Uploaded January 2020 | Updated September 2026, 1 week ago
The direct pathway is a circuit in the basal ganglia best-known for its hypothesized role in movement. In this video, I discuss the structures that are considered part of the direct pathway, and explain how they are thought to work together to facilitate movement.
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TRANSCRIPT:
The basal ganglia are a group of structures that are generally considered to include the caudate and putamen (which are collectively known as the striatum), the globus pallidus, subthalamic nucleus, and substantia nigra. The globus pallidus is further divided into internal and external segments, and the substantia nigra is divided into the substantia nigra pars compacta and substantia nigra pars reticulata. The direct pathway is a circuit in the basal ganglia best-known for its hypothesized role in movement.
The direct pathway model involves glutamate neurons that project from the thalamus to motor regions of the cerebral cortex. These excitatory projections are thought to be involved with stimulating movement. Neurons from the globus pallidus internal and substantia nigra pars reticulata, however, project to the thalamus and maintain a steady release of the neurotransmitter GABA which acts to inhibit the thalamic neurons and suppress movement. This mechanism is thought to be important in keeping unwanted movements from occurring. When we want to make a movement, however, information about the movement is sent from the cortex to the striatum via the corticostriatal pathway. Glutamate neurons in this pathway excite neurons in the striatum, and the activated striatal neurons release GABA in the globus pallidus internal and substantia nigra pars reticulata, inhibiting the activity of these regions and stopping the inhibition of neurons in the thalamus that are involved with movement. This effectively opens a gate for movement to occur. Activity along this pathway tends to occur just prior to a movement, and thus has been linked to the facilitation of movement.
The substantia nigra pars compacta is thought to modulate the activity of the direct pathway. Neurons from the substantia nigra pars compacta travel to the striatum via the nigrostriatal pathway, and release dopamine in the striatum. One effect of this seems to be the facilitation of activity in the direct pathway.
References:
Lanciego JL, Luquin N, Obeso JA. Functional neuroanatomy of the basal ganglia. Cold Spring Harb Perspect Med. 2012 Dec 1;2(12):a009621. doi: 10.1101/cshperspect.a009621.
Purves D, Augustine GJ, Fitzpatrick D, Hall WC, Lamantia AS, Mooney RD, Platt ML, White LE, eds. Neuroscience. 6th ed. New York. Sinauer Associates; 2018.
Special thanks to Nicole Lookfong for help with fact-checking the script for this video.
The direct pathway is a circuit in the basal ganglia best-known for its hypothesized role in movement. In this video, I discuss the structures that are considered part of the direct pathway, and explain how they are thought to work together to facilitate movement.
đź§ Take your learning further with my free, self-paced Introduction to Neuroscience course featuring my videos, articles, and hundreds of quiz questions: neuroscientificallychallenged.com/course
If you're looking for accessible and entertaining ways to learn more about the brain, check out my books:
📚Your Brain, Explained: What Neuroscience Reveals About Your Brain and its Quirks: amazon.com/Your-Brain-Explained-Neuroscience-Reveals/dp/1473696569
📚Bizarre: The Most Peculiar Cases of Human Behavior and What They Tell Us About How the Brain Works: amazon.com/Bizarre-Peculiar-Cases-Human-Behavior/dp/139980121X
TRANSCRIPT:
The basal ganglia are a group of structures that are generally considered to include the caudate and putamen (which are collectively known as the striatum), the globus pallidus, subthalamic nucleus, and substantia nigra. The globus pallidus is further divided into internal and external segments, and the substantia nigra is divided into the substantia nigra pars compacta and substantia nigra pars reticulata. The direct pathway is a circuit in the basal ganglia best-known for its hypothesized role in movement.
The direct pathway model involves glutamate neurons that project from the thalamus to motor regions of the cerebral cortex. These excitatory projections are thought to be involved with stimulating movement. Neurons from the globus pallidus internal and substantia nigra pars reticulata, however, project to the thalamus and maintain a steady release of the neurotransmitter GABA which acts to inhibit the thalamic neurons and suppress movement. This mechanism is thought to be important in keeping unwanted movements from occurring. When we want to make a movement, however, information about the movement is sent from the cortex to the striatum via the corticostriatal pathway. Glutamate neurons in this pathway excite neurons in the striatum, and the activated striatal neurons release GABA in the globus pallidus internal and substantia nigra pars reticulata, inhibiting the activity of these regions and stopping the inhibition of neurons in the thalamus that are involved with movement. This effectively opens a gate for movement to occur. Activity along this pathway tends to occur just prior to a movement, and thus has been linked to the facilitation of movement.
The substantia nigra pars compacta is thought to modulate the activity of the direct pathway. Neurons from the substantia nigra pars compacta travel to the striatum via the nigrostriatal pathway, and release dopamine in the striatum. One effect of this seems to be the facilitation of activity in the direct pathway.
References:
Lanciego JL, Luquin N, Obeso JA. Functional neuroanatomy of the basal ganglia. Cold Spring Harb Perspect Med. 2012 Dec 1;2(12):a009621. doi: 10.1101/cshperspect.a009621.
Purves D, Augustine GJ, Fitzpatrick D, Hall WC, Lamantia AS, Mooney RD, Platt ML, White LE, eds. Neuroscience. 6th ed. New York. Sinauer Associates; 2018.
Special thanks to Nicole Lookfong for help with fact-checking the script for this video.



![2-Minute Neuroscience: Color Blindness
Color blindness is a condition in which a person has difficulty seeing or distinguishing certain colors. In this video, I explain the biological mechanisms underlying color blindness and how it is inherited.
đź§ Take your learning further with my free, self-paced Introduction to Neuroscience course featuring my videos, articles, and hundreds of quiz questions: https://neuroscientificallychallenged.com/course
If youre looking for accessible and entertaining ways to learn more about the brain, check out my books:
📚Your Brain, Explained: What Neuroscience Reveals About Your Brain and its Quirks: https://www.amazon.com/Your-Brain-Explained-Neuroscience-Reveals/dp/1473696569/
📚Bizarre: The Most Peculiar Cases of Human Behavior and What They Tell Us About How the Brain Works: https://www.amazon.com/Bizarre-Peculiar-Cases-Human-Behavior/dp/139980121X/
TRANSCRIPT
Color blindness is a condition in which a person has difficulty seeing or distinguishing certain colors. It typically does not involve a complete loss of color vision. Color blindness can be due to various causes, but the most common forms are inherited and caused by genetic differences that affect the function of cone photoreceptors in the retina. The most common type of color blindness is red-green color blindness, where individuals have difficulty distinguishing red and green hues.
Normal color vision relies on three types of cones—each sensitive to different ranges of wavelengths corresponding roughly to blue, green, and red. Some individuals have all three cones but have abnormalities in cone sensitivity that cause irregularities in color perception; this is referred to as anomalous trichromacy and is the mildest form of color blindness. When only two of the three cone cells are functional, it results in a type of color blindness known as dichromacy. The rarest and most severe form of color blindness is called monochromacy and involves a complete loss of color vision.
Red-green color blindness is much more common in males because the mutations that typically cause it are found on the x chromosome. If females possess such a mutation on one x chromosome, it is likely to be balanced out by a functional gene on the other x chromosome. Because males only have one x chromosome, a mutation is more likely to result in color blindness.
Color blindness can be diagnosed using color vision tests, and although it cannot be cured, various technologies like color-enhancing lenses can help in some situations.
REFERENCES
Breedlove SM, Watson NV. Behavioral Neuroscience. 10th ed. New York (NY): Oxford University Press; 2023.
Carroll J, Conway BR. Color vision. Handb Clin Neurol. 2021;178:131-153. doi: 10.1016/B978-0-12-821377-3.00005-2. PMID: 33832674.
Meister M, Tessier‑Lavigne M. Low‑Level Visual Processing: The Retina. In: Kandel ER, Koester JD, Mack SH, Siegelbaum SA, editors. Principles of Neural Science. 6th ed. New York (NY): McGraw‑Hill; 2021.
Naifeh N, Kaufman EJ. Color Vision. 2022 Oct 31. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 29261952.
Simunovic MP. Colour vision deficiency. Eye (Lond). 2010 May;24(5):747-55. doi: 10.1038/eye.2009.251. Epub 2009 Nov 20. PMID: 19927164.
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