Parkinson disease
(PD) is a neurodegenerative disorder of the motor
activity of the brain, regulated by dopaminergic neurons of substantia
nigra, resulting in an increased density of histaminergic fibers.
This study was aimed to evaluate the effects of H1 antagonist’s
ebastine and levocetirizine in PD per se and in combination. Animals
were divided into 9 groups (
n
= 10). Group 1 received
carboxymethyl cellulose CMC (1 mL/kg). Group II was treated with haloperidol
(1 mg/kg) (diseased group). Group III was treated with levodopa/carbidopa
(levo 20 mg/kg). Groups IV and V were treated with ebastine at dose
levels of 2 and 4 mg/kg, respectively. Groups VI and VII were treated
with levocetirizine at dose levels of 0.5 and 1 mg/kg, respectively.
Group VIII was treated with ebastine (4 mg/kg) + levo (20 mg/kg) in
combination. Group IX was treated with levocetirizine (1 mg/kg) +
levo (20 mg/kg). PD was induced with haloperidol (1 mg/kg iv, once
daily for 23 days) for a duration of 30 min. Behavioral tests like
rotarod, block and triple horizontal bars, actophotometer, and open
field were performed. Biochemical markers of oxidative stress, i.e.,
SOD, CAT, GSH, MDA, dopamine, serotonin, and nor-adrenaline and nitrite,
were determined. Histamine, mRNA expression of α-synuclein,
and TNF-α level in the serum and brain of mice were analyzed.
Endogenous biochemical markers were increased except mRNA expression
of α-synuclein, which was reduced. In combination therapy with
the standard drug, ebastine (4 mg/kg) significantly improved the cataleptic
state and dopamine levels, but no significant difference in the renal
and liver functioning tests was observed. This study concluded that
ebastine (4 mg/kg) might work in the treatment of PD as it improves
the cataleptic state in haloperidol-induced catalepsy.