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Curcumin: Novel Treatment in Neonatal Hypoxic-Ischemic Brain Injury

Artikel i vetenskaplig tidskrift
Författare Eridan Rocha-Ferreira
C. Sisa
S. Bright
T. Fautz
M. Harris
I. C. Riquelme
C. Agwu
T. Kurulday
B. Mistry
D. Hill
S. Lange
M. Hristova
Publicerad i Frontiers in Physiology
Volym 10
Sidor 19
ISSN 1664-042X
Publiceringsår 2019
Publicerad vid Institutionen för neurovetenskap och fysiologi
Sidor 19
Språk en
Länkar dx.doi.org/10.3389/fphys.2019.01351
Ämnesord curcumin, hypoxia, ischemia, neuroprotection, neonate, oxidative stress, mitochondrial stat3, turmeric curcuma, oxidative stress, nitric-oxide, stem-cells, rat-brain, differentiation, activation, prohibitin, expression, Physiology
Ämneskategorier Pediatrik, Neurologi

Sammanfattning

Hypoxic-ischemic encephalopathy (HIE) is a major cause of mortality and morbidity in neonates, with an estimated global incidence of 3/1,000 live births. HIE brain damage is associated with an inflammatory response and oxidative stress, resulting in the activation of cell death pathways. At present, therapeutic hypothermia is the only clinically approved treatment available for HIE. This approach, however, is only partially effective. Therefore, there is an unmet clinical need for the development of novel therapeutic interventions for the treatment of HIE. Curcumin is an antioxidant reactive oxygen species scavenger, with reported anti-tumor and anti-inflammatory activity. Curcumin has been shown to attenuate mitochondrial dysfunction, stabilize the cell membrane, stimulate proliferation, and reduce injury severity in adult models of spinal cord injury, cancer, and cardiovascular disease. The role of curcumin in neonatal HIE has not been widely studied due to its low bioavailability and limited aqueous solubility. The aim of this study was to investigate the effect of curcumin treatment in neonatal HIE, including time of administration and dose-dependent effects. Our results indicate that curcumin administration prior to HIE in neonatal mice elevated cell and tissue loss, as well as glial activation compared to HI alone. However, immediate post-treatment with curcumin was significantly neuroprotective, reducing grey and white matter tissue loss, TUNEL+ cell death, microglia activation, reactive astrogliosis, and iNOS oxidative stress when compared to vehicle-treated littermates. This effect was dose-dependent, with 200 mu g/g body weight as the optimal dose-regimen, and was maintained when curcumin treatment was delayed by 60 or 120 min post-HI. Cell proliferation measurements showed no changes between curcumin and HI alone, suggesting that the protective effects of curcumin on the neonatal brain following HI are most likely due to curcumin's anti-inflammatory and antioxidant properties, as seen in the reduced glial and iNOS activity. In conclusion, this study suggests curcumin as a potent neuroprotective agent with potential for the treatment of HIE. The delayed application of curcumin further increases its clinical relevance.

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