III.1.2. Result of the antioxidant potential of our plant
extracts
III.1.2.1. Polyphenol
content of our extracts
The polyphenol content of our extracts is represented on table
XIV below.
Table XIV :
Polyphenols content results
|
FOEF
|
FOHF
|
FOET
|
FOHT
|
Concentration (mg catechin Eq)
|
718.142 #177; 12.910a
|
486.876 #177; 8.606b
|
149.105 #177; 38.730c
|
207.922 #177; 4.303d
|
Table XIV above shows that all extracts had polyphenols with
FOEF having a higher content (718.142 mg catechin Eq). We also note a
significant difference (P<0.05) in polyphenols content for all the
extracts.
III.1.2.2. DPPH (1,
1-Diphenyl-2-Picrilhydrazyl) antiradical activity of extracts
Figure 11 below represent the inhibition percentages obtain
after an evaluation of antiradical activity of the ethanolic and hydroethanolic
fruits and twigs extracts respectively.
Antiradical activity of twigs extracts
Antiradical activity of fruits extracts
Figure 11 :
Antiradical activity of extracts using the DPPH method
Figure 11 above shows that for both plant parts, the
hydroethanolic solvent was the best system with a high antiradical activity
compared to ethanolic solvent system (p<0.05) and
the scavenging activity increases as concentration increases. Moreover the
inhibition profile of the hydroethanolic fruits was the best with an IC 50 of
0.701 mg/ml as compared to the others and this IC 50 was significantly
different (p<0.05) from all the other extracts.
III.1.3. The effect of extracts on starch digestion in vitro.
Figure 12 below represents the variation of the inhibition of
activity of á-amylase (digestive enzyme) activity in the
presence of different concentrations of extracts.
Figure 12 :
Effect of extracts on the inhibition of pancreatic á-amylase
activity
From figure 12 above, we observed that the percentage
inhibition of the alpha amylase activity increased with increase in
concentration for both extracts with that of hydroethanolic fruits being
significantly higher compared to that of hydroethanolic twigs. Also, when the
concept of IC50 values was used, hydroethanolic fruit extract showed the best
result with an IC50 of 0.4727 mg/ml as compared to that of the twigs having an
IC50 of 0.7473mg/ml. á-Amylase inhibitory activity was measured at
various concentrations and the inhibition was observed at all doses (Fig. 12).
When comparing the total water soluble phenolic concentration of hydroethanolic
extracts with the á-amylase inhibitory activity, a correlation was
observed.
III.1.4. Acute toxicity study of the hydroethanolic fruits and
twigs extracts
III.1.4.1. Effect of extracts on the behaviour of experimental
animals
The behavioural reactions of rats under acute toxicity are
represented in table XV.
Table XV: Behaviour of rats during acute
toxicity study (48hours)
Observations
|
Negative control
|
FOHT
|
FOHF
|
General mobility
|
Normal
|
Normal 30min after
|
Normal 4hrs after
|
sleep
|
Normal
|
Normal
|
Normal
|
feeding
|
Normal
|
Normal 1hr after
|
Normal 6hrs after
|
faeces
|
Normal
|
Normal
|
Normal
|
Sensibility to sound
|
Jump immediately
|
Jump immediately
|
Jump immediately
|
death
|
No dead
|
No dead
|
No dead
|
From the above result we observe that these extracts at
5000mg/Kg of BW taken at a single dose do not lead to death. The other
parameters remain comparable to the negative control.
|