Publications by authors named "A Macias-Camero"

Persistent and unresolved inflammation is a common underlying factor observed in several and seemingly unrelated human diseases, including cardiovascular and neurodegenerative diseases. Particularly, in atopic conditions, acute inflammatory responses such as those triggered by insect venom, food or drug allergies possess also a life-threatening potential. However, respiratory allergies predominantly exhibit late immune responses associated with chronic inflammation, that can eventually progress into a severe phenotype displaying similar features as those observed in other chronic inflammatory diseases, as is the case of uncontrolled severe asthma.

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The human gut microbiome establishes and matures during infancy, and dysregulation at this stage may lead to pathologies later in life. We conducted a multi-omics study comprising three generations of family members to investigate the early development of the gut microbiota. Fecal samples from 200 individuals, including infants (0-12 months old; 55% females, 45% males) and their respective mothers and grandmothers, were analyzed using two independent metabolomics platforms and metagenomics.

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Pectins are dietary fibers that are attributed with several beneficial immunomodulatory effects. Depending on the degree of esterification (DE), pectins can be classified as high methoxyl pectin (HMP) or low methoxyl pectin (LMP). The aim of this study was to investigate the effects of pectin methyl-esterification on intestinal microbiota and its immunomodulatory properties in naive mice.

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Article Synopsis
  • The type-1 cannabinoid receptor (CBR) plays a crucial role in modulating brain function by regulating neurotransmitter release in nerve terminals.
  • A study found that CBR interacts specifically with a protein called growth-associated protein of 43 kDa (GAP43) at mossy cell axon boutons in the hippocampus, affecting excitatory synapses.
  • This interaction inhibits the anti-convulsant effects of cannabinoids by disrupting CBR's ability to suppress transmission in hippocampal circuits, highlighting GAP43's role as a regulatory partner for CBR.
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