Cingulum (brain)

Last updated
Cingulum
Sobo 1909 671 - Cingulum.png
Medial surface of right cerebral hemisphere. Some of major association tracts are depicted. Cingulum is at center, in red.
Tractography - Cingulum - animation.gif
Tractography of cingulum. Animation.
Details
Identifiers
Latin cingulum
NeuroNames 1445
TA98 A14.1.09.555
A05.1.03.044
TA2 5597
FMA 260761
Anatomical terms of neuroanatomy

In neuroanatomy, the cingulum or cingulum bundle is an association tract, a nerve tract that projects from the cingulate gyrus to the entorhinal cortex in the brain, allowing for communication between components of the limbic system. [1] It forms the white matter core of the cingulate gyrus, following it from the subcallosal gyrus of the frontal lobe beneath the rostrum of corpus callosum to the parahippocampal gyrus and uncus of the temporal lobe. [2]

Contents

Neurons of the cingulum receive afferent fibers from the parts of the thalamus that are associated with the spinothalamic tract. This, in addition to the fact that the cingulum is a central structure in learning to correct mistakes, indicates that the cingulum is involved in appraisal of pain and reinforcement of behavior that reduces it. [3]

Cingulotomy, the surgical severing of the anterior cingulum, is a form of psychosurgery used to treat depression and OCD.

The cingulum was one of the earliest identified brain structures.

Anatomy and function

The cingulum is described from various brain images as a C-shaped structure within the brain that wraps around the frontal lobe to the temporal lobe right above the corpus callosum. It is located beneath the cingulate gyrus within the medial surface of the brain therefore encircling the entire brain. There are two primary parts of the cingulate cortex: the posterior cingulate cortex and the anterior cingulate cortex. The anterior is linked to emotion, especially apathy and depression. Here function and structure changes are related meaning any change within this structure would lead to a function change, particularly behavioral because of its function involving emotions. Damage to this area can have various effects on mental disorders and mental health. The posterior section is more related to cognitive functions. This can include attention, visual and spatial skills, working memory and general memory. Because of its location, the cingulum is very important to brain structure connectivity and the integration of information that it receives. [4]

Relation to cognitive impairment

In recent years the cingulum has been associated with various brain disorders and diseases. One such area of interest is the disruption of white matter in the posterior cingulum causing mild cognitive impairment. Using diffusion MRI techniques, researchers have associated mild cognitive impairment with damage to the cingulum. The cingulum is a frontal association tract that could play a critical role because it connects sites repeatedly implicated in cognitive control. [5] The middle segment of the cingulum contains connections with premotor and motor cortical areas. Another place of importance that explains the cingulum and its relation to mild cognitive impairment is the fact that the cingulum connects to the hippocampus. The cingulum takes memory information and integrates this to other parts of the brain. Damage to the cingulum also simultaneously damages the hippocampus. This is vital because the hippocampus is pivotal in memory storage. Damage to gray matter, bodies of neurons, or white matter of axons in the cingulum therefore can affect humans cognitively because of this damage. Also variations in microstructure of a group of fibers in the rostral cingulum have been shown to be extremely sensitive to performance of cognitive control tasks. White matter pathology of the cingulum represents one of the earliest changes in development of age-related dementia and is currently aiding researchers worldwide to discover more about this relationship. [6]

Additional images

Related Research Articles

<span class="mw-page-title-main">Language center</span> Speech processing areas of the brain

In neuroscience and psychology, the term language center refers collectively to the areas of the brain which serve a particular function for speech processing and production. Language is a core system that gives humans the capacity to solve difficult problems and provides them with a unique type of social interaction. Language allows individuals to attribute symbols to specific concepts, and utilize them through sentences and phrases that follow proper grammatical rules. Finally, speech is the mechanism by which language is orally expressed.

<span class="mw-page-title-main">Limbic system</span> Set of brain structures involved in emotion and motivation

The limbic system, also known as the paleomammalian cortex, is a set of brain structures located on both sides of the thalamus, immediately beneath the medial temporal lobe of the cerebrum primarily in the forebrain.

<span class="mw-page-title-main">Cingulate cortex</span> Part of the brain within the cerebral cortex

The cingulate cortex is a part of the brain situated in the medial aspect of the cerebral cortex. The cingulate cortex includes the entire cingulate gyrus, which lies immediately above the corpus callosum, and the continuation of this in the cingulate sulcus. The cingulate cortex is usually considered part of the limbic lobe.

<span class="mw-page-title-main">Brodmann area</span> Region of the brain

A Brodmann area is a region of the cerebral cortex, in the human or other primate brain, defined by its cytoarchitecture, or histological structure and organization of cells. The concept was first introduced by the German anatomist Korbinian Brodmann in the early 20th century. Brodmann mapped the human brain based on the varied cellular structure across the cortex and identified 52 distinct regions, which he numbered 1 to 52. These regions, or Brodmann areas, correspond with diverse functions including sensation, motor control, and cognition.

<span class="mw-page-title-main">Temporal lobe</span> One of the four lobes of the mammalian brain

The temporal lobe is one of the four major lobes of the cerebral cortex in the brain of mammals. The temporal lobe is located beneath the lateral fissure on both cerebral hemispheres of the mammalian brain.

<span class="mw-page-title-main">Frontal lobe</span> Part of the brain

The frontal lobe is the largest of the four major lobes of the brain in mammals, and is located at the front of each cerebral hemisphere. It is parted from the parietal lobe by a groove between tissues called the central sulcus and from the temporal lobe by a deeper groove called the lateral sulcus. The most anterior rounded part of the frontal lobe is known as the frontal pole, one of the three poles of the cerebrum.

<span class="mw-page-title-main">Fornix (neuroanatomy)</span> Bundle of nerve fibers in the brain

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.

<span class="mw-page-title-main">Prefrontal cortex</span> Part of the brain responsible for personality, decision-making, and social behavior

In mammalian brain anatomy, the prefrontal cortex (PFC) covers the front part of the frontal lobe of the cerebral cortex. It is the association cortex in the frontal lobe. The PFC contains the Brodmann areas BA8, BA9, BA10, BA11, BA12, BA13, BA14, BA24, BA25, BA32, BA44, BA45, BA46, and BA47.

<span class="mw-page-title-main">Lobes of the brain</span> Parts of the cerebrum

The lobes of the brain are the major identifiable zones of the human cerebral cortex, and they comprise the surface of each hemisphere of the cerebrum. The two hemispheres are roughly symmetrical in structure, and are connected by the corpus callosum. They traditionally have been divided into four lobes, but are today considered as having six lobes each. The lobes are large areas that are anatomically distinguishable, and are also functionally distinct to some degree. Each lobe of the brain has numerous ridges, or gyri, and furrows, the sulci that constitute further subzones of the cortex. The expression "lobes of the brain" usually refers only to those of the cerebrum, not to the distinct areas of the cerebellum.

<span class="mw-page-title-main">Posterior cingulate cortex</span> Caudal part of the cingulate cortex of the brain

The posterior cingulate cortex (PCC) is the caudal part of the cingulate cortex, located posterior to the anterior cingulate cortex. This is the upper part of the "limbic lobe". The cingulate cortex is made up of an area around the midline of the brain. Surrounding areas include the retrosplenial cortex and the precuneus.

<span class="mw-page-title-main">Indusium griseum</span>

The indusium griseum, consists of a thin membranous layer of grey matter in contact with the upper surface of the corpus callosum and continuous laterally with the grey matter of the cingulate cortex and inferiorly with the hippocampus. It is vestigial in humans and is a remnant of the former position of the hippocampus in lower animals.

The perirhinal cortex is a cortical region in the medial temporal lobe that is made up of Brodmann areas 35 and 36. It receives highly processed sensory information from all sensory regions, and is generally accepted to be an important region for memory. It is bordered caudally by postrhinal cortex or parahippocampal cortex and ventrally and medially by entorhinal cortex.

<span class="mw-page-title-main">Retrosplenial cortex</span> Part of the brains cerebral cortex

The retrosplenial cortex (RSC) is a cortical area in the brain comprising Brodmann areas 29 and 30. It is secondary association cortex, making connections with numerous other brain regions. The region's name refers to its anatomical location immediately behind the splenium of the corpus callosum in primates, although in rodents it is located more towards the brain surface and is relatively larger. Its function is currently not well understood, but its location close to visual areas and also to the hippocampal spatial/memory system suggest it may have a role in mediating between perceptual and memory functions, particularly in the spatial domain. However, its exact contribution to either space or memory processing has been hard to pin down.

The trisynaptic circuit or trisynaptic loop is a relay of synaptic transmission in the hippocampus. The trisynaptic circuit is a neural circuit in the hippocampus, which is made up of three major cell groups: granule cells in the dentate gyrus, pyramidal neurons in CA3, and pyramidal neurons in CA1. The hippocampal relay involves 3 main regions within the hippocampus which are classified according to their cell type and projection fibers. The first projection of the hippocampus occurs between the entorhinal cortex (EC) and the dentate gyrus (DG). The entorhinal cortex transmits its signals from the parahippocampal gyrus to the dentate gyrus via granule cell fibers known collectively as the perforant path. The dentate gyrus then synapses on pyramidal cells in CA3 via mossy cell fibers. CA3 then fires to CA1 via Schaffer collaterals which synapse in the subiculum and are carried out through the fornix. Collectively the dentate gyrus, CA1 and CA3 of the hippocampus compose the trisynaptic loop.

The neuroanatomy of memory encompasses a wide variety of anatomical structures in the brain.

Recognition memory, a subcategory of explicit memory, is the ability to recognize previously encountered events, objects, or people. When the previously experienced event is reexperienced, this environmental content is matched to stored memory representations, eliciting matching signals. As first established by psychology experiments in the 1970s, recognition memory for pictures is quite remarkable: humans can remember thousands of images at high accuracy after seeing each only once and only for a few seconds.

The biology of obsessive–compulsive disorder (OCD) refers biologically based theories about the mechanism of OCD. Cognitive models generally fall into the category of executive dysfunction or modulatory control. Neuroanatomically, functional and structural neuroimaging studies implicate the prefrontal cortex (PFC), basal ganglia (BG), insula, and posterior cingulate cortex (PCC). Genetic and neurochemical studies implicate glutamate and monoamine neurotransmitters, especially serotonin and dopamine.

<span class="mw-page-title-main">Nerve tract</span> Bundle of nerve fibers (axons) connecting nuclei of the central nervous system

A nerve tract is a bundle of nerve fibers (axons) connecting nuclei of the central nervous system. In the peripheral nervous system, this is known as a nerve fascicle, and has associated connective tissue. The main nerve tracts in the central nervous system are of three types: association fibers, commissural fibers, and projection fibers. A nerve tract may also be referred to as a commissure, decussation, or neural pathway. A commissure connects the two cerebral hemispheres at the same levels, while a decussation connects at different levels.

Alcohol-related brain damage alters both the structure and function of the brain as a result of the direct neurotoxic effects of alcohol intoxication or acute alcohol withdrawal. Increased alcohol intake is associated with damage to brain regions including the frontal lobe, limbic system, and cerebellum, with widespread cerebral atrophy, or brain shrinkage caused by neuron degeneration. This damage can be seen on neuroimaging scans.

References

  1. Bubb, EJ; Metzler-Baddeley, C; Aggleton, JP (September 2018). "The cingulum bundle: Anatomy, function, and dysfunction". Neuroscience and Biobehavioral Reviews. 92: 104–127. doi:10.1016/j.neubiorev.2018.05.008. PMC   6090091 . PMID   29753752.
  2. J. Edward Bruni, Donald Montemurro, Human Neuroanatomy: A Text, Brain Atlas and Laboratory Dissection Guide, Oxford University Press, 2009[ full citation needed ]
  3. Per Brodal: The Central Nervous System[ full citation needed ]
  4. Jared Tanner Ph.D.: An overview of and introduction to the cingulum, 2010[ full citation needed ]
  5. Metzler-Baddeley, C; Jones, DK; Steventon, J; Westacott, L; Aggleton, JP; O'Sullivan, MJ (December 2012). "Cingulum microstructure predicts cognitive control in older age and mild cognitive impairment". J Neurosci. 32 (49): 17612–9. doi: 10.1523/JNEUROSCI.3299-12.2012 . PMC   6621654 . PMID   23223284. Open Access logo PLoS transparent.svg (full free text)
  6. Delano-Wood, L; Stricker, NH; Sorg, SF; Nation, DA; Jak, AJ; Woods, SP; et al. (2012). "Posterior cingulum white matter disruption and its associations with verbal memory and stroke risk in mild cognitive impairment". J Alzheimers Dis. 29 (3): 589–603. doi:10.3233/JAD-2012-102103. PMC   3341099 . PMID   22466061. Open Access logo PLoS transparent.svg (full free text in PMC)
  7. Bubb, Emma J.; Metzler-Baddeley, Claudia; Aggleton, John P. (2018). "The cingulum bundle: Anatomy, function, and dysfunction". Neuroscience & Biobehavioral Reviews. 92. Elsevier BV: 104–127. doi:10.1016/j.neubiorev.2018.05.008. ISSN   0149-7634. PMC   6090091 . PMID   29753752.