Modulation of Kupffer cell activity by Tinospora cordifolia in liver damage.

Kupffer cells are major determinants of outcome of liver injury. Their activity was therefore studied in a model of chronic liver disease. The effect of Tinospora cordifolia, an indigenous agent with proven hepatoprotective activity, was evaluated on Kupffer cell function, using carbon clearance tes...

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Main Authors: Nagarkatti D, Rege N, Desai N, Dahanukar S
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 1994-04-01
Series:Journal of Postgraduate Medicine
Subjects:
Online Access:http://www.jpgmonline.com/article.asp?issn=0022-3859;year=1994;volume=40;issue=2;spage=65;epage=7;aulast=Nagarkatti
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spelling doaj-84783a9d55fd45e1ac6c5cc5e7ed6a8c2020-11-25T01:46:24ZengWolters Kluwer Medknow PublicationsJournal of Postgraduate Medicine0022-38590972-28231994-04-01402657Modulation of Kupffer cell activity by Tinospora cordifolia in liver damage.Nagarkatti DRege NDesai NDahanukar SKupffer cells are major determinants of outcome of liver injury. Their activity was therefore studied in a model of chronic liver disease. The effect of Tinospora cordifolia, an indigenous agent with proven hepatoprotective activity, was evaluated on Kupffer cell function, using carbon clearance test as a parameter. Rats were divided into two major groups. In Gp I which served as normal control t1/2 of carbon was 9.48 +/- 4.14 min. GpII received horse-serum in a dose of 0.5 ml/100 gm b.w. i.p. for a period of 12 weeks and was divided into three sub-groups. In Gp IIA at the end of 12 weeks half-life of carbon was found to be significantly increased to 19.86 +/- 7.95 min (p < 0.01). Indicating suppressed Kupffer cell function in chronic liver damage. In Gp IIB treated with vehicle for 4 more weeks there was significant prolongation of half-life to 38.32 +/- 10.61 min (p < 0.01), indicating perpetuation of damage in absence of damaging agent. Whereas in Gp IIc, treated with Tinospora cordifolia t 1/2 was decreased to 14.24 7.74 min (p < .01), as compared to vehicle control indicating a significant improvement in Kupffer cell function and a trend towards normalization.http://www.jpgmonline.com/article.asp?issn=0022-3859;year=1994;volume=40;issue=2;spage=65;epage=7;aulast=NagarkattiAnalysis of VarianceAnimalCarbonpharmacokineticsDisease ModelsAnimalFemaleKupffer CellsphysiologyLiver FailuremetabolismphysiopathologytherapyMaleMetabolic Clearance RatePlantsMedicinalRats
collection DOAJ
language English
format Article
sources DOAJ
author Nagarkatti D
Rege N
Desai N
Dahanukar S
spellingShingle Nagarkatti D
Rege N
Desai N
Dahanukar S
Modulation of Kupffer cell activity by Tinospora cordifolia in liver damage.
Journal of Postgraduate Medicine
Analysis of Variance
Animal
Carbon
pharmacokinetics
Disease Models
Animal
Female
Kupffer Cells
physiology
Liver Failure
metabolism
physiopathology
therapy
Male
Metabolic Clearance Rate
Plants
Medicinal
Rats
author_facet Nagarkatti D
Rege N
Desai N
Dahanukar S
author_sort Nagarkatti D
title Modulation of Kupffer cell activity by Tinospora cordifolia in liver damage.
title_short Modulation of Kupffer cell activity by Tinospora cordifolia in liver damage.
title_full Modulation of Kupffer cell activity by Tinospora cordifolia in liver damage.
title_fullStr Modulation of Kupffer cell activity by Tinospora cordifolia in liver damage.
title_full_unstemmed Modulation of Kupffer cell activity by Tinospora cordifolia in liver damage.
title_sort modulation of kupffer cell activity by tinospora cordifolia in liver damage.
publisher Wolters Kluwer Medknow Publications
series Journal of Postgraduate Medicine
issn 0022-3859
0972-2823
publishDate 1994-04-01
description Kupffer cells are major determinants of outcome of liver injury. Their activity was therefore studied in a model of chronic liver disease. The effect of Tinospora cordifolia, an indigenous agent with proven hepatoprotective activity, was evaluated on Kupffer cell function, using carbon clearance test as a parameter. Rats were divided into two major groups. In Gp I which served as normal control t1/2 of carbon was 9.48 +/- 4.14 min. GpII received horse-serum in a dose of 0.5 ml/100 gm b.w. i.p. for a period of 12 weeks and was divided into three sub-groups. In Gp IIA at the end of 12 weeks half-life of carbon was found to be significantly increased to 19.86 +/- 7.95 min (p < 0.01). Indicating suppressed Kupffer cell function in chronic liver damage. In Gp IIB treated with vehicle for 4 more weeks there was significant prolongation of half-life to 38.32 +/- 10.61 min (p < 0.01), indicating perpetuation of damage in absence of damaging agent. Whereas in Gp IIc, treated with Tinospora cordifolia t 1/2 was decreased to 14.24 7.74 min (p < .01), as compared to vehicle control indicating a significant improvement in Kupffer cell function and a trend towards normalization.
topic Analysis of Variance
Animal
Carbon
pharmacokinetics
Disease Models
Animal
Female
Kupffer Cells
physiology
Liver Failure
metabolism
physiopathology
therapy
Male
Metabolic Clearance Rate
Plants
Medicinal
Rats
url http://www.jpgmonline.com/article.asp?issn=0022-3859;year=1994;volume=40;issue=2;spage=65;epage=7;aulast=Nagarkatti
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