Chronic Hyperosmotic Stress Converts GABAergic Inhibition into Excitation in Vasopressin and Oxytocin Neurons in the Rat
Male
Neurons
0301 basic medicine
Patch-Clamp Techniques
Sodium-Potassium-Chloride Symporters
Vasopressins
Sodium
Hypothalamus
Action Potentials
Neural Inhibition
Bicuculline
Oxytocin
Electric Stimulation
Rats
Rats, Sprague-Dawley
03 medical and health sciences
Sodium Potassium Chloride Symporter Inhibitors
Osmotic Pressure
Stress, Physiological
Animals
Solute Carrier Family 12, Member 2
Bumetanide
DOI:
10.1523/jneurosci.1440-11.2011
Publication Date:
2011-09-15T03:39:41Z
AUTHORS (15)
ABSTRACT
In mammals, the increased secretion of arginine–vasopressin (AVP) (antidiuretic hormone) and oxytocin (natriuretic hormone) is a key physiological response to hyperosmotic stress. In this study, we examined whether chronic hyperosmotic stress weakens GABAAreceptor-mediated synaptic inhibition in rat hypothalamic magnocellular neurosecretory cells (MNCs) secreting these hormones. Gramicidin-perforated recordings of MNCs in acute hypothalamic slices prepared from control rats and ones subjected to the chronic hyperosmotic stress revealed that this challenge not only attenuated the GABAergic inhibition but actually converted it into excitation. The hyperosmotic stress caused a profound depolarizing shift in the reversal potential of GABAergic response (EGABA) in MNCs. ThisEGABAshift was associated with increased expression of Na+–K+–2Cl−cotransporter 1 (NKCC1) in MNCs and was blocked by the NKCC inhibitor bumetanide as well as by decreasing NKCC activity through a reduction of extracellular sodium. Blocking central oxytocin receptors during the hyperosmotic stress prevented the switch to GABAergic excitation. Finally, intravenous injection of the GABAAreceptor antagonist bicuculline lowered the plasma levels of AVP and oxytocin in rats under the chronic hyperosmotic stress. We conclude that the GABAergic responses of MNCs switch between inhibition and excitation in response to physiological needs through the regulation of transmembrane Cl−gradients.
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