Enkephalin: Difference between revisions

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===Stress response regulation===
===Stress response regulation===
Several studies showed the importance of enkephalins in anxiety and stress. A polymorphism in the gene encoding neutral endopeptidase involved in enkephalin metabolism, was identified in patients with anxiety disorders <ref name="henry">Henry, M. S., Gendron, L., Tremblay, M. E., & Drolet, G. (2017). Enkephalins: Endogenous Analgesics with an Emerging Role in Stress Resilience. Neural plasticity, 2017, 1546125. https://doi.org/10.1155/2017/1546125</ref> <ref>Comings, D. E., Dietz, G., Gade-Andavolu, R., Blake, H., Muhleman, D., Huss, M., Saucier, G., & MacMurray, J. P. (2000). Association of the neutral endopeptidase (MME) gene with anxiety. Psychiatric genetics, 10(2), 91–94. https://doi.org/10.1097/00041444-200010020-00007</ref>. Moreover, an enkephalin KO mice model had increased anxiety with the elevated plus maze (EPM), open field (OF) and light-dark box (LDB) tests, as well as an exaggerated startle response (SR), which is an unconscious defensive response to unexpected or threatened stimuli, and a reduced duration in the social interaction test (SI) <ref name="henry"/> <ref>Ragnauth, A., Schuller, A., Morgan, M., Chan, J., Ogawa, S., Pintar, J., Bodnar, R. J., & Pfaff, D. W. (2001). Female preproenkephalin-knockout mice display altered emotional responses. Proceedings of the National Academy of Sciences of the United States of America, 98(4), 1958–1963. https://doi.org/10.1073/pnas.041598498</ref> <ref>Bilkei-Gorzo, A., Racz, I., Michel, K., Zimmer, A., Klingmüller, D., & Zimmer, A. (2004). Behavioral phenotype of pre-proenkephalin-deficient mice on diverse congenic backgrounds. Psychopharmacology, 176(3-4), 343–352. https://doi.org/10.1007/s00213-004-1904-9</ref> <ref>König, M., Zimmer, A. M., Steiner, H., Holmes, P. V., Crawley, J. N., Brownstein, M. J., & Zimmer, A. (1996). Pain responses, anxiety and aggression in mice deficient in pre-proenkephalin. Nature, 383(6600), 535–538. https://doi.org/10.1038/383535a0</ref>. This suggests that a reduced enkephalin neurotransmission relates with the expression of anxiety. However, in other studies it appears that enkephalins enhanced the reactivity to chronic stress, as enkephalin KO mice were resistant to anxiety and depression-like behaviors after a chronic mild unpredictable stress <ref name="henry"/> <ref>Melo, I., Drews, E., Zimmer, A., & Bilkei-Gorzo, A. (2014). Enkephalin knockout male mice are resistant to chronic mild stress. Genes, brain, and behavior, 13(6), 550–558. https://doi.org/10.1111/gbb.12139</ref>. It seems that enkephalins have different effects on anxiety and stress and this might depend on the central nervous system region. In response to stress, Corticotropin-Releasing Factor (CRF) is released and stimulates the production of endogenous opioids such as endorphins and enkephalins. Enkephalin has been found to modulate the release of CRF from the paraventricular nucleus of the hypothalamus <ref name="cullen"/>. More knowledge on enkephalin pathways and their role is needed in order to fully understand stress regulation and a variety of stress- and anxiety- related  disorders.
Several studies showed the importance of enkephalins in anxiety and stress. A polymorphism in the gene encoding neutral endopeptidase involved in enkephalin metabolism, was identified in patients with anxiety disorders <ref name="henry">Henry, M. S., Gendron, L., Tremblay, M. E., & Drolet, G. (2017). Enkephalins: Endogenous Analgesics with an Emerging Role in Stress Resilience. Neural plasticity, 2017, 1546125. https://doi.org/10.1155/2017/1546125</ref> <ref>Comings, D. E., Dietz, G., Gade-Andavolu, R., Blake, H., Muhleman, D., Huss, M., Saucier, G., & MacMurray, J. P. (2000). Association of the neutral endopeptidase (MME) gene with anxiety. Psychiatric genetics, 10(2), 91–94. https://doi.org/10.1097/00041444-200010020-00007</ref>. Moreover, an enkephalin KO mice model had increased anxiety with the elevated plus maze (EPM), open field (OF) and light-dark box (LDB) tests, as well as an exaggerated startle response (SR), which is an unconscious defensive response to unexpected or threatened stimuli, and a reduced duration in the social interaction test (SI) <ref name="henry"/> <ref>Ragnauth, A., Schuller, A., Morgan, M., Chan, J., Ogawa, S., Pintar, J., Bodnar, R. J., & Pfaff, D. W. (2001). Female preproenkephalin-knockout mice display altered emotional responses. Proceedings of the National Academy of Sciences of the United States of America, 98(4), 1958–1963. https://doi.org/10.1073/pnas.041598498</ref> <ref>Bilkei-Gorzo, A., Racz, I., Michel, K., Zimmer, A., Klingmüller, D., & Zimmer, A. (2004). Behavioral phenotype of pre-proenkephalin-deficient mice on diverse congenic backgrounds. Psychopharmacology, 176(3-4), 343–352. https://doi.org/10.1007/s00213-004-1904-9</ref> <ref>König, M., Zimmer, A. M., Steiner, H., Holmes, P. V., Crawley, J. N., Brownstein, M. J., & Zimmer, A. (1996). Pain responses, anxiety and aggression in mice deficient in pre-proenkephalin. Nature, 383(6600), 535–538. https://doi.org/10.1038/383535a0</ref>. This suggests that a reduced enkephalin neurotransmission relates with the expression of anxiety. However, in other studies it appears that enkephalins enhanced the reactivity to chronic stress, as enkephalin KO mice were resistant to anxiety and depression-like behaviors after a chronic mild unpredictable stress <ref name="henry"/> <ref>Melo, I., Drews, E., Zimmer, A., & Bilkei-Gorzo, A. (2014). Enkephalin knockout male mice are resistant to chronic mild stress. Genes, brain, and behavior, 13(6), 550–558. https://doi.org/10.1111/gbb.12139</ref>. It seems that enkephalins have different effects on anxiety and stress and this might depend on the central nervous system region. In response to stress, Corticotropin-Releasing Factor (CRF) is released and stimulates the production of endogenous opioids such as endorphins and enkephalins. Enkephalin has been found to modulate the release of CRF from the paraventricular nucleus of the hypothalamus <ref name="cullen"/>. More knowledge on enkephalin pathways and their role is needed in order to fully understand stress regulation and a variety of stress- and anxiety- related  disorders.
===Formation of social memory===
Enkephalin has a depressant or inhibitory function of neuronal communication, and it is produced by VIP neurons <ref>Blasco-Ibáñez JM, Martínez-Guijarro FJ, Freund TF. Enkephalin-containing interneurons are specialized to innervate other interneurons in the hippocampal CA1 region of the rat and guinea-pig. Eur J Neurosci. 1998;10:1784–95.</ref>, located in a small area of the hippocampus called CA2, which is known to be involved in the formation of social memory <ref>Oliva A, Fernández-Ruiz A, Leroy F, Siegelbaum SA. Hippocampal CA2 sharp-wave ripples reactivate and promote social memory. Nature. 2020;587:264–9.</ref>. In mice, it is observed that VIP neurons show greater activity during the encounter with an unknown individual than against another relative and also when faced with a new object <ref>Leroy, F., de Solis, C.A., Boyle, L.M. et al. Enkephalin release from VIP interneurons in the hippocampal CA2/3a region mediates heterosynaptic plasticity and social memory. Mol Psychiatry (2021). https://doi.org/10.1038/s41380-021-01124-y</ref>. With the release of enkephalin by VIP interneurons in CA2, a special type of plasticity is induced, called ITDP (Input-timing-dependent plasticity), which is essential for the formation of social memory <ref>Leroy F, Brann DH, Meira T, Siegelbaum SA. Input-timing-dependent Plasticity in the Hippocampal CA2 region and its potential role in social memory. Neuron. 2017;95:1089–102.e5.</ref>.


== Pathophysiology ==
== Pathophysiology ==