TY - JOUR
T1 - Melatonin-based therapeutics for atherosclerotic lesions and beyond
T2 - Focusing on macrophage mitophagy
AU - Ajoolabady, Amir
AU - Bi, Yaguang
AU - McClements, David J.
AU - Lip, Gregory Y.H.
AU - Richardson, Des R.
AU - Reiter, Russel J.
AU - Klionsky, Daniel J.
AU - Ren, Jun
N1 - Funding Information:
DJK is supported by NIH GM131919. JR is supported by the Natural Science Foundation of China ( 82130011 ). Others had no grants associated with this work,
Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2022/2
Y1 - 2022/2
N2 - Atherosclerosis refers to a unique form of chronic proinflammatory anomaly of the vasculature, presented as rupture-prone or occlusive lesions in arteries. In advanced stages, atherosclerosis leads to the onset and development of multiple cardiovascular diseases with lethal consequences. Inflammatory cytokines in atherosclerotic lesions contribute to the exacerbation of atherosclerosis. Pharmacotherapies targeting dyslipidemia, hypercholesterolemia, and neutralizing inflammatory cytokines (TNF-α, IL-1β, IL-6, IL-17, and IL-12/23) have displayed proven promises although contradictory results. Moreover, adjuvants such as melatonin, a pluripotent agent with proven anti-inflammatory, anti-oxidative and neuroprotective properties, also display potentials in alleviating cytokine secretion in macrophages through mitophagy activation. Here, we share our perspectives on this concept and present melatonin-based therapeutics as a means to modulate mitophagy in macrophages and, thereby, ameliorate atherosclerosis.
AB - Atherosclerosis refers to a unique form of chronic proinflammatory anomaly of the vasculature, presented as rupture-prone or occlusive lesions in arteries. In advanced stages, atherosclerosis leads to the onset and development of multiple cardiovascular diseases with lethal consequences. Inflammatory cytokines in atherosclerotic lesions contribute to the exacerbation of atherosclerosis. Pharmacotherapies targeting dyslipidemia, hypercholesterolemia, and neutralizing inflammatory cytokines (TNF-α, IL-1β, IL-6, IL-17, and IL-12/23) have displayed proven promises although contradictory results. Moreover, adjuvants such as melatonin, a pluripotent agent with proven anti-inflammatory, anti-oxidative and neuroprotective properties, also display potentials in alleviating cytokine secretion in macrophages through mitophagy activation. Here, we share our perspectives on this concept and present melatonin-based therapeutics as a means to modulate mitophagy in macrophages and, thereby, ameliorate atherosclerosis.
KW - Atherosclerosis
KW - Macrophages
KW - Melatonin
KW - Mitophagy
KW - Therapeutics
UR - http://www.scopus.com/inward/record.url?scp=85122513221&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85122513221&partnerID=8YFLogxK
U2 - 10.1016/j.phrs.2022.106072
DO - 10.1016/j.phrs.2022.106072
M3 - Review article
C2 - 35007709
AN - SCOPUS:85122513221
SN - 1043-6618
VL - 176
JO - Pharmacological Research
JF - Pharmacological Research
M1 - 106072
ER -