Corticosterone

Corticosterone
Corticosterone molecule
Names
IUPAC name
(11β)-​11,​21-​dihydroxypregn-​4-​ene-​3,​20-​dione
Identifiers
50-22-6 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:16827 N
ChEMBL ChEMBL110739 N
ChemSpider 5550 YesY
DrugBank DB04652 N
ECHA InfoCard 100.000.018
2869
MeSH Corticosterone
PubChem 5753
UNII W980KJ009P N
Properties
C21H30O4
Molar mass 346.47 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Corticosterone, also known as 17-deoxycortisol and 11β,21-dihydroprogesterone,[1] is a 21-carbon steroid hormone of the corticosteroid type produced in the cortex of the adrenal glands. It is of minor importance in humans, except in the very rare case of congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency.[2]

Roles

In many species, including amphibians, reptiles, rodents and birds, corticosterone is a main glucocorticoid,[3] involved in regulation of energy, immune reactions, and stress responses.

However, in humans, cortisol is the primary glucocorticoid that is produced primarily in the zona fasciculata of the adrenal cortex. Corticosterone has only weak glucocorticoid and mineralocorticoid potencies in humans and is important mainly as an intermediate in the steroidogenic pathway from pregnenolone to aldosterone. Corticosterone is converted to aldosterone by aldosterone synthase, found only in the mitochondria of glomerulosa cells. Glomerulosa cells are found in the Zona glomerulosa, which is the most superficial region of endocrine cells in the adrenal cortex.

Corticosterone is the precursor molecule to the mineralocorticoid aldosterone, one of the major homeostatic modulators of sodium and potassium levels in vivo.

Release or generation mechanisms

One example of a release pathway relates to UV-B stimulation on the skins of certain amphibians such as the Rough-skinned Newt, Taricha granulosa; this trigger seems to cause the internal generation of corticosterone in that species.[4]

Corticosterone in birds

A sizable amount of research has been done on the effects of corticosterone in birds. A brief survey of this research is below.

Corticosterone both inhibits protein synthesis and degrades proteins. Birds with increased levels of corticosterone will have slower feather growth during their molting period and an extended period of poor flight. As a result, many birds have reduced levels of corticosterone when they moult so as to prevent the degradation of their new feathers.[5]

Corticosterone has further developmental effects on birds. Increased levels of corticosterone in chicks leads to increased begging for food and aggressiveness. In the short term this leads to higher chance of obtaining food, but in the long term, increased corticosterone in early life compromises the birds cognitive functioning (problem solving, association of visual cue with food, etc.).[6]

Parental response to chicks increased begging is to increase time foraging for food. This leaves the nest of chicks without protection for increased durations of time.[7] To counter this, during extended periods of food shortage, some species of chicks may suppress corticosterone activity and thus reduce the negative effects elevated corticosterone induces.[8]

Effect on memory

Corticosterone has multiple effects on memory. The main effects are seen through the impact of stress on emotional memories as well as long term memory (LTM).

With emotional memories, corticosterone is largely associated with fear memory recognition. Studies have shown that when fear memories are reactivated or consolidated, levels of corticosterone increased. The increase in corticosterone is linked to anxiety relief. This finding depends on the time at which the administration of corticosterone took place as compared to when the fear conditioning took place; corticosterone can either facilitate or interrupt conditioned fear.[9]

Not only does corticosterone have effects on emotional memories but memory recognition and consolidation as well.

With respect to recognition and long term memories, corticosterone has variable effects. Studies show that the modification of certain chemical and brain processes that affect corticosterone levels can also impact stress effects on memory. In studies on rats, the fluctuations of corticosterone concentration are shown to prevent stress’ impairment of recognition memory in lower amounts. These lower levels seem to be linked to the rescue of stress-induced attenuation of CA1 long-term potentiation.[10] When researchers looked at stress effects on LTM, they found many outcomes. In multiple studies, the formation of LTM (tested 24 h later) was found to be enhanced by corticosterone in some studies, while the persistence of LTM (tested at least 1 wk later) was only assisted by corticosterone in the late phase of memory consolidation and reconsolidation.[11][12] Stress facilitates the consolidation but disrupts the reconsolidation of emotional memory. As mentioned previously, the persistence of LTM is selectively enhanced when stress and corticosterone are administered during the late phase after acquisition, but it is disrupted when stress and corticosterone are administered during the late phase after retrieval of memory.[12] With regards to the persistence of LTM, there is a restricted time window between acquisition or retrieval where persistence is affected. These studies found that while persistence of LTM is selectively affected based on stage of memory, the formation of LTM is left intact after a certain length of time. Up to this point, studies have not agreed as to whether or not these processes are dependent on corticosterone or what even happens based on corticosterone in these processes and how memory is ultimately affected.

In the end, corticosterone affects many processes in terms of memory as well as different types of memories themselves.

See also

References

  1. ↑ R.A. Hill; H.L.J. Makin; D.N. Kirk; G.M. Murphy (23 May 1991). Dictionary of Steroids. CRC Press. pp. 189–. ISBN 978-0-412-27060-4.
  2. ↑ http://emedicine.medscape.com/article/117140-overview#a5
  3. ↑ "e.hormone | The Hormones : Corticoids". Retrieved 2009-04-09.
  4. ↑ C. Michael Hogan (2008) Rough-skinned Newt (Taricha granulosa), Globaltwitcher, ed. Nicklas Stromberg
  5. ↑ Romero, L.M., Strochlic, D., Wingfield, J.C. (2005). Corticosterone inhibits feather growth: Potential mechanism explaining seasonal down regulation of corticosterone during molt. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 142, 65-73.
  6. ↑ Kitaysky, A.S., Kitaiskaia, E.V., Piatt, J.F., Wingfield, J.C. (2003). Benefits and costs of increased levels of corticosterone in seabird chicks. Hormones and Behavior, 43, 140-149.
  7. ↑ Kitaysky, A.S., Piatt, J.F., Wingfield, J.C. (2000). Corticosterone facilitates begging and affects resource allocation in the black-legged kittiwake. Behavioral Endocrinology, 12, 619-625.
  8. ↑ Kitaysky, A.S., Kitaishaia, E.V., Wingfield, J.C., Piatt, J.F. (2001). Dietary restriction causes chronic elevation of corticosterone and enhances stress response in red-legged kittiwake chicks. Journal of Comparative Physiology B, 8, 701-709
  9. ↑ A. Albrecht et al. 2013. Long-Lasting Increase of Corticosterone After Fear Memory Reactivation: Anxiolytic Effects and Network Activity Modulation in the Ventral Hippocampus. Neuropsychopharmacology. 38: 386-394.
  10. ↑ H. Tamano et al. 2013. Preventative effect of theanine intake on stress-induced imparirments of hippocampal long-term potentiation and recognition memory. Brain Research Bulletin. 95: 1-6.
  11. ↑ S. Moore et al. 2013. Conversion of short-term to long-term memory in the novel object recognition paradigm. Neurobiology of Learning and Memory. 105: 174-185.
  12. 1 2 C. Yang et al. 2013. Stress within a Restricted Time Window Selectively Affects the Persistence of Long-Term Memory. PLoS One. 8(3): e59075.

Additional images

  1. ↑ Häggström, Mikael; Richfield, David (2014). "Diagram of the pathways of human steroidogenesis". WikiJournal of Medicine. 1 (1). doi:10.15347/wjm/2014.005. ISSN 2002-4436.
This article is issued from Wikipedia - version of the 11/4/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.