Inflammasomes are key intracellular multimeric proteins able to initiate the cellular inflammatory signaling pathway. NLRP3 inflammasome represents one of the main protein complexes involved in the development of inflammatory events, and its activity has been largely demonstrated to be connected with inflammatory or autoinflammatory disorders, including diabetes, gouty arthritis, liver fibrosis, Alzheimer’s disease, respiratory syndromes, atherosclerosis, and cancer initiation. In recent years, it has been demonstrated how dietary intake and nutritional status represent important environmental elements that can modulate metabolic inflammation, since food matrices are an important source of several bioactive compounds. In this review, an updated status of knowledge regarding food bioactive compounds as NLRP3 inflammasome modulators is discussed. Several chemical classes, namely polyphenols, organosulfurs, terpenes, fatty acids, proteins, amino acids, saponins, sterols, polysaccharides, carotenoids, vitamins, and probiotics, have been shown to possess NLRP3 inflammasome-modulating activity through in vitro and in vivo assays, mainly demonstrating an anti-NLRP3 inflammasome activity. Plant foods are particularly rich in important bioactive compounds, each of them can have different effects on the pathway of inflammatory response, confirming the importance of the nutritional pattern (food model) as a whole rather than any single nutrient or functional compound.

Modulatory properties of food and nutraceutical components targeting NLRP3 inflammasome activation / Spano, M.; Di Matteo, G.; Ingallina, C.; Ambroselli, D.; Carradori, S.; Gallorini, M.; Giusti, A. M.; Salvo, A.; Grosso, M.; Mannina, L.. - In: NUTRIENTS. - ISSN 2072-6643. - 14:3(2022), pp. 491-529. [10.3390/nu14030490]

Modulatory properties of food and nutraceutical components targeting NLRP3 inflammasome activation

Spano M.
Primo
;
Di Matteo G.
Secondo
;
Ingallina C.;Ambroselli D.;Giusti A. M.;Salvo A.
Penultimo
;
Mannina L.
Ultimo
2022

Abstract

Inflammasomes are key intracellular multimeric proteins able to initiate the cellular inflammatory signaling pathway. NLRP3 inflammasome represents one of the main protein complexes involved in the development of inflammatory events, and its activity has been largely demonstrated to be connected with inflammatory or autoinflammatory disorders, including diabetes, gouty arthritis, liver fibrosis, Alzheimer’s disease, respiratory syndromes, atherosclerosis, and cancer initiation. In recent years, it has been demonstrated how dietary intake and nutritional status represent important environmental elements that can modulate metabolic inflammation, since food matrices are an important source of several bioactive compounds. In this review, an updated status of knowledge regarding food bioactive compounds as NLRP3 inflammasome modulators is discussed. Several chemical classes, namely polyphenols, organosulfurs, terpenes, fatty acids, proteins, amino acids, saponins, sterols, polysaccharides, carotenoids, vitamins, and probiotics, have been shown to possess NLRP3 inflammasome-modulating activity through in vitro and in vivo assays, mainly demonstrating an anti-NLRP3 inflammasome activity. Plant foods are particularly rich in important bioactive compounds, each of them can have different effects on the pathway of inflammatory response, confirming the importance of the nutritional pattern (food model) as a whole rather than any single nutrient or functional compound.
2022
food; modulation activity; NLRP3 inflammasome; nutrients; animals; dietary supplements; humans; inflammation; NLR family, pyrin domain-containing 3 protein; atherosclerosis; inflammasomes
01 Pubblicazione su rivista::01g Articolo di rassegna (Review)
Modulatory properties of food and nutraceutical components targeting NLRP3 inflammasome activation / Spano, M.; Di Matteo, G.; Ingallina, C.; Ambroselli, D.; Carradori, S.; Gallorini, M.; Giusti, A. M.; Salvo, A.; Grosso, M.; Mannina, L.. - In: NUTRIENTS. - ISSN 2072-6643. - 14:3(2022), pp. 491-529. [10.3390/nu14030490]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1632237
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