Toxins,
Journal Year:
2024,
Volume and Issue:
16(11), P. 495 - 495
Published: Nov. 17, 2024
The
gut
dysbiosis
present
in
chronic
kidney
disease
(CKD)
has
been
associated
with
anemia.
Factors
such
as
the
accumulation
of
gut-derived
uremic
toxins,
increased
barrier
permeability-induced
inflammation,
and
a
reduced
intestinal
production
short-chain
fatty
acids
(SCFAs),
all
changes
microbiota
composition
CKD,
may
lead
to
development
or
worsening
anemia
renal
patients.
Understanding
addressing
these
mechanisms
related
CKD
patients
can
help
delay
improve
its
control
this
population.
One
approach
is
avoid
reduce
use
drugs
linked
phosphate
binders,
oral
iron
supplementation,
antibiotics,
others,
unless
they
are
indispensable.
Another
involves
introducing
dietary
that
promote
healthier
and/or
using
prebiotics,
probiotics,
symbiotics
setting.
These
measures
increase
presence
SCFA-producing
saccharolytic
bacteria
proteolytic
bacteria,
thereby
lowering
toxins
inflammation.
By
ameliorating
CKD-related
dysbiosis,
strategies
also
enhance
response
erythropoiesis-stimulating
agents
(ESAs)
ESA-resistant
In
review,
we
have
explored
relationship
between
propose
feasible
solutions,
both
those
already
known
potential
future
treatments.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(7), P. 3694 - 3694
Published: March 26, 2024
Metabolic-associated
fatty
liver
disease
(MAFLD)
includes
several
metabolic
dysfunctions
caused
by
dysregulation
in
the
brain–gut–liver
axis
and,
consequently,
increases
cardiovascular
risks
and
dysfunction.
In
MAFLD,
type
2
diabetes
mellitus,
obesity,
syndrome
are
frequently
present;
these
conditions
related
to
lipogenesis
systemic
inflammation.
This
study
aimed
review
connection
between
MAFLD.
The
inflammatory
process,
cellular
alterations
hepatocytes
stellate
cells,
hypercaloric
diet,
sedentarism
aggravate
prognosis
of
patients
with
Thus,
understand
modulation
physiopathology
it
is
necessary
include
organokines
involved
this
process
(adipokines,
myokines,
osteokines,
hepatokines)
their
clinical
relevance
project
future
perspectives
condition
bring
light
new
possibilities
therapeutic
approaches.
Adipokines
responsible
for
activation
distinct
signaling
different
tissues,
such
as
insulin
pro-inflammatory
cytokines,
which
important
balancing
substances
avoid
MAFLD
its
progression.
Myokines
improve
quantity
quality
adipose
contributing
avoiding
development
Finally,
hepatokines
decisive
improving
or
not
progression
through
regulation
anti-inflammatory
organokines.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(9), P. 4654 - 4654
Published: April 25, 2024
The
supply
and
control
of
iron
is
essential
for
all
cells
vital
many
physiological
processes.
All
functions
activities
are
expressed
in
conjunction
with
iron-binding
molecules.
For
example,
natural
chelators
such
as
transferrin
chelator–iron
complexes
haem
play
major
roles
metabolism
human
physiology.
Similarly,
the
mainstay
treatments
most
common
diseases
metabolism,
namely
deficiency
anaemia
overload,
involve
iron–chelator
iron-chelating
drugs
deferiprone
(L1),
deferoxamine
(DF)
deferasirox.
Endogenous
citric
acid
glutathione
exogenous
ascorbic
also
important
homeostasis.
Recent
advances
treatment
effective
ferric
tri-maltol
complex
(feraccru
or
accrufer)
transfusional
overload
using
L1
L1/DF
combinations
have
decreased
associated
mortality
morbidity
improved
quality
life
millions
patients.
Many
other
chelating
ciclopirox,
dexrazoxane
EDTA
used
daily
by
patients
diseases.
their
metabolites
iron-chelation
capacity
hydroxyurea,
tetracyclines,
anthracyclines
aspirin,
well
dietary
molecules
gallic
acid,
caffeic
quercetin,
ellagic
maltol
phytochelators,
known
to
interact
affect
related
Different
interactions
observed
presence
essential,
xenobiotic,
diagnostic
theranostic
metal
ions
competing
iron.
Clinical
trials
Parkinson’s,
Alzheimer’s
neurodegenerative
diseases,
HIV
infections,
cancer,
diabetic
nephropathy
inflammation,
highlight
importance
chelation
therapy
clinical
conditions.
proposed
use
modulating
ferroptosis
signifies
a
new
era
design
therapeutic
strategies
introduction
artificial
intelligence
guidance
optimal
outcomes
personalised
medicine
expected
increase
further
impact
medicine,
survival
metabolic
disorders
Dietary
protein
absorption
in
neonatal
mammals
and
fishes
relies
on
the
function
of
a
specialized
conserved
population
highly
absorptive
lysosome
rich
enterocytes
(LREs).
The
gut
microbiome
has
been
shown
to
enhance
nutrients,
such
as
lipids,
by
intestinal
epithelial
cells.
However,
whether
is
also
affected
poorly
understood.
Here,
we
investigate
connections
between
microbes
zebrafish
gut.
Using
live
microscopy-based
quantitative
assays,
find
that
slow
pace
uptake
degradation
LREs.
While
do
not
affect
number
absorbing
LRE
cells,
lower
expression
endocytic
digestion
machinery
transgene
assisted
cell
isolation
single
RNA-sequencing,
characterize
all
cells
take
up
dietary
protein.
We
bacteria-sensing
metabolic
pathways
LREs,
some
secretory
types
share
components
with
custom-formulated
diets,
investigated
influence
diet
activity
microbiome.
Impaired
along
protein-deficient
diet,
alters
microbial
community
leads
increased
abundance
bacterial
genera
have
capacity
reduce
Together,
these
results
reveal
diet-dependent
reciprocal
interactions
LREs
regulate
absorption.
Dietary
protein
absorption
in
neonatal
mammals
and
fishes
relies
on
the
function
of
a
specialized
conserved
population
highly
absorptive
lysosome-rich
enterocytes
(LREs).
The
gut
microbiome
has
been
shown
to
enhance
nutrients,
such
as
lipids,
by
intestinal
epithelial
cells.
However,
whether
is
also
affected
poorly
understood.
Here,
we
investigate
connections
between
microbes
zebrafish
gut.
Using
live
microscopy-based
quantitative
assays,
find
that
slow
pace
uptake
degradation
LREs.
While
do
not
affect
number
absorbing
LRE
cells,
lower
expression
endocytic
digestion
machinery
transgene-assisted
cell
isolation
single
RNA-sequencing,
characterize
all
cells
take
up
dietary
protein.
We
bacteria-sensing
metabolic
pathways
LREs,
some
secretory
types
share
components
with
custom-formulated
diets,
investigated
influence
diet
activity
microbiome.
Impaired
along
protein-deficient
diet,
alters
microbial
community
leads
an
increased
abundance
bacterial
genera
have
capacity
reduce
Together,
these
results
reveal
diet-dependent
reciprocal
interactions
LREs
regulate
absorption.
Dietary
protein
absorption
in
neonatal
mammals
and
fishes
relies
on
the
function
of
a
specialized
conserved
population
highly
absorptive
lysosome-rich
enterocytes
(LREs).
The
gut
microbiome
has
been
shown
to
enhance
nutrients,
such
as
lipids,
by
intestinal
epithelial
cells.
However,
whether
is
also
affected
poorly
understood.
Here,
we
investigate
connections
between
microbes
zebrafish
gut.
Using
live
microscopy-based
quantitative
assays,
find
that
slow
pace
uptake
degradation
LREs.
While
do
not
affect
number
absorbing
LRE
cells,
lower
expression
endocytic
digestion
machinery
transgene-assisted
cell
isolation
single
RNA-sequencing,
characterize
all
cells
take
up
dietary
protein.
We
bacteria-sensing
metabolic
pathways
LREs,
some
secretory
types
share
components
with
custom-formulated
diets,
investigated
influence
diet
activity
microbiome.
Impaired
along
protein-deficient
diet,
alters
microbial
community
leads
an
increased
abundance
bacterial
genera
have
capacity
reduce
Together,
these
results
reveal
diet-dependent
reciprocal
interactions
LREs
regulate
absorption.