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Triptolide Attenuates Muscular Inflammation and Oxidative Stress in a Delayed-Onset Muscle Soreness Animal Model

Bibliographic Data

ID15515489
AuthorsChe‐Chia Hsu (0000-0001-7294-3364, National Cheng Kung University Hospital), Che-Chia Hsu (Department of Orthopaedics, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan 70428, Taiwan), Chin-Chuan Tsai (Department of Traditional Chinese Medicine, E-Da Dachang Hospital, Kaohsiung 82445, Taiwan), Chin‐Chuan Tsai (E-Da Hospital), Po‐Yen Ko (0000-0002-2879-5584, National Cheng Kung University Hospital), Po-Yen Ko (Department of Orthopaedics, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan 70428, Taiwan), Ting-Hsien Kwan (Chia-Yi Christian Hospital), Ming‐Yie Liu (0000-0003-4561-9758, National Cheng Kung University), Ming-Yie Liu (National Cheng Kung University), Po‐Ting Wu (0000-0001-5534-8993, National Cheng Kung University Hospital, corresponding author), I‐Ming Jou (0000-0001-6877-481X, E-Da Hospital, corresponding author), I-Ming Jou (Department of Orthopaedics, E-Da Hospital, Kaohsiung 82445, Taiwan)
Year2022
Volume19
Issue24
Pages16685-16685
Publication date2022-12-12
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueInternational Journal of Environmental Research and Public Health (JOURNAL)
Journal identifiersISSN: 1661-7827 • E-ISSN: 1660-4601
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/ijerph192416685
PMID36554566
OpenAlexW4312127060
LanguageEN
References cited42

Delayed-onset muscle soreness (DOMS) is associated with exercise-induced muscle damage and inflammation, which is mainly caused by prolonged eccentric exercise in humans. Triptolide, an extract from the Chinese herb Tripterygium wilfordii Hook F, has been used for treating autoimmune and inflammatory diseases in clinical practice. However, whether triptolide attenuates acute muscle damage is still unclear. Here, we examined the effect of triptolide on carrageenan-induced DOMS in rats. Rats were injected with 3% of carrageenan into their muscles to induce acute left gastrocnemius muscular damage, and triptolide treatment attenuated carrageenan-induced acute muscular damage without affecting hepatic function. Triptolide can significantly decrease lipid hydroperoxide and nitric oxide (NO) levels, proinflammatory cytokine production, and the activation of nuclear factor (NF)-ĸB, as well as increase a reduced form of glutathione levels in carrageenan-treated rat muscles. At the enzyme levels, triptolide reduced the inducible nitric oxide synthase (iNOS) expression and muscular myeloperoxidase (MPO) activity in carrageenan-treated DOMS rats. In conclusion, we show that triptolide can attenuate muscular damage by inhibiting muscular oxidative stress and inflammation in a carrageenan-induced rat DOMS model

Apoptosis · Carrageenan · Delayed onset muscle soreness · Inflammation · Muscle damage · Nitric oxide · Nitric oxide synthase · Oxidative stress · Pathology · Proinflammatory cytokine · Tripterygium wilfordii · Triptolide · Autoimmune and Inflammatory Disorders Research · Chemistry · Exercise and Physiological Responses · Medicine · Natural Compounds in Disease Treatment · Biochemistry · Endocrinology · Internal Medicine · Pharmacology

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