Investigative Ophthalmology & Visual Science,
Journal Year:
2022,
Volume and Issue:
63(1), P. 37 - 37
Published: Jan. 27, 2022
Purpose:
The
oxygen-induced
retinal
neovascularization
mouse
model
closely
approximates
pathological
changes
associated
with
human
neovascularization-associated
diseases,
including
retinopathies.
We
used
this
and
endothelial
cells
(HRECs)
under
hypoxia
to
explore
the
relationship
between
taurine
upregulated
gene-1
(TUG1),
vascular
growth
factor
(VEGF),
miR-299-3p
on
retinopathy
of
prematurity
(ROP).
Methods:
An
(OIR)
was
established;
mice
were
divided
into
a
normal
control
group,
OIR
TUG1
group
(lentivirus
control),
TUG1-knockdown
group.
apoptosis
evaluated
using
TUNEL
assay.
Angiogenic,
apoptotic,
inflammatory
factors
detected
by
Western
blot,
immunohistochemistry,
immunofluorescence
analyses.
HRECs
cultured
assessed
for
VEGF
expression,
apoptosis,
tubule
formation,
migration
ability.
TUG1,
VEGF,
via
dual
luciferase
reporter
gene
Results:
Intravitreal
injection
lentivirus
reduced
response
in
tissue
markedly
retina.
Overexpression
miR-299
rate,
tube
ability
hypoxia-treated
cells,
thereby
inhibiting
formation
new
blood
vessels.
assay
suggested
that
has
binding
sites
VEGF.
Conclusions:
reduces
expression
VEGFA
competitively
adsorbing
facilitates
regulation
neovascularization,
suggesting
it
may
serve
as
therapeutic
target
neovascular
diseases.
Nanomaterials,
Journal Year:
2022,
Volume and Issue:
12(2), P. 238 - 238
Published: Jan. 12, 2022
Phytopharmaceuticals
have
been
widely
used
globally
since
ancient
times
and
acknowledged
by
healthcare
professionals
patients
for
their
superior
therapeutic
value
fewer
side-effects
compared
to
modern
medicines.
However,
phytopharmaceuticals
need
a
scientific
methodical
approach
deliver
components
thereby
improve
patient
compliance
treatment
adherence.
Dose
reduction,
improved
bioavailability,
receptor
selective
binding,
targeted
delivery
of
can
be
likely
achieved
molding
them
into
specific
nano-formulations.
In
recent
decades,
nanotechnology-based
emerged
as
potential
candidates
the
various
communicable
non-communicable
diseases.
Nanotechnology
combined
with
broadens
perspective
overcomes
problems
associated
plant
medicine.
The
current
review
highlights
application
nano-phytopharmaceuticals
in
neurological,
cardiovascular,
pulmonary,
gastro-intestinal
disorders.
We
conclude
that
emerge
promising
therapeutics
many
pathological
conditions
good
higher
acceptance.
Chinese Medicine,
Journal Year:
2024,
Volume and Issue:
19(1)
Published: Feb. 28, 2024
Abstract
Object
Bufei
Yishen
formula
(BYF),
a
traditional
Chinese
medicine
alleviates
COPD
symptoms
and
suppresses
airway
epithelial
inflammation.
In
this
study,
we
determined
whether
BYF
protects
the
barrier
from
destruction
in
rats.
Methods
The
protective
effects
of
on
were
examined
rat
model.
BEAS-2B
cells
exposed
to
cigarette
smoke
extract
(CSE)
determine
effect
function.
Transcriptomic
network
analyses
conducted
identify
mechanisms.
Results
Oral
reduced
severity
rats
by
suppressing
decline
lung
function,
pathological
changes,
inflammation,
protected
function
upregulating
apical
junction
proteins,
including
occludin
(OCLN),
zonula
occludens
(ZO)-1,
E-cadherin
(E-cad).
treatment
permeability,
increased
TEER
as
well
OCLN,
ZO-1,
E-cad
CSE.
Furthermore,
58
compounds
identified
used
predict
421
potential
targets.
addition,
expression
572
differentially
expressed
genes
(DEGs)
was
CSE-exposed
cells.
A
analysis
targets
DEGs
revealed
that
regulates
multiple
pathways,
which
Sirt1,
AMPK,
Foxo3,
autophagy
pathways
may
be
most
important
with
respect
Moreover,
vitro
experiments
confirmed
nobiletin,
one
active
BYF,
protein
levels,
E-cad.
It
also
LC3B
phosphorylated
AMPK
levels
decreased
phosphorylation
FoxO3a.
Conclusions
enhancing
through
regulation
SIRT1/AMPK/FOXO3
signaling
pathway.
Phytomedicine,
Journal Year:
2023,
Volume and Issue:
118, P. 154980 - 154980
Published: July 17, 2023
Airway
epithelial
barrier
dysfunction
is
highly
related
to
the
pathogenesis
of
chronic
obstructive
pulmonary
disease
(COPD).
Effective-component
combination
(ECC)
derived
from
Bufei
Yishen
formula
(BYF)
an
effective
treatment
regimen
for
patients
with
COPD
and
has
previously
been
found
attenuate
airway
inflammation
in
rats.To
determine
mechanism
underlying
protective
effects
ECC-BYF
against
disruption
COPD.The
on
were
investigated
a
rat
model.
BEAS-2B
cells
stimulated
cigarette
smoke
extract
(CSE)
direct
function
aryl
hydrocarbon
receptor
(AHR)/
epidermal
growth
factor
(EGFR)
signaling.The
results
revealed
that
attenuated
rats
maintained
by
upregulating
expression
apical
junction
proteins,
including
occludin
(OCC),
zonula
occludens
(ZO)-1,
E-cadherin
(E-cad).
In
cells,
decreased
permeability,
increased
transepithelial
electrical
resistance,
prevented
decrease
OCC,
ZO-1,
E-cad
induced
CSE
exposure.
addition,
transcriptomics
network
analysis
may
be
multiple
signaling
pathways,
ErbB,
AHR,
PI3K-Akt-mTOR
pathways.
suppressed
protein
levels
p-EGFR
p-ERK1/2
mRNA
CYP1A1
CSE-exposed
as
well
p-EGFR,
p-ERK1/2,
lungs
COPD.
AHR
agonist
FICZ
weakened
effect
suppressing
increase
ZO-1
OCC
preventing
inhibitory
EGFR
phosphorylation.This
first
study
demonstrate
function.
The
associated
suppression
AHR/EGFR
pathway
promote
adhesion.
Pharmaceutics,
Journal Year:
2021,
Volume and Issue:
13(2), P. 177 - 177
Published: Jan. 28, 2021
Obstructive
airway
diseases,
e.g.,
chronic
obstructive
pulmonary
disease
(COPD)
and
asthma,
represent
leading
causes
of
morbidity
mortality
worldwide.
However,
the
efficacy
currently
available
inhaled
therapeutics
is
not
sufficient
for
arresting
progression
decreasing
mortality,
hence
providing
an
urgent
need
development
novel
therapeutics.
Local
delivery
to
airways
via
inhalation
promising
drugs,
because
it
allows
directly
target
site
action
minimizes
systemic
drug
exposure.
In
addition,
modalities
like
RNA
provide
entirely
new
opportunities
highly
specific
treatment
diseases.
Here,
we
review
state
art
conventional
drugs
used
COPD
asthma
with
focus
on
quality
attributes
medicines,
outline
therapeutic
potential
safety
drugs.
Subsequently,
present
recent
advances
in
manufacturing
thermostable
solid
dosage
forms
administration,
important
inhalable
dry
powder
formulations,
obstacles
translation
clinic.
Delivery
challenges
technologies
overcome
them
are
also
discussed.
Finally,
future
prospects
RNA-based
highlight
major
knowledge
gaps,
which
require
further
investigation
advance
medicine
towards
bedside.
International Journal of COPD,
Journal Year:
2022,
Volume and Issue:
Volume 17, P. 1219 - 1236
Published: May 1, 2022
Ferroptosis
and
immune
infiltration
are
involved
in
the
pathogenesis
of
chronic
obstructive
pulmonary
disease
(COPD).
We
aim
to
identify
ferroptosis-related
hub
genes
analyze
their
association
with
COPD
through
bioinformatics
methods.The
mRNA
microarray
data
GSE38974
were
downloaded
from
Gene
Expression
Omnibus
obtain
differentially
expressed
(DEGs).
The
DEGs
intersected
(FRGs)
FerrDb
FRGs.
GO
KEGG
enrichment
protein-protein
interaction
(PPI)
analyses
FRGs
conducted
R
software
STRING
database.
key
module
screened
by
Cytoscape
software.
MiRNAs,
transcription
factors
signal
molecules
predicted
miRNet
NetworkAnalyst.
correlation
Comparative
Toxicomics
Database
(CTD)
receiver
operating
characteristic
(ROC)
curves
analyzed.
Immune
was
evaluated
CIBERSORT
algorithm.
Spearman
between
infiltrated
cells.Fifteen
identified,
which
enriched
some
terms
involving
airway
inflammatory
responses
structural
remodeling.
Five
selected
including
HIF1A,
IL6,
PTGS2,
CDKN1A
ATM.
Inference
scores
CTD
indicated
COPD.
Two
miRNAs,
five
one
molecule
predicted.
combination
could
be
a
fine
diagnostic
indicator
(AUC:
0.981,
CI:
0.940-1.000).
evaluation
showed
that
monocytes
M0
macrophages
upregulated
lung
tissues,
while
CD8
T
cells,
activated
NK
M2
macrophages,
resting
dendritic
cells
mast
downregulated.
significantly
associated
cells.We
identified
(HIF1A,
ATM)
COPD,
found
they
may
influence
regulating
ferroptosis
thus
affecting
infiltrating
cells.
Drug Delivery and Translational Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 18, 2025
Small
interfering
RNA
(siRNA)
and
messenger
(mRNA)
have
drawn
considerable
attention
in
recent
years
due
to
their
ability
modulate
the
expression
of
specific
disease-related
proteins.
However,
it
is
difficult
find
safe,
robust,
effective
delivery
systems
suitable
for
pulmonary
treat
lung
diseases.
In
this
study,
two
cationic
peptides,
namely
LAH4-L1
PEG12KL4,
were
employed
as
non-viral
vectors
siRNA
mRNA
delivery.
Four
formulations
(i.e.
LAH4-L1/siRNA;
PEG12KL4/siRNA;
LAH4-L1/mRNA
PEG12KL4/mRNA)
investigated.
Microfluidic
mixing
method
was
utilised
fabricate
complexes
a
controllable
reproducible
manner.
Upon
optimisation
microfluidic
protocol,
vibrating
mesh
nebuliser
aerosolise
complexes,
transfection
efficiency
evaluated
on
A549
BEAS-2B
cells.
Following
nebulisation,
inhalable
mist
generated
all
with
mass
median
aerodynamic
diameter
below
5
μm.
Although
hydrodynamic
particle
sizes
significantly
reduced
around
100
nm
after
nebulisation
regardless
original
size
prior
binding
vitro
peptide
successfully
preserved
no
significant
differences
compared
same
system
before
nebulisation.
The
current
result
indicates
that
both
PEG12KL4
hold
potential
future
clinical
application
through