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The ganglia and trunks are connected to adjacent spinal nerves by gray rami communicantes throughout the length of the sympathetic trunk and by white rami communicantes in the thoracic and upper lumbar parts of the trunk (T1 to L2). Neuronal fibers found in the sympathetic trunks include preganglionic and postganglionic sympathetic fibers and visceral afferent fibers.
The splanchnic nerves are important components in the innervation of the abdominal viscera. They pass from the sympathetic trunk or sympathetic ganglia associated with the trunk, to the prevertebral plexus and ganglia anterior to the abdominal aorta.
There are two different types of splanchnic nerves, depending on the type of visceral efferent fiber they are carrying:
The thoracic, lumbar, and sacral splanchnic nerves carry preganglionic sympathetic fibers from the sympathetic trunk to ganglia in the prevertebral plexus, and also visceral afferent fibers.
The pelvic splanchnic nerves carry preganglionic parasympathetic fibers from anterior rami of S2, S3, and S4 spinal nerves to an extension of the prevertebral plexus in the pelvis (the inferior hypogastric plexus or pelvic plexus).
Three thoracic splanchnic nerves pass from sympathetic ganglia along the sympathetic trunk in the thorax to the prevertebral plexus and ganglia associated with the abdominal aorta in the abdomen (Fig. 4.136):
The greater splanchnic nerve arises from the fifth to the ninth (or tenth) thoracic ganglia and travels to the celiac ganglion in the abdomen (a prevertebral ganglion associated with the celiac trunk).
The lesser splanchnic nerve arises from the ninth and tenth (or tenth and eleventh) thoracic ganglia and travels to the aorticorenal ganglion.
The least splanchnic nerve, when present, arises from the twelfth thoracic ganglion and travels to the renal plexus.
There are usually two to four lumbar splanchnic nerves, which pass from the lumbar part of the sympathetic trunk or associated ganglia and enter the prevertebral plexus (Fig. 4.136).
Similarly, the sacral splanchnic nerves pass from the sacral part of the sympathetic trunk or associated ganglia and enter the inferior hypogastric plexus, which is an extension of the prevertebral plexus into the pelvis.
The pelvic splanchnic nerves (parasympathetic root) are unique. They are the only splanchnic nerves that carry parasympathetic fibers. In other words, they do not originate from the sympathetic trunks. Rather, they originate directly from the anterior rami of S2 to S4. Preganglionic parasympathetic fibers originating in the sacral spinal cord pass from the S2 to S4 spinal nerves to the inferior hypogastric plexus (Fig. 4.136). Once in this plexus, some of these fibers pass upward, enter the abdominal prevertebral plexus, and distribute with the arteries supplying the hindgut. This provides the pathway for innervation of the distal one-third of the transverse colon, the descending colon, and the sigmoid colon by preganglionic parasympathetic fibers.
The abdominal prevertebral plexus is a collection of nerve fibers that surrounds the abdominal aorta and is continuous onto its major branches. Scattered throughout the length of the abdominal prevertebral plexus are cell bodies of postganglionic sympathetic fibers. Some of these cell bodies are organized into distinct ganglia, while others are more random in their distribution. The ganglia are usually associated with specific branches of the abdominal aorta and named after these branches.
The three major divisions of the abdominal prevertebral plexus and associated ganglia are the celiac, aortic, and superior hypogastric plexuses (Fig. 4.137).
The celiac plexus is the large accumulation of nerve fibers and ganglia associated with the roots of the celiac trunk and superior mesenteric artery immediately below the aortic hiatus of the diaphragm. Ganglia associated with the celiac plexus include two celiac ganglia, a single superior mesenteric ganglion, and two aorticorenal ganglia.
The aortic plexus consists of nerve fibers and associated ganglia on the anterior and lateral surfaces of the abdominal aorta extending from just below the origin of the superior mesenteric artery to the bifurcation of the aorta into the two common iliac arteries. The major ganglion in this plexus is the inferior mesenteric ganglion at the root of the inferior mesenteric artery.
The superior hypogastric plexus contains numerous small ganglia and is the final part of the abdominal prevertebral plexus before the prevertebral plexus continues into the pelvic cavity.
Each of these major plexuses gives origin to a number of secondary plexuses, which may also contain small ganglia. These plexuses are usually named after the vessels with which they are associated. For example, the celiac plexus is usually described as giving origin to the superior mesenteric plexus and the renal plexus, as well as other plexuses that extend out along the various branches of the celiac trunk. Similarly, the aortic plexus has secondary plexuses consisting of the inferior mesenteric plexus, the spermatic plexus, and the external iliac plexus.
Inferiorly, the superior hypogastric plexus divides into the hypogastric nerves, which descend into the pelvis and contribute to the formation of the inferior hypogastric or pelvic plexus (Fig. 4.137).
The abdominal prevertebral plexus receives: preganglionic parasympathetic and visceral afferent fibers from the vagus nerves [X], preganglionic sympathetic and visceral afferent fibers from the thoracic and lumbar splanchnic nerves, and preganglionic parasympathetic fibers from the pelvic splanchnic nerves.
Parasympathetic innervation of the abdominal part of the gastrointestinal tract and of the spleen, pancreas, gallbladder, and liver is from two sources鈥攖he vagus nerves [X] and the pelvic splanchnic nerves.
The vagus nerves [X] enter the abdomen associated with the esophagus as the esophagus passes through the diaphragm (Fig. 4.138) and provide parasympathetic innervation to the foregut and midgut.
After entering the abdomen as the anterior and posterior vagal trunks, they send branches to the abdominal prevertebral plexus. These branches contain preganglionic parasympathetic fibers and visceral afferent fibers, which are distributed with the other components of the prevertebral plexus along the branches of the abdominal aorta.
The pelvic splanchnic nerves, carrying preganglionic parasympathetic fibers from S2 to S4 spinal cord levels, enter the inferior hypogastric plexus in the pelvis. Some of these fibers move upward into the inferior mesenteric part of the prevertebral plexus in the abdomen (Fig. 4.138). Once there, these fibers are distributed with branches of the inferior mesenteric artery and provide parasympathetic innervation to the hindgut.
The enteric system is a division of the visceral part of the nervous system and is a local neuronal circuit in the wall of the gastrointestinal tract. It consists of motor and sensory neurons organized into two interconnected plexuses (the myenteric and submucosal plexuses) between the layers of the gastrointestinal wall, and the associated nerve fibers that pass between the plexuses and from the plexuses to the adjacent tissue (Fig. 4.139).
The enteric system regulates and coordinates numerous gastrointestinal tract activities, including gastric secretory activity, gastrointestinal blood flow, and the contraction and relaxation cycles of smooth muscle (peristalsis).
Although the enteric system is generally independent of the central nervous system, it does receive input from postganglionic sympathetic and preganglionic parasympathetic neurons that modifies its activities.
Sympathetic innervation of the stomachThe pathway of sympathetic innervation of the stomach is as follows:
A preganglionic sympathetic fiber originating at the T6 level of the spinal cord enters an anterior root to leave the spinal cord.
At the level of the intervertebral foramen, the anterior root (which contains the preganglionic fiber) and a posterior root join to form a spinal nerve.
Outside the vertebral column, the preganglionic fiber leaves the anterior ramus of the spinal nerve through the white ramus communicans.
The white ramus communicans, containing the preganglionic fiber, connects to the sympathetic trunk.
Entering the sympathetic trunk, the preganglionic fiber does not synapse but passes through the trunk and enters the greater splanchnic nerve.
The greater splanchnic nerve passes through the crura of the diaphragm and enters the celiac ganglion.
In the celiac ganglion, the preganglionic fiber synapses with a postganglionic neuron.
The postganglionic fiber joins the plexus of nerve fibers surrounding the celiac trunk and continues along its branches.
The postganglionic fiber travels through the plexus of nerves accompanying the branches of the celiac trunk supplying the stomach and eventually reaches its point of distribution.
This input from the sympathetic system may modify the activities of the gastrointestinal tract controlled by the enteric nervous system.
The posterior abdominal region is posterior to the abdominal part of the gastrointestinal tract, the spleen, and the pancreas (Fig. 4.140). This area, bounded by bones and muscles making up the posterior abdominal wall, contains numerous structures that not only are directly involved in the activities of the abdominal contents but also use this area as a conduit between body regions. Examples include the abdominal aorta and its associated nerve plexuses, the inferior vena cava, the sympathetic trunks, and lymphatics. There are also structures originating in this area that are critical to the normal function of other regions of the body (i.e., the lumbar plexus of nerves), and there are organs that associate with this area during development and remain in it in the adult (i.e., the kidneys and suprarenal glands).
Lumbar vertebrae and the sacrumProjecting into the midline of the posterior abdominal area are the bodies of the five lumbar vertebrae (Fig. 4.141). The prominence of these structures in this region is due to the secondary curvature (a forward convexity) of the lumbar part of the vertebral column.
The lumbar vertebrae can be distinguished from cervical and thoracic vertebrae because of their size. They are much larger than any other vertebrae in any other region. The vertebral bodies are massive and progressively increase in size from vertebra LI to LV. The pedicles are short and stocky, the transverse processes are long and slender, and the spinous processes are large and stubby. The articular processes are large and oriented medially and laterally, which promotes flexion and extension in this part of the vertebral column.
Between each lumbar vertebra is an intervertebral disc, which completes this part of the midline boundary of the posterior abdominal wall.
The midline boundary of the posterior abdominal wall, inferior to the lumbar vertebrae, consists of the upper margin of the sacrum (Fig. 4.141). The sacrum is formed by the fusion of the five sacral vertebrae into a single, wedge-shaped bony structure that is broad superiorly and narrows inferiorly. Its concave anterior surface and its convex posterior surface contain anterior and posterior sacral foramina for the anterior and posterior rami of spinal nerves to pass through.
The ilia, which are components of each pelvic bone, attach laterally to the sacrum at the sacro-iliac joints (Fig. 4.141). The upper part of each ilium expands outward into a thin wing-like area (the iliac fossa). The medial side of this region of each iliac bone, and the related muscles, are components of the posterior abdominal wall.
Superiorly, ribs XI and XII complete the bony framework of the posterior abdominal wall (Fig. 4.141). These ribs are unique in that they do not articulate with the sternum or other ribs, they have a single articular facet on their heads, and they do not have necks or tubercles.
Rib XI is posterior to the superior part of the left kidney, and rib XII is posterior to the superior part of both kidneys. Also, rib XII serves as a point of attachment for numerous muscles and ligaments.
Muscles forming the medial, lateral, inferior, and superior boundaries of the posterior abdominal region fill in the bony framework of the posterior abdominal wall (Table 4.2). Medially are the psoas major and minor muscles, laterally is the quadratus lumborum muscle, inferiorly is the iliacus muscle, and superiorly is the diaphragm (Figs. 4.142 and 4.143).
Medially, the psoas major muscles cover the anterolateral surface of the bodies of the lumbar vertebrae, filling in the space between the vertebral bodies and the transverse processes (Fig. 4.142). Each of these muscles arises from the bodies of vertebra TXII and all five lumbar vertebrae, from the intervertebral discs between each vertebra, and from the transverse processes of the lumbar vertebrae. Passing inferiorly along the pelvic brim, each muscle continues into the anterior thigh, under the inguinal ligament, to attach to the lesser trochanter of the femur.
The psoas major muscle flexes the thigh at the hip joint when the trunk is stabilized and flexes the trunk against gravity when the body is supine. It is innervated by anterior rami of nerves L1 to L3.
Associated with the psoas major muscle is the psoas minor muscle, which is sometimes absent. Lying on the surface of the psoas major when present, this slender muscle arises from vertebrae TXII and LI and the intervening intervertebral disc; its long tendon inserts into the pectineal line of the pelvic brim and the iliopubic eminence.
The psoas minor is a weak flexor of the lumbar vertebral column and is innervated by the anterior ramus of nerve L1.
Laterally, the quadratus lumborum muscles fill the space between rib XII and the iliac crest on both sides of the vertebral column (Fig. 4.142). They are overlapped medially by the psoas major muscles; along their lateral borders are the transversus abdominis muscles.
Each quadratus lumborum muscle arises from the transverse process of vertebra LV, the iliolumbar ligament, and the adjoining part of the iliac crest. The muscle attaches superiorly to the transverse process of the first four lumbar vertebrae and the inferior border of rib XII.
The quadratus lumborum muscles depress and stabilize the twelfth ribs and contribute to lateral bending of the trunk. Acting together, the muscles may extend the lumbar part of the vertebral column. They are innervated by anterior rami of T12 and L1 to L4 spinal nerves.
Inferiorly, an iliacus muscle fills the iliac fossa on each side (Fig. 4.142). From this expansive origin covering the iliac fossa, the muscle passes inferiorly, joins with the psoas major muscle, and attaches to the lesser trochanter of the femur. As they pass into the thigh, these combined muscles are referred to as the iliopsoas muscle.
Like the psoas major muscle, the iliacus flexes the thigh at the hip joint when the trunk is stabilized and flexes the trunk against gravity when the body is supine. It is innervated by branches of the femoral nerve.
Superiorly, the diaphragm forms the boundary of the posterior abdominal region. This musculotendinous sheet also separates the abdominal cavity from the thoracic cavity.
Structurally, the diaphragm consists of a central tendinous part into which the circumferentially arranged muscle fibers attach (Fig. 4.143). The diaphragm is anchored to the lumbar vertebrae by musculotendinous crura, which blend with the anterior longitudinal ligament of the vertebral column:
The right crus is the longest and broadest of the crura and is attached to the bodies of vertebrae LI to LIII and the intervening intervertebral discs (Fig. 4.144).
Similarly, the left crus is attached to vertebrae LI and LII and the associated intervertebral disc.
The crura are connected across the midline by a tendinous arch (the median arcuate ligament), which passes anterior to the aorta (Fig. 4.144).
Lateral to the crura, a second tendinous arch is formed by the fascia covering the upper part of the psoas major muscle. This is the medial arcuate ligament, which is attached medially to the sides of vertebrae LI and LII and laterally to the transverse process of vertebra LI (Fig. 4.144).
A third tendinous arch, the lateral arcuate ligament, is formed by a thickening in the fascia that covers the quadratus lumborum. It is attached medially to the transverse process of vertebra LI and laterally to rib XII (Fig. 4.144).
The medial and lateral arcuate ligaments serve as points of origin for some of the muscular components of the diaphragm.
Structures passing through or around the diaphragmNumerous structures pass through or around the diaphragm (Fig. 4.143):
The aorta passes posterior to the diaphragm and anterior to the vertebral bodies at the lower level of vertebra TXII; it is between the two crura of the diaphragm and posterior to the median arcuate ligament, just to the left of midline.
Accompanying the aorta through the aortic hiatus is the thoracic duct and, sometimes, the azygos vein.
The esophagus passes through the musculature of the right crus of the diaphragm at the level of vertebra TX, just to the left of the aortic hiatus.
Passing through the esophageal hiatus with the esophagus are the anterior and posterior vagal trunks, the esophageal branches of the left gastric artery and vein, and a few lymphatic vessels.
The third large opening in the diaphragm is the caval opening, through which the inferior vena cava passes from the abdominal cavity to the thoracic cavity (Fig. 4.143) at approximately vertebra TVIII in the central tendinous part of the diaphragm.
Accompanying the inferior vena cava through the caval opening is the right phrenic nerve.
The left phrenic nerve passes through the muscular part of the diaphragm just anterior to the central tendon on the left side.
Additional structures pass through small openings either in or just outside the diaphragm as they pass from the thoracic cavity to the abdominal cavity (Fig. 4.143):
The greater, lesser, and least (when present) splanchnic nerves pass through the crura, on either side.
The hemi-azygos vein passes through the left crus.Passing posterior to the medial arcuate ligament, on either side, are the sympathetic trunks.
Passing anterior to the diaphragm, just deep to the ribs, are the superior epigastric vessels.
Other vessels and nerves (i.e., the musculophrenic vessels and intercostal nerves) also pass through the diaphragm at various points.
The classic appearance of the right and left domes of the diaphragm is caused by the underlying abdominal contents pushing these lateral areas upward, and by the fibrous pericardium, which is attached centrally, causing a flattening of the diaphragm in this area (Fig. 4.145).
The domes are produced by: the liver on the right, with some contribution from the right kidney and the right suprarenal gland, and the fundus of the stomach and spleen on the left, with contributions from the left kidney and the left suprarenal gland.
Although the height of these domes varies during breathing, a reasonable estimate in normal expiration places the left dome at the fifth intercostal space and the right dome at rib V. This is important to remember when percussing the thorax.
During inspiration, the muscular part of the diaphragm contracts, causing the central tendon of the diaphragm to be drawn inferiorly. This results in some flattening of the domes, enlargement of the thoracic cavity, and a reduction in intrathoracic pressure. The physiological effect of these changes is that air enters the lungs and venous return to the heart is enhanced.
There is blood supply to the diaphragm on its superior and inferior surfaces:
Superiorly, the musculophrenic and pericardiacophrenic arteries, both branches of the internal thoracic artery, and the superior phrenic artery, a branch of the thoracic aorta, supply the diaphragm.
Inferiorly, the inferior phrenic arteries, branches of the abdominal aorta, supply the diaphragm (see Fig. 4.143).
Venous drainage is through companion veins to these arteries.Innervation of the diaphragm is primarily by the phrenic nerves. These nerves, from the C3 to C5 spinal cord levels, provide all motor innervation to the diaphragm and sensory fibers to the central part. They pass through the thoracic cavity, between the mediastinal pleura and the pericardium, to the superior surface of the diaphragm. At this point, the right phrenic nerve accompanies the inferior vena cava through the diaphragm and the left phrenic nerve passes through the diaphragm by itself (see
Fig. 4.143). Additional sensory fibers are supplied to the peripheral areas of the diaphragm by intercostal nerves.
The bean-shaped kidneys are retroperitoneal in the posterior abdominal region (Fig. 4.149). They lie in the extraperitoneal connective tissue immediately lateral to the vertebral column. In the supine position, the kidneys extend from approximately vertebra TXII superiorly to vertebra LIII inferiorly, with the right kidney somewhat lower than the left because of its relationship with the liver. Although they are similar in size and shape, the left kidney is a longer and more slender organ than the right kidney, and nearer to the midline.
Relationships to other structuresThe anterior surface of the right kidney is related to numerous structures, some of which are separated from the kidney by a layer of peritoneum and some of which are directly against the kidney (Fig. 4.150):
A small part of the superior pole is covered by the right suprarenal gland.
Moving inferiorly, a large part of the rest of the upper part of the anterior surface is against the liver and is separated from it by a layer of peritoneum.
Medially, the descending part of the duodenum is retroperitoneal and contacts the kidney.
The inferior pole of the kidney, on its lateral side, is directly associated with the right colic flexure and, on its medial side, is covered by a segment of the intraperitoneal small intestine.
The anterior surface of the left kidney is also related to numerous structures, some with an intervening layer of peritoneum and some directly against the kidney (Fig. 4.150):
A small part of the superior pole, on its medial side, is covered by the left suprarenal gland.
The rest of the superior pole is covered by the intraperitoneal stomach and spleen.
Moving inferiorly, the retroperitoneal pancreas covers the middle part of the kidney.
On its lateral side, the lower half of the kidney is covered by the left colic flexure and the beginning of the descending colon, and, on its medial side, by the parts of the intraperitoneal jejunum.
Posteriorly, the right and left kidneys are related to similar structures (Fig. 4.151). Superiorly is the diaphragm and inferior to this, moving in a medial to lateral direction, are the psoas major, quadratus lumborum, and transversus abdominis muscles.
The superior pole of the right kidney is anterior to rib XII, while the same region of the left kidney is anterior to ribs XI and XII. The pleural sacs and specifically the costodiaphragmatic recesses therefore extend posterior to the kidneys.
Also passing posterior to the kidneys are the subcostal vessels and nerves and the iliohypogastric and ilio-inguinal nerves.