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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 />

69

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