Nutraceuticals,
Journal Year:
2024,
Volume and Issue:
4(3), P. 395 - 408
Published: July 17, 2024
The
enteric
nervous
system
(ENS)
interacts
bidirectionally
with
the
local
immune
system,
responding
to
inflammation
within
gastrointestinal
(GI)
tract.
In
a
previous
study
same
samples,
several
gene
targets
were
identified
as
being
differentially
expressed
in
inflamed
colonic
tissue
of
pigs
challenged
dextran
sodium
sulphate
(DSS).
Additionally,
animals
basal
DSS
group,
exhibited
reduced
growth
and
increased
fecal
pathology
scores,
while
relative
abundance
beneficial
taxa
was
harmful
bacteria
increased.
While
changes
innate
response
barrier
function
are
widely
cited
regarding
inflammatory
bowel
disease
(IBD),
effects
on
structures
less
well
understood.
Hence,
objectives
this
to:
(1)
evaluate
expression
range
functionally
diverse
neuroactive
receptors,
transporters
neurotrophic
factors
RNA
derived
from
pigs;
(2)
examine
associations
these
components
inflammatory,
matrix
remodeling
targets.
Mature
split
into
two
experimental
groups:
diet
(n
=
10);
+
11).
orally
once
daily
for
four
days
sacrificed
humanely.
Colonic
collected
analysis.
Most
evaluated
present
at
low
levels
or
some
cases
undetectable
by
QPCR,
including
dopamine
receptor
DRD5
serotonin
HTR3A.
receptors
(DRD1,
DRD3,
DRD4),
(HTR4),
other
selected
(GRM7,
GABRA2)
down-regulated
DSS-challenged
group
(p
<
0.05).
notably,
DRD2,
up-regulated
four-fold,
suggesting
an
active
process
involving
Relationships
(previously
published)
data
samples
suggest
that
DRD1
DRD2
influenced
different
pathways
may
also
be
interlinked
and,
more
specifically,
genes
relevant
epithelial
mesenchymal
transition
(CDH1,
CDH2,
IL6,
IL13,
IL10,
MMP1,
MMP2)
important
fibrotic
pathogenesis
IBD.
Frontiers in Physiology,
Journal Year:
2022,
Volume and Issue:
13
Published: Dec. 13, 2022
Stress-induced
abnormalities
in
gut
monoamine
levels
(e.g.,
serotonin,
dopamine,
norepinephrine)
have
been
linked
to
gastrointestinal
(GI)
dysfunction,
as
well
the
worsening
of
symptoms
GI
disorders.
However,
influence
stress
on
changes
across
entire
intestinal
biogeography
has
not
well-characterized,
especially
days
following
exposure.
Therefore,
aim
this
study
was
comprehensively
assess
neurochemical
signatures
rat
tract
after
exposure
an
acute
stressor.
To
end,
adult
male
F344
rats
were
subjected
episode
unpredictable
tail
shocks
(acute
stress)
or
left
undisturbed.
Forty-eight
hours
later
euthanized
either
a
12
h
period
fasting
30
min
food
access
evaluate
profiles
during
peri-
and
early
postprandial
periods.
Monoamine-related
neurochemicals
measured
via
UHPLC
regions
small
intestine
(duodenum,
jejunum,
ileum),
large
(cecum,
proximal
colon,
distal
colon),
cecal
contents,
fecal
liver.
The
results
suggest
relatively
wide-spread
increase
measures
serotonin
activity
can
be
observed
48
stress,
however
some
evidence
found
supporting
localized
differences
metabolization.
Moreover,
reduced
catecholamine-related
concentrations
most
notably
ileum,
lesser
extent
contents.
Next,
stress-related
consistent
with
profiles.
dopamine
elevated
association
which
did
parallel
findings
any
other
area.
Finally,
together
only
had
minor
effects
Taken
together,
these
data
nuanced
monoaminergic
exist
stressor,
highlighting
importance
assessments
that
consider
when
investigating
biological
outcomes
may
relevant
pathophysiology.
Microscopy Research and Technique,
Journal Year:
2024,
Volume and Issue:
87(9), P. 2103 - 2112
Published: April 29, 2024
Abstract
The
striped
dolphin
(
Stenella
coeruleoalba
)
is
a
medium‐sized
pelagic
with
single
external
nasal
opening
(blowhole)
located
in
the
rostral
and
dorsal
regions
of
skull.
cavity
divided
into
three
sections:
olfactory,
respiratory,
vestibular
areas.
surface
epithelium
lining
regio
vestibularis
first
tissue
nose
to
be
directly
affected
by
environmental
antigens.
Cetaceans
have
significant
amount
mucosa‐associated
lymphoid
(MALT)
throughout
their
bodies.
found
mucosa
known
as
nose‐
or
nasopharynx‐associated
(NALT).
NALT
has
not
yet
been
studied
dolphins,
but
it
identified
documented
humans
laboratory
rodents.
This
study
utilized
toll‐like
receptor
2
(TLR2),
CD4,
Langerin/CD207,
inducible
nitric
oxide
synthase
characterize,
for
time,
immune
cells
mucosal
S
.
using
confocal
microscopy
immunofluorescence
techniques.
findings
revealed
scattered
immunoreactive
tested
antibodies,
present
both
epithelial
vestibulum
underlying
connective
tissue.
enhances
our
comprehension
system
cetaceans.
Research
Highlights
provides
new
insights
research
deepens
knowledge
skin
Gastroenterology Insights,
Journal Year:
2024,
Volume and Issue:
15(3), P. 541 - 554
Published: June 28, 2024
Inflammatory
bowel
diseases
(IBDs)
represent
multifactorial
chronic
inflammatory
conditions
of
the
gastrointestinal
tract.
The
main
IBDs
are
Crohn’s
disease
(CD)
and
ulcerative
colitis
(UC).
CD
may
cause
perforation,
stricture
or
transmural
inflammation,
which
can
occur
discontinuously
in
entire
tract
(GIT).
UC
leads
to
mucosal
inflammation
as
well
atrophy
rectum
colon.
Innate
immunity
is
considered
first
line
defense
against
microbial
invasion;
among
Toll-like
receptors,
TLR2
most
important
for
mycobacterial
infection.
has
been
reported
have
a
lot
functions
infectious
other
pathologies,
such
acute
diseases.
Alfa-Smooth
Muscle
Actin
(α-SMA)
an
biomarker
IBDs.
All
myofibroblasts
express
α-SMA,
found
be
upregulated
UC.
Paraformaldehyde-fixed
intestinal
tissues,
from
patients
with
UC,
were
analyzed
by
immunostaining
α-SMA.
Our
results
showed
that,
samples
obtained
inflamed
mucosa,
TLR2-positive
epithelial
cells
concentrated
on
surface
scattered
immune
connective
tissue;
furthermore,
numerous
α-SMA-positive
(subepithelial
myofibroblasts)
detected
lamina
propria
around
glands,
while
some
co-localizing
α-SMA
could
macrophages.
In
patients,
enterocytes
villus
observed.
control
samples,
low
positivity
was
observed
subepithelial
propria.
These
data
recall
during
state;
addition,
expression
change
epithelium
IBDs,
demonstrating
that
alterations
innate
system
response
contribute
pathogenesis
these
Nutraceuticals,
Journal Year:
2024,
Volume and Issue:
4(3), P. 395 - 408
Published: July 17, 2024
The
enteric
nervous
system
(ENS)
interacts
bidirectionally
with
the
local
immune
system,
responding
to
inflammation
within
gastrointestinal
(GI)
tract.
In
a
previous
study
same
samples,
several
gene
targets
were
identified
as
being
differentially
expressed
in
inflamed
colonic
tissue
of
pigs
challenged
dextran
sodium
sulphate
(DSS).
Additionally,
animals
basal
DSS
group,
exhibited
reduced
growth
and
increased
fecal
pathology
scores,
while
relative
abundance
beneficial
taxa
was
harmful
bacteria
increased.
While
changes
innate
response
barrier
function
are
widely
cited
regarding
inflammatory
bowel
disease
(IBD),
effects
on
structures
less
well
understood.
Hence,
objectives
this
to:
(1)
evaluate
expression
range
functionally
diverse
neuroactive
receptors,
transporters
neurotrophic
factors
RNA
derived
from
pigs;
(2)
examine
associations
these
components
inflammatory,
matrix
remodeling
targets.
Mature
split
into
two
experimental
groups:
diet
(n
=
10);
+
11).
orally
once
daily
for
four
days
sacrificed
humanely.
Colonic
collected
analysis.
Most
evaluated
present
at
low
levels
or
some
cases
undetectable
by
QPCR,
including
dopamine
receptor
DRD5
serotonin
HTR3A.
receptors
(DRD1,
DRD3,
DRD4),
(HTR4),
other
selected
(GRM7,
GABRA2)
down-regulated
DSS-challenged
group
(p
<
0.05).
notably,
DRD2,
up-regulated
four-fold,
suggesting
an
active
process
involving
Relationships
(previously
published)
data
samples
suggest
that
DRD1
DRD2
influenced
different
pathways
may
also
be
interlinked
and,
more
specifically,
genes
relevant
epithelial
mesenchymal
transition
(CDH1,
CDH2,
IL6,
IL13,
IL10,
MMP1,
MMP2)
important
fibrotic
pathogenesis
IBD.