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Rosa moschata ameliorates haloperidol-induced Parkinson's disease via reduction of neurodegeneration and oxidative stress
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Objective:
To investigate the effect of
Rosa moschata
(
R. moschata
) extract on haloperidol-induced Parkinson’s disease (PD) in rats.
Methods:
Haloperidol (1 mg/kg) was given to rats intraperitoneally for 3 weeks for induction of PD.
R. moschata
extract (150, 300 and 600 mg/kg) was administered orally for 21 days. The neuroprotective role of
R. moschata
leaf extract in PD was explored by performing neurobehavioral tests and RT-PCR analysis and measuring neurotransmitters and oxidative stress biomarkers.
Results:
An improvement in motor functions and muscle strength was observed in PD rats treated with
R. moschata
extract. The levels of dopamine, serotonin, noradrenaline, superoxide dismutase, catalase, glutathione, and superoxide dismutase were significantly increased (
P
< 0.001), whereas acetylcholinesterase and malondialdehyde levels were markedly decreased by treatment with
R. moschata
extract (
P
< 0.001). The extract also markedly downregulated the mRNA expressions of
IL-1β
,
α-synuclein
,
IL-1α
, and
TNF-α
in brain tissue. Moreover, histopathological analysis indicated that neurofibrillary tangles and plaques were noticeably decreased in a dose-dependent manner in PD rats treated with
R. moschata
extract.
Conclusions:
R. moschata
extract alleviates haloperidol-induced PD in rats by reducing oxidative stress and neurodegeneration. It may be used for management and treatment of PD. However, additional studies are required to confirm its efficacy and molecular mechanisms.
Title: Rosa moschata ameliorates haloperidol-induced Parkinson's disease via reduction of neurodegeneration and oxidative stress
Description:
Objective:
To investigate the effect of
Rosa moschata
(
R.
moschata
) extract on haloperidol-induced Parkinson’s disease (PD) in rats.
Methods:
Haloperidol (1 mg/kg) was given to rats intraperitoneally for 3 weeks for induction of PD.
R.
moschata
extract (150, 300 and 600 mg/kg) was administered orally for 21 days.
The neuroprotective role of
R.
moschata
leaf extract in PD was explored by performing neurobehavioral tests and RT-PCR analysis and measuring neurotransmitters and oxidative stress biomarkers.
Results:
An improvement in motor functions and muscle strength was observed in PD rats treated with
R.
moschata
extract.
The levels of dopamine, serotonin, noradrenaline, superoxide dismutase, catalase, glutathione, and superoxide dismutase were significantly increased (
P
< 0.
001), whereas acetylcholinesterase and malondialdehyde levels were markedly decreased by treatment with
R.
moschata
extract (
P
< 0.
001).
The extract also markedly downregulated the mRNA expressions of
IL-1β
,
α-synuclein
,
IL-1α
, and
TNF-α
in brain tissue.
Moreover, histopathological analysis indicated that neurofibrillary tangles and plaques were noticeably decreased in a dose-dependent manner in PD rats treated with
R.
moschata
extract.
Conclusions:
R.
moschata
extract alleviates haloperidol-induced PD in rats by reducing oxidative stress and neurodegeneration.
It may be used for management and treatment of PD.
However, additional studies are required to confirm its efficacy and molecular mechanisms.
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