Paolo Bergamo

Dr. Paolo Bergamo

CNR Institute of Biosciences and Bioresource, Naples, Campania, Italy
orcid

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2015 in Journal of Biological Chemistry
Verified
Journal Article
Open access
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JMJunki Miyamoto
Junki Miyamoto
TMTaichi Mizukure
Taichi Mizukure
SPSi-Bum Park
Si-Bum Park
SKShigenobu Kishino
Shigenobu Kishino
IKIkuo Kimura
Ikuo Kimura
STSoichi Tanabe
Soichi Tanabe
Gut microbial metabolites of polyunsaturated fatty acids have attracted much attention because of their various physiological properties. Dysfunction of tight junction (TJ) in the intestine contributes to the pathogenesis of many disorders such as inflammatory bowel disease. We evaluated the effects of five novel gut microbial metabolites on tumor necrosis factor (TNF)-α-induced barrier impairment in Caco-2 cells and dextran sulfate sodium-induced colitis in mice. 10-Hydroxy-cis-12-octadecenoic acid (HYA), a gut microbial metabolite of linoleic acid, suppressed TNF-α and dextran sulfate sodium-induced changes in the expression of TJ-related molecules, occludin, zonula occludens-1, and myosin light chain kinase. HYA also suppressed the expression of TNF receptor 2 (TNFR2) mRNA and protein expression in Caco-2 cells and colonic tissue. In addition, HYA suppressed the protein expression of TNFR2 in murine intestinal epithelial cells. Furthermore, HYA significantly up-regulated G protein-coupled receptor (GPR) 40 expression in Caco-2 cells. It also induced [Ca2+]i responses in HEK293 cells expressing human GPR40 with higher sensitivity than linoleic acid, its metabolic precursor. The barrier-recovering effects of HYA were abrogated by a GPR40 antagonist and MEK inhibitor in Caco-2 cells. Conversely, 10-hydroxyoctadacanoic acid, which is a gut microbial metabolite of oleic acid and lacks a carbon-carbon double bond at Δ12 position, did not show these TJ-restoring activities and down-regulated GPR40 expression. Therefore, HYA modulates TNFR2 expression, at least partially, via the GPR40-MEK-ERK pathway and may be useful in the treatment of TJ-related disorders such as inflammatory bowel disease.

15 August 2002 in Journal of Agricultural and Food Chemistry
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Journal Article
Closed access
MCMarina Carbonaro
Marina Carbonaro
MMMaria Mattera
Maria Mattera
SNStefano Nicoli
Stefano Nicoli
Paolo BergamoPaolo Bergamo
Paolo Bergamo
MCMarsilio Cappelloni
Marsilio Cappelloni

1 September 2007 in Gastroenterology
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Journal Article
Closed access
CGCarmen Gianfrani
Carmen Gianfrani
Rosa Anna SicilianoRosa Anna Siciliano
Rosa Anna Siciliano
AFAngelo Facchiano
Angelo Facchiano
ACAlessandra Camarca
Alessandra Camarca
MMMaria F. Mazzeo
Maria F. Mazzeo
MRMauro Rossi
Mauro Rossi


28 March 2021 in Nutrients
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Journal Article
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Maria Pina MollicaMaria Pina Mollica
Maria Pina Mollica
Giovanna TrincheseGiovanna Trinchese
Giovanna Trinchese
Fabiano CimminoFabiano Cimmino
Fabiano Cimmino
EPEduardo Penna
Eduardo Penna
Gina CavaliereGina Cavaliere
Gina Cavaliere
Marianna CrispinoMarianna Crispino
Marianna Crispino
Milk contains several important nutrients that are beneficial for human health. This review considers the nutritional qualities of essential fatty acids (FAs), especially omega-3 (ω-3) and omega-6 (ω-6) polyunsaturated fatty acids (PUFAs) present in milk from ruminant and non-ruminant species. In particular, the impact of milk fatty acids on metabolism is discussed, including its effects on the central nervous system. In addition, we presented data indicating how animal feeding—the main way to modify milk fat composition—may have a potential impact on human health, and how rearing and feeding systems strongly affect milk quality within the same animal species. Finally, we have presented the results of in vivo studies aimed at supporting the beneficial effects of milk FA intake in animal models, and the factors limiting their transferability to humans were discussed.