Beneficial Effects of Ginger Root Extract on Pain Behaviors, Inflammation, and Mitochondrial Function in the Colon and Different Brain Regions of Male and Female Neuropathic Rats: A Gut–Brain Axis Study
Julianna Santos,
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Hemalata Deshmukh,
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Moamen M. Elmassry
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et al.
Nutrients,
Journal Year:
2024,
Volume and Issue:
16(20), P. 3563 - 3563
Published: Oct. 21, 2024
Neuroinflammation
and
mitochondrial
dysfunction
have
been
implicated
in
the
progression
of
neuropathic
pain
(NP)
but
can
be
mitigated
by
supplementation
with
gingerol-enriched
ginger
(GEG).
However,
exact
benefits
GEG
for
each
sex
treating
neuroinflammation
homeostasis
different
brain
regions
colon
remain
to
determined.
Language: Английский
Alzheimer’s disease and diabetes-associated cognitive dysfunction: the microglia link?
Metabolic Brain Disease,
Journal Year:
2025,
Volume and Issue:
40(1)
Published: Jan. 4, 2025
Language: Английский
Peanuts (Arachis hypogea L.) in Food Industry and their Benefits for Human Health – a Review of the Current Literature
Nathalia. M. Mendes,
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Yandra Cervelim Nunes,
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Enzo Pereira de Lima
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et al.
Journal of Food Composition and Analysis,
Journal Year:
2025,
Volume and Issue:
unknown, P. 107574 - 107574
Published: April 1, 2025
Language: Английский
Peanut Shell Extract Improves Markers of Glucose Homeostasis in Diabetic Mice by Modulating Gut Dysbiosis and Suppressing Inflammatory Immune Response
Matthew Bender,
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Julianna Santos,
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Jannette M. Dufour
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et al.
Nutrients,
Journal Year:
2024,
Volume and Issue:
16(23), P. 4158 - 4158
Published: Nov. 30, 2024
There
is
strong
evidence
that
the
tripartite
interaction
between
glucose
homeostasis,
gut
microbiota,
and
host
immune
system
plays
a
critical
role
in
pathophysiology
of
type
2
diabetes
mellitus
(T2DM).
We
reported
previously
peanut
shell
extract
(PSE)
improves
mitochondrial
function
db/db
mice
by
suppressing
oxidative
stress
inflammation
liver,
brain,
white
adipose
tissue.
This
study
evaluated
impacts
PSE
supplementation
on
liver
histology,
intestinal
microbiome
composition,
innate
response
diabetic
mice.
Fourteen
were
randomly
assigned
to
group
(DM,
AIN-93G
diet)
(1%
wt/wt
for
5
weeks.
Six
C57BL/6J
received
diet
weeks
(control
group).
Parameters
homeostasis
included
serum
insulin,
HOMA-IR,
HOMA-B,
analysis
pancreatic
tissues
insulin
glucagon.
assessed
colon
using
microarray.
Gut
composition
cecal
contents
was
analyzed
16S
rRNA
gene
amplicon
sequencing.
improved
(decreased
concentration,
HOMA-B)
reduced
hepatic
lipidosis
reversed
DM-induced
shifts
relative
abundance
sequence
variants
Enterorhabdus,
Staphylococcus,
Anaerotruncus,
Akkermansia.
Relative
DM
mice,
had
suppressed
expression
levels
Cd8α,
Csf2,
Irf23
increased
Tyk2,
Myd88,
Gusb
liver.
demonstrates
T2DM-associated
disorders
part
due
suppression
inflammation.
Language: Английский