TY - JOUR
T1 - High bioavailability curcumin : an anti-inflammatory and neurosupportive bioactive nutrient for neurodegenerative diseases characterized by chronic neuroinflammation
AU - Ullah, Faheem
AU - Liang, Andy
AU - Rangel, Alejandra
AU - Gyengesi, Erika
AU - Niedermayer, Garry
AU - Munch, Gerald
PY - 2017
Y1 - 2017
N2 - Neuroinflammation is a pathophysiological process present in a number of neurodegenerative disorders, such as Alzheimer’s disease, Huntington’s disease, Parkinson’s disease, stroke, traumatic brain injury including chronic traumatic encephalopathy and other age-related CNS disorders. Although there is still much debate about the initial trigger for some of these neurodegenerative disorders, during the progression of disease, broad range anti-inflammatory drugs including cytokine suppressive anti-inflammatory drugs (CSAIDs) might be promising therapeutic options to limit neuroinflammation and improve the clinical outcome. One of the most promising CSAIDs is curcumin, which modulates the activity of several transcription factors (e.g., STAT, NF-κB, AP-1) and their pro-inflammatory molecular signaling pathways. However, normal curcumin preparations demonstrate low bioavailability in vivo. To increase bioavailability, preparations of high bioavailability curcumin have been introduced to achieve therapeutically relevant concentrations in target tissues. This literature review aims to summarize the pharmacokinetic and toxicity profile of different curcumin formulations.
AB - Neuroinflammation is a pathophysiological process present in a number of neurodegenerative disorders, such as Alzheimer’s disease, Huntington’s disease, Parkinson’s disease, stroke, traumatic brain injury including chronic traumatic encephalopathy and other age-related CNS disorders. Although there is still much debate about the initial trigger for some of these neurodegenerative disorders, during the progression of disease, broad range anti-inflammatory drugs including cytokine suppressive anti-inflammatory drugs (CSAIDs) might be promising therapeutic options to limit neuroinflammation and improve the clinical outcome. One of the most promising CSAIDs is curcumin, which modulates the activity of several transcription factors (e.g., STAT, NF-κB, AP-1) and their pro-inflammatory molecular signaling pathways. However, normal curcumin preparations demonstrate low bioavailability in vivo. To increase bioavailability, preparations of high bioavailability curcumin have been introduced to achieve therapeutically relevant concentrations in target tissues. This literature review aims to summarize the pharmacokinetic and toxicity profile of different curcumin formulations.
KW - anti-inflammatory agents
KW - curcumin
KW - inflammation
KW - microglia
KW - nervous system
KW - pharmacokinetics
UR - http://handle.westernsydney.edu.au:8081/1959.7/uws:39022
U2 - 10.1007/s00204-017-1939-4
DO - 10.1007/s00204-017-1939-4
M3 - Article
SN - 0340-5761
VL - 91
SP - 1623
EP - 1634
JO - Archives of Toxicology
JF - Archives of Toxicology
IS - 4
ER -