Key result
Baicalin treatment in rats with acute pancreatitis significantly decreased NF-kappaB activation (P<.05), TNF-alpha expression (P<.01), and pancreatic pathological damage (P<.01).
p-value: p=< .01
Baicalin attenuates experimental pancreatitis; hypothesis-generating, with translation to human disease remaining untested.
Forty Wistar rats were divided into 5 groups, including the control group, the acute pancreatitis group (AP group, induced by intraperitoneal injections of caerulein), and the AP group treated with baicalin, the AP group treated with LPS, and the AP group treated with LPS and baicalin. Pathological damage of pancreatic tissue was scored with hematoxylin and eosin (HE) staining. The mRNA expression of TNF-alpha was measured with semiquantitative RT-PCR, and activation of NF-kappaB was detected with flow cytometry assay. It was shown in the results that the expression of TNF-alpha mRNA, activation of NF-kappaB, and pathological score of AP group were all obviously higher than those of control group (P < .01). In AP group treated with LPS, further rise of these values were observed (P < .01). In the AP group treated with baicalin, activation of NF-kappaB decreased (P < .05), and expression of TNF-alpha mRNA also obviously decreased (P < .01), while pancreatic pathological damage was alleviated at the same time (P < .01); similar results were observed in AP group treated with LPS and baicalin (P < .01), which indicated that baicalin might be applied to inhibit NF-kappaB activating and TNF-alpha expressing so as to treat AP.
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Xue et al. (2006) studied Caerulein-induced acute pancreatitis (n=40). Baicalin vs. Control group, AP group, and AP + LPS group was evaluated on Expression of TNF-alpha mRNA, activation of NF-kappaB, and pathological score (p=< .01). Baicalin treatment in rats with acute pancreatitis significantly decreased NF-kappaB activation (P<.05), TNF-alpha expression (P<.01), and pancreatic pathological damage (P<.01).
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