Comparison of Pharmacokinetics of Six Bioactive Constituents from Paeoniae Radix Rubra in Normal and Toxic Heat and Blood Stasis Syndrome Rats by Uhplc-Qqq-Ms/Ms
Lin-Han Xiang,
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Xu-Yan Guo,
No information about this author
Meng-Ge Feng
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et al.
Published: Jan. 1, 2025
Ethnopharmacological
relevanceIn
the
clinical
practice
of
traditional
Chinese
medicine,
concept
toxic
heat
and
blood
stasis
syndrome
(THBSS)
is
commonly
observed
in
many
critical
diseases.
Although
herbal
medicine
Paeoniae
Radix
Rubra
(PRR)
has
been
employed
for
treating
various
diseases
associated
with
THBSS,
difference
pharmacokinetic
characteristics
its
bioactive
constituents
between
such
pathological
state
normal
remains
unknown.Aim
studyTo
elucidate
profiles
six
from
PRR
following
oral
administration
a
comparative
study
THBSS
rats.Materials
methodsOne
group
rats
was
administered
at
dosage
12.6
g/kg,
while
three
additional
groups
were
dosages
6.3,
12.6,
18.9
respectively.
UHPLC-QQQ-MS/MS
technology
utilized
to
conduct
analysis
paeoniflorin
(PAE),
oxypaeoniflorin
(O-PAE),
galloylpaeoniflorin
(G-PAE),
benzoylpaeoniflorin
(B-PAE),
salicylic
acid
(SA),
3,3'-di-O-methylellagic
(DMA)
on
rat
plasma
samples.ResultsThe
method
successfully
developed
simultaneous
determination
these
compounds
plasma.
In
rats,
PAE,
O-PAE,
G-PAE
exhibit
multimodal
patterns
relatively
prolonged
durations.
B-PAE
rapidly
absorbed
eliminated,
mean
MRT(0-t),
Tmax,
t1/2,
CLz/F
values
1.96
h,
0.42
115.37
L/h/kg,
respectively,
resulting
short
existence
body.
SA
DMA
higher
bioavailability
vivo
exposure
(mean
AUC(0-t)
13604.49
39813.75
ng/mL·h)
despite
their
low
contents
PRR,
having
lowest
elimination
rate
(t1/2
30.74
h).
Notably,
behaviors
G-PAE,
are
significantly
altered
(p
<
0.05).
The
Cmax
increased
by
60%,
87%,
55%,
AUC(0-∞)
O-PAE
35%,
MRT(0-∞)
36%,
Tmax
extended
185%
200%.
Additionally,
may
possess
linear
within
range
other
analytes
do
not
linearity.ConclusionsThis
represents
inaugural
investigation
into
pharmacokinetics
rats.
alterations
be
attributed
changed
flow
dynamics,
microvascular
permeability,
disorder
gut
microflora,
or
reduced
drug
metabolism.
Furthermore,
this
offers
valuable
insights
subsequent
research
pharmacokinetic-pharmacodynamic
relationship
use
THBSS.
Language: Английский
Drug-Induced Liver Injury and the Urgent Need for Improved Diagnostic Test
Medical Reports,
Journal Year:
2025,
Volume and Issue:
unknown, P. 100170 - 100170
Published: Jan. 1, 2025
Language: Английский
Inulin Hydrogel Loaded with Self-Assembled Nanoparticles of Curcumin and Glycyrrhizic Acid for Inflammatory Bowel Disease Treatment Via Anti-Inflammation, Antioxidation, and Microbiota Modulation
Jiaxin Wu,
No information about this author
Leyan Wang,
No information about this author
Lu Han
No information about this author
et al.
Published: Jan. 1, 2025
Language: Английский
Modulating the Gut Microbiota to Combat Drug-Induced Liver Injury: A New Frontier in Hepatic Health
IntechOpen eBooks,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 19, 2025
Drug-induced
liver
injury
(DILI)
encompasses
a
spectrum
of
damage
caused
by
pharmaceuticals
or
their
metabolites,
ranging
from
mild,
asymptomatic
dysfunction
to
severe,
acute
failure.
The
diagnosis
DILI
primarily
depends
on
thorough
understanding
its
clinical
presentation
and
the
careful
exclusion
alternative
etiologies
injury.
This
chapter
provides
comprehensive
analysis
epidemiology,
pathogenesis,
therapeutic
approaches
DILI,
aiming
deepen
this
complex
condition.
Furthermore,
it
investigates
emerging
role
gut
microbiota
in
pathogenesis
offering
novel
insights
potential
avenues
for
future
interventions.
Language: Английский