The Digestive System - Study Notes
The Digestive System - Study Notes
Lecturer: Dr. R. Ahangari
University of Central Florida, Orlando
Reference: Human Physiology by Linda S. Constanzo, WebMed
Physiology of the Gastrointestinal (GI) Tract
- The GI tract is designed for nutrition provision through multiple activities including:
- Movement of Food: Transport of food through the GI tract.
- Secretion of Digestive Juices: Involves digestion of food.
- Absorption: Absorption of digestive products, water, and electrolytes.
- Circulation: Circulation of blood through the GI organs to remove absorbed substances.
- Control Mechanisms: Regulation of these functions through nervous and hormonal systems.
Alimentary Tract Overview
- Oral Cavity: Initial breakdown of food begins here.
- Esophagus: Serves as a passage for food to the stomach.
- Stomach: Functions for storage and performs a second breakdown of food.
- Accessory Organs: Includes liver, pancreas, and gall bladder aiding digestion.
- Intestines: Comprises small and large intestines, responsible for further digestion and absorption.
Principles of Gastrointestinal Motility
- GI Wall Components:
- Composed of major and minor muscle layers and valves.
- Electrical Activity: Responsible for coordinating muscle contractions in the GI tract.
Structures and Innervation of the GI Tract
- Mucous Membrane: Specialized epithelial cells for secretion or absorption.
- Muscularis Mucosa: Layer of muscle fibers beneath lamina propria that affects surface area for secretion/absorption.
- Muscle Layer: Consists of:
- Inner Circular Layer:
- Function: Contraction decreases the diameter of the GI lumen.
- Outer Longitudinal Layer:
- Function: Causes shortening of a segment of the GI tract.
- Serosa (Adventitia): The external peritoneal covering layer.
Intrinsic (Enteric) Innervation of the Digestive Tract
- Plexuses: The digestive system is supplied by two different plexuses:
- Submucosal Plexus of Meissner
- Myenteric Plexus of Auerbach
- Function: These plexuses integrate and coordinate the motility as well as secretory and endocrine functions of the GI tract.
- Sympathetic Fibers: Interspersed between these two plexuses.
Extrinsic Innervation of the GI Tract
- Efferent Fibers: Carry information from the brainstem and spinal cord to the GI tract.
- Afferent Fibers: Carry sensory information (via chemoreceptors and mechanoreceptors) from the GI tract back to the brainstem and spinal cord.
- Parasympathetic Innervation:
- Includes Vagus nerve (CN X) and pelvic splanchnic nerve (S2-4).
- Effect: Excitatory on GI functions, synapse in myenteric and submucosal plexuses.
- Vagus Nerve: Supplies the esophagus, stomach, pancreas, and intestines to the upper parts of the large intestine.
- Pelvic Splanchnic Nerve: Supplies lower parts of the large intestine and pelvic organs.
- Sympathetic Innervation:
- Originates from the spinal cord through abdominal splanchnic nerves (T5-L2).
- Preganglionic cholinergic fibers synapse in prevertebral ganglia.
- Postganglionic adrenergic fibers inhibit peristalsis and gastric secretion, causing pyloric contraction and conveying pain signals from the stomach.
Gastrointestinal Motility
- Contractile Tissue: The predominant type in the GI tract is unitary smooth muscle.
- Exceptions: Pharynx, upper third of the esophagus, and the external anal sphincter are composed of striated muscle.
- Muscle Contraction Types:
- Circular Muscle Contraction: Reduces the diameter of the GI segment.
- Longitudinal Muscle Contraction: Reduces the length of the GI segment.
- Types of Contractions:
- Phasic Contraction: Found in the esophagus, gastric antrum, and small intestine; these contract and relax periodically.
- Tonic Contraction: Located in lower esophageal sphincter, the orad stomach, ileocecal, and internal anal sphincters.
Membrane Potentials in Intestinal Smooth Muscle
- Slow Waves:
- Description:
- Oscillating membrane potentials inherent to smooth muscle cells of some GI parts.
- Occur spontaneously, originating in interstitial cells of Cajal (the pacemaker for GI smooth muscle).
- Not action potentials but influence the pattern of action potentials.
- Mechanism: Slow wave production cycle involves the activation and deactivation of cell membrane. Depolarization (Calcium ions inward) increases the probability of action potentials occurring, which leads to muscle contraction.
- Repolarization Phase: Caused by potassium (K+) ions outward.
Frequency of Slow Waves
- Varies along the GI tract but remains constant within segments:
- Stomach: Lowest frequency (3 cycles/min).
- Duodenum: Highest frequency (12 cycles/min).
- Ileum: Medium frequency (9 cycles/min).
- The action potentials on top of the slow waves are influenced by neural and hormonal inputs.
Spike Potentials and Action Potentials
- Spike Potentials: Represent action potentials triggered at -40 mV.
- Resting Membrane Potential: Ranges between -50 to -60 mV.
- Factors Influencing Spike Count: The number of spikes is proportional to the threshold rise and duration of time above threshold (1-10 per burst).
- Duration: Action potential duration in GI muscles is 10-40 times longer than in large nerve fibers (approximately 10-20 ms) due to calcium-sodium channel activity.
Resting Membrane Voltage Characteristics
- Normal Values: Average resting membrane voltage is about -56 mV.
- Depolarization Factors:
- Stretching of the muscle.
- Acetylcholine release.
- Stimulation from the parasympathetic nervous system.
- Specific gastrointestinal hormones.
- Hyperpolarization Factors:
- Norepinephrine/epinephrine release.
- Stimulation from the sympathetic nervous system.
Calcium Ions and Muscle Contraction
- Mechanism of Action: In GI smooth muscle, calcium works through calmodulin rather than troponin C as the calcium regulator, coordinating the binding of myosin and actin filaments.
Tonic Contraction of GI Smooth Muscle
- Definition: Even in the absence of action potentials, sub-threshold slow waves result in weak contractions.
- Characteristics:
- GI smooth muscle does not completely relax, exhibiting a basal level of contraction (tonic contraction).
- Controlled by:
- Nervous input (not related to slow waves).
- Hormonal influence.
- Potentially by calcium entry influenced by varying resting membrane potential.
- Peristalsis: This occurs in relation to the underlying tone of the smooth muscle.