Food Bioscience,
Journal Year:
2024,
Volume and Issue:
57, P. 103587 - 103587
Published: Jan. 6, 2024
Reactive
oxygen
species
may
induce
oxidation
of
macromolecules
in
foods
and
during
digestion
the
gastrointestinal
tract,
negatively
impacting
human
health.
Antioxidants
present
plant
foods,
including
carotenoids,
tocochromanols,
ascorbic
acid,
as
well
(poly)phenols
iridoids,
counteract
macromolecules.
The
aims
study
were
to
determine
contents
acid
from
Gaultheria
spp.
berries
investigate
cytoprotective
antioxidant
activities
fruit
extracts
monotropein
esters
berries.
Moreover,
underlying
mechanisms
action
epithelial
cells
after
vitro
was
also
investigated.
content
ranged
3
24
mg/100
g
fw,
carotenoids
9
56
μg/100
total
tocochromanols
0.29
0.45
fw.
pre-incubation
gastric
(AGS)
intestinal
(Caco-2)
with
significantly
increased
viability
stressed
10
mM
H2O2
100
AAPH,
respectively,
compared
control
cells.
Furthermore,
digested
relative
mRNA
Nrf2/Keap1/ARE
signaling
pathway
enzymes
such
superoxide
dismutase
(SOD),
glutathione
peroxidase
(GPX)
reductase,
catalase
(CAT).
Caco-2
protein
expression
GPX,
CAT,
Keap1,
Nrf2,
incremented
SOD
activity
In
conclusion,
protect
against
oxidative
stress
digestive
processes.
Antibiotics,
Journal Year:
2023,
Volume and Issue:
12(7), P. 1157 - 1157
Published: July 7, 2023
Broccoli,
Brassica
oleracea
var.
italica,
has
recently
gained
considerable
attention
due
to
its
remarkable
nutritional
composition
and
numerous
health
benefits.
In
this
review,
the
aspects
of
broccoli
are
examined,
highlighting
rich
nutrient
content
essential
bioactive
compounds.
The
cruciferous
vegetable
is
a
source
several
important
nutrients,
including
fiber,
vitamins
(A,
C,
K),
minerals
(calcium,
potassium,
iron),
antioxidants.
It
also
been
shown
contain
compounds
such
as
glucosinolates,
sulforaphane,
indole-3-carbinol,
all
which
have
significant
health-promoting
effects.
These
chemicals
known
potent
antioxidant,
anti-inflammatory,
anticancer
This
review
article
aims
comprehensively
examine
diverse
spectrum
nutrients
contained
in
explore
medicinal
potential
promote
human
health.
Nutrients,
Journal Year:
2023,
Volume and Issue:
15(4), P. 1035 - 1035
Published: Feb. 19, 2023
Food-derived
bioactive
peptides
(BAPs)
obtained
from
edible
insect-protein
hold
multiple
activities
promising
the
potential
to
target
complex
pathological
mechanisms
responsible
for
chronic
health
conditions
such
as
hypertension
development.
In
this
study,
enzymatic
protein
hydrolysates
non-mulberry
silkworm
Antheraea
assama
(Muga)
and
Philosomia
ricini
(Eri)
pupae,
specifically
Alcalase
(A.
assama)
Papain
(P.
ricini)
after
60
240
min,
exhibited
highest
ACE-inhibitory
antioxidant
properties.
The
hydrolysates’
fractions
(<3,
3–10
>10
kDa),
Alc_M60min_F3
(≤3
kDa)
Pap_E240min_F3
showed
activities,
respectively.
Further
RP-HPLC
purified
sub-fractions
F4
F6
ACE
inhibition
well
potent
anti-oxinflammatory
in
lipopolysaccharide
(LPS)-treated
endothelial
cells.
Indeed,
peptide
were
effective
preventing
p65
nuclear
translocation
3
h
of
LPS
stimulation
along
with
p38
MAPK
phosphorylation
HUVEC
addition,
pretreatment
significantly
prevented
LPS-induced
upregulation
COX-2
expression
IL-1β
secretion,
while
NRF2
(nuclear
factor
erythroid
2-related
2)-regulated
enzymes
HO-1
NQO1
was
induced
by
both
fractions.
derived
pupae
have
potentialities
be
explored
nutritional
approaches
against
related
cardiovascular
diseases.
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: May 31, 2024
Abstract
Satureja
is
an
aromatic
plant
that
used
for
flavoring,
perfume,
and
food
manufacturing
due
to
its
pleasant
essential
oil.
Modern
medicine
research
revealed
several
biological
activities
of
oil,
including
antifungal,
antibacterial,
antiviral,
antioxidant,
anticancer,
anti-inflammatory.
However,
the
functional
properties
fatty
acid
have
not
been
explored.
This
study
examined
profile,
lipid
nutritional
quality,
anti-amylase,
anti-lipase
capacities
.
The
efficiency
on
anti-oxidative
anti-inflammatory
parameters
in
LPS-induced
macrophage
through
Nrf2/NF-kB/NADH
oxidase
pathway
was
examined.
whole
extract
prepared
with
chloroform/methanol/water
solution.
Fatty
acids
methyl
ester
from
were
methanol/sulfuric
reagent.
profile
analyzed
using
gas
chromatography-mass
spectrometry.
Total
antioxidant
determined
by
ABTS
decolorization.
Lipase
amylase
monitoring
decomposition
p
-nitrophenyl
butyrate
starch.
cell
line
grown
DMEM
media
presence
acid.
hydrogen
peroxide
production
treated
cells
monitored
FOX
NADH
activity
measured
breakdown.
expression
NOX,
NF-kB,
NRF2,
tested
real-time
PCR.
main
components
linolenic
(24.67–37.32%),
palmitic
(10.65–20.29%),
linoleic
(8.31–13.39%),
oleic
(4.42–14.35%),
stearic
(2.76–8.77%)
palmitoleic
(1.77–4.95%).
Given
omega-3
PUFA
(23.58–37.32%),
SFA
(21.53–26.70%),
omega-6
(10.86–16.14%),
omega-9
MUFA
omega-7
(1.77–4.95%)
comprise
majority
acids.
has
a
promising
unsaturation
index
(120.77–164.27),
PUFA/MUFA
(2.07–6.41),
hypocholesterolemic
(2.44–3.47),
health-promoting
(2.03–2.42),
PUFA/SFA
(1.37–1.94),
nutritive
value
(0.53–1.71),
MUFA/SFA
(0.30–0.80)
omega-6/omega-3
(0.34–0.65),
atherogenicity
(0.41–0.49),
thrombogenicity
(0.17–0.27).
displayed
strong
capacity
(with
IC
50
ranging
354
428
µg/mL),
anti-amylase
370
390
µg/mL).
LPS
induced
NF-kB
synthesis
cells.
In
LPS-stimulated
macrophages,
reduced
NOX
expression,
peroxide,
increased
NRF2
at
0.04
mg/mL.
conclusion,
potent
anti-lipase,
activities.
mechanisms
lowering
oxidative
stress
markers
depended
down-regulating
superoxide-producing
enzymes
gene
protein
levels.
polyunsaturated
could
be
recommended
healthy
products
combined
dietary
therapy
treat
obesity,
diabetes,
stress.
Food Frontiers,
Journal Year:
2024,
Volume and Issue:
5(5), P. 1866 - 1908
Published: July 7, 2024
Abstract
The
escalating
global
cancer
burden
underscores
the
urgent
need
for
more
effective
therapeutic
strategies.
Phytochemicals,
naturally
occurring
compounds
in
plants,
have
garnered
attention
their
potential
chemoprevention
and
chemotherapy.
Their
ability
to
modulate
molecular
mechanisms
influence
cell
signaling
pathways
offers
a
promising
avenue
management.
This
review
aims
synthesize
current
knowledge
on
phytochemicals’
chemopreventive
chemotherapeutic
potential,
focusing
of
action
impacts
involved
cancer.
A
systematic
literature
search
was
conducted
across
major
databases,
including
PubMed/Medline,
Web
Science,
Scopus,
Google
Scholar.
strategy
uses
Medical
Subject
Headings
(MeSH)
free‐text
terms
using
Boolean
operators
capture
relevant
studies.
Inclusion
criteria
targeted
original
research
reviews
effects
phytochemicals
cancer,
with
specific
focus
mechanisms.
flavonoids,
polyphenols,
terpenoids,
demonstrated
significant
anticancer
properties
by
inducing
cycle
arrest,
apoptosis,
autophagy.
They
critical
pathways,
such
as
cyclooxygenase‐2,
nuclear
factor
kappa
B,
various
growth
factor‐related
rectify
epigenetic
alterations,
contributing
effects.
Phytochemicals
represent
valuable
resource
developing
novel
prevention
treatment
strategies;
actions
underscore
combat.
Further
is
warranted
translate
these
findings
into
clinical
applications,
optimizing
phytochemical‐based
interventions
Pharmaceutics,
Journal Year:
2023,
Volume and Issue:
15(6), P. 1578 - 1578
Published: May 23, 2023
Phytochemicals,
produced
as
secondary
plant
metabolites,
have
shown
interesting
potential
therapeutic
activities
against
neurodegenerative
diseases
and
cancer.
Unfortunately,
poor
bioavailability
rapid
metabolic
processes
compromise
their
use,
several
strategies
are
currently
proposed
for
overcoming
these
issues.
The
present
review
summarises
enhancing
the
central
nervous
system's
phytochemical
efficacy.
Particular
attention
has
been
paid
to
use
of
phytochemicals
in
combination
with
other
drugs
(co-administrations)
or
administration
prodrugs
conjugates,
particularly
when
approaches
supported
by
nanotechnologies
exploiting
conjugation
appropriate
targeting
molecules.
These
aspects
described
polyphenols
essential
oil
components,
which
can
improve
loading
nanocarriers,
be
part
nanocarriers
designed
targeted
co-delivery
achieve
synergistic
anti-glioma
anti-neurodegenerative
effects.
vitro
models,
able
simulate
blood-brain
barrier,
neurodegeneration
glioma,
useful
optimizing
innovative
formulations
before
vivo
via
intravenous,
oral,
nasal
routes,
is
also
summarised.
Among
compounds,
quercetin,
curcumin,
resveratrol,
ferulic
acid,
geraniol,
cinnamaldehyde
efficaciously
formulated
attain
brain-targeting
characteristics,
may
therefore
therapeutically
glioma
diseases.
RSC Advances,
Journal Year:
2024,
Volume and Issue:
14(33), P. 23744 - 23771
Published: Jan. 1, 2024
Introduction:
Pharmacotherapeutic
targets
for
breast
cancer
include
the
estrogen
receptor
(ER),
progesterone
(PR),
and
human
epidermal
growth
factor
(EGFR).
Inhibitors
of
these
receptors
could
be
interesting
therapeutic
candidates
treatment
management
(BC).
Aim:
This
study
used
GC-MS
HPLC
to
identify
bioactive
compounds
in
Pleurotus
ostreatus
(P.
ostreatus)
extracts
applied
silico
methods
potent
EGFR,
ER,
PR
inhibitors
from
as
potential
drug
candidates.
Method:
were
chemicals
P.
aqueous
(PO-A),
methanol
(PO-M),
ethanol
(PO-E),
chloroform
(PO-C),
n-hexane
(PO-H).
The
PR,
EGFR
model
optimization
molecular
docking
compounds/control
binding
pocket
simulated
using
AutoDock
Vina
PyRx.
drug-likeness,
pharmacokinetic,
pharmacodynamic
features
prospective
leads
all
anticipated.
Result:
results
indicated
existence
29
PO-A,
36
PO-M
PO-E,
42
PO-C,
22
PO-H
extracts.
With
only
o-tolylamino-acetic
acid
(4-nitro-benzylidene)-hydrazide
(-7.5
kcal
mol-1)
ethanolic
extract
bind
receptor.
on
other
hand,
identified
several
with
higher
affinities
than
control.
Ergotaman-3',6',18-trione
(-8.1
mol-1),
5,10-diethoxy-2,3,7,8-tetrahydro-1H,6H-dipyrrolo[1,2-a:1',2'-d]pyrazine
(-7.8
extract;
(-8.4
had
better
affinity
compared
(-7.7
mol-1).
Likewise,
ergotaman-3',6',18-trione
(-9.7
phenol,
2,4-bis(1,1-dimethyl
ethyl)
(-8.2
control,
gefitinib
(-7.9
regards
EGFR.
None
or
outperformed
control
any
proteins.
Phenols
flavonoids
such
quercetin,
luteolin,
rutin,
chrysin,
apigenin,
ellagic
acid,
naringenin
their
Conclusion:
class
phenols
lead
molecules
due
ability
strongly
proteins'
receptors.
These
showed
promising
drug-like
properties;
they
safe
new
creating
anticancer
medicines.