most blood (approximately 70%) resides on the venous side of circulation, enabling adjustment to metabolic demands.

Capacitance and Cardiovascular Control

  • Passive vs. Active Capacitance

    • Passive Capacitance: Involves changes in venous volume due to blood flow without active constriction.

    • Active Capacitance: Involves vasoconstriction from sympathetic stimulation to manage blood flow.

    • The relationship between compliance and capacitance is crucial, underpinning both normal physiology and responses to stress (e.g., hemorrhage).

Varicose Veins

  • Symptoms

    • Heavy or aching legs

    • Ankle swelling

    • Skin discoloration from metabolite accumulation

  • Complications

    • Increased risk of fainting (syncope)

    • Intolerance to prolonged standing

    • Possible development of eczema or thrombophlebitis (leading to serious conditions like pulmonary embolism, deep vein thrombosis, stroke, or myocardial infarction).

  • Treatment Options

    • Compression stockings

    • Leg elevation

    • Anti-inflammatory or anticoagulant drugs

    • Surgical options for vein removal.

Study Questions

  • Comparative Anatomy

    • Discuss the anatomical differences among arteries, veins, and capillaries, relating these features to their respective functions.

  • Capillary Types

    • Provide examples from the body where each type of capillary is found.

  • Compliance vs. Capacitance

    • Explain the differences in mechanics and their implications on venous versus arterial function.

  • Pathological Conditions

    • Identify two disorders related to lymphatic or venous dysfunction and describe the underlying mechanisms involved.