Study on the effects and mechanism of total glucosides of paeony on enhancing efficacy and reducing toxicity of Tripterygium wilfordii polyglycoside in the treatment of eczema
返回论文页
|更新时间:2023-02-24
|
Study on the effects and mechanism of total glucosides of paeony on enhancing efficacy and reducing toxicity of Tripterygium wilfordii polyglycoside in the treatment of eczema
ZHANG Minghao,WANG Zhen,GAO Yiying,et al.Study on the effects and mechanism of total glucosides of paeony on enhancing efficacy and reducing toxicity of Tripterygium wilfordii polyglycoside in the treatment of eczema[J].ZHONGGUO YAOFANG,2023,34(04):444-449.
ZHANG Minghao,WANG Zhen,GAO Yiying,et al.Study on the effects and mechanism of total glucosides of paeony on enhancing efficacy and reducing toxicity of Tripterygium wilfordii polyglycoside in the treatment of eczema[J].ZHONGGUO YAOFANG,2023,34(04):444-449. DOI: 10.6039/j.issn.1001-0408.2023.04.12.
Study on the effects and mechanism of total glucosides of paeony on enhancing efficacy and reducing toxicity of Tripterygium wilfordii polyglycoside in the treatment of eczema
To investigate the effects of total glucosides of paeony (TGP) on enhancing efficacy and reducing toxicity of
Tripterygium wilfordii
polyglycoside (TWP) in the treatment of eczema.
METHODS
2
Totally 50 SD male rats were collected to establish eczema model by sensitizing with 2,4-dinitrofluorobenzene-acetone olive oil solution (volume ratio was 4∶1) on the abdominal area and provoking on the back and ear. Model rats were randomly divided into model group, loratadine group (0.9 mg/kg), TWP group (9.45 mg/kg), TGP group (162 mg/kg) and compatibility group (TWP 9.45 mg/kg+TGP 162 mg/kg), with 10 rats in each group. Other 10 rats were collected to set as normal group. Three days after the first sensitization, administration groups were given relevant medicine intragastrically, and normal group and model group were given constant volume of 0.1% CMC-Na solution intragastrically, once a day, for consecutive 21 d. Twenty-four hours later after the final administration, the general condition of rats in each group was observed, and the eczema area and severity index (EASI) were scored; ear swelling degree of rats was measured, and the skin histomorphology observation and pathological score were performed; protein expressions of p38 mitogen-activated protein kinase (p38 MAPK), phosphorylated p38 MAPK (p-p38 MAPK) and phosphorylation level of p38 MAPK in rat skin tissue were detected; the levels of inflammatory indexes (interleukin-4, interferon-γ), liver and kidney function indexes [glutamic-pyruvic transaminase (GPT), glutamic-oxaloacetic transaminase (GOT), serum creatinine (SCr) and blood urea nitrogen (BUN)] and oxidant stress indexes [total superoxide dismutase (T-SOD) and malondialdehyde (MDA)] were measured.
RESULTS
2
Compared with normal group, EASI score, ear swelling degree, pathological score, protein expressions of p38 MAPK and p-p38 MAPK, phosphorylation level of p38 MAPK, the levels of inflammatory indexes and BUN were all increased significantly in model group (
P
<0.05). Compared with model group, EASI scores, ear swelling degree, pathological scores, protein expressions of p38 MAPK and p-p38 MAPK, phosphorylation levels of p38 MAPK and levels of inflammatory indexes were all improved significantly in administration groups (
P
<0.05). The levels of GPT, GOT, SCr and BUN were increased significantly in TWP group, while the serum levels of GOT and SCr in TGP group and serum level of SCr in loratadine group were all decreased significantly (
P
<0.05). The levels of T-SOD in liver and kidney tissue were all decreased significantly in TWP group and compatibility group, while the levels of MDA were increased significantly (
P
<0.05). The compatibility group showed more obvious effect in improving the ear swelling degree, pathological score, p38 MAPK expression and its phosphorylation level and levels of inflammatory indexes, and could reverse the abnormality of liver and kidney indexes caused by TWP (
P
<0.05).
CONCLUSIONS
2
The combination of TGP and TWP has the effects of anti-inflammatory, synergistic and hepatorenal detoxification in eczema model rats. Its mechanism may be associated with down-regulating the expression of serum proinflammatory indexes and inhibiting the activation of p38 MAPK pathway.
关键词
白芍总苷雷公藤多苷湿疹增效减毒p38丝裂原激活的蛋白激酶通路大鼠
Keywords
Tripterygium wilfordii polyglycosideeczemaenhancing efficacy and reducing toxicityp38 MAPK pathwayrat
FUKUDA S,MIDORO K,KAMEI T,et al. Inhibition of allergic dermal inflammation by the novel imidazopyridazine derivative TAK-427 in a Guinea pig experimental model of eczema[J]. J Pharmacol Exp Ther,2002,303(3):1283-1290.
KUNNAS T,NIKKARI S T. Association of the collagen type Ⅳ alpha 1 chain gene rs3783107 GG genotype with hypertension,asthma,and eczema:the Tampere adult population cardiovascular risk study[J]. Genet Test Mol Biomarkers,2020,24(1):6-9.
MAGRO C,CROWSON A N,FRANKS L,et al. The histologic and molecular correlates of COVID-19 vaccine-induced changes in the skin[J]. Clin Dermatol,2021,39(6):966-984.
MALLABO M R B,CORPUZ M J A T,SALONGA R B,et al. Inhibitory effect of sulfated polysaccharide from Codium edule P.C. silva against 2,4-dinitrofluorobenzene(DNFB)-induced allergic contact dermatitis on female BALB/c mice[J]. Adv Pharm Bull,2022,12(2):410-418.
MANRESA M C. Animal models of contact dermatitis:2,4-dinitrofluorobenzene-induced contact hypersensitivity[J]. Methods Mol Biol,2021,2223:87-100.
NIE N N,BAI C,SONG S N,et al. Bifidobacterium plays a protective role in TNF-α-induced inflammatory response in Caco-2 cell through NF-κB and p38MAPK pathways[J]. Mol Cell Biochem,2020,464(1/2):83-91.
LIU D L,WANG K,SU D Y,et al. TMEM16A regulates pulmonary arterial smooth muscle cells proliferation via p38MAPK/ERK pathway in high pulmonary blood flow-induced pulmonary arterial hypertension[J]. J Vasc Res,2020,58(1):27-37.
ARYANI H P,SANTOSO B,PURWANTO B,et al. The effect of low-calorie high protein diet on insulin,TNF-α and P38MAPK levels in insulin-resistant PCOS mice models[J]. Syst Rev Pharm,2020,11:597-605.