Habenula
Habenula | |
---|---|
Identifiers | |
MeSH | D019262 |
NeuroNames | 294 |
NeuroLex ID | birnlex_1611 |
TA98 | A14.1.08.003 |
TA2 | 5662 |
FMA | 62032 |
Anatomical terms of neuroanatomy |
The habenula (diminutive of Latin habena meaning rein) is a small bilateral neuronal structure in the brain of vertebrates, that has also been called a microstructure since it is no bigger than a pea. The naming as little rein describes its elongated shape in the epithalamus, where it borders the third ventricle, and lies in front of the pineal gland.[1]
Although it is a microstructure each habenular nucleus is divided into two distinct regions of nuclei, a medial habenula (MHb), and a lateral habenula (LHb) both having different neuronal populations, inputs, and outputs.[2][3] The medial habenula can be subdivided into five subnuclei, the lateral habenula into four subnuclei.[4] Research has shown morphological complexity in the MHb and LHb. Different inputs to the MHb are discriminated between the different subnuclei.[5] In the two regions of nuclei there is a difference in gene expression giving different functions to each.[6]
The habenula is a conserved structure across vertebrates. In mammals it is highly symmetric, and in fish, amphibians and reptiles it is highly asymmetric in size, molecular composition, and connections.[1] The habenular nuclei are a major component in the limbic system pathways.[1] The fasciculus retroflexus pathway between the habenula and the interpeduncular nucleus is one of the first major nerve tracts to form in the developing brain.[1]
The habenula is a central structure that connects forebrain regions to midbrain regions, and acts as a hub or node for the integration of emotional and sensory processing.[2] It integrates information from the limbic system, sensory and basal ganglia to guide appropriate and effective responses.[5] The habenula is involved in the regulation of monoamine neurotransmittters notably dopamine and serotonin.[2][3] Both of these neurotransmitters are strongly associated with anxiety disorders, and avoidance behaviours.[2] The functions of the habenula are also involved in motivation, emotion, learning, and pain.[2] The MHb plays an important role in depression, stress, memory, and nicotine withdrawal, as well as a role in cocaine, methamphetamine and alcohol addiction.[6] The MHb shows a high level of nicotinic acetylcholine receptors (nAChRs), that are involved in many forms of addiction. Previously their expression was only noted in other structures associated with addiction. Their expression in the MHb has become a later focus of research.[6]
Anatomy
Each habenular nucleus has two divisions, a medial habenular nucleus (MHb), and a lateral habenular nucleus (LHb). Studies have shown that the medial habenula can be subdivided into five subnuclei, and the lateral habenula into four subnuclei.
Lateral habenula
The primary input regions to the lateral habenula (LHb) are the lateral
Neurons in the lateral habenula are 'reward-negative' as they are activated by stimuli associated with unpleasant events, the absence of the reward or the presence of punishment especially when this is unpredictable.[11] Reward information to the lateral habenula comes from the internal part of the globus pallidus.[12]
The outputs of the lateral habenula target dopaminergic regions (substantia nigra pars compacta and the ventral tegmental area), serotonergic regions (median raphe and dorsal raphe nuclei), and a cholinergic region (the laterodorsal tegmental nucleus).[8] This output inhibits dopamine neurons in substantia nigra pars compacta and the ventral tegmental area, with activation in the lateral habenula linking to deactivation in them, and vice versa, deactivation in the lateral habenula with their activation.[13] The lateral habenula functions to oppose the action of the laterodorsal tegmental nucleus in the acquisition of avoidance responses but not the processing of avoidance later on when it is a memory, motivation or its execution.[14] Research suggests that lateral habenula may play a crucial role in decision making.[15]
There has also shown to be an association with aberrant LHb activity and depression.[16]
Medial habenula
The medial habenula (MHb) receives connections from the posterior
Asymmetry
Asymmetry in the habenula was first noted in 1883 by Nikolaus Goronowitsch.[7] Various species exhibit left-right asymmetric differentiation of habenular neurons. In many fishes and amphibians, the habenula on one side is significantly larger and better organized into distinct nuclei in the dorsal diencephalon than its smaller pair. The sidedness of such differentiation (whether the left or the right is more developed) varies with the species. In birds and mammals, however, both habenulae are more symmetrical (although not entirely) and consist of a medial and a lateral nucleus on each side which is in fish and amphibians equivalent to dorsal habenula and the ventral habenula, respectively.[19][8][20]
Olfactory coding
In some
Functions
These nuclei are hypothesized to be involved in regulation of monoamines, such as dopamine and serotonin.[22][23]
The habenular nuclei are involved in pain processing, reproductive behavior, nutrition,
Depression
Both the medial and lateral habenula show reduced volume in those with depression. Neuron cell numbers were also reduced on the right side.[26] Such changes are not seen in those with schizophrenia.[26] Deep brain stimulation of the major afferent bundle (i.e., stria medullaris thalami) of the lateral habenula has been used for treatment of depression where it is severe, protracted and therapy-resistant.[27][28]
N-Methyl-D-aspartate (NMDA) receptor-dependent burst firing in the lateral habenula has been associated with depression in animal studies,[29] and it has been shown that the general anesthetic ketamine blocks this firing by acting as a receptor antagonist.[30] Ketamine has been the subject of numerous studies after having shown fast-acting antidepressant effects in humans (in a 0.5 mg/bw kg dose).[31]
Motivation and addiction
Recent exploration of the habenular nuclei has begun to associate the structure with an organism's current mood, feeling of motivation, and reward recognition.
LHb is especially important in understanding the reward and motivation relationship as it relates to addictive behaviors.[32] The LHb inhibits dopaminergic neurons, decreasing the release of dopamine.[35] It was determined by several animal studies that receiving a reward coincided with elevated dopamine levels, but once the learned association was learned by the animal, dopamine levels remain elevated, only decreasing when the reward is removed.[20][23][32][35] Therefore, dopamine levels only increase with unpredicted rewards and with a "positive prediction error".[20] Moreover, it was determined that removal of an anticipated award activated LHb, inhibited dopamine levels.[20] This finding helps explain why addictive drugs are associated with elevated dopamine levels.[20]
Nicotine and nAChRs
According to the
History
The habenular is a well conserved structure that appeared in vertebrates more than 360 million years ago.[4] The habenular commissure was described for the first time in 1555 by Andreas Vesalius[40] and the habenula nuclei in 1872 by Theodor Hermann Meynert.[41]
References
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- ^ a b c Fakhoury, Marc; López, Domínguez. "The Role of Habenula in Motivation and Reward". Advances in Neuroscience.
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External links
- Stained brain slice images which include the "Habenula" at the BrainMaps project
- NIF Search - Habenula via the Neuroscience Information Framework
- Neuroanatomy lab sectional atlas