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Third ventricle | |
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![]() Third ventricle shown in red | |
![]() Blue – lateral ventricles Cyan – interventricular foramina (Monro) Yellow – third ventricle Red – cerebral aqueduct (Sylvius) Purple – fourth ventricle Green – continuous with the central canal (apertures to subarachnoid space are not visible) | |
Details | |
Identifiers | |
Latin | ventriculus tertius cerebri |
MeSH | D020542 |
NeuroNames | 446 |
NeuroLex ID | birnlex_714 |
TA98 | A14.1.08.410 |
TA2 | 5769 |
FMA | 78454 |
Anatomical terms of neuroanatomy |
The third ventricle is one of the four connected ventricles of the ventricular system within the mammalian brain. It is a slit-like cavity formed in the diencephalon between the two thalami, in the midline between the right and left lateral ventricles, and is filled with cerebrospinal fluid (CSF). [1]
Running through the third ventricle is the interthalamic adhesion, which contains thalamic neurons and fibers that may connect the two thalami.
The third ventricle is a narrow, laterally flattened, vaguely rectangular region, filled with cerebrospinal fluid, and lined by ependyma. It is connected at the superior anterior corner to the lateral ventricles, by the interventricular foramina, and becomes the cerebral aqueduct (aqueduct of Sylvius) at the posterior caudal corner. Since the interventricular foramina are on the lateral edge, the corner of the third ventricle itself forms a bulb, known as the anterior recess (it is also known as the bulb of the ventricle). The roof of the ventricle comprises choroid plexus, forming the inferior central portion of the tela choroidea; immediately above the superior central portion of the tela choroidea is the fornix.
The lateral side of the ventricle is marked by a sulcus – the hypothalamic sulcus – from the inferior side of the interventricular foramina to the anterior side of the cerebral aqueduct. The lateral border posterior/superior of the sulcus constitutes the thalamus, while anterior/inferior of the sulcus it constitutes the hypothalamus. The interthalamic adhesion usually tunnels through the thalamic portion of the ventricle, joining together the left and right halves of the thalamus, although it is sometimes absent, or split into more than one tunnel through the ventricle; it is currently unknown whether any nerve fibres pass between the left and right thalamus via the adhesion (it has more resemblance to a herniation than a commissure).
The posterior border of the ventricle primarily constitutes the epithalamus. The superior part of the posterior border constitutes the habenular commissure, while more centrally it the pineal gland, which regulates sleep and reacts to light levels. Caudal of the pineal gland is the posterior commissure; nerve fibres reach the posterior commissure from the adjacent midbrain, but their onward connection is currently uncertain. The commissures create concavity to the shape of the posterior ventricle border, causing the suprapineal recess above the habenular, and the deeper pineal recess between the habenular and posterior commissures; the recesses being so-named due to the pineal recess being bordered by the pineal gland.
The anterior wall of the ventricle forms the lamina terminalis, within which the vascular organ monitors and regulates the osmotic concentration of the blood; the cerebrum lies beyond the lamina, and causes it to have a slightly concave shape. The optic recess – marks the inferior end of the lamina terminalis, with the optic chiasm forming the immediately adjacent floor.
The portion of the floor immediately posterior of the optic chiasm distends inferiorly, and slightly anteriorly, to form a funnel (the infundibulum); the recess leading to the funnel is known as the infundibular recess. The border of the funnel is the tuber cinereum, which constitutes a bundle of nerve fibres from the hypothalamus. The funnel ends in the posterior lobe of the pituitary gland, which is thus neurally connected to the hypothalamus via the tuber cinereum. A venous sinus (the circular sinus) surrounds the superior portion of the tuber cinereum; the circular sinus is in fact simply a portion of the two lateral cavernous sinuses, joined together by a posterior and anterior intercavernous sinus.
The mammillary bodies form the floor posterior of the tuber cinereum, acting as the link between the fornix and the hypothalamus. Posterior of the mamillary bodies, the ventricle becomes the opening of the cerebral aqueduct, the inferior borders becoming the crus cerebri (sometimes historically called the cerebral peduncle) of the midbrain.
The third ventricle, like other parts of the ventricular system of the brain, develops from the neural canal of the neural tube. Specifically, it originates from the most rostral portion of the neural tube which initially expands to become the prosencephalon. The lamina terminalis is the rostral termination of the neural tube. After about five weeks, different portions of the prosencephalon begin to take distinct developmental paths from one another – the more rostral portion becomes the telencephalon, while the more caudal portion becomes the diencephalon. [2] The telencephalon gradually expands laterally to a much greater extent than it does dorsally or ventrally, and its connection to the remainder of the neural tube reduces to the interventricula foramina. The diencephalon expands more evenly, but caudally of the diencephalon the canal remains narrow. The third ventricle is the space formed by the expanding canal of the diencephalon.
The hypothalamic region of the ventricle develops from the ventral portion of the neural tube, while the thalamic region develops from the dorsal portion; the wall of the tube thickens and becomes the hypothalamus and thalamus respectively. The hypothalamic area of the ventricle begins to distend ventrally during the 5th week of development, creating the infundibulum and posterior pituitary; an outgrowth from the stomodeum (the future mouth) gradually extends towards it, to form the anterior pituitary.
The optic recess is noticeable by the end of the 6th week, by which time a bend is distinguishable in the dorsal portion of the ventricle border. Rostral of the bend, the medial dorsal portion of the ventrical begins to flatten, and become secretory (i.e. choroid plexus), forming the roof of the ventricle. Caudal of the bend, the ventricle border forms the epithalamus, and begins to distend towards the parietal bone (in lower vertebrates, it distends more specifically to the parietal eye); the border of the distention forms the pineal gland.
The floor of the third ventricle is formed by hypothalamic structures and this can be opened surgically between the mamillary bodies and the pituitary gland in a procedure called an endoscopic third ventriculostomy. An endoscopic third ventriculostomy can be performed in order to release extra fluid caused by hydrocephalus.
Several studies have found evidence of ventricular enlargement to be associated with major depression, particularly enlargement of the third ventricle. [3] These observations are interpreted as indicating a loss of neural tissue in brain regions adjacent to the enlarged ventricle, leading to suggestions that cytokines and related mediators of neurodegeneration may play a role in giving rise to the disease. [4] [5] [6]
A chordoid glioma is a rare tumour that can arise in the third ventricle. [7]
The central nervous system (CNS) is the part of the nervous system consisting of the brain and spinal cord, the retina and optic nerve, and the olfactory nerve and epithelia. The CNS is so named because the brain integrates the received information and coordinates and influences the activity of all parts of the bodies of bilaterally symmetric and triploblastic animals—that is, all multicellular animals except sponges and diploblasts. It is a structure composed of nervous tissue positioned along the rostral to caudal axis of the body and may have an enlarged section at the rostral end which is a brain. Only arthropods, cephalopods and vertebrates have a true brain, though precursor structures exist in onychophorans, gastropods and lancelets.
The pituitary gland is an endocrine gland in vertebrates. In humans, the pituitary gland is located at the base of the brain, protruding off the bottom of the hypothalamus. The human pituitary gland is oval shaped, about the size of a chickpea, and weighs 0.5 grams (0.018 oz) on average.
The medulla oblongata or simply medulla is a long stem-like structure which makes up the lower part of the brainstem. It is anterior and partially inferior to the cerebellum. It is a cone-shaped neuronal mass responsible for autonomic (involuntary) functions, ranging from vomiting to sneezing. The medulla contains the cardiac, respiratory, vomiting and vasomotor centers, and therefore deals with the autonomic functions of breathing, heart rate and blood pressure as well as the sleep–wake cycle.
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The brainstem is the stalk-like part of the brain that interconnects the cerebrum and diencephalon with the spinal cord. In the human brain, the brainstem is composed of the midbrain, the pons, and the medulla oblongata. The midbrain is continuous with the thalamus of the diencephalon through the tentorial notch.
The glossopharyngeal nerve, also known as the ninth cranial nerve, cranial nerve IX, or simply CN IX, is a cranial nerve that exits the brainstem from the sides of the upper medulla, just anterior to the vagus nerve. Being a mixed nerve (sensorimotor), it carries afferent sensory and efferent motor information. The motor division of the glossopharyngeal nerve is derived from the basal plate of the embryonic medulla oblongata, whereas the sensory division originates from the cranial neural crest.
In neuroanatomy, the ventricular system is a set of four interconnected cavities known as cerebral ventricles in the brain. Within each ventricle is a region of choroid plexus which produces the circulating cerebrospinal fluid (CSF). The ventricular system is continuous with the central canal of the spinal cord from the fourth ventricle, allowing for the flow of CSF to circulate.
The pineal gland is a small endocrine gland in the brain of most vertebrates. In the darkness the pineal gland produces melatonin, a serotonin-derived hormone, which modulates sleep patterns following the diurnal cycles. The shape of the gland resembles a pine cone, which gives it its name. The pineal gland is located in the epithalamus, near the center of the brain, between the two hemispheres, tucked in a groove where the two halves of the thalamus join. It is one of the neuroendocrine secretory circumventricular organs in which capillaries are mostly permeable to solutes in the blood.
The midbrain or mesencephalon is the rostral-most portion of the brainstem connecting the diencephalon and cerebrum with the pons. It consists of the cerebral peduncles, tegmentum, and tectum.
The fornix is a C-shaped bundle of nerve fibers in the brain that acts as the major output tract of the hippocampus. The fornix also carries some afferent fibers to the hippocampus from structures in the diencephalon and basal forebrain. The fornix is part of the limbic system. While its exact function and importance in the physiology of the brain are still not entirely clear, it has been demonstrated in humans that surgical transection—the cutting of the fornix along its body—can cause memory loss. There is some debate over what type of memory is affected by this damage, but it has been found to most closely correlate with recall memory rather than recognition memory. This means that damage to the fornix can cause difficulty in recalling long-term information such as details of past events, but it has little effect on the ability to recognize objects or familiar situations.
In the human brain, the diencephalon is a division of the forebrain. It is situated between the telencephalon and the midbrain. The diencephalon has also been known as the tweenbrain in older literature. It consists of structures that are on either side of the third ventricle, including the thalamus, the hypothalamus, the epithalamus and the subthalamus.
The fourth ventricle is one of the four connected fluid-filled cavities within the human brain. These cavities, known collectively as the ventricular system, consist of the left and right lateral ventricles, the third ventricle, and the fourth ventricle. The fourth ventricle extends from the cerebral aqueduct to the obex, and is filled with cerebrospinal fluid (CSF).
The lateral ventricles are the two largest ventricles of the brain and contain cerebrospinal fluid. Each cerebral hemisphere contains a lateral ventricle, known as the left or right lateral ventricle, respectively.
The posterior cerebral artery (PCA) is one of a pair of cerebral arteries that supply oxygenated blood to the occipital lobe, part of the back of the human brain. The two arteries originate from the distal end of the basilar artery, where it bifurcates into the left and right posterior cerebral arteries. These anastomose with the middle cerebral arteries and internal carotid arteries via the posterior communicating arteries.
Circumventricular organs (CVOs) are structures in the brain characterized by their extensive and highly permeable capillaries, unlike those in the rest of the brain where there exists a blood–brain barrier (BBB) at the capillary level. Although the term "circumventricular organs" was originally proposed in 1958 by Austrian anatomist Helmut O. Hofer concerning structures around the brain ventricular system, the penetration of blood-borne dyes into small specific CVO regions was discovered in the early 20th century. The permeable CVOs enabling rapid neurohumoral exchange include the subfornical organ (SFO), the area postrema (AP), the vascular organ of lamina terminalis, the median eminence, the pituitary neural lobe, and the pineal gland.
The tuber cinereum is the portion of hypothalamus forming the floor of the third ventricle situated between the optic chiasm, and the mammillary bodies. The tuberal region is one of the three regions of the hypothalamus, the other two being the chiasmatic region and the mamillary region.
The hypothalamic sulcus is a groove in the lateral wall of the third ventricle, marking the boundary between the thalamus and hypothalamus. The upper and lower portions of the lateral wall of the third ventricle correspond to the alar lamina and basal lamina, respectively, of the lateral wall of the fore-brain vesicle and are separated from each other by a furrow, the hypothalamic sulcus, which extends from the interventricular foramen to the cerebral aqueduct.
The stria medullaris (SM), is a part of the epithalamus and forms a bilateral white matter tract of the initial segment of the dorsal diencephalic conduction system (DDCS). It contains afferent fibers from the septal nuclei, lateral preoptico-hypothalamic region, and anterior thalamic nuclei to the habenula. It forms a horizontal ridge on the medial surface of the thalamus on the border between dorsal and medial surfaces of thalamus. The SM, in conjunction with the habenula and the habenular commissure, forms the habenular trigone. It is considered to be the primary afferent of the DDCS.
This article describes anatomical terminology that is used to describe the central and peripheral nervous systems - including the brain, brainstem, spinal cord, and nerves.