Award details

The regulation of circadian and ultradian rhythmicity of circulating glucocorticoid hormones and their roles in the optimisation of limbic activity

Reference	BB/G004307/1
Principal Investigator / Supervisor	Professor Hugh Piggins
Co-Investigators / Co-Supervisors
Institution	The University of Manchester
Department	Life Sciences
Funding type	Research
Value (£)	500,958
Status	Completed
Type	Research Grant
Start date	19/09/2008
End date	18/09/2011
Duration	36 months

Abstract

Although the role of the SCN in the regulation of circadian function has been appreciated for many years, the role and regulation of peripheral clocks both in the CNS and in peripheral tissues is poorly understood. What is clear is that many of these peripheral oscillators cannot maintain their episodic activity in the absence of the SCN, and thus there must be some form neural or circulating signal that can coordinate these slave oscillators. Since one of the major clock genes / period 1 (per 1) has glucocorticoid response elements in its five prime - upstream sequence, and its expression can be induced by glucocorticoids, this would suggest that circulating glucocorticoids which are secreted in both an ultradian and circadian rhythm, may be an important factor in setting the activity of these oscillators. We should like to test this hypothesis by: 1. Clarifying the effect of the SCN on ultradian as well and circadian rhythmicity of glucocorticoid secretion. 2. Revealing the effects of altering the glucocorticoid circadian rhythm on per 1 and/or per 2 activity. 3. Investigating how blocking the activation of per 1 and/or per 2 by glucocorticoid effects synaptic plasticity 4. Examining the role of PER 1 activation in cognitive function

Summary

Biological rhythms are critical for good health and the optimal function of many physiological systems. The daily-circadian-regulation of body rhythms is controlled by a group of cells in the suprachiasmatic nucleus (SCN) of the hypothalamus. These cells employ a specific molecular machinery of so-called clock genes, which use a self-regulating feedback system to maintain an approximate 24-hour rhythm of activity. This central clock / whose activity is fine tuned by external cues such as light / regulates multiple physiological systems including endocrine, metabolic, cardiovascular, cognitive and behavioural outputs. The discovery that clock genes are also found in other areas of the brain and in many peripheral tissues challenges the concept of a single SCN pacemaker. Unlike the SCN however, the clock genes in these other areas do not necessarily express independent long-term rhythms and need the SCN to entrain and maintain their rhythms. This immediately demands that we address the question of how the SCN can control these slave oscillators. One obvious candidate as a controller of the clock genes outside the SCN is the glucocorticoid secreted by the adrenal cortex, which is secreted in a circadian rhythm. This rhythm is under the control of the SCN, and we have recently shown that signalling through this system depends on both its circadian rhythm and the pulse character of its secretion. Furthermore, we know that a critically important clock gene / period 1 (per 1) / has the molecular signature that allows it to be regulated by glucocorticoids. In this application therefore, we want to define how the SCN effects glucocorticoid secretory dynamics, and how changes in these dynamics alter the regulation of clock genes in areas of the brain vital for cognitive function and anxiety behaviour. We shall then go on to investigate how these changes in clock genes alter the efficiency of neurones to interact (synaptic plasticity) and how this in turn alters the memory abilities of conscious animals.

Committee	Closed Committee - Animal Sciences (AS)
Research Topics	Neuroscience and Behaviour
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

Associated awards:

BB/G00403X/1 The regulation of circadian and ultradian rhythmicity of circulating glucocorticoid hormones and their role in the optimisation of limbic activity

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