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RESULTS                                             prominent preventive effect was observed in the group
                                                              pre-treated with FSME.
          AZA treatment resulted in a significant increase in hepatic
          MDA level concomitant with a significant decline in hepatic   In the present study, serum triglyceride level showed
          GSH content and TAC as compared to control rats [Figure 1].   insignificant change among the different studied groups,
          However, the administration of either CFME or FSME alone   but serum cholesterol level increased significantly in
          revealed insignificant changes in the mentioned parameters   AZA-treated rats as compared with the control group. The
          when compared to control rats except in rats that received   animals those were administrated with CFME or FSME alone
          FSME where a significant increase in hepatic GSH was   showed an insignificant change in serum cholesterol level
          observed. Pre-administration with CFME or FSME significantly   as compared with the control group. The administration
          reversed the elevation in hepatic MDA level and also reversed   of CFME in combination with AZA offered little protection
          the decrease in hepatic GSH content and TAC-induced by AZA   against AZA-induced changes in cholesterol level, whereas
          treatment toward the normal values of the controls.  the administration of FSME to rats succeeded in ameliorating
                                                              significantly the AZA-induced changes in the mentioned
          The selected and specialized serum markers of liver functions   parameter [Figure 4].
          among the different groups are shown in Figures 2 and 3. It
          is clearly indicated that CFME or FSME had no effect on AST,   AZA treatment resulted in a significant decrease in BWG (%),
          ALT, and ALP activities as well as total- and direct-bilirubin   when compared to control rats [Figure 5a]. The administrated
          levels when compared with the control group. The treatment   with CFME produced a non-significant decrease in BWG, but
          of rats with AZA alone resulted in significant increases in   FSME administration caused a significant decrease in BWG
          AST, ALT, and ALP activities, direct-bilirubin levels and a   when compared to control rats. Pre-treatment with CFME
          non-significant increase in total-bilirubin level. However,   before AZA treatment did not ameliorate the decrease in BWG
          the administration of CFME or FSME to rats succeeded   induced by AZA treatment, while as pre-administration with
          significantly in preventing the AZA-induced changes in   FSME before AZA treatment induced a significant increase in
          the above mentioned parameters. In addition, the more   BWG when compared to the AZA-treated group.


















                         a                                     b

















                                             c
          Figure 1: (a) Hepatic malondialdehyde (MDA) level; (b) hepatic reduced glutathione (GSH) level; and (c) total antioxidant capacity (TAC) in rats treated daily for 28
          consecutive days with chamomile fl owers methanolic extract (CFME), fennel seeds methanolic extract (FSME), azathioprine (AZA), CFME + AZA, and FSME + AZA.
          Data represent the mean ± standard error (n = 8). *P ≤ 0.05 compared to normal control rats;  P ≤ 0.05 compared to AZA-treated rats
                                                                     †
          128                                                       Hepatoma Research | Volume 1 | Issue 3 | October 15, 2015
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