Hostname: page-component-586b7cd67f-rdxmf Total loading time: 0 Render date: 2024-11-26T12:59:28.690Z Has data issue: false hasContentIssue false

Does growth restriction increase the vulnerability to acute ventilation-induced brain injury in newborn lambs? Implications for future health and disease

Published online by Cambridge University Press:  09 August 2017

B. J. Allison*
Affiliation:
The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia Department of Obstetrics and Gynecology, Monash University, Clayton, VIC, Australia
S. B. Hooper
Affiliation:
The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia Department of Obstetrics and Gynecology, Monash University, Clayton, VIC, Australia
E. Coia
Affiliation:
The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia Department of Obstetrics and Gynecology, Monash University, Clayton, VIC, Australia
G. Jenkin
Affiliation:
The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia Department of Obstetrics and Gynecology, Monash University, Clayton, VIC, Australia
A. Malhotra
Affiliation:
The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia Department of Pediatrics, Monash Newborn, Monash Medical Centre, Monash University, Melbourne, VIC, Australia
V. Zahra
Affiliation:
The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia Department of Obstetrics and Gynecology, Monash University, Clayton, VIC, Australia
A. Sehgal
Affiliation:
Department of Pediatrics, Monash Newborn, Monash Medical Centre, Monash University, Melbourne, VIC, Australia
M. Kluckow
Affiliation:
Department of Neonatology, Royal North Shore Hospital, University of Sydney, Sydney, NSW, Australia
A. W. Gill
Affiliation:
Centre for Neonatal Research and Education, The University of Western Australia, WA, Australia
T. Yawno
Affiliation:
The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia Department of Obstetrics and Gynecology, Monash University, Clayton, VIC, Australia
G. R. Polglase
Affiliation:
The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia Department of Obstetrics and Gynecology, Monash University, Clayton, VIC, Australia
M. Castillo-Melendez
Affiliation:
The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia Department of Obstetrics and Gynecology, Monash University, Clayton, VIC, Australia
S. L. Miller
Affiliation:
The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC, Australia Department of Obstetrics and Gynecology, Monash University, Clayton, VIC, Australia
*
*Address for correspondence: B. Allison, PhD, The Ritchie Centre, Hudson Institute of Medical Research, 27-31 Wright Street, Clayton, VIC 3168, Australia. (Email: [email protected])

Abstract

Fetal growth restriction (FGR) and preterm birth are frequent co-morbidities, both are independent risks for brain injury. However, few studies have examined the mechanisms by which preterm FGR increases the risk of adverse neurological outcomes. We aimed to determine the effects of prematurity and mechanical ventilation (VENT) on the brain of FGR and appropriately grown (AG, control) lambs. We hypothesized that FGR preterm lambs are more vulnerable to ventilation-induced acute brain injury. FGR was surgically induced in fetal sheep (0.7 gestation) by ligation of a single umbilical artery. After 4 weeks, preterm lambs were euthanized at delivery or delivered and ventilated for 2 h before euthanasia. Brains and cerebrospinal fluid (CSF) were collected for analysis of molecular and structural indices of early brain injury. FGRVENT lambs had increased oxidative cell damage and brain injury marker S100B levels compared with all other groups. Mechanical ventilation increased inflammatory marker IL-8 within the brain of FGRVENT and AGVENT lambs. Abnormalities in the neurovascular unit and increased blood–brain barrier permeability were observed in FGRVENT lambs, as well as an altered density of vascular tight junctions markers. FGR and AG preterm lambs have different responses to acute injurious mechanical ventilation, changes which appear to have been developmentally programmed in utero.

Type
Original Article
Copyright
© Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2017 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Barker, DJP. Adult consequences of fetal growth restriction. Clin Obstet Gynecol. 2006; 49, 270.CrossRefGoogle ScholarPubMed
2. Wu, YW, Croen, LA, Shah, SJ, Newman, TB, Najjar, DV. Cerebral palsy in a term population: risk factors and neuroimaging findings. Pediatr. 2006; 118, 690697.CrossRefGoogle Scholar
3. Hack, M, Breslau, N, Weissman, B, et al. Effect of very low birth weight and subnormal head size on cognitive abilities at school age. N Engl J Med. 1991; 325, 231237.Google Scholar
4. Ferriero, DM. Neonatal brain injury. N Engl J Med. 2004; 351, 19851995.Google Scholar
5. Miller, SL, Huppi, PS, Mallard, C. The consequences of fetal growth restriction on brain structure and neurodevelopmental outcome. J Physiol. 2016; 594, 807823.Google Scholar
6. Castillo-Melendez, M, Yawno, T, Allison, BJ, et al. Cerebrovascular adaptations to chronic hypoxia in the growth restricted lamb. Int J Dev Neuro. 2015; 45, 5565.Google Scholar
7. Tolcos, M, Bateman, E, O’Dowd, R, et al. Intrauterine growth restriction affects the maturation of myelin. Exp Neurol. 2011; 232, 5365.Google Scholar
8. Kok, JH, Lya den Ouden, A, Verloove-Vanhorick, SP, Brand, R. Outcome of very preterm small for gestational age infants: the first nine years of life. BJOG. 1998; 105, 162168.Google Scholar
9. Jobe, AH, Hillman, N, Polglase, GR, et al. Injury and inflammation from resuscitation of the preterm infant. Neonatology. 2008; 94, 190196.CrossRefGoogle ScholarPubMed
10. Polglase, GR, Miller, SL, Barton, SK, et al. Initiation of resuscitation with high tidal volumes causes cerebral hemodynamic disturbance, brain inflammation and injury in preterm lambs. PLoS One. 2012; 7, e39535.Google Scholar
11. Khwaja, O, Volpe, JJ. Pathogenesis of cerebral white matter injury of prematurity. Arch Dis Child Fetal Neonatal Ed. 2007; 93, F153F161.Google Scholar
12. Sutherland, AE, Crossley, KJ, Allison, BJ, et al. The effects of intrauterine growth restriction and antenatal glucocorticoids on ovine fetal lung development. Pediatr Res. 2012; 71, 689696.Google Scholar
13. Allison, BJ, Hooper, SB, Coia, E, et al. Ventilation induced lung injury is not exacerbated by growth restriction in preterm lambs. Am J Physiol Lung Cell Mole Physiol. 2015; 310, L213L223.Google Scholar
14. Polglase, GR, Hooper, SB, Gill, AW, et al. Cardiovascular and pulmonary consequences of airway recruitment in preterm lambs. J Appl Physiol. 2009; 106, 13471355.Google Scholar
15. Polglase, GR, Hooper, SB, Gill, AW, et al. Intrauterine inflammation causes pulmonary hypertension and cardiovascular sequelae in preterm lambs. J Appl Physiol. 2010; 108, 17571765.Google Scholar
16. Barton, SK, McDougall, A, Melville, JM. Differential short‐term regional effects of early high dose erythropoietin on white matter in preterm lambs after mechanical ventilation. J Peds. 2016; 594, 14371449.Google Scholar
17. Wallace, MJ, Probyn, ME, Zahra, VA, et al. Early biomarkers and potential mediators of ventilation-induced lung injury in very preterm lambs. Respir Res. 2009; 10, 19.Google Scholar
18. Baburamani, AA, Lo, C, Castillo-Melendez, M, Walker, DW. Morphological evaluation of the cerebral blood vessels in the late gestation fetal sheep following hypoxia in utero. Microvasc Res. 2013; 85, 19.CrossRefGoogle ScholarPubMed
19. Baschat, AA. Neurodevelopment following fetal growth restriction and its relationship with antepartum parameters of placental dysfunction. Ultrasound Obstet Gynecol . 2011; 37, 501514.Google Scholar
20. Miller, SL, Yan, EB, Castillo-Melendez, M, Jenkin, G, Walker, DW. Melatonin provides neuroprotection in the late-gestation fetal sheep brain in response to umbilical cord occlusion. Dev Neurosci. 2005; 27, 200210.Google Scholar
21. Chong, ZZ, Li, F, Maiese, K. Oxidative stress in the brain: novel cellular targets that govern survival during neurodegenerative disease. Prog Neurobiol. 2005; 75, 207246.Google Scholar
22. Rogers, S, Witz, G, Anwar, M, Hiatt, M, Hegyi, T. Antioxidant capacity and oxygen radical diseases in the preterm newborn. Arch Pediatr Adolesc Med. 2000; 154, 544548.Google Scholar
23. Volpe, JJ. Neurobiology of periventricular leukomalacia in the premature infant. Pediatr Res. 2001; 50, 553562.Google Scholar
24. Miller, SL, Yawno, T, et al. Antenatal antioxidant treatment with melatonin to decrease newborn neurodevelopmental deficits and brain injury caused by fetal growth restriction. J Pineal Res. 2014; 56, 283294.Google Scholar
25. Miller, SL, Chai, M, Loose, J, et al. The effects of maternal betamethasone administration on the intrauterine growth-restricted fetus. Endocrinology. 2007; 148, 12881295.Google Scholar
26. Biri, A, Bozkurt, N, Turp, A, et al. Role of oxidative stress in intrauterine growth restriction. Gynecol Obstet Invest. 2007; 64, 187192.CrossRefGoogle ScholarPubMed
27. Aridas, JDS, Yawno, T, Sutherland, AE, et al. Detecting brain injury in neonatal hypoxic ischemic encephalopathy: closing the gap between experimental and clinical research. Exp Neurol. 2014; 261, 281290.Google Scholar
28. Gonçalves, C-A, Leite, MC, Nardin, P. Biological and methodological features of the measurement of S100B, a putative marker of brain injury. Clin Biochem. 2008; 41, 755763.CrossRefGoogle ScholarPubMed
29. Boutsikou, T, Mastorakos, G, Kyriakakou, M, et al. Circulating levels of inflammatory markers in intrauterine growth restriction. Mediators Inflamm.. 2010; 2010, 17.Google Scholar
30. Nagdyman, N, Kömen, W, Ko, H-K, Müller, C, Obladen, M. Early biochemical indicators of hypoxic-ischemic encephalopathy after birth asphyxia. Pediatr Res. 2001; 49, 502506.Google Scholar
31. Nagdyman, N, Grimmer, I, Scholz, T, Müller, C, Obladen, M. Predictive value of brain-specific proteins in serum for neurodevelopmental outcome after birth asphyxia. Pediatr Res. 2003; 54, 270275.CrossRefGoogle ScholarPubMed
32. Denieffe, S, Kelly, RJ, McDonald, C, Lyons, A, Lynch, MA. Classical activation of microglia in CD200-deficient mice is a consequence of blood brain barrier permeability and infiltration of peripheral cells. Brain Behav Immun. 2013; 34, 8697.Google Scholar
33. Martinez, FO. Macrophage activation and polarization. Front Biosci.. 2008; 13, 453.Google Scholar
34. Barton, SK, Melville, JM, Tolcos, M, et al. Human amnion epithelial cells modulate ventilation-induced white matter pathology in preterm lambs. Dev Neurosci. 2015; 37, 338348.Google Scholar
35. Stolp, HB, Johansson, PA, Habgood, MD, et al. Effects of neonatal systemic inflammation on blood-brain barrier permeability and behaviour in juvenile and adult rats. Cardiovasc Psychiatry Neurol. 2011; 2011, 10.Google Scholar
36. Schwab, JM, Postler, E, Nguyen, TD, et al. Connective tissue growth factor is expressed by a subset of reactive astrocytes in human cerebral infarction. Neuropathol Appl Neurobiol. 2000; 26, 434440.Google Scholar
37. Liu, Y, Liu, Z, Li, X, et al. Accumulation of connective tissue growth factor+cells during the early phase of rat traumatic brain injury. Ann Diagn Pathol. 2014; 9, 141.CrossRefGoogle ScholarPubMed
38. Ueberham, U, Ueberham, E, Gruschka, H, Arendt, T. Connective tissue growth factor in Alzheimer’s disease. Neuroscience. 2003; 116, 16.Google Scholar
39. Förster, C, Silwedel, C, Golenhofen, N, et al. Occludin as direct target for glucocorticoid‐induced improvement of blood–brain barrier properties in a murine in vitro system. J Physiol. 2005; 565, 475486.CrossRefGoogle Scholar
40. Thompson, C, Syddall, H, Rodin, I, Osmond, C, Barker, DJP. Birth weight and the risk of depressive disorder in late life. Br J Psych. 2001; 179, 450455.Google Scholar
Supplementary material: Image

Allison supplementary material

Figure S1

Download Allison supplementary material(Image)
Image 92.5 KB
Supplementary material: Image

Allison supplementary material

Figure S2

Download Allison supplementary material(Image)
Image 134.4 KB
Supplementary material: Image

Allison supplementary material

Figure S3

Download Allison supplementary material(Image)
Image 1.1 MB
Supplementary material: File

Allison supplementary material

Allison supplementary material 1

Download Allison supplementary material(File)
File 34.9 KB
Supplementary material: PDF

Allison supplementary material

Allison supplementary material 2

Download Allison supplementary material(PDF)
PDF 106.1 KB
Supplementary material: File

Allison supplementary material

Tables S1-S3

Download Allison supplementary material(File)
File 26.2 KB
Supplementary material: PDF

Allison supplementary material

Tables S1-S3

Download Allison supplementary material(PDF)
PDF 80.4 KB