4.6 Article

Osmotherapy With Hypertonic Saline Attenuates Global Cerebral Edema Following Experimental Cardiac Arrest via Perivascular Pool of Aquaporin-4

期刊

CRITICAL CARE MEDICINE
卷 44, 期 8, 页码 E702-E710

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/CCM.0000000000001671

关键词

aquaporins; cardiac arrest; cerebral edema; global cerebral ischemia; hypertonic saline; osmotherapy

资金

  1. Public Health Service National Institutes of Health grant [NS046379]
  2. National Institutes of Health (NIH)
  3. Public Health Service NIH grant [NS046379]

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Objectives: We tested the hypothesis that osmotherapy with hypertonic saline attenuates cerebral edema following experimental cardiac arrest and cardiopulmonary resuscitation by exerting its effect via the perivascular pool of aquaporin-4. We used mice with targeted disruption of the gene encoding alpha-syntrophin (alpha-Syn(-/-)) that demonstrate diminished perivascular aquaporin-4 pool but retain the non-endfoot and ependymal pools. Design: Laboratory animal study. Setting: University animal research laboratory. Interventions: Isoflurane-anesthetized adult male wild-type C57B/6 or alpha a-Syn(-/-) mice were subjected to cardiac arrest/cardiopulmonary resuscitation and treated with either a continuous IV infusion of 0.9% saline or various concentrations of hypertonic saline. Serum osmolality, regional brain water content, blood-brain barrier disruption, and aquaporin-4 protein expression were determined at 24 hours after cardiac arrest/cardiopulmonary resuscitation. Measurements and Main Results: Hypertonic saline (7.5%) treatment significantly attenuated water content in the caudoputamen complex and cortex compared with 0.9% saline treatment in wildtype mice subjected to cardiac arrest/cardiopulmonary resuscitation. In contrast, in alpha-Syn(-/-) mice subjected to cardiac arrest/cardiopulmonary resuscitation, 7.5% hypertonic saline treatment did not attenuate water content. Treatment with 7.5% hypertonic saline attenuated blood-brain barrier disruption at 24 hours following cardiac arrest/cardiopulmonary resuscitation in wild-type mice but not in alpha-Syn(-/-) mice. Total aquaporin-4 protein expression was not different between 0.9% saline and hypertonic saline-treated wild-type mice. Conclusions: Following experimental cardiac arrest/cardiopulmonary resuscitation: 1) continuous hypertonic saline therapy maintained to achieve serum osmolality of approximate to 350 mOsm/L is beneficial for the treatment of cerebral edema; 2) perivascular pool of aquaporin-4 plays a critical role in water egress from brain; and 3) hypertonic saline attenuates blood-brain barrier disruption via perivascular aquaporin-4 pool.

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