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The expression of glycogen synthase in the small intestine of untreated STZ-induced diabetic rats was significantly (p<0.05) decreased by comparison with those of the non-diabetic control rats after the 5-week experimental period. Interestingly, treatment of STZ-induced diabetic rats with OA and MA significantly (p<0.05) increased the expression of glycogen synthase in the small intestine. Similarly, rats treated with the standard anti-diabetic drugs, metformin and insulin showed significant (p<0.05) increases in the intestinal expression of glycogen synthase after the 5-week period (see Figure 24).

85

0 1 2 3 4

  

ND DC OA MA MET INS

D e n si ty G ly co g e n s y n th a se/ -a c ti n

Figure 24. Comparison of the effects of OA and MA administered in STZ-diabetic rats twice every third day for 5 weeks on small intestine glycogen synthase expression with untreated STZ- diabetic rats and those treated with the standard drugs metformin and insulin. Values are presented as means, and vertical bars indicate SEM of means (n = 6 in each group).♦=p<0.05 by comparison to the non-diabetic control.  =p<0.05 by comparison to the STZ-induced diabetic control.

86 3.9.2 α-amylase and α-glucosidase

The small intestine α-amylase and α-glucosidase expression of untreated STZ-induced diabetic rats were significantly (p<0.05) increased by comparison with those of the non-diabetic control rats after the 5-week experimental period. However, treatment of STZ-induced diabetic rats with OA and MA significantly (p<0.05) decreased the intestinal expression these carbohydrate hydrolyzing enzymes. STZ-diabetic rats treated with standard drugs metformin and insulin showed a similar response pattern of results (see Figure 25 and Figure 26).

87

ND DC OA MA MET INS

0 1 2 3

D en si ty ( -a m y la se/ -a c ti n )

Figure 25. Comparison of the effects of OA and MA administered in STZ-diabetic rats twice every third day for 5 weeks on small intestine α-amylase expression with untreated STZ-diabetic rats and those treated with the standard drugs metformin and insulin. Values are presented as means, and vertical bars indicate SEM of means (n = 6 in each group).♦=p<0.05 by comparison to the non-diabetic control.  =p<0.05 by comparison to the STZ-induced diabetic control.

88

ND DC OA MA MET INS

0 1 2 3

D en si ty ( -g lu co si d a se / -a ct in )

Figure 26. Comparison of the effects of OA and MA administered in STZ-diabetic rats twice every third day for 5 weeks on small intestine α-glucosidase expression with untreated STZ- diabetic rats and those treated with the standard drugs metformin and insulin. Values are presented as means, and vertical bars indicate SEM of means (n = 6 in each group).♦=p<0.05 by comparison to the non-diabetic control.  =p<0.05 by comparison to the STZ-induced diabetic control.

89 3.9.3 SGLT1 and GLUT2

The small intestine expression of SGLT1 and GLUT2 in STZ-induced diabetic rats were significantly (p<0.05) increased by comparison with those of the non-diabetic rats after the 5- week experimental period. On the other hand, treatment of STZ-induced diabetic rats with OA and MA significantly (p<0.05) decreased the intestinal expressions of SGLT1 and GLUT2. STZ- diabetic rats treated with standard drugs metformin and insulin showed a similar response pattern of results (see Figure 27 and Figure 28).

90

ND DC OA MA MET INS

0 2 4 6 8

 

Den si ty ( S G L T1 / -a ct in )

Figure 27. Comparison of the effects of OA and MA administered in STZ-diabetic rats twice every third day for 5 weeks on small intestine SGLT1 expression with untreated STZ-diabetic rats and those treated with the standard drugs metformin and insulin. Values are presented as means, and vertical bars indicate SEM of means (n = 6 in each group).♦=p<0.05 by comparison to the non-diabetic control.  =p<0.05 by comparison to the STZ-induced diabetic control.

91

ND DC OA MA MET INS

0.0 0.5 1.0 1.5 2.0 2.5

  

De n si ty ( G LU T 2 / -a c ti n )

Figure 28. Comparison of the effects of OA and MA administered in STZ-diabetic rats twice every third day for 5 weeks on small intestine GLUT2 expression with untreated STZ-diabetic rats and those treated with the standard drugs metformin and insulin. Values are presented as means, and vertical bars indicate SEM of means (n = 6 in each group).♦=p<0.05 by comparison to the non-diabetic control.  =p<0.05 by comparison to the STZ-induced diabetic control.

92 3.9.4 Ghrelin

The expression of ghrelin in the gastric fundus, small and large intestine of STZ-induced diabetic rats was significantly (p<0.05) increased by comparison with those of the non-diabetic rats after the 5-week experimental period. On the other hand, treatment of STZ-induced diabetic rats with OA and MA significantly (p<0.05) decreased the expression of ghrelin in the gastric fundus as well as in the small and large intestine. Additionally, STZ-diabetic rats treated with standard drugs metformin and insulin showed a similar response pattern of results (see Figure 29, Figure 30 and Figure 31).

93

0 4 8 12

  

ND DC OA MA MET INS

D en si ty ( G h rel in / -a ct in )

Figure 29. Comparison of the effects of OA and MA administered in STZ-diabetic rats twice every third day for 5 weeks on gastric fundus ghrelin expression with untreated STZ-diabetic rats and those treated with the standard drugs metformin and insulin. Values are presented as means, and vertical bars indicate SEM of means (n = 6 in each group).♦=p<0.05 by comparison to the non-diabetic control.  =p<0.05 by comparison to the STZ-induced diabetic control.

Ghrelin