Neural top–down control of physiology concerns the direct regulation by the brain of physiological functions (in addition to smooth muscle and glandular ones). Cellular functions include the immune system’s production of T-lymphocytes and antibodies, and nonimmune related homeostatic functions such as liver gluconeogenesis, sodium reabsorption, osmoregulation, and brown adipose tissue nonshivering thermogenesis. This regulation occurs through the sympathetic and parasympathetic system (the autonomic nervous system), and their direct innervation of body organs and tissues that starts in the brainstem. There is also a noninnervation hormonal control through the hypothalamus and pituitary (HPA). These lower brain areas are under control of cerebral cortex ones. Such cortical regulation differs between its left and right sides. Pavlovian conditioning shows that brain control over basic cell level physiological function can be learned.

Higher brain

Cerebral cortex

Sympathetic and parasympathetic nervous systems and the hypothalamus are regulated by the higher brain.[1][2][3][4] Through them, the higher cerebral cortex areas can control the immune system, and the body’s homeostatic and stress physiology. Areas doing this include the insular cortex,[5][6][7] the orbital, and the medial prefrontal cortices.[8][9] These cerebral areas also control smooth muscle and glandular physiological processes through the sympathetic and parasympathetic nervous system including blood circulation, urogenital, gastrointestinal[10] functions, pancreatic gut secretions,[11] respiration, coughing, vomiting, piloerection, pupil dilation, lacrimation and salivation.[12]

Lateralization

The sympathetic nervous system is predominantly controlled by the right side of the brain (focused upon the insular cortex), while the left side predominantly controls the parasympathetic nervous system.[4] The cerebral cortex in rodents shows lateral specialization in its regulation of immunity with immunosuppression being controlled by the right hemisphere, and immunopotention by the left one.[9][13] Humans show similar lateral specialized control of the immune system from the evidence of strokes,[14] surgery to control epilepsy,[15] and the application of TMS.[16]

Brainstem

The higher brain top down control of physiology is mediated by the sympathetic and parasympathetic nervous systems in the brainstem,[1][2][3][4] and the hypothalamus.[1][17][18] The sympathetic nervous system arises in brainstem nuclei that project down into intermediolateral columns of thoracolumbar spinal cord neurons in spinal segments T1–L2. The parasympathetic nervous system in the motor nuclei of cranial nerves III, VII, IX, (control over the pupil and salivary glands) and X (vagus –many functions including immunity) and sacral spinal segments (gastrointestinal and urogenital systems).[12] Another control occurs through top down control by the medial areas of the prefrontal cortex.[1][17][18] upon the hypothalamus which has a nonnerve control of the body through hormonal secretions of the pituitary.

Immunity

The brain controls immunity both indirectly through HPA glucocorticoid secretions from the pituitary, and by various direct innervations.[19]

  • Antibodies. There is sympathetic innervation of the thymus gland.[20] Sympathetic control exists over antibody production,[21] and the modulation of cytokine concentrations.[22]
  • Cellular immunity. An intact sympathetic nervous system is required to maintain full cellular immunoregulation as denervated mice do not produce and activate, for example, splenic suppressor T cells, or thymic NKT cells.[23]
  • Organ inflammation. Sympathetic innervation of various organs[19] contacts macrophages and dendritic cells and can increase local inflammation including the kidney[24] gut,[25] the skin,[26] and the synovial joints[27]
  • Antiinflammation. The vagus nerve carries a parasympathetic cholinergic antiinflammatory pathway that reduces proinflammatory cytokines such as TNF by spleen macrophages in the red pulp and the marginal zone and so the activation of inflammation.[28][29] This control is in part controlled by direct innervation of body organs such as the spleen.[30] However, the existence of the parasympathetic antiinflammatory nerve pathway is controversial with one reviewer stating: “there is no evidence for an anti-inflammatory role of the efferent vagus nerve that is independent of the sympathetic nervous system.”[31]

Metabolism

The liver receives both sympathetic and parasympathetic nervous system innervation.[32]

Other

Conditioning

The brains of animals can anticipatorily learn to control cell level physiology such as immunity through Pavlovian conditioning. In this conditioning, a neutral stimulus saccharin is paired in a drink with an agent, cyclophosphamide, that produces an unconditioned response (immunosuppression). After learning this pairing, the taste of saccharin by itself through neural top down control created immunosuppression, as a new conditioned response.[42] This work was originally done on rats, however, the same conditioning can also occur in humans.[43] The conditioned response happens in the brain with the ventromedial nucleus of the hypothalamus providing the output pathway to the immune system, the amygdala, the input of visceral information, and the insular cortex acquires and creates the conditioned response.[5] The production of different components of the immune system can be controlled as conditioned responses:

  • Antibodies[43][44][45]
  • IL-2[46][47]
  • B, CD8+ T cells and CD4+ naive and memory T cells, and granulocytes.[48] Such conditioning in rats can last a year.[49]

Nonimmune functions can also be conditioned:

See also

References

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  4. 1 2 3 Craig, A. D. (B. (2005). "Forebrain emotional asymmetry: A neuroanatomical basis?". Trends in Cognitive Sciences. 9 (12): 566–571. doi:10.1016/j.tics.2005.10.005. PMID 16275155. S2CID 16892662.
  5. 1 2 Pacheco-Lopez, G.; Niemi, M. B.; Kou, W.; Härting, M.; Fandrey, J.; Schedlowski, M. (2005). "Neural Substrates for Behaviorally Conditioned Immunosuppression in the Rat". Journal of Neuroscience. 25 (9): 2330–2337. doi:10.1523/JNEUROSCI.4230-04.2005. PMC 6726099. PMID 15745959.
  6. ↑ Ramírez-Amaya, V.; Alvarez-Borda, B.; Ormsby, C. E.; Martínez, R. D.; Pérez-Montfort, R.; Bermúdez-Rattoni, F. (1996). "Insular cortex lesions impair the acquisition of conditioned immunosuppression". Brain, Behavior, and Immunity. 10 (2): 103–114. doi:10.1006/brbi.1996.0011. PMID 8811934. S2CID 24813018.
  7. ↑ Ramı́Rez-Amaya, V.; Bermudez-Rattoni, F. (1999). "Conditioned Enhancement of Antibody Production is Disrupted by Insular Cortex and Amygdala but Not Hippocampal Lesions". Brain, Behavior, and Immunity. 13 (1): 46–60. doi:10.1006/brbi.1998.0547. PMID 10371677. S2CID 20527835.
  8. ↑ Ohira, H.; Isowa, T.; Nomura, M.; Ichikawa, N.; Kimura, K.; Miyakoshi, M.; Iidaka, T.; Fukuyama, S.; Nakajima, T.; Yamada, J. (2008). "Imaging brain and immune association accompanying cognitive appraisal of an acute stressor". NeuroImage. 39 (1): 500–514. doi:10.1016/j.neuroimage.2007.08.017. PMID 17913515. S2CID 26357564.
  9. 1 2 Vlajković, S.; Nikolić, V.; Nikolić, A.; Milanović, S.; Janković, B. D. (1994). "Asymmetrical modulation of immune reactivity in left- and right-biased rats after ipsilateral ablation of the prefrontal, parietal and occipital brain neocortex". The International Journal of Neuroscience. 78 (1–2): 123–134. doi:10.3109/00207459408986051. PMID 7829286.
  10. 1 2 Pocai, A.; Obici, S.; Schwartz, G. J.; Rossetti, L. (2005). "A brain-liver circuit regulates glucose homeostasis". Cell Metabolism. 1 (1): 53–61. doi:10.1016/j.cmet.2004.11.001. PMID 16054044.
  11. ↑ Love, J. A.; Yi, E.; Smith, T. G. (2007). "Autonomic pathways regulating pancreatic exocrine secretion". Autonomic Neuroscience. 133 (1): 19–34. doi:10.1016/j.autneu.2006.10.001. PMID 17113358. S2CID 24929003.
  12. 1 2 Brading, A. (1999). The autonomic nervous system and its effectors. Oxford: Blackwell Science. ISBN 978-0-632-02624-1.
  13. ↑ Barnéoud, P.; Neveu, P. J.; Vitiello, S.; Mormède, P.; Le Moal, M. (1988). "Brain neocortex immunomodulation in rats". Brain Research. 474 (2): 394–398. doi:10.1016/0006-8993(88)90458-1. PMID 3145098. S2CID 23658789.
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  16. ↑ Clow, A.; Lambert, S.; Evans, P.; Hucklebridge, F.; Higuchi, K. (2003). "An investigation into asymmetrical cortical regulation of salivary S-IgA in conscious man using transcranial magnetic stimulation". International Journal of Psychophysiology. 47 (1): 57–64. doi:10.1016/S0167-8760(02)00093-4. PMID 12543446.
  17. 1 2 Radley, J. J.; Arias, C. M.; Sawchenko, P. E. (2006). "Regional Differentiation of the Medial Prefrontal Cortex in Regulating Adaptive Responses to Acute Emotional Stress". Journal of Neuroscience. 26 (50): 12967–12976. doi:10.1523/JNEUROSCI.4297-06.2006. PMC 6674963. PMID 17167086.
  18. 1 2 Kern, S.; Oakes, T. R.; Stone, C. K.; McAuliff, E. M.; Kirschbaum, C.; Davidson, R. J. (2008). "Glucose metabolic changes in the prefrontal cortex are associated with HPA axis response to a psychosocial stressor". Psychoneuroendocrinology. 33 (4): 517–529. doi:10.1016/j.psyneuen.2008.01.010. PMC 2601562. PMID 18337016.
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  53. 1 2 Stockhorst, U.; Mahl, N.; Krueger, M.; Huenig, A.; Schottenfeldnaor, Y.; Huebinger, A.; Berresheim, H.; Steingrueber, H.; Scherbaum, W. (2004). "Classical conditioning and conditionability of insulin and glucose effects in healthy humans". Physiology & Behavior. 81 (3): 375–388. doi:10.1016/j.physbeh.2003.12.019. PMID 15135009. S2CID 2498317.
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