Received:20 October 2019,
Published:30 March 2020
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Ayijiamali SHAYITI, Kasimujiang AXIMUJIANG, Chenbo XU, et al. Effect of Compound Huankuile Suspension on ulcerative colitis in rats and the therapeutic mechanism[J]. Journal of Third Military Medical University, 2020, 42(6): 616-623.
Ayijiamali SHAYITI, Kasimujiang AXIMUJIANG, Chenbo XU, et al. Effect of Compound Huankuile Suspension on ulcerative colitis in rats and the therapeutic mechanism[J]. Journal of Third Military Medical University, 2020, 42(6): 616-623. DOI: 10.16016/j.1000-5404.201910144.
Objective
2
To investigate the effect of Huankuile (HKL) suspension
a compound traditional Chinese herbal medicinal preparation
for treating ulcerative colitis (UC) in rats and explore its therapeutic mechanism.
Methods
2
Fifty male Wistar rats were randomized into normal control group
UC model group
HKL suspension intervention group
and 5-amino acid (5-ASA) intervention group. Except for those in the normal control group
all the rats were subjected to colonic enema with 2
4
6-trinitrobenzene sulfonic acid (TNBS) and ethanol to induce UC
followed by drug treatment for 14 d. The colonic injury index (CMDI) and pathological scores of the colon tissues were assessed
and the histopathological changes in the colon was observed with HE staining. The mRNA and protein expression levels of interleukin-6 (IL-6)
IL-17
IL-10
and transforming growth factor-β1 (TGF-β1) in the colon tissues were detected using real-time PCR and ELISA.
Results
2
Compared with those in the normal control group
the rats in the UC model group had markedly higher CMDI and pathological scores in the colon tissues (
P
<
0.05)
which were significantly reduced by intervention with HKL and 5-ASA (
P
<
0.05). The rats with US showed significantly increased expression of IL-6
IL-17
and IL-10 at both mRNA and protein levels in the colon tissue (
P
<
0.05) without significant changes in TGF-β1 mRNA expression but with significantly de
creased TGF-β1 protein expression (
P
<
0.05). Treatment with HKL and 5-ASA obviously lowered the mRNA and protein level of IL-6 and IL-17 and the protein expression of IL-10 (
P
<
0.05) and increased the expression level of TGF-β1 mRNA (
P
<
0.05) in the colon tissue of the rats with UC; but only treatment with HKL resulted in significant changes in the expression levels of IL-10 mRNA and TGF-β1 protein in the rats with UC (
P
<
0.05). HKL and 5-ASA showed no significant differences in their therapeutic effects on UC or in their effects on the expressions of the inflammatory factors (
P
>
0.05).
Conclusion
2
HKL can effectively improve the symptoms and colonic injury in rats with TNBS-induced UC possibly by down-regulating the pro-inflammatory factors IL-6 and IL-17 and up-regulating the anti-inflammatory factor TGF-β1.
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