Polyphenol Microbial Metabolites Exhibit Gut and Blood⁻Brain Barrier Permeability and Protect Murine Microglia against LPS-Induced Inflammation.
Shelby L JohnsonRiley D KirkNicholas A DaSilvaHang MaNavindra P SeeramMatthew J BertinPublished in: Metabolites (2019)
Increasing evidence supports the beneficial effects of polyphenol-rich diets, including the traditional Mediterranean diet, for the management of cardiovascular disease, obesity and neurodegenerative diseases. However, a common concern when discussing the protective effects of polyphenol-rich diets against diseases is whether these compounds are present in systemic circulation in their intact/parent forms in order to exert their beneficial effects in vivo. Here, we explore two common classes of dietary polyphenols, namely isoflavones and lignans, and their gut microbial-derived metabolites for gut and blood-brain barrier predicted permeability, as well as protection against neuroinflammatory stimuli in murine BV-2 microglia. Polyphenol microbial metabolites (PMMs) generally showed greater permeability through artificial gut and blood-brain barriers compared to their parent compounds. The parent polyphenols and their corresponding PMMs were evaluated for protective effects against lipopolysaccharide-induced inflammation in BV-2 microglia. The lignan-derived PMMs, equol and enterolactone, exhibited protective effects against nitric oxide production, as well as against pro-inflammatory cytokines (IL-6 and TNF-α) in BV-2 microglia. Therefore, PMMs may contribute, in large part, to the beneficial effects attributed to polyphenol-rich diets, further supporting the important role of gut microbiota in human health and disease prevention.
Keyphrases
- inflammatory response
- blood brain barrier
- lps induced
- lipopolysaccharide induced
- cerebral ischemia
- weight loss
- human health
- ms ms
- microbial community
- cardiovascular disease
- nitric oxide
- oxidative stress
- risk assessment
- type diabetes
- metabolic syndrome
- insulin resistance
- climate change
- white matter
- coronary artery disease
- resting state
- spinal cord injury
- neuropathic pain
- cardiovascular events
- nitric oxide synthase
- body mass index
- spinal cord
- subarachnoid hemorrhage