TY - JOUR
T1 - Caffeoylquinic acids
T2 - chemistry, biosynthesis, occurrence, analytical challenges, and bioactivity
AU - Alcázar Magaña, Armando
AU - Kamimura, Naofumi
AU - Soumyanath, Amala
AU - Stevens, Jan F.
AU - Maier, Claudia S.
N1 - Funding Information:
The authors acknowledge the BENFRA Center (NIH/NCCIH U19AT010829) and The OSU Mass Spectrometry Center. The purchase of the AB Sciex 5600 was made possible by NIH grant S10RR027878. AAM acknowledges The Plant Journal and the Phytochemical Society of North America (PSNA) for the Early Career Award 2020. The authors declare that they have no conflicts of interest.
Funding Information:
The authors acknowledge the BENFRA Center (NIH/NCCIH U19AT010829) and The OSU Mass Spectrometry Center. The purchase of the AB Sciex 5600 was made possible by NIH grant S10RR027878. AAM acknowledges and the Phytochemical Society of North America (PSNA) for the Early Career Award 2020. The Plant Journal
Publisher Copyright:
© 2021 Society for Experimental Biology and John Wiley & Sons Ltd.
PY - 2021/9
Y1 - 2021/9
N2 - Caffeoylquinic acids (CQAs) are specialized plant metabolites we encounter in our daily life. Humans consume CQAs in mg-to-gram quantities through dietary consumption of plant products. CQAs are considered beneficial for human health, mainly due to their anti-inflammatory and antioxidant properties. Recently, new biosynthetic pathways via a peroxidase-type p-coumaric acid 3-hydroxylase enzyme were discovered. More recently, a new GDSL lipase-like enzyme able to transform monoCQAs into diCQA was identified in Ipomoea batatas. CQAs were recently linked to memory improvement; they seem to be strong indirect antioxidants via Nrf2 activation. However, there is a prevalent confusion in the designation and nomenclature of different CQA isomers. Such inconsistencies are critical and complicate bioactivity assessment since different isomers differ in bioactivity and potency. A detailed explanation regarding the origin of such confusion is provided, and a recommendation to unify nomenclature is suggested. Furthermore, for studies on CQA bioactivity, plant-based laboratory animal diets contain CQAs, which makes it difficult to include proper control groups for comparison. Therefore, a synthetic diet free of CQAs is advised to avoid interferences since some CQAs may produce bioactivity even at nanomolar levels. Biotransformation of CQAs by gut microbiota, the discovery of new enzymatic biosynthetic and metabolic pathways, dietary assessment, and assessment of biological properties with potential for drug development are areas of active, ongoing research. This review is focused on the chemistry, biosynthesis, occurrence, analytical challenges, and bioactivity recently reported for mono-, di-, tri-, and tetraCQAs.
AB - Caffeoylquinic acids (CQAs) are specialized plant metabolites we encounter in our daily life. Humans consume CQAs in mg-to-gram quantities through dietary consumption of plant products. CQAs are considered beneficial for human health, mainly due to their anti-inflammatory and antioxidant properties. Recently, new biosynthetic pathways via a peroxidase-type p-coumaric acid 3-hydroxylase enzyme were discovered. More recently, a new GDSL lipase-like enzyme able to transform monoCQAs into diCQA was identified in Ipomoea batatas. CQAs were recently linked to memory improvement; they seem to be strong indirect antioxidants via Nrf2 activation. However, there is a prevalent confusion in the designation and nomenclature of different CQA isomers. Such inconsistencies are critical and complicate bioactivity assessment since different isomers differ in bioactivity and potency. A detailed explanation regarding the origin of such confusion is provided, and a recommendation to unify nomenclature is suggested. Furthermore, for studies on CQA bioactivity, plant-based laboratory animal diets contain CQAs, which makes it difficult to include proper control groups for comparison. Therefore, a synthetic diet free of CQAs is advised to avoid interferences since some CQAs may produce bioactivity even at nanomolar levels. Biotransformation of CQAs by gut microbiota, the discovery of new enzymatic biosynthetic and metabolic pathways, dietary assessment, and assessment of biological properties with potential for drug development are areas of active, ongoing research. This review is focused on the chemistry, biosynthesis, occurrence, analytical challenges, and bioactivity recently reported for mono-, di-, tri-, and tetraCQAs.
KW - Nrf2 activation
KW - caffeoylquinic acids
KW - chlorogenic acid
KW - cognitive decline
KW - neuroprotective activity
KW - specialized plant metabolites
UR - http://www.scopus.com/inward/record.url?scp=85111321139&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85111321139&partnerID=8YFLogxK
U2 - 10.1111/tpj.15390
DO - 10.1111/tpj.15390
M3 - Review article
C2 - 34171156
AN - SCOPUS:85111321139
SN - 0960-7412
VL - 107
SP - 1299
EP - 1319
JO - Plant Journal
JF - Plant Journal
IS - 5
ER -