Dopaminergic pathways
Dopaminergic pathways (dopamine pathways, dopaminergic projections) in the
The four major dopaminergic pathways are the mesolimbic pathway, the mesocortical pathway, the nigrostriatal pathway, and the tuberoinfundibular pathway. The mesolimbic pathway and the mesocortical pathway form the mesocorticolimbic system. Two other dopaminergic pathways to be considered are the hypothalamospinal tract and the incertohypothalamic pathway.
Parkinson's disease, attention deficit hyperactivity disorder (ADHD), substance use disorders (addiction), and restless legs syndrome (RLS) can be attributed to dysfunction in specific dopaminergic pathways.
The dopamine neurons of the dopaminergic pathways synthesize and release the
Pathways
Major
Six of the dopaminergic pathways are listed below.[5][6][7]
Pathway name | Description | Associated processes | Associated disorders | |
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Mesocorticolimbic system |
The mesolimbic pathway transmits dopamine from the prefix in the word "mesolimbic" refers to the midbrain, or "middle brain", since "meso" means "middle" in Greek .
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The mesocortical pathway transmits dopamine from the VTA to the prefrontal cortex. The "meso" prefix in "mesocortical" refers to the VTA, which is located in the midbrain, and "cortical" refers to the cortex. |
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Nigrostriatal pathway | The nigrostriatal pathway transmits dopaminergic neurons from the zona compacta of the substantia nigra[8] to the caudate nucleus and putamen.
The dorsal striatum .
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Tuberoinfundibular pathway | The tuberoinfundibular pathway transmits dopamine from the hypothalamus to the pituitary gland.
This pathway controls the secretion of certain hormones, including prolactin, from the pituitary gland.[9] "Infundibular" in the word "tuberoinfundibular" refers to the cup or infundibulum, out of which the pituitary gland develops. |
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Hypothalamospinal tract | The tuberoinfundibular pathway not only regulates hormonal balance but also influences locomotor networks in the brainstem and spinal cord. Modulating motor control and coordination, showcasing the interconnected nature of neural circuits in the brain. |
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Incertohypothalamic pathway | This pathway from the zona incerta influences the hypothalamus and locomotor centers in the brainstem. |
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Minor
- Hypothalamospinal
- Incertohypothalamic
- Zona incerta → Hypothalamus
- Zona incerta → Brainstem VTA → Amygdala (mesoamygdaloid pathway)[6]
- VTA → Hippocampus[6]
- VTA → Cingulate cortex[6]
- VTA → Olfactory bulb[6]
- SNc → Subthalamic nucleus[11]
Function
Mesocorticolimbic system
The
Mesocortical pathway
The
Mesolimbic pathway
Referred to as the reward pathway,
Nigrostriatal pathway
The
Tuberoinfundibular pathway
The tuberoinfundibular pathway transmits dopamine from the hypothalamus to the pituitary gland. This neural circuit plays a pivotal role in the regulation of hormonal balance and, specifically, in modulating the secretion of prolactin from the pituitary gland, which is responsible for breast milk production in females. Hyperprolactinemia is an associated condition caused by an excessive amount of prolactin production that is common in pregnant women.[31] After childbirth, the tuberoinfundibular pathway resumes its role in regulating prolactin levels. The decline in estrogen levels postpartum contributes to the restoration of dopaminergic inhibition, preventing sustained hyperprolactinemia in non-pregnant and non-nursing individuals.[32]
Cortico-basal ganglia-thalamo-cortical loop
The dopaminergic pathways that project from the
These models of the basal ganglia are thought to be relevant to the study of
Regulation
The
Neurotransmitter | Origin | Type of Connection | Sources |
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Glutamate | Excitatory projections into the VTA and SNc | [41] | |
GABA
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Inhibitory projections into the VTA and SNc | [41] |
Serotonin | Modulatory effect, depending on receptor subtype Produces a biphasic effect on VTA neurons |
[41] | |
Norepinephrine |
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Modulatory effect, depending on receptor subtype The excitatory and inhibitory effects of the LC on the VTA and SNc are time-dependent |
[41][42] |
Endocannabinoids
|
Excitatory effect on dopaminergic neurons from inhibiting GABAergic inputs Inhibitory effect on dopaminergic neurons from inhibiting glutamatergic inputs May interact with orexins via CB1–OX1 receptor heterodimers to regulate neuronal firing |
[40][41][43][45] | |
Acetylcholine |
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Modulatory effect, depending on receptor subtype | [41] |
Orexin | Excitatory effect on dopaminergic neurons via signaling through OX2) to regulate neuronal firing
Increases both tonic and phasic firing of dopaminergic neurons in the VTA May interact with endocannabinoids via CB1–OX1 receptor heterodimers |
[43][44][45] |
See also
Notes
- ^ retrograde neurotransmission, the dendrites of the postsynaptic neuron release neurotransmitters that signal through receptors that are located on the axon terminal of the presynaptic neuron.[43]
Endocannabinoids signal between neurons through retrograde neurotransmission at synapses;[43] consequently, the dopaminergic neurons that project out of the VTA and SNc release endocannabinoids from their dendrites onto the axon terminals of their inhibitory GABAergic and excitatory glutamatergic inputs to inhibit their effects on dopamine neuronal firing.[40][43]
References
- PMID 17905440.
- ^ "Beyond the Reward Pathway". Learn Genetics. University of Utah. Archived from the original on 2010-02-09. Retrieved 2009-10-23.
- ^ ISBN 978-0-7817-0166-2. Archived from the originalon 5 February 2018.
- ^ ISBN 978-0-387-30351-2.
- ^ PMID 20149820.
Recent studies on intracranial self-administration of neurochemicals (drugs) found that rats learn to self-administer various drugs into the mesolimbic dopamine structures–the posterior ventral tegmental area, medial shell nucleus accumbens and medial olfactory tubercle. ... In the 1970s it was recognized that the olfactory tubercle contains a striatal component, which is filled with GABAergic medium spiny neurons receiving glutamatergic inputs form cortical regions and dopaminergic inputs from the VTA and projecting to the ventral pallidum just like the nucleus accumbens
Figure 3: The ventral striatum and self-administration of amphetamine - ^ ISBN 9780071481274.
Neurons from the SNc densely innervate the dorsal striatum where they play a critical role in the learning and execution of motor programs. Neurons from the VTA innervate the ventral striatum (nucleus accumbens), olfactory bulb, amygdala, hippocampus, orbital and medial prefrontal cortex, and cingulate cortex. VTA DA neurons play a critical role in motivation, reward-related behavior, attention, and multiple forms of memory. ... Thus, acting in diverse terminal fields, dopamine confers motivational salience ("wanting") on the reward itself or associated cues (nucleus accumbens shell region), updates the value placed on different goals in light of this new experience (orbital prefrontal cortex), helps consolidate multiple forms of memory (amygdala and hippocampus), and encodes new motor programs that will facilitate obtaining this reward in the future (nucleus accumbens core region and dorsal striatum). ... DA has multiple actions in the prefrontal cortex. It promotes the "cognitive control" of behavior: the selection and successful monitoring of behavior to facilitate attainment of chosen goals. Aspects of cognitive control in which DA plays a role include working memory, the ability to hold information "on line" in order to guide actions, suppression of prepotent behaviors that compete with goal-directed actions, and control of attention and thus the ability to overcome distractions. ... Noradrenergic projections from the LC thus interact with dopaminergic projections from the VTA to regulate cognitive control.
- ISBN 9780071481274.
Relationship of the hypothalamus and the pituitary gland. The anterior pituitary, or adenohypophysis, receives rich blood flow from the capillaries of the portal hypophyseal system. This system delivers factors released by hypothalamic neurons into portal capillaries at the median eminence. The figure shows one such projection, from the tuberal (arcuate) nuclei via the tuberoinfundibular tract to the median eminence.
- ISBN 9780128036082.
- ISBN 9780128093245.
- ^ S2CID 36698721.
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- ISBN 9780071481274.
• Executive function, the cognitive control of behavior, depends on the prefrontal cortex, which is highly developed in higher primates and especially humans.
• Working memory is a short-term, capacity-limited cognitive buffer that stores information and permits its manipulation to guide decision-making and behavior. ...
These diverse inputs and back projections to both cortical and subcortical structures put the prefrontal cortex in a position to exert what is often called "top-down" control or cognitive control of behavior. ... The prefrontal cortex receives inputs not only from other cortical regions, including association cortex, but also, via the thalamus, inputs from subcortical structures subserving emotion and motivation, such as the amygdala (Chapter 14) and ventral striatum (or nucleus accumbens; Chapter 15). ...
In conditions in which prepotent responses tend to dominate behavior, such as in drug addiction, where drug cues can elicit drug seeking (Chapter 15), or in attention deficit hyperactivity disorder (ADHD; described below), significant negative consequences can result. ... ADHD can be conceptualized as a disorder of executive function; specifically, ADHD is characterized by reduced ability to exert and maintain cognitive control of behavior. Compared with healthy individuals, those with ADHD have diminished ability to suppress inappropriate prepotent responses to stimuli (impaired response inhibition) and diminished ability to inhibit responses to irrelevant stimuli (impaired interference suppression). ... Functional neuroimaging in humans demonstrates activation of the prefrontal cortex and caudate nucleus (part of the striatum) in tasks that demand inhibitory control of behavior. ... Early results with structural MRI show thinning of the cerebral cortex in ADHD subjects compared with age-matched controls in prefrontal cortex and posterior parietal cortex, areas involved in working memory and attention. - ^ PMID 19587853.
- ^ PMID 21205279.
- PMID 21989194.
- S2CID 12241566.
- S2CID 24568869– via SpringerLink.
- ^ PMID 23141060.
- S2CID 36091832.
- PMID 25950633.
To summarize: the emerging realization that many diverse pleasures share overlapping brain substrates; better neuroimaging maps for encoding human pleasure in orbitofrontal cortex; identification of hotspots and separable brain mechanisms for generating 'liking' and 'wanting' for the same reward; identification of larger keyboard patterns of generators for desire and dread within NAc, with multiple modes of function; and the realization that dopamine and most 'pleasure electrode' candidates for brain hedonic generators probably did not cause much pleasure after all.
- PMID 23375169.
- OCLC 1191071328.)
{{cite book}}
: CS1 maint: location missing publisher (link - PMID 25950633.
- PMID 17670959.
- PMID 29899667.
- PMID 27611585.
- ISBN 9780128052914.
- S2CID 237507806.
- PMID 11589124– via Elsevier.
- PMID 24648786.
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- ^ PMID 21270784.
- PMID 23740050.
- PMID 18838041.
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- PMID 26080439.
- ^ PMID 19305743.
Thus, it is conceivable that low levels of CB1 receptors are located on glutamatergic and GABAergic terminals impinging on DA neurons [127, 214], where they can fine-tune the release of inhibitory and excitatory neurotransmitter and regulate DA neuron firing.
Consistently, in vitro electrophysiological experiments from independent laboratories have provided evidence of CB1 receptor localization on glutamatergic and GABAergic axon terminals in the VTA and SNc. - ^ PMID 21872647.
- ^ PMID 24904299.
It has been shown that electrical stimulation of LC results in an excitation followed by a brief inhibition of midbrain dopamine (DA) neurons through an α1 receptor dependent mechanism (Grenhoff et al., 1993).
- ^ PMID 24391536.
Direct CB1-HcrtR1 interaction was first proposed in 2003 (Hilairet et al., 2003). Indeed, a 100-fold increase in the potency of hypocretin-1 to activate the ERK signaling was observed when CB1 and HcrtR1 were co-expressed ... In this study, a higher potency of hypocretin-1 to regulate CB1-HcrtR1 heteromer compared with the HcrtR1-HcrtR1 homomer was reported (Ward et al., 2011b). These data provide unambiguous identification of CB1-HcrtR1 heteromerization, which has a substantial functional impact. ... The existence of a cross-talk between the hypocretinergic and endocannabinoid systems is strongly supported by their partially overlapping anatomical distribution and common role in several physiological and pathological processes. However, little is known about the mechanisms underlying this interaction. ... Acting as a retrograde messenger, endocannabinoids modulate the glutamatergic excitatory and GABAergic inhibitory synaptic inputs into the dopaminergic neurons of the VTA and the glutamate transmission in the NAc. Thus, the activation of CB1 receptors present on axon terminals of GABAergic neurons in the VTA inhibits GABA transmission, removing this inhibitory input on dopaminergic neurons (Riegel and Lupica, 2004). Glutamate synaptic transmission in the VTA and NAc, mainly from neurons of the PFC, is similarly modulated by the activation of CB1 receptors (Melis et al., 2004).
• Figure 1: Schematic of brain CB1 expression and orexinergic neurons expressing OX1 (HcrtR1) or OX2 (HcrtR2)
• Figure 2: Synaptic signaling mechanisms in cannabinoid and orexin systems
• Figure 3: Schematic of brain pathways involved in food intake - ^ PMID 19815001.
- ^ PMID 24530395.
Orexin receptor subtypes readily formed homo- and hetero(di)mers, as suggested by significant BRET signals. CB1 receptors formed homodimers, and they also heterodimerized with both orexin receptors. ... In conclusion, orexin receptors have a significant propensity to make homo- and heterodi-/oligomeric complexes. However, it is unclear whether this affects their signaling. As orexin receptors efficiently signal via endocannabinoid production to CB1 receptors, dimerization could be an effective way of forming signal complexes with optimal cannabinoid concentrations available for cannabinoid receptors.