Publications by authors named "Henri Schulte"

Background: Bronchopulmonary dysplasia (BPD) is a chronic lung condition of premature neonates, yet without an established pharmacological treatment. The BPD rabbit model exposed to 95% oxygen has been used in recent years for drug testing. However, the toxicity of the strong hyperoxic hit precludes a longer-term follow-up due to high mortality after the first week of life.

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For medical students the dissection course is the preferred method to learn gross anatomy. However, the added value of active cadaver dissection on knowledge gain in multimodal curricula offering a diversity of e-learning resources is unknown. The Covid-19-related lockdown forced educators to replace the dissection course by e-learning resources.

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Article Synopsis
  • Bronchopulmonary dysplasia (BPD) is a serious lung condition commonly seen in premature babies, and this study focused on creating a hyperoxia-based model of BPD using preterm rabbits to analyze lung changes.
  • Researchers observed that after seven days of hyperoxia exposure, the rabbits showed significant reductions in lung function, including decreased inspiratory capacity and increased lung resistance, alongside indications of pulmonary hypertension.
  • Stereological analysis revealed that hyperoxic rabbits had fewer alveoli and reduced alveolar surface area, along with thickened alveolar walls and fluid buildup, mirroring the lung damage seen in human BPD.
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Background: Ischaemic postconditioning (IPoC) refers to brief periods of reocclusion of blood supply following an ischaemic event. This has been shown to ameliorate ischaemia reperfusion injury in different tissues, and it may represent a feasible therapeutic strategy for ischaemia reperfusion injury following strangulating small intestinal lesions in horses. The objective of this study was to assess the degree cell death, inflammation, oxidative stress, and heat shock response in an equine experimental jejunal ischaemia model with and without IPoC.

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Lung function declines with advancing age. To improve our understanding of the structure-function relationships leading to this decline, we investigated structural alterations in the lung and their impact on micromechanics and lung function in the aging mouse. Lung function analysis was performed in 3, 6, 12, 18, and 24 months old C57BL/6 mice ( = 7-8/age), followed by lung fixation and stereological sample preparation.

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