Medial forebrain bundle

The medial forebrain bundle (MFB), is a neural pathway containing fibers from the basal olfactory regions, the periamygdaloid region and the septal nuclei, as well as fibers from brainstem regions, including the ventral tegmental area.

Medial forebrain bundle
Anatomical diagram of medial forebrain bundle. These neural fibres connect the septal area in forebrain with medial hypothalamus.
Details
Identifiers
Latinfasciculus medialis telencephali
MeSHD008474
NeuroNames433
NeuroLex IDbirnlex_908
TAA14.1.08.955
FMA62064
Anatomical terms of neuroanatomy

Anatomy

The MFB passes through the lateral hypothalamus and the basal forebrain in a rostral-caudal direction. The MFB has its main projections to these regions of Brodmann areas (BA) 8, 9, 10, 11, 11m. The superior frontal region of MFB projects to BA 8, 9, 10; the rostral middle frontal projects to dorsolateral prefrontal cortex (BA 9, 10); lateral orbitofrontal of MFB shows its projections to nucleus accumbens septi (NAC) and ventral striatum as subcortical reward associated structures.[1]

It contains both ascending and descending fibers. The mesolimbic pathway, which is a collection of dopaminergic neurons that projects from the ventral tegmental area to the nucleus accumbens, is a component pathway of the MFB.[2]

The MFB is one of the two major pathways connecting the limbic forebrain, midbrain, and hindbrain. The other one is the dorsal diencephalic conduction (DDC) system. The two pathways seem to have parallel neural circuits, and share similar physiology and function.[3]

Function

It is commonly accepted that the MFB is a part of the reward system, involved in the integration of reward and pleasure.[4] Electrical stimulation of the medial forebrain bundle is believed to cause sensations of pleasure. This hypothesis is based upon intracranial self-stimulation (ICSS) studies. Animals will work for MFB ICSS, and humans report that MFB ICSS is intensely pleasurable.[5]

Another research technique that was used in determining the function of the MFB was microdialysis.[6] Reinforcing electrical stimulation of the MFB using this method has shown to cause a release in dopamine in the nucleus accumbens. Other microdialysis studies that have been performed have shown that the presence of natural reinforcers such as food, water, and a sex partner, have found to cause a release in dopamine in the nucleus accumbens. This shows that the electrical stimulation of the MFB causes a similar effect compared to natural reinforcers.

The medial forebrain bundle has been shown to be linked to an individual's grief/sadness system through regulation of the individual's seeking/pleasure system.[7]

Potential role in diagnosis/treatment

The medial forebrain bundle may serve as a target in treating treatment-resistant depression.[8] Since the MFB connects areas of the brain which are involved with motivated behavior, mood regulation, and antidepressant response the stimulation of the MFB through deep brain stimulation could be an effective form of treatment. Subjects that receive the deep brain stimulation treatment in the medial forebrain bundle have been reported to have high remission rates with normative functioning and no adverse side effects.

The medial forebrain bundle may also serve to study abuse-related drug effects through intracranial self-stimulation.[9] ICSS targets the MFB at the level of the lateral hypothalamus and elicits a range of responses from the subject through stimulation to acquire a baseline of responses. From this baseline the subject is then exposed to varying levels of stimuli in that are high/low in amplitude and frequency. These responses are then compared to the baseline of the subject to detect for sensitivity to the stimuli. Based on the sensitivity of the response from the subject, a level of inference on the drug abuse potential can be made.


Animal research

In animal studies studying the effects of Levodopa-induced dyskinesia, a major complication in the treatment of Parkinson's disease, lesions in the medial forebrain bundle show a maximum level of severity and sensitivity to levodopa and provide insight into the mechanisms of Levodopa-induced dyskinesia.[10] Other lesions in the mouse, particularly in the striatum 6-OHDA, show a variable sensitivity to levodopa and shows the difference in lesion severity based on location.

In a study with rats, using intracranial self-stimulation implanted in the medial forebrain bundle, rats treated with nicotine and methamphetamine showed an increased speed at which they pressed a lever to induce self-stimulation.[11] The study indicates that the medial forebrain bundle may be directly linked to motivational behavior that is induced by drugs.

In a research on rats, the deep brain stimulation (DBS) on the MFB causes an increase in dopamine for 40 seconds which is above baseline but after 40 seconds, it wasn't increased above baseline.[12]

gollark: It could probably be worked in during restarts.
gollark: Apparently Netflix have a thing to randomly crash production machines to ensure everything still works if they do.
gollark: In the case of RAID1ing SSDs, 120GB ones are probably cheap enough that it makes sense for this.
gollark: As I said, you obviously *want* high uptime, but sometimes the tradeoffs aren't worth it.
gollark: "Dedicated server" basically just means it's on a dedicated machine.

References
  1. Coenen VA, Schumacher LV, Kaller C, Schlaepfer TE, Reinacher PC, Egger K, et al. (2018). "The anatomy of the human medial forebrain bundle: Ventral tegmental area connections to reward-associated subcortical and frontal lobe regions". NeuroImage. Clinical. 18: 770–783. doi:10.1016/j.nicl.2018.03.019. PMC 5964495. PMID 29845013.
  2. You ZB, Chen YQ, Wise RA (2001). "Dopamine and glutamate release in the nucleus accumbens and ventral tegmental area of rat following lateral hypothalamic self-stimulation". Neuroscience. 107 (4): 629–39. doi:10.1016/s0306-4522(01)00379-7. PMID 11720786.
  3. Bianco IH, Wilson SW (April 2009). "The habenular nuclei: a conserved asymmetric relay station in the vertebrate brain". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 364 (1519): 1005–20. doi:10.1098/rstb.2008.0213. PMC 2666075. PMID 19064356.
  4. Hernandez G, Hamdani S, Rajabi H, Conover K, Stewart J, Arvanitogiannis A, Shizgal P (August 2006). "Prolonged rewarding stimulation of the rat medial forebrain bundle: neurochemical and behavioral consequences". Behavioral Neuroscience. 120 (4): 888–904. doi:10.1037/0735-7044.120.4.888. PMID 16893295.
  5. http://www.salon.com/2013/03/23/science_fiction_turns_real_genetically_engineering_animals_for_war/
  6. Carlson. Neil. Physiology of Behavior (11th Edition). Pearson, 2012. Online.
  7. Coenen VA, Schlaepfer TE, Maedler B, Panksepp J (October 2011). "Cross-species affective functions of the medial forebrain bundle-implications for the treatment of affective pain and depression in humans". Neuroscience and Biobehavioral Reviews. 35 (9): 1971–81. doi:10.1016/j.neubiorev.2010.12.009. PMID 21184778.
  8. Gálvez JF, Keser Z, Mwangi B, Ghouse AA, Fenoy AJ, Schulz PE, et al. (April 2015). "The medial forebrain bundle as a deep brain stimulation target for treatment resistant depression: A review of published data". Progress in Neuro-Psychopharmacology & Biological Psychiatry. 58: 59–70. doi:10.1016/j.pnpbp.2014.12.003. PMID 25530019.
  9. Negus SS, Miller LL. Intracranial self-stimulation to evaluate potential abuse of drugs. "Pharmocol Rev." 66.3 (2014):869-917. Online
  10. Francardo V, Cenci MA (January 2014). "Investigating the molecular mechanisms of L-DOPA-induced dyskinesia in the mouse". Parkinsonism & Related Disorders. 20 Suppl 1: S20-2. doi:10.1016/S1353-8020(13)70008-7. PMID 24262181.
  11. Sagara H, Sendo T, Gomita Y (October 2010). "Evaluation of motivational effects induced by intracranial self-stimulation behavior". Acta Medica Okayama. 64 (5): 267–75. doi:10.18926/AMO/40501. PMID 20975759.
  12. Klanker M, Feenstra M, Willuhn I, Denys D (November 2017). "Deep brain stimulation of the medial forebrain bundle elevates striatal dopamine concentration without affecting spontaneous or reward-induced phasic release". Neuroscience. 364: 82–92. doi:10.1016/j.neuroscience.2017.09.012. PMID 28918253.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.