Therapeutic hypothermia provides incomplete neuroprotection after hypoxia-ischemia (HI)-induced brain injury in neonates. We previously showed that cortical neuron and white matter apoptosis are promoted by hypothermia and early rewarming in a piglet model of HI. The unfolded protein response (UPR) may be one of the potential mediators of this cell death. Here, neonatal piglets underwent HI or sham surgery followed by 29 h of normothermia, 2 h of normothermia + 27 h of hypothermia or 18 h of hypothermia + rewarming. Piglets recovered for 29 h. Immunohistochemistry for endoplasmic reticulum to nucleus signaling-1 protein (ERN1), a marker of UPR activation, was used to determine the ratios of ERN1+ macroglia and neurons in the motor subcortical white matter and cerebral cortex. The ERN1+ macroglia were immunophenotyped as oligodendrocytes and astrocytes by immunofluorescent colabeling. Temperature (p = 0.046) and HI (p < 0.001) independently affected the ratio of ERN1+ macroglia. In sham piglets, sustained hypothermia (p = 0.011) and rewarming (p = 0.004) increased the ERN1+ macroglia ratio above that in normothermia. HI prior to hypothermia diminished the UPR. Ratios of ERN1+ macroglia correlated with white matter apoptotic profile counts in shams (r = 0.472; p = 0.026), thereby associating UPR activation with white matter apoptosis during hypothermia and rewarming. Accordingly, macroglial cell counts decreased in shams that received sustained hypothermia (p = 0.009) or rewarming (p = 0.007) compared to those in normothermic shams. HI prior to hypothermia neutralized the macroglial cell loss. Neither HI nor temperature affected ERN1+ neuron ratios. In summary, delayed hypothermia and rewarming activate the macroglial UPR, which is associated with white matter apoptosis. HI may decrease the macroglial endoplasmic reticulum stress response after hypothermia and rewarming.

1.
Azzopardi D, Strohm B, Marlow N, et al: Effects of hypothermia for perinatal asphyxia on childhood outcomes. N Engl J Med 2014;371:140-149.
2.
Shankaran S, Pappas A, McDonald SA, et al: Childhood outcomes after hypothermia for neonatal encephalopathy. N Engl J Med 2012;366:2085-2092.
3.
Shankaran S, Laptook AR, Ehrenkranz RA, et al: Whole-body hypothermia for neonates with hypoxic-ischemic encephalopathy. N Engl J Med 2005;353:1574-1584.
4.
Wang B, Armstrong JS, Lee JH, et al: Rewarming from therapeutic hypothermia induces cortical neuron apoptosis in a swine model of neonatal hypoxic-ischemic encephalopathy. J Cereb Blood Flow Metab 2015;35:781-793.
5.
Wang B, Armstrong JS, Reyes M, et al: White matter apoptosis is increased by delayed hypothermia and rewarming in a neonatal piglet model of hypoxic ischemic encephalopathy. Neuroscience 2016;316:296-310.
6.
Van Schie PE, Schijns J, Becher JG, Barkhof F, van Weissenbruch MM, Vermeulen RJ: Long-term motor and behavioral outcome after perinatal hypoxic-ischemic encephalopathy. Eur J Paediatr Neurol 2015;19:354-359.
7.
Cavalleri F, Lugli L, Pugliese M, et al: Prognostic value of diffusion-weighted imaging summation scores or apparent diffusion coefficient maps in newborns with hypoxic-ischemic encephalopathy. Pediatr Radiol 2014;44:1141-1154.
8.
Sun H, Tang Y, Li L, Guan X, Wang D: Effects of local hypothermia on neuronal cell apoptosis after intracerebral hemorrhage in rats. J Nutr Health Aging 2015;19:291-298.
9.
Zhu X, Zelmer A, Kapfhammer JP, Wellmann S: Cold-inducible RBM3 inhibits PERK phosphorylation through cooperation with NF90 to protect cells from endoplasmic reticulum stress. FASEB J 2016;30:624-634.
10.
Prieto Robles C, Argibay Lago A, Hernanz Del Rio A, Rodriguez Castano IM, Fernandez-Rodriguez D: Optimization of glucose metabolism in patients undergoing therapeutic hypothermia after sudden cardiac arrest. Rev Enferm 2015;38:46-50.
11.
Yu A, Li P, Tang T, Wang J, Chen Y, Liu L: Roles of Hsp70s in stress responses of microorganisms, plants, and animals. Biomed Res Int 2015;2015:510319.
12.
Badiola N, Penas C, Minano-Molina A, et al: Induction of ER stress in response to oxygen-glucose deprivation of cortical cultures involves the activation of the PERK and IRE-1 pathways and of caspase-12. Cell Death Dis 2011;2:e149.
13.
Nakka VP, Gusain A, Raghubir R: Endoplasmic reticulum stress plays critical role in brain damage after cerebral ischemia/reperfusion in rats. Neurotox Res 2010;17:189-202.
14.
Smith HL, Li W, Cheetham ME: Molecular chaperones and neuronal proteostasis. Semin Cell Dev Biol 2015;40:142-152.
15.
Rzechorzek NM, Connick P, Patani R, Selvaraj BT, Chandran S: Hypothermic preconditioning of human cortical neurons requires proteostatic priming. EBioMedicine 2015;2:528-535.
16.
Lin W, Popko B: Endoplasmic reticulum stress in disorders of myelinating cells. Nat Neurosci 2009;12:379-385.
17.
Gow A, Wrabetz L: CHOP and the endoplasmic reticulum stress response in myelinating glia. Curr Opin Neurobiol 2009;19:505-510.
18.
Kumar R, Krause GS, Yoshida H, Mori K, DeGracia DJ: Dysfunction of the unfolded protein response during global brain ischemia and reperfusion. J Cereb Blood Flow Metab 2003;23:462-471.
19.
Larson AC, Jamrogowicz JL, Kulikowicz E, et al: Cerebrovascular autoregulation after rewarming from hypothermia in a neonatal swine model of asphyxic brain injury. J Appl Physiol (1985) 2013;115:1433-1442.
20.
Lee JK, Brady KM, Mytar JO, et al: Cerebral blood flow and cerebrovascular autoregulation in a swine model of pediatric cardiac arrest and hypothermia. Crit Care Med 2011;39:2337-2345.
21.
Lee JK, Yang ZJ, Wang B, et al: Noninvasive autoregulation monitoring in a swine model of pediatric cardiac arrest. Anesth Analg 2012;114:825-836.
22.
Chonghaile TN, Gupta S, John M, Szegezdi E, Logue SE, Samali A: BCL-2 modulates the unfolded protein response by enhancing splicing of X-box binding protein-1. Biochem Biophys Res Commun 2015;466:40-45.
23.
Hyrskyluoto A, Bruelle C, Lundh SH, et al: Ubiquitin-specific protease-14 reduces cellular aggregates and protects against mutant huntingtin-induced cell degeneration: involvement of the proteasome and ER stress-activated kinase IRE1alpha. Hum Mol Genet 2014;23:5928-5939.
24.
Lafrenaye AD, Todani M, Walker SA, Povlishock JT: Microglia processes associate with diffusely injured axons following mild traumatic brain injury in the micro pig. J Neuroinflammation 2015;12:186.
25.
Martin LJ, Al-Abdulla NA, Brambrink AM, Kirsch JR, Sieber FE, Portera-Cailliau C: Neurodegeneration in excitotoxicity, global cerebral ischemia, and target deprivation: a perspective on the contributions of apoptosis and necrosis. Brain Res Bull 1998;46:281-309.
26.
Tagin M, Zhu C, Gunn AJ: Beneficence and nonmaleficence in treating neonatal hypoxic-ischemic brain injury. Dev Neurosci 2015;37:305-310.
27.
Gunn AJ, Gluckman PD: Head cooling for neonatal encephalopathy: the state of the art. Clin Obstet Gynecol 2007;50:636-651.
28.
Thornton C, Hagberg H: Role of mitochondria in apoptotic and necroptotic cell death in the developing brain. Clin Chim Acta 2015;451:35-38.
29.
Bainbridge A, Tachtsidis I, Faulkner SD, et al: Brain mitochondrial oxidative metabolism during and after cerebral hypoxia-ischemia studied by simultaneous phosphorus magnetic-resonance and broadband near-infrared spectroscopy. Neuroimage 2014;102:173-183.
30.
Thoresen M, Penrice J, Lorek A, et al: Mild hypothermia after severe transient hypoxia-ischemia ameliorates delayed cerebral energy failure in the newborn piglet. Pediatr Res 1995;37:667-670.
31.
Martin LJ, Brambrink AM, Price AC, et al: Neuronal death in newborn striatum after hypoxia-ischemia is necrosis and evolves with oxidative stress. Neurobiol Dis 2000;7:169-191.
32.
Mueller-Burke D, Koehler RC, Martin LJ: Rapid NMDA receptor phosphorylation and oxidative stress precede striatal neurodegeneration after hypoxic ischemia in newborn piglets and are attenuated with hypothermia. Int J Dev Neurosci 2008;26:67-76.
33.
Agnew DM, Koehler RC, Guerguerian AM, et al: Hypothermia for 24 hours after asphyxic cardiac arrest in piglets provides striatal neuroprotection that is sustained 10 days after rewarming. Pediatr Res 2003;54:253-262.
34.
Ni X, Yang ZJ, Wang B, et al: Early antioxidant treatment and delayed hypothermia after hypoxia-ischemia have no additive neuroprotection in newborn pigs. Anesth Analg 2012;115:627-637.
35.
Zhu J, Wang B, Lee JH, et al: Additive neuroprotection of a 20-HETE inhibitor with delayed therapeutic hypothermia after hypoxia-ischemia in neonatal piglets. Dev Neurosci 2015;37:376-389.
36.
Hofmann S, Cherkasova V, Bankhead P, Bukau B, Stoecklin G: Translation suppression promotes stress granule formation and cell survival in response to cold shock. Mol Biol Cell 2012;23:3786-3800.
37.
Harding HP, Zhang Y, Ron D: Protein translation and folding are coupled by an endoplasmic-reticulum-resident kinase. Nature 1999;397:271-274.
38.
Lu M, Lawrence DA, Marsters S, et al: Opposing unfolded-protein-response signals converge on death receptor 5 to control apoptosis. Science 2014;345:98-101.
39.
Sun X, Crawford R, Liu C, Luo T, Hu B: Development-dependent regulation of molecular chaperones after hypoxia-ischemia. Neurobiol Dis 2015;82:123-131.
40.
Chavez-Valdez R, Flock DL, Martin LJ, Northington FJ: Endoplasmic reticulum pathology and stress response in neurons precede programmed necrosis after neonatal hypoxia-ischemia. Int J Dev Neurosci 2016;48:58-70.
41.
Knight JR, Bastide A, Roobol A, et al: Eukaryotic elongation factor 2 kinase regulates the cold stress response by slowing translation elongation. Biochem J 2015;465:227-238.
42.
Zhao H, Chen Y: Effects of mild hypothermia therapy on the levels of glutathione in rabbit blood and cerebrospinal fluid after cardiopulmonary resuscitation. Iran J Basic Med Sci 2015;18:194-198.
43.
Yuan X, Ghosh N, McFadden B, et al: Hypothermia modulates cytokine responses after neonatal rat hypoxic-ischemic injury and reduces brain damage. ASN Neuro 2014;6: 1759091414558418.
44.
Bickler PE, Clark JP, Gabatto P, Brosnan H: Hypoxic preconditioning and cell death from oxygen/glucose deprivation co-opt a subset of the unfolded protein response in hippocampal neurons. Neuroscience 2015;310:306-321.
45.
Fischer H, Koenig U, Eckhart L, Tschachler E: Human caspase 12 has acquired deleterious mutations. Biochem Biophys Res Commun 2002;293:722-726.
46.
Tekes A, Poretti A, Scheurkogel MM, et al: Apparent diffusion coefficient scalars correlate with near-infrared spectroscopy markers of cerebrovascular autoregulation in neonates cooled for perinatal hypoxic-ischemic injury. AJNR Am J Neuroradiol 2015;36:188-193.
47.
Howlett JA, Northington FJ, Gilmore MM, et al: Cerebrovascular autoregulation and neurologic injury in neonatal hypoxic-ischemic encephalopathy. Pediatr Res 2013;74:525-535.
48.
Burton VJ, Gerner G, Cristofalo E, et al: A pilot cohort study of cerebral autoregulation and 2-year neurodevelopmental outcomes in neonates with hypoxic-ischemic encephalopathy who received therapeutic hypothermia. BMC Neurol 2015;15:209.
49.
Hori D, Everett AD, Lee JK, et al: Rewarming rate during cardiopulmonary bypass is associated with release of glial fibrillary acidic protein. Ann Thorac Surg 2015;100:1353-1358.
50.
Bisschops LL, Hoedemaekers CW, Mollnes TE, van der Hoeven JG: Rewarming after hypothermia after cardiac arrest shifts the inflammatory balance. Crit Care Med 2012;40:1136-1142.
51.
Dohi K, Miyamoto K, Fukuda K, et al: Status of systemic oxidative stress during therapeutic hypothermia in patients with post-cardiac arrest syndrome. Oxid Med Cell Longev 2013;2013:562429.
52.
Alva N, Palomeque J, Carbonell T: Oxidative stress and antioxidant activity in hypothermia and rewarming: can RONS modulate the beneficial effects of therapeutic hypothermia? Oxid Med Cell Longev 2013;2013:957054.
53.
Guerra R, Vera-Aguilar E, Uribe-Ramirez M, et al: Exposure to inhaled particulate matter activates early markers of oxidative stress, inflammation and unfolded protein response in rat striatum. Toxicol Lett 2013;222:146-154.
54.
Llorente IL, Burgin TC, Perez-Rodriguez D, Martinez-Villayandre B, Perez-Garcia CC, Fernandez-Lopez A: Unfolded protein response to global ischemia following 48 h of reperfusion in the rat brain: the effect of age and meloxicam. J Neurochem 2013;127:701-710.
55.
Millson GC, Hunter GD: Protein synthesis in normal and scrapie mouse brain. J Neurochem 1968;15:447-453.
56.
Agematsu K, Korotcova L, Morton PD, Gallo V, Jonas RA, Ishibashi N: Hypoxia diminishes the protective function of white-matter astrocytes in the developing brain. J Thorac Cardiovasc Surg 2016;151:265-272. e3.
57.
Oberheim NA, Takano T, Han X, et al: Uniquely hominid features of adult human astrocytes. J Neurosci 2009;29:3276-3287.
58.
Araque A, Carmignoto G, Haydon PG, Oliet SH, Robitaille R, Volterra A: Gliotransmitters travel in time and space. Neuron 2014;81:728-739.
59.
Lu XM, Shear DA, Deng-Bryant Y, et al: Comprehensive evaluation of neuroprotection achieved by extended selective brain cooling therapy in a rat model of penetrating ballistic-like brain injury. Ther Hypothermia Temp Manag 2016;6:30-39.
60.
Ohnishi M, Urasaki T, Ochiai H, et al: Selective enhancement of wnt4 expression by cyclic AMP-associated cooperation between rat central astrocytes and microglia. Biochem Biophys Res Commun 2015;467:367-372.
61.
Jelsing J, Hay-Schmidt A, Dyrby T, Hemmingsen R, Uylings HB, Pakkenberg B: The prefrontal cortex in the Gottingen minipig brain defined by neural projection criteria and cytoarchitecture. Brain Res Bull 2006;70:322-336.
62.
Davidson JO, Yuill CA, Zhang FG, Wassink G, Bennet L, Gunn AJ: Extending the duration of hypothermia does not further improve white matter protection after ischemia in term-equivalent fetal sheep. Sci Rep 2016;6:25178.
63.
Martinez-Biarge M, Bregant T, Wusthoff CJ, et al: White matter and cortical injury in hypoxic-ischemic encephalopathy: antecedent factors and 2-year outcome. J Pediatr 2012;161:799-807.
64.
Yang Q, Gao H, Dong R, Wu YQ: Sequential changes of endoplasmic reticulum stress and apoptosis in myocardial fibrosis of diabetes mellitus-induced rats. Mol Med Rep 2016;13:5037-5044.
Copyright / Drug Dosage / Disclaimer
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
You do not currently have access to this content.