Available online at www.pharmresfoundation.com ISSN: 2229-3787 ...
Available online at www.pharmresfoundation.com ISSN: 2229-3787 ...
Available online at www.pharmresfoundation.com ISSN: 2229-3787 ...
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<strong>Available</strong> <strong>online</strong> <strong>at</strong> <strong>www</strong>.pharmresfound<strong>at</strong>ion.<strong>com</strong> <strong>ISSN</strong>: <strong>2229</strong>-<strong>3787</strong><br />
Table 1: Hep<strong>at</strong>oprotective Activity of C. inerme extracts on acetaminophen-induced Hep<strong>at</strong>otoxicity in mice.<br />
Serum biochemical parameter<br />
Groups Tre<strong>at</strong>ment<br />
AST<br />
ALT<br />
ALP Total bilirubin<br />
IU/L<br />
IU/L<br />
IU/L<br />
mg/dl<br />
Group 1 1 % Gum Acacia 49.50±1.36 65.33±1.40 83.42±1.75 2.23±0.08<br />
Group 2 Acetaminophen<br />
( 250 mg/kg) i.p.<br />
Group 3 Acetaminophen 250 mg/kg<br />
i.p. + Silymarin (50 mg/kg)<br />
a, b<br />
62.67±1.03<br />
a, b<br />
70.25±1.87<br />
a, b<br />
113.17±1.30<br />
a, b, c<br />
2.72±0.12<br />
Group 4 Acetaminophen 250 mg/kg<br />
i.p. CIME (200 mg/kg)<br />
a, b<br />
93.00±1.74<br />
a, b<br />
193.75±1.71<br />
a, b<br />
401.50±1.33<br />
a, b, c<br />
0.28±0.024<br />
Group 5 Acetaminophen 250 mg/kg<br />
i.p. + CIME (300 mg/kg)<br />
a, b<br />
78.25±1.40<br />
a, b<br />
151.50±1.60<br />
a, b<br />
367.25±2.04<br />
a, b, c<br />
0.25±0.019<br />
Group 6 Acetaminophen 250 mg/kg<br />
i.p. + CIPE (200 mg/kg)<br />
a, b<br />
110.75±1.75<br />
a, b<br />
196.25±1.66<br />
a, b<br />
486.75±1.02<br />
a, b, c<br />
0.29±0.017<br />
Group 7 Acetaminophen 250 mg/kg<br />
i.p. + CIPE (300 mg/kg)<br />
a, b<br />
76.75±1.17<br />
a, b<br />
179.50±1.90<br />
a, b<br />
397.50±2.02<br />
a, b, c<br />
0.26±0.019<br />
a b c<br />
P < 0.001, P < 0.01 and P < 0.05.<br />
All the values are expressed as Mean ± SEM.; n =6. The d<strong>at</strong>a was analyzed by evalu<strong>at</strong>ed by One-way analysis of variance<br />
(ANOVA) followed by Dunnett’s t-test, Group-2 <strong>com</strong>pared with normal group-1 with a P < 0.001. Experimental groups from-3 to<br />
7 <strong>com</strong>pared with group-2 with b P < 0.01 and c P < 0.05.<br />
158.50±1.33 a<br />
The liver sections of the mice tre<strong>at</strong>ed with<br />
CIME (200 and 300 mg/kg) of groups 4 and 5 showed<br />
signs of protection as was evident by the absence of<br />
necrosis and vacuoles (Fig. 4 and 5) while the liver<br />
sections of the mice tre<strong>at</strong>ed with CIPE (200 and 300<br />
mg/kg) of groups 6 and 7 showed reduction in f<strong>at</strong>ty<br />
degener<strong>at</strong>ion and absence of necrosis (Fig. 6 and 7).<br />
Fig. 1: Histop<strong>at</strong>hology of liver of Neg<strong>at</strong>ive control<br />
group. T.S. of liver revealed normochrom<strong>at</strong>ic<br />
hep<strong>at</strong>ocytes (H), occasionally apoptosis, cart wheel<br />
nucleus (CWN) and lipid vacuoles (CV). A good mitotic<br />
index has been observed. H and E, 100x.<br />
129.42±1.76 a<br />
257.83±1.27 a<br />
4.02±0.20 a<br />
Fig. 2: Histop<strong>at</strong>hology of liver of Positive control group.<br />
T.S. of liver revealed hyper chrom<strong>at</strong>ic and highly<br />
damaged hep<strong>at</strong>ocytes (H). Large numbers of lipid<br />
vacuoles (LV) have been observed which propelled<br />
nucleus to the periphery of the cell. Frequent apoptosis<br />
(Apop) and necrosis (CWN) with poor mitotic index<br />
have been observed. H and E, 100x.<br />
DISCUSSION<br />
In acute toxicity study, oral administr<strong>at</strong>ion of<br />
both CIME and CIPE did not produce any mortality in<br />
mice up to a dose level of 3 g/kg body weight. This<br />
may be due to broad non-toxic range of the plant,<br />
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