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Ann Biol Sci, 2017

ISSN: 2348-1927

August 23-24, 2017 | Toronto, Canada

Annual Conference on

MICROBIAL PATHOGENESIS, INFECTIOUS DISEASE,

ANTIMICROBIALS AND DRUG RESISTANCE

Background & Objective:

The side effects of NSAIDS drugs

have caused increasing interest of scientists in herbal

medicines as alternative treatment. In this study, the anti-

inflammatoryeffect of seedand fruit of datepalmhydroalcolic

extracts, due to having antioxidants, was studied.

Materials & Methods:

In this study, the extracts of date

palm seed and fruit were prepared by maceration method

in 70% alcohol. Eighty (80) male rats Wistar, divided into

10 groups of eight (8) in each, 4 groups received different

doses (100, 200, 400 and 600 mg/kg) of seed extract and

4 other groups different doses (100, 200, 400 and 600 mg/

kg) of fruits extract of the palm and the positive control

aspirin (300 mg/kg) and the negative control group saline

(5 ml/kg) via injection intraperitoneally. Half an hour later

all animals received 100 µl of 1% carrageenan into the rats’

hind paw subcutaneous. The changes in rats paw edema was

measured by plethysmometer every hour for five hours.

Results:

The effect of all of the doses of date palm seed

extract on edema were less than Aspirin (P<0.05). But

there was no significant difference between the group that

received 400 and 600 mg/kg date palm fruit extract when

compared with aspirin group. The dose 400 mg/kg of fruit

extract showed the most anti-inflammatory effect and it was

assigned as the best dose.

Conclusion:

It is likely that with further studies on different

model of animals and also on human model the palm fruit

extract could be used for pain treatment.

e

:

siavash.farma@gmail.com

The preventive effect of date palm (

Phoenix dactylifera

) seed and fruit hydroalcoholic extracts on

Carrageenan-induced inflammation in male rat’s hind paw

Ardeshir Arzi, Siavash Azarbani, Hanieh Zarringhalam, Zahra Nazari

and

Mohsen Rezaei

Jondishapour University of Medical Sciense, Iran

Arch Clin Microbiol, 8:5

DOI: 10.4172/1989-8436-C1-003