Tri-iodothyronine as a stimulator of liver regeneration after partial and subtotal hepatectomy.

Standard

Tri-iodothyronine as a stimulator of liver regeneration after partial and subtotal hepatectomy. / Bockhorn, Maximilian; Frilling, A; Benko, T; Best, J; Sheu, S-Y; Trippler, M; Schlaak, J F; Broelsch, C E.

in: EUR SURG RES, Jahrgang 39, Nr. 1, 1, 2007, S. 58-63.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Bockhorn, M, Frilling, A, Benko, T, Best, J, Sheu, S-Y, Trippler, M, Schlaak, JF & Broelsch, CE 2007, 'Tri-iodothyronine as a stimulator of liver regeneration after partial and subtotal hepatectomy.', EUR SURG RES, Jg. 39, Nr. 1, 1, S. 58-63. <http://www.ncbi.nlm.nih.gov/pubmed/17213727?dopt=Citation>

APA

Bockhorn, M., Frilling, A., Benko, T., Best, J., Sheu, S-Y., Trippler, M., Schlaak, J. F., & Broelsch, C. E. (2007). Tri-iodothyronine as a stimulator of liver regeneration after partial and subtotal hepatectomy. EUR SURG RES, 39(1), 58-63. [1]. http://www.ncbi.nlm.nih.gov/pubmed/17213727?dopt=Citation

Vancouver

Bockhorn M, Frilling A, Benko T, Best J, Sheu S-Y, Trippler M et al. Tri-iodothyronine as a stimulator of liver regeneration after partial and subtotal hepatectomy. EUR SURG RES. 2007;39(1):58-63. 1.

Bibtex

@article{0780bf32c9c546c9951068251567f6e9,
title = "Tri-iodothyronine as a stimulator of liver regeneration after partial and subtotal hepatectomy.",
abstract = "BACKGROUND: Tri-iodothyronine (T3) has been shown to be a hepatic mitogen. We investigated whether exogenous application of T3 improves liver regeneration after 70% partial hepatectomy (PH) and confers a survival advantage after 90% subtotal hepatectomy (SH) in rats and whether this is associated with the stimulation of angiogenesis. METHODS: Rats were subjected to PH or SH 10 days after injection of a single dose of T3. Liver body weight ratio (LBR), hepatic proliferation (Ki-67), biochemical markers as well as vascular endothelial growth factor (VEGF) expression were assessed by immunohistochemistry. Gene expression of pathogenic relevant genes was determined by customized cDNA arrays and quantitative RT-PCR. RESULTS: T3-treated rats showed an increased LBR and Ki-67 index after PH and SH, which reached statistical significance compared to placebo-treated rats (p <0.05). On the transcriptional level, T3-treated rats had an increased expression of VEGF as demonstrated by immunohistochemistry, which was associated with a higher expression of its receptor Flt-1. CONCLUSIONS: Exogenous administration of T3 ameliorates liver regeneration after 70% PH and 90% SH, possibly due to stimulation of angiogenesis. Therefore, its clinical use might be of interest due to its excellent general practicability.",
author = "Maximilian Bockhorn and A Frilling and T Benko and J Best and S-Y Sheu and M Trippler and Schlaak, {J F} and Broelsch, {C E}",
year = "2007",
language = "Deutsch",
volume = "39",
pages = "58--63",
journal = "EUR SURG RES",
issn = "0014-312X",
publisher = "S. Karger AG",
number = "1",

}

RIS

TY - JOUR

T1 - Tri-iodothyronine as a stimulator of liver regeneration after partial and subtotal hepatectomy.

AU - Bockhorn, Maximilian

AU - Frilling, A

AU - Benko, T

AU - Best, J

AU - Sheu, S-Y

AU - Trippler, M

AU - Schlaak, J F

AU - Broelsch, C E

PY - 2007

Y1 - 2007

N2 - BACKGROUND: Tri-iodothyronine (T3) has been shown to be a hepatic mitogen. We investigated whether exogenous application of T3 improves liver regeneration after 70% partial hepatectomy (PH) and confers a survival advantage after 90% subtotal hepatectomy (SH) in rats and whether this is associated with the stimulation of angiogenesis. METHODS: Rats were subjected to PH or SH 10 days after injection of a single dose of T3. Liver body weight ratio (LBR), hepatic proliferation (Ki-67), biochemical markers as well as vascular endothelial growth factor (VEGF) expression were assessed by immunohistochemistry. Gene expression of pathogenic relevant genes was determined by customized cDNA arrays and quantitative RT-PCR. RESULTS: T3-treated rats showed an increased LBR and Ki-67 index after PH and SH, which reached statistical significance compared to placebo-treated rats (p <0.05). On the transcriptional level, T3-treated rats had an increased expression of VEGF as demonstrated by immunohistochemistry, which was associated with a higher expression of its receptor Flt-1. CONCLUSIONS: Exogenous administration of T3 ameliorates liver regeneration after 70% PH and 90% SH, possibly due to stimulation of angiogenesis. Therefore, its clinical use might be of interest due to its excellent general practicability.

AB - BACKGROUND: Tri-iodothyronine (T3) has been shown to be a hepatic mitogen. We investigated whether exogenous application of T3 improves liver regeneration after 70% partial hepatectomy (PH) and confers a survival advantage after 90% subtotal hepatectomy (SH) in rats and whether this is associated with the stimulation of angiogenesis. METHODS: Rats were subjected to PH or SH 10 days after injection of a single dose of T3. Liver body weight ratio (LBR), hepatic proliferation (Ki-67), biochemical markers as well as vascular endothelial growth factor (VEGF) expression were assessed by immunohistochemistry. Gene expression of pathogenic relevant genes was determined by customized cDNA arrays and quantitative RT-PCR. RESULTS: T3-treated rats showed an increased LBR and Ki-67 index after PH and SH, which reached statistical significance compared to placebo-treated rats (p <0.05). On the transcriptional level, T3-treated rats had an increased expression of VEGF as demonstrated by immunohistochemistry, which was associated with a higher expression of its receptor Flt-1. CONCLUSIONS: Exogenous administration of T3 ameliorates liver regeneration after 70% PH and 90% SH, possibly due to stimulation of angiogenesis. Therefore, its clinical use might be of interest due to its excellent general practicability.

M3 - SCORING: Zeitschriftenaufsatz

VL - 39

SP - 58

EP - 63

JO - EUR SURG RES

JF - EUR SURG RES

SN - 0014-312X

IS - 1

M1 - 1

ER -