Literature DB >> 26378209

Cell swelling increases the severity of spreading depression in Locusta migratoria.

Kristin E Spong1, Brittany Chin2, Kelsey L M Witiuk2, R Meldrum Robertson2.   

Abstract

Progressive accumulation of extracellular potassium ions can trigger propagating waves of spreading depression (SD), which are associated with dramatic increases in extracellular potassium levels ([K(+)]o) and arrest in neural activity. In the central nervous system the restricted nature of the extracellular compartment creates an environment that is vulnerable to disturbances in ionic homeostasis. Here we investigate how changes in the size of the extracellular space induced by alterations in extracellular osmolarity affect locust SD. We found that hypotonic exposure increased susceptibility to experimentally induced SD evidenced by a decrease in the latency to onset and period between individual events. Hypertonic exposure was observed to delay the onset of SD or prevent the occurrence altogether. Additionally, the magnitude of extracellular K(+) concentration ([K(+)]o) disturbance during individual SD events was significantly greater and they were observed to propagate more quickly under hypotonic conditions compared with hypertonic conditions. Our results are consistent with a conclusion that hypotonic exposure reduced the size of the extracellular compartment by causing cell swelling and thus facilitated the accumulation of K(+) ions. Lastly, we found that pharmacologically reducing the accumulation of extracellular K(+) using the K(+) channel blocker tetraethylammonium slowed the rate of SD propagation while increasing [K(+)]o through inhibition of the Na-K-2Cl cotransporter increased propagation rates. Overall our findings indicate that treatments or conditions that act to reduce the accumulation of extracellular K(+) help to protect against the development of SD and attenuate the spread of ionic disturbance adding to the evidence that diffusion of K(+) is a leading event during locust SD.
Copyright © 2015 the American Physiological Society.

Entities:  

Keywords:  cell swelling; hypertonic; hypotonic; potassium; spreading depression

Mesh:

Substances:

Year:  2015        PMID: 26378209      PMCID: PMC4686288          DOI: 10.1152/jn.00804.2015

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  32 in total

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2.  K+ homeostasis and central pattern generation in the metathoracic ganglion of the locust.

Authors:  Corinne I Rodgers; John D Labrie; R Meldrum Robertson
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3.  Loss of potassium homeostasis underlies hyperthermic conduction failure in control and preconditioned locusts.

Authors:  Tomas G A Money; Corinne I Rodgers; Stuart M K McGregor; R Meldrum Robertson
Journal:  J Neurophysiol       Date:  2009-04-22       Impact factor: 2.714

Review 4.  Roles for novel pharmacological blockers of aquaporins in the treatment of brain oedema and cancer.

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6.  Coma in response to environmental stress in the locust: a model for cortical spreading depression.

Authors:  Corinne I Rodgers; Gary A B Armstrong; R Meldrum Robertson
Journal:  J Insect Physiol       Date:  2010-04-07       Impact factor: 2.354

7.  Potassium fluxes across the blood brain barrier of the cockroach, Periplaneta americana.

Authors:  Andrea L Kocmarek; Michael J O'Donnell
Journal:  J Insect Physiol       Date:  2010-10-15       Impact factor: 2.354

Review 8.  The role of spreading depression, spreading depolarization and spreading ischemia in neurological disease.

Authors:  Jens P Dreier
Journal:  Nat Med       Date:  2011-04-07       Impact factor: 53.440

9.  Suppression of spreading depression-like events in locusts by inhibition of the NO/cGMP/PKG pathway.

Authors:  Gary A B Armstrong; Corinne I Rodgers; Tomas G A Money; R Meldrum Robertson
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10.  Stress preconditioning of spreading depression in the locust CNS.

Authors:  Corinne I Rodgers; Gary A B Armstrong; Kelly L Shoemaker; John D LaBrie; Christopher D Moyes; R Meldrum Robertson
Journal:  PLoS One       Date:  2007-12-26       Impact factor: 3.240

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  3 in total

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Journal:  J Neurophysiol       Date:  2016-06-29       Impact factor: 2.714

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Journal:  J Neurophysiol       Date:  2016-06-22       Impact factor: 2.714

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