Clinical study on Ganbi decoction in treating antituberculotic agent-caused liver injury

Xian Yin-sheng; Wang Zuo-ren; Gong Xian-feng; Huang Bao-zhong

doi:10.1007/BF02857355

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Clinical study on Ganbi decoction in treating antituberculotic agent-caused liver injury

OriginalPaper | Updated：2021-08-27

- Clinical study on Ganbi decoction in treating antituberculotic agent-caused liver injury
- Clinical study on Ganbi decoction in treating antituberculotic agent-caused liver injury
- 中国结合医学杂志（英文版） 2006年12卷第2期页码：107-111
- Affiliations：
  
  1. Department of Surgery on Liver and Gallbladder, The First Hospital of Xi’an Jiaotong University,Xi’an
  2. Xi’an Tuberculosis Hospital,China
  3. Xi’an Hospital of Traditional Chinese Medicine,China
- Author bio：
- Funds：
- DOI：10.1007/BF02857355
  中图分类号：
- 纸质出版日期：2006，
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Yin-sheng, X., Zuo-ren, W., Xian-feng, G. et al. Clinical study on Ganbi decoction in treating antituberculotic agent-caused liver injury., Chin. J. Integr. Med. 12, 107–111 (2006). https://doi.org/10.1007/BF02857355

Xian Yin-sheng, Wang Zuo-ren, Gong Xian-feng, et al. Clinical study on Ganbi decoction in treating antituberculotic agent-caused liver injury[J]. Chinese Journal of Integrative Medicine, 2006,12(2):107-111.
Yin-sheng, X., Zuo-ren, W., Xian-feng, G. et al. Clinical study on Ganbi decoction in treating antituberculotic agent-caused liver injury., Chin. J. Integr. Med. 12, 107–111 (2006). https://doi.org/10.1007/BF02857355 DOI：

Xian Yin-sheng, Wang Zuo-ren, Gong Xian-feng, et al. Clinical study on Ganbi decoction in treating antituberculotic agent-caused liver injury[J]. Chinese Journal of Integrative Medicine, 2006,12(2):107-111. DOI： 10.1007/BF02857355.

摘要

Objective: To study the effect and mechanism of Ganbi decoction (GBD) in treating patients with antituberculotic agent caused liver injury (ATB-LI).Methods: One hundred and twenty-eight patients with ATB-LI were randomly assigned to the treated group (n = 66) and the control group (n = 62) with the envelop method. Meanwhile

60 healthy persons were selected as the healthy control group. The treated group was treated by GBD one dose every day with the constituents modified depending on patients’ symptoms

and the control group was treated with glucuronolactone tablets and inosine injection. One week was taken as one treatment course. The changes of clinical syndromes

physical signs

T-lymphycyte sub-groups and serum level of nitric oxide (NO) were observed before and after treatment and the recovery time of liver function was recorded. The outcome was compared with that in the healthy control group.Results: In the treated group

28 patients (42.4%) were cured

30 (45.5%) improved and 8 (12.1%) ineffectively cured

the total effective rate being 87.9% (58/66). In the control group

17 patients (27.4%) were cured

24 (38.7%) improved

and 21 (33.9%) ineffectively cured

the total effective rate being 66. 1 % (41/62). The total effective rate in the treated group was significantly higher than that in the control group (P< 0. 05). Liver function was improved in both groups

recovery time in the treated group was 12.0 ±7.0 days

which was significantly shorter than that in the control group (16.0 ±8.0 days)

showing significant difference between the two groups (P< 0.05). The levels of CD3

CD4 and CD8 were significantly higher and level of NO significantly lower in the two groups of patients than those in the healthy control group (P< 0.05)

but these parameters were improved more significantly in the treated group after treatment

when compared with those before treatment or with those in the control group

all showing significant difference (P< 0.05).Conclusion: GBD could prevent ATB-LI

and its mechanism could be by way of reducing NO production induced by endotoxin of macrophage and stimulating the proliferation of T-lymphycyte to elevate immunity.

Abstract

60 healthy persons were selected as the healthy control group. The treated group was treated by GBD one dose every day with the constituents modified depending on patients’ symptoms

and the control group was treated with glucuronolactone tablets and inosine injection. One week was taken as one treatment course. The changes of clinical syndromes

physical signs

28 patients (42.4%) were cured

30 (45.5%) improved and 8 (12.1%) ineffectively cured

the total effective rate being 87.9% (58/66). In the control group

17 patients (27.4%) were cured

24 (38.7%) improved

and 21 (33.9%) ineffectively cured

recovery time in the treated group was 12.0 ±7.0 days

which was significantly shorter than that in the control group (16.0 ±8.0 days)

showing significant difference between the two groups (P< 0.05). The levels of CD3

CD4 and CD8 were significantly higher and level of NO significantly lower in the two groups of patients than those in the healthy control group (P< 0.05)

but these parameters were improved more significantly in the treated group after treatment

when compared with those before treatment or with those in the control group

all showing significant difference (P< 0.05).Conclusion: GBD could prevent ATB-LI

and its mechanism could be by way of reducing NO production induced by endotoxin of macrophage and stimulating the proliferation of T-lymphycyte to elevate immunity.

关键词

Ganbi Decoctionanti-tuberculosis agentliver injury

Keywords

Ganbi Decoctionanti-tuberculosis agentliver injury

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