• DOI:10.1152/ajpregu.00388.2012
• Corpus ID: 23527154

Acute on chronic exposure to endotoxin in preterm fetal sheep.

@article{Mathai2013AcuteOC,
  title={Acute on chronic exposure to endotoxin in preterm fetal sheep.},
  author={Sam Mathai and Lindsea Booth and Joanne O. Davidson and Paul P. Drury and Mhoyra Fraser and Ellen C. Jensen and Sherly A. George and Andrew S. Naylor and Alistair Jan Gunn and Laura Bennet},
  journal={American journal of physiology. Regulatory, integrative and comparative physiology},
  year={2013},
  volume={304 3},
  pages={
          R189-97
        }
}

• S. Mathai, L. Booth, +7 authors L. Bennet
• Published 1 February 2013
• Medicine
• American journal of physiology. Regulatory, integrative and comparative physiology

Acute, high-dose exposure to endotoxin lipopolysaccharide (LPS) in preterm fetal sheep can trigger periventricular white matter lesions (PVL), in association with severe hypotension/hypoxemia and significant mortality. Intriguingly, however, chronic or repeated exposure to LPS can induce tachyphylaxis. We therefore tested the hypothesis that progressive, acute on chronic fetal infection would be associated with white matter injury with little fetal mortality. Chronically instrumented preterm (0.7 gestational age) fetal sheep were exposed to a continuous low-dose LPS infusion (100 ng over 24 h, followed by 250 ng/24 h for 96 h) or saline. Boluses of 1 μg LPS or saline were given at 48, 72, and 96 h; sheep were killed at day 10. Six of 11 fetal sheep exposed to saline infusion + LPS boluses died 4-7 h after the first bolus. In contrast, there was no fetal mortality after saline infusions alone (n = 9), low-dose LPS infusion + saline boluses (n = 5), or low-dose LPS + LPS boluses (n = 9). Low-dose LPS infusion + LPS boluses was associated with greater microglial induction than low-dose LPS + saline boluses but a similar area of periventricular white matter inflammation. One fetus developed severe focal white matter necrosis after LPS infusion + boluses. The acute cardiovascular compromise associated with high-dose, acute exposure to LPS is markedly attenuated by previous low-dose infusions, with limited apparent exacerbation of periventricular white matter injury compared with low-dose infusion alone.