Abstract:
The increasing prevalence of asthma in developing countries during the last decade
continues to represent a significant public health problem, causing both economic
and social burdens. It remains an area of considerable unmet medical need which
affects 235–330 million and kills about 300,000 people worldwide. Low and middle
income countries make up more than 80% of the mortality and the prevalence of
Asthma in Kenya is 15.8%. Treatment of asthma is hindered by severe side effects
and high cost of the treatment. Methanol and aqueous extracts of Acacia
xanthophloea, Strychnos henningsii and Microglossa pyrifolia have shown efficacy
on antimicrobial and antioxidant properties but have not been investigated for anti asthmatic activities. This study was aimed at evaluating the anti-asthmatic activities
of extracts of Acacia xanthophloea, Strychnos henningsii and Microglossa pyrifolia
on asthma-induced mice. A total of 81 female Swiss Albino mice grouped into 9
major groups with 9 mice each, aged 8weeks old and weighing 20 +/- 2g, were
asthma-induced by Intraperitoneal injection of 1% Ovalbumin (grade VI; Sigma,
Steinheim, Germany) followed by treatment using methanol and water extracts of A
xanthophloea, S henningsii and M pyrifolia in concentrations of 50, 100 and
200mg/kg body weight except for positive control group of mice which was induced
and not treated. Standard reference drug control group was given 10mg/kg
Prednisolone. After treatment, serum total Immunoglobin E (IgE) levels were
determine using mouse OVA specific IgE Enzyme Linked Immunosorbent Assay
(ELISA) (Legend MaxTM). Bronchoalveolar lavage fluid eosinophils level was also
determined using Diff-Quick staining Technique. Cytotoxicity determination of the
plant extracts was tested on Vero E6 cells using MTT viability assay. Phytochemical
Screening of the plant extracts was done using thin layer chromatography. Data were
analyzed and expressed as Means and Standard Deviation and the parametric data
was statistically analyzed using one way Analysis of Variance (ANOVA) followed
with unpaired student‟s t-test at p-value < 0.001, GraphPad software was used.
Cytotoxicity results were analyzed by Almar blue assay software to determine the
Cytotoxic concentration 50 (CC50). The key results showed that the extracts were
able to reduce the serum total IgE levels and Balf eosinophils level by upto100% in
reference to the positive control. The standard drug Prednisolone also demonstrated
the same effects. Based on this study the extracts tested therefore have the ability to
reduce IgE and eosinophils levels in an asthmatic attack. TLC revealed presence of
Phenols, Alkaloids, and Flavonoids in the methanol and aqueous extracts of the
medicinal plants. These results can be used as a guideline in setting other
experiments using human cells or human subjects since this was a pilot study