Experimental study on the suppression of sodium nitroprussiate-induced chondrocyte apoptosis by Tougu Xiaotong Capsule (透骨消痛胶囊)-containing serum
Back to article page
OriginalPaper|Updated:2021-08-27
|
Experimental study on the suppression of sodium nitroprussiate-induced chondrocyte apoptosis by Tougu Xiaotong Capsule (透骨消痛胶囊)-containing serum
Experimental study on the suppression of sodium nitroprussiate-induced chondrocyte apoptosis by Tougu Xiaotong Capsule (透骨消痛胶囊)-containing serum
中国结合医学杂志(英文版)2011年17卷第6期 页码:436-443
Affiliations:
1. Academy of Integrative Medicine of Fujian University of Traditional Chinese Medicine,Fuzhou,China
2. Fujian Provincial Key Lab for Integrative Medical Study on Senile Diseases,Fuzhou,China
Author bio:
Funds:
Supported by the National Natural Science Foundation of China (No. 81072826), Major Project Foundation of Fujian Provincial Administration of Science and Technology (No. 2009Y0029), and the Developmental Fund of CHEN Keji Integrative Medicine (No. CKJ2010013)
Li, Xh., Wu, Mx., Ye, Hz. et al. Experimental study on the suppression of sodium nitroprussiate-induced chondrocyte apoptosis by Tougu Xiaotong Capsule (透骨消痛胶囊)-containing serum., Chin. J. Integr. Med. 17, 436–443 (2011). https://doi.org/10.1007/s11655-011-0751-x
Xi-hai Li, Ming-xia Wu, Hong-zhi Ye, et al. Experimental study on the suppression of sodium nitroprussiate-induced chondrocyte apoptosis by Tougu Xiaotong Capsule (透骨消痛胶囊)-containing serum[J]. Chinese Journal of Integrative Medicine, 2011,17(6):436-443.
Li, Xh., Wu, Mx., Ye, Hz. et al. Experimental study on the suppression of sodium nitroprussiate-induced chondrocyte apoptosis by Tougu Xiaotong Capsule (透骨消痛胶囊)-containing serum., Chin. J. Integr. Med. 17, 436–443 (2011). https://doi.org/10.1007/s11655-011-0751-xDOI:
Xi-hai Li, Ming-xia Wu, Hong-zhi Ye, et al. Experimental study on the suppression of sodium nitroprussiate-induced chondrocyte apoptosis by Tougu Xiaotong Capsule (透骨消痛胶囊)-containing serum[J]. Chinese Journal of Integrative Medicine, 2011,17(6):436-443. DOI: 10.1007/s11655-011-0751-x.
Experimental study on the suppression of sodium nitroprussiate-induced chondrocyte apoptosis by Tougu Xiaotong Capsule (透骨消痛胶囊)-containing serum
摘要
To study the mechanism of action of Tougu Xiaotong Capsule (透骨消痛胶囊
TGXTC) ex vivo in suppressing chondrocyte (CD) apoptosis induced by sodium nitroprussiate (SNP). Thirty New Zealand rabbits
2 months old
were randomized by lottery into five groups
six in each: the blank group treated with saline
the positive control group treated with Zhuanggu Guanjie Pill (壮骨关节丸
70 mg/kg)
and the three experimental groups
EGA
EGB
and EGC
treated with low dose (35 mg/kg)
moderate dose (70 mg/kg)
and high dose (140 mg/kg) of TGXTC
respectively. All treatments were administered via gastrogavage twice a day for 3 days. Arterial blood was collected from the abdominal aorta and drug or drug metabolites-containing serum was prepared. CDs obtained from knee joints of 16 four-week-old New Zealand rabbits were cultured to the third passage and confirmed by toluidine blue staining. SNP of various final concentrations (0
0.5
1.0
and 2.0 mmol/L) was used to induce CD apoptosis
and the dosage-effect relationship of SNP in inducing CD apoptosis was determined. Serum samples from the blank
control
and three dosages of TGXTC-treated rabbits were tested in the CD culture in the presence of SNP. Cell apoptosis was determined by Hoechst 33342 staining
viability of CDs was quantified by MTT
CD apoptosis rate was determined by annexin V-FITC/PI staining
levels of p53 and Bcl-2 mRNA expression in CDs were determined with RT-PCR
and contents of caspase-3 and caspase-9 proteins were determined by colorimetry. CD apoptosis was induced by SNP at all concentrations tested and in a dose-dependent manner. The SNP concentration of 1 mmol/L and treatment duration of 24 h appeared to be optimal and were selected for the study. Serum samples from the positive control rabbits and from the two higher doses of TGXTC-treated rabbits showed reduction of SNP-induced CD apoptosis
decrease in p53 mRNA expression
inhibition of catalytic activities of caspase-3 and caspase-9
and increase in Bcl-2 mRNA expression when compared with the serum from the blank group (P<0.05). TGXTC-containing sera antagonized SNP-induced CD apoptosis and the molecular basis for the action was associated with up-regulation of Bcl-2
down-regulation of p53 expression
and inhibition of caspase-3 and caspase-9 catalytic activities.
Abstract
To study the mechanism of action of Tougu Xiaotong Capsule (透骨消痛胶囊
TGXTC) ex vivo in suppressing chondrocyte (CD) apoptosis induced by sodium nitroprussiate (SNP). Thirty New Zealand rabbits
2 months old
were randomized by lottery into five groups
six in each: the blank group treated with saline
the positive control group treated with Zhuanggu Guanjie Pill (壮骨关节丸
70 mg/kg)
and the three experimental groups
EGA
EGB
and EGC
treated with low dose (35 mg/kg)
moderate dose (70 mg/kg)
and high dose (140 mg/kg) of TGXTC
respectively. All treatments were administered via gastrogavage twice a day for 3 days. Arterial blood was collected from the abdominal aorta and drug or drug metabolites-containing serum was prepared. CDs obtained from knee joints of 16 four-week-old New Zealand rabbits were cultured to the third passage and confirmed by toluidine blue staining. SNP of various final concentrations (0
0.5
1.0
and 2.0 mmol/L) was used to induce CD apoptosis
and the dosage-effect relationship of SNP in inducing CD apoptosis was determined. Serum samples from the blank
control
and three dosages of TGXTC-treated rabbits were tested in the CD culture in the presence of SNP. Cell apoptosis was determined by Hoechst 33342 staining
viability of CDs was quantified by MTT
CD apoptosis rate was determined by annexin V-FITC/PI staining
levels of p53 and Bcl-2 mRNA expression in CDs were determined with RT-PCR
and contents of caspase-3 and caspase-9 proteins were determined by colorimetry. CD apoptosis was induced by SNP at all concentrations tested and in a dose-dependent manner. The SNP concentration of 1 mmol/L and treatment duration of 24 h appeared to be optimal and were selected for the study. Serum samples from the positive control rabbits and from the two higher doses of TGXTC-treated rabbits showed reduction of SNP-induced CD apoptosis
decrease in p53 mRNA expression
inhibition of catalytic activities of caspase-3 and caspase-9
and increase in Bcl-2 mRNA expression when compared with the serum from the blank group (P<0.05). TGXTC-containing sera antagonized SNP-induced CD apoptosis and the molecular basis for the action was associated with up-regulation of Bcl-2
down-regulation of p53 expression
and inhibition of caspase-3 and caspase-9 catalytic activities.
Johnson EO, Charchandi A, Babis GC, Soucacos PN. Apoptosis in osteoarthritis: morphology, mechanisms, and potential means for therapeutic intervention. J Surg Orthop Adv 2008;17:147–152.
Saito S, Murakoshi K, Kotake S, Kamatani N, Tomatsu T. Granzyme B induces apoptosis of chondrocytes with natural killer cell-like cytotoxicity in rheumatoid arthritis. J Rheumatol 2008;35:1932–1943.
Dave M, Attur M, Palmer G, Al-Mussawir HE, Kennish L, Patel J, et al. The antioxidant resveratrol protects against chondrocyte apoptosis via effects on mitochondrial polarization and ATP production. Arthritis Rheum 2008;58:2786–2797.
Areshkov PA, Kavsan VM. Chitinase 3-like protein 2 (CHI3L2, YKL-39) activates phosphorylation of extracellular signal-regulated kinases ERK1/ERK2 in human embryonic kidney (HEK293) and human glioblastoma (U87 MG) cells. Tsitol Genet 2010;44:3–9.
Ye HZ, LI XH, Liang WN, Zheng CS, Chen WL, Liu XX. Effects of Tougu Xiaotong Granule (TXG)-containing serum on proliferation of rabbit chondrocytes in vitro. Chin J Clin Pharmacol Ther (Chin) 2009;14:624–628.
Wu ZZ, Liu XX, Li XH. Tougu Xiaotong Granule induces the differentiation of bone marrow mesenchymal stem cells to chondrocytes. J Clin Rehabil Tissue Eng Res (Chin) 2009;13:6456–6460.
Liu XX, Li XH, Zhou JT. Research on mechanism of Tougu Xiaotong Granule in preventing and treating knee osteoarthritis. Chin J Integr Med 2007;27:50–54.
Zheng CS, Xu XJ, Liu XX, Ye HZ. Computational pharmacology of Jingzhi Tougu Xiaotong Granule in preventing and treating osteoarthritis. Acta Physico-Chimica Sin (Chin) 2010;26:775–783.
The Ministry of Science and Technology of the People’s Republic of China. Guidance suggestions for the care and use of laboratory animals. http://www.most.gov.cv/fggw/zfwj/zfwj2006/200609/t20060930_54389.htm.
Huang JH, Huang XH, Chen ZY, Zheng QS, Sun RY. Dose conversion among different animals and healthy volunteers in pharmacological study. Chin J Clin Pharmacol Ther (Chin) 2004;9:1069–1072.
Li XH, Du M, Liu XX, Chen WL, Wu MX, Lin JM, et al. Millimeter wave treatment promotes chondrocyte proliferation by upregulating the expression of cyclin-dependent kinase 2 and cyclin A. Int J Mol Med 2010;26:77–84.
Li XH, Du M, Liu XX, Chen WL, Wu MX, Lin JM, et al. Millimeter wave treatment inhibits NO-induced apoptosis of chondrocytes through the p38 MAPK pathway. Int J Mol Med 2010;25:393–399.
Zheng CS, Ye HZ, Xu XJ, Liu XX. Computational pharmacology study of Tougu Xiaotong Granule in preventing and treating knee osteoarthritis. Chin J Integr Med 2009;15:371–376.
Lin MN, Liu XX. Tougu Xiaotong Decoction for treating 30 cases of osteoarthritis of the knee. Fujian J Tradit Chin Med (Chin) 2005;36:15–16.
Han I, Park HJ, Seong SC, Lee S, Kim IG, Lee MC. Role of transglutaminase 2 in apoptosis induced by hydrogen peroxide in human chondrocytes. J Orthop Res 2011;29:252–257.
Farkas B, Kvell K, Czömpöly T, Illés T, Bárdos T. Increased chondrocyte death after steroid and local anesthetic combination. Clin Orthop Relat Res 2010;468:3112–3120.
Liu JT, Guo X, Ma WJ, Zhang YG, Xu P, Yao JF, et al. Mitochondrial function is altered in articular chondrocytes of an endemic osteoarthritis, Kashin-Beck disease. Osteoarthritis Cartilage 2010;18:1218–1226.
Kim J, Xu M, Xo R, Mates A, Wilson GL, Pearsall AW 4th, et al. Mitochondrial DNA damage is involved in apoptosis caused by pro-inflammatory cytokines in human OA chondrocytes. Osteoarthritis Cartilage 2010;18:424–432.
Wang C, Lau TT, Loh WL, Su K, Wang DA. Cytocompatibility study of a natural biomaterial crosslinker-Genipin with therapeutic model cells. J Biomed Mater Res B Appl Biomater 2011;97:58–65.
Gaber S, Fischerauer EE, Fröhlich E, Janezic G, Amerstorfer F, Weinberg AM. Chondrocyte apoptosis enhanced at the growth plate: a physeal response to a diaphyseal fracture. Cell Tissue Res 2009;335:539–549.
Li XQ, Shao SH, Fu GL, Han XH, Gao H. Study on norcantharidin-induced apoptosis in SMMC-7721 cells through mitochondrial pathways. Chin J Integr Med 2010;16:448–452.
Del Carlo M Jr, Loeser RF. Cell death in osteoarthritis. Curr Rheumatol Rep 2008;10:37–42.
Glucan HBP-A increase type II collagen expression of chondrocytes in vitro and tissue engineered cartilage in vivo
Effect of Ermiao Recipe (二妙方) with medicinal guide Angelicae Pubescentis Radix on promoting the homing of bone marrow stem cells to treat cartilage damage in osteoarthritis rats
Zhuanggu Jianxi Decoction (壮骨健膝方) limits interleukin-1 β-induced degeneration chondrocytes via the caveolin-p38 MAPK signal pathway
Metabolic regulatory and anti-oxidative effects of modified bushen huoxue decoction (补肾活血方) on experimental rabbit model of osteoarthritis
Effects of Baduanjin (八段锦) exercise on knee osteoarthritis: A one-year study
相关作者
暂无数据
相关机构
Institute of Chinese Materia Medica of Shanghai University of Traditional Chinese Medicine
Research Institute of Orthopaedics, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
Wangjing Hospital, China Academy of Chinese Medical Sciences
Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences