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Published on: November 20, 2015
Effects of Phosphatidylserine Source of Docosahexaenoic Acid on Cerebellar Development in Preterm Pigs
Daniel Chizhikov1,2, Randal K Buddington1,3, Igor Y Iskusnykh4
1School of Health Studies, University of Memphis, Memphis, TN 38152, USA.
Insights
Supplementing preterm pig formula with phosphatidylserine-docosahexaenoic acid (PS-DHA) enhanced cerebellar development by increasing granule cell proliferation and survival, crucial for cognitive and motor function.
Area of Science:
- Neuroscience
- Developmental Biology
- Pediatrics
Background:
- Preterm birth significantly impacts infant neurodevelopment, particularly cerebellar development, affecting cognitive and motor functions.
- Previous studies indicated that phosphatidylserine-docosahexaenoic acid (PS-DHA) supplementation improved cerebellar weight in preterm pigs.
- The specific effects of PS-DHA on cerebellar cell populations and developmental processes remained unclear.
Purpose of the Study:
- To investigate the impact of PS-DHA on the development of specific cerebellar cell populations in preterm pigs.
- To determine if PS-DHA enhances key developmental processes within the cerebellum.
Main Methods:
- Preterm pigs were fed a milk replacer with either PS-DHA or sunflower oil (control) for ten days.
- Cerebellar tissues were analyzed post-necropsy using immunohistochemistry to assess cell populations.
- Key cerebellar cell types and developmental markers were quantified.
Main Results:
- PS-DHA consumption led to an expansion of undifferentiated granule cell precursors and increased proliferation in the external granule cell layer (EGL).
- Significantly fewer apoptotic cells were observed in the internal granule cell layer (IGL) of PS-DHA supplemented pigs.
- No significant effects were found on differentiating granule cells, EGL thickness, Purkinje cell density, Bergmann glial fibers, or Purkinje cell diameter.
Conclusions:
- PS-DHA supports cerebellar development in preterm infants by promoting granule cell proliferation, a process often impaired by preterm birth.
- PS-DHA enhances the survival of granule cells within the internal granule cell layer.
- These findings highlight PS-DHA as a potential therapeutic candidate for improving brain development in preterm infants.
Abstract:
Preterm birth, a major contributor to infant mortality and morbidity, impairs development of the cerebellum, the brain region involved in cognitive processing and motor function. Previously, we showed that at term-equivalent age, preterm pigs that received formula supplemented with docosahexaenoic acid (DHA) esterified to phosphatidylserine (PS) had cerebellar weights similar to those of newborn term pigs and were heavier than control preterm pigs. However, whether PS-DHA promotes the development of specific cerebellar cell populations or enhances key developmental processes remains unknown. Here we investigated the effects of the PS-DHA on development of the cerebellum in preterm pigs delivered via caesarean section and reared for ten days on a milk replacer with either PS-DHA (experimental group) or sunflower oil (control group). Upon necropsy, key cerebellar populations were analyzed using immunohistochemistry. Consumption of PS-DHA was associated with the expansion of undifferentiated granule cell precursors and increased proliferation in the external granule cell layer (EGL). Preterm pigs that received PS-DHA also had significantly fewer apoptotic cells in the internal granule cell layer (IGL) that contains differentiated granule neurons. PS-DHA did not affect the number of differentiating granule cells in the inner EGL, thickness of the inner EGL, density of Purkinje cells, or Bergmann glial fibers, or diameter of Purkinje cells. Thus, PS-DHA may support cerebellar development in preterm subjects by enhancing proliferation of granule cells, a process specifically inhibited by preterm birth, and increasing the survival of granule cells in the IGL. These findings suggest that PS-DHA is a promising candidate for clinical studies directed at enhancing brain development.

