GTPCH is not a rate-limiting factor for hemorrhagic shock-induced hepatic nitric oxide biosynthesis

Ching Rong Cheng, Chun Jen Huang, Yen Ta Lu, Yung Wei Hsu, Peishan Tsai, Nuan Yen Su, Jeffrey W. Skimming

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Background: Hemorrhagic shock upregulates inducible nitric oxide (NO) synthase (iNOS) expression and the resultant NO overproduction. Liver is one of the major organs that is responsible for increased NO production after trauma-hemorrhage and resuscitation. Guanosine triphosphate cyclohydrolase I (GTPCH) is the rate-limiting enzyme for the synthesis of tetrahydrobiopterin (BH4), a necessary co-factor for iNOS activity. Very little is known about the effects of hemorrhagic shock on hepatic GTPCH expression. Methods: Fifteen male Sprague-Dawley rats were randomly assigned to one of three groups, i.e. a sham instrumented (Sham) group, a sustained hemorrhagic shock (HS) group, and a hemorrhagic shock with resuscitation (HS/RES) group (n = 5 in each group). Controlled hemorrhagic shock was induced and the mean arterial pressure (MAP) was kept between 40-45 mmHg for sixty minutes in both HS and HS/RES groups. Then resuscitation with infusion of shed autologous blood and normal saline was performed in HS/RES group. Microdialysis probes were put in the liver and the right atrium for collection of serial samples. NO concentrations in dialysate samples were measured using chemiluminescence. Hepatic iNOS and GTPCH mRNA concentrations were analyzed using semi-quantitative reverse transcription and polymerase chain reaction (RT-PCR). Results: Hemorrhagic shock induced both the hepatic and circulating NO biosynthesis as well as hepatic iNOS mRNA expression. Resuscitation with shed blood/normal saline normalized this upregulation. However, no difference was found in mean hepatic GTPCH mRNA concentrations between groups in this experiment. Conclusions: We provide the evidence that hemorrhagic shock-induced NO biosynthesis involves upregulation of iNOS transcription in liver tissue and GTPCH transcription is unaffected by either hemorrhagic shock or resuscitation. Furthermore, microdialysis is an ideal technique for serial sampling and that events can be followed.

Original languageEnglish
Pages (from-to)109-116
Number of pages8
JournalActa Anaesthesiologica Sinica
Volume40
Issue number3
Publication statusPublished - Sep 2002
Externally publishedYes

Fingerprint

Hemorrhagic Shock
Guanosine Triphosphate
Nitric Oxide
Liver
Resuscitation
Up-Regulation
Microdialysis
Messenger RNA
Dialysis Solutions
Nitric Oxide Synthase Type II
Luminescence
Heart Atria
Reverse Transcription
Sprague Dawley Rats
Arterial Pressure
Hemorrhage

Keywords

  • GTP cyclohydrolase
  • Microdialysis
  • Nitric-oxide synthase
  • Rats
  • Shock, hemorrhagic

ASJC Scopus subject areas

  • Anesthesiology and Pain Medicine

Cite this

Cheng, C. R., Huang, C. J., Lu, Y. T., Hsu, Y. W., Tsai, P., Su, N. Y., & Skimming, J. W. (2002). GTPCH is not a rate-limiting factor for hemorrhagic shock-induced hepatic nitric oxide biosynthesis. Acta Anaesthesiologica Sinica, 40(3), 109-116.

GTPCH is not a rate-limiting factor for hemorrhagic shock-induced hepatic nitric oxide biosynthesis. / Cheng, Ching Rong; Huang, Chun Jen; Lu, Yen Ta; Hsu, Yung Wei; Tsai, Peishan; Su, Nuan Yen; Skimming, Jeffrey W.

In: Acta Anaesthesiologica Sinica, Vol. 40, No. 3, 09.2002, p. 109-116.

Research output: Contribution to journalArticle

Cheng, CR, Huang, CJ, Lu, YT, Hsu, YW, Tsai, P, Su, NY & Skimming, JW 2002, 'GTPCH is not a rate-limiting factor for hemorrhagic shock-induced hepatic nitric oxide biosynthesis', Acta Anaesthesiologica Sinica, vol. 40, no. 3, pp. 109-116.
Cheng, Ching Rong ; Huang, Chun Jen ; Lu, Yen Ta ; Hsu, Yung Wei ; Tsai, Peishan ; Su, Nuan Yen ; Skimming, Jeffrey W. / GTPCH is not a rate-limiting factor for hemorrhagic shock-induced hepatic nitric oxide biosynthesis. In: Acta Anaesthesiologica Sinica. 2002 ; Vol. 40, No. 3. pp. 109-116.
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T1 - GTPCH is not a rate-limiting factor for hemorrhagic shock-induced hepatic nitric oxide biosynthesis

AU - Cheng, Ching Rong

AU - Huang, Chun Jen

AU - Lu, Yen Ta

AU - Hsu, Yung Wei

AU - Tsai, Peishan

AU - Su, Nuan Yen

AU - Skimming, Jeffrey W.

PY - 2002/9

Y1 - 2002/9

N2 - Background: Hemorrhagic shock upregulates inducible nitric oxide (NO) synthase (iNOS) expression and the resultant NO overproduction. Liver is one of the major organs that is responsible for increased NO production after trauma-hemorrhage and resuscitation. Guanosine triphosphate cyclohydrolase I (GTPCH) is the rate-limiting enzyme for the synthesis of tetrahydrobiopterin (BH4), a necessary co-factor for iNOS activity. Very little is known about the effects of hemorrhagic shock on hepatic GTPCH expression. Methods: Fifteen male Sprague-Dawley rats were randomly assigned to one of three groups, i.e. a sham instrumented (Sham) group, a sustained hemorrhagic shock (HS) group, and a hemorrhagic shock with resuscitation (HS/RES) group (n = 5 in each group). Controlled hemorrhagic shock was induced and the mean arterial pressure (MAP) was kept between 40-45 mmHg for sixty minutes in both HS and HS/RES groups. Then resuscitation with infusion of shed autologous blood and normal saline was performed in HS/RES group. Microdialysis probes were put in the liver and the right atrium for collection of serial samples. NO concentrations in dialysate samples were measured using chemiluminescence. Hepatic iNOS and GTPCH mRNA concentrations were analyzed using semi-quantitative reverse transcription and polymerase chain reaction (RT-PCR). Results: Hemorrhagic shock induced both the hepatic and circulating NO biosynthesis as well as hepatic iNOS mRNA expression. Resuscitation with shed blood/normal saline normalized this upregulation. However, no difference was found in mean hepatic GTPCH mRNA concentrations between groups in this experiment. Conclusions: We provide the evidence that hemorrhagic shock-induced NO biosynthesis involves upregulation of iNOS transcription in liver tissue and GTPCH transcription is unaffected by either hemorrhagic shock or resuscitation. Furthermore, microdialysis is an ideal technique for serial sampling and that events can be followed.

AB - Background: Hemorrhagic shock upregulates inducible nitric oxide (NO) synthase (iNOS) expression and the resultant NO overproduction. Liver is one of the major organs that is responsible for increased NO production after trauma-hemorrhage and resuscitation. Guanosine triphosphate cyclohydrolase I (GTPCH) is the rate-limiting enzyme for the synthesis of tetrahydrobiopterin (BH4), a necessary co-factor for iNOS activity. Very little is known about the effects of hemorrhagic shock on hepatic GTPCH expression. Methods: Fifteen male Sprague-Dawley rats were randomly assigned to one of three groups, i.e. a sham instrumented (Sham) group, a sustained hemorrhagic shock (HS) group, and a hemorrhagic shock with resuscitation (HS/RES) group (n = 5 in each group). Controlled hemorrhagic shock was induced and the mean arterial pressure (MAP) was kept between 40-45 mmHg for sixty minutes in both HS and HS/RES groups. Then resuscitation with infusion of shed autologous blood and normal saline was performed in HS/RES group. Microdialysis probes were put in the liver and the right atrium for collection of serial samples. NO concentrations in dialysate samples were measured using chemiluminescence. Hepatic iNOS and GTPCH mRNA concentrations were analyzed using semi-quantitative reverse transcription and polymerase chain reaction (RT-PCR). Results: Hemorrhagic shock induced both the hepatic and circulating NO biosynthesis as well as hepatic iNOS mRNA expression. Resuscitation with shed blood/normal saline normalized this upregulation. However, no difference was found in mean hepatic GTPCH mRNA concentrations between groups in this experiment. Conclusions: We provide the evidence that hemorrhagic shock-induced NO biosynthesis involves upregulation of iNOS transcription in liver tissue and GTPCH transcription is unaffected by either hemorrhagic shock or resuscitation. Furthermore, microdialysis is an ideal technique for serial sampling and that events can be followed.

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KW - Shock, hemorrhagic

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