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Am J Physiol Endocrinol Metab 281: E269-E274, 2001;
0193-1849/01 $5.00
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Vol. 281, Issue 2, E269-E274, August 2001

Involvement of thioredoxin in the regulation of growth hormone secretion in rat pituitary cell cultures

Ikue Hata1, Yosuke Shigematsu2, Yusei Ohshima1, Hirokazu Tsukahara1, Kazuo Fujisawa1, Masahiro Hiraoka1, Hajime Nakamura3, Hiroshi Masutani3, Junji Yodoi3, Fumikazu Kotsuji4, Masakatsu Sudo1, and Mitsufumi Mayumi1

Departments of 1 Pediatrics, 2 Basic Nursing, and 4 Gynecology, Fukui Medical University, Fukui 910-1193; and 3 Institute for Virus Research, Kyoto University, Kyoto 606-8507, Japan

We report here an examination of the effect of thioredoxin (TRX) on the secretion of growth hormone (GH) from rat anterior pituitary cells in vitro. Treatment of rat pituitary cells with growth hormone-releasing factor (GRF), but not GH, led to a significant increase in intracellular TRX protein levels. GRF, recombinant human TRX (rhTRX), and a combination thereof were all shown to induce immediate GH secretion from pituitary cells, as evidenced by perifusion experiments. RhTRX, but not other reducing agents such as beta -mercaptoethanol and N-acetyl-L-cysteine, augmented GRF-stimulated and -unstimulated GH secretion from rat pituitary cells in a dose-dependent manner. RhTRX did not significantly affect the GH mRNA expression of pituitary cells stimulated in the presence or absence of GRF. In addition, rhTRX-augmented GH secretion was not significantly affected by the presence of cycloheximide. Collectively, these findings suggest that TRX is induced by stimulation with GRF and plays a regulatory role in GH secretion from rat anterior pituitary cells by enhancing the secretion of stored GH, rather than by the synthesis of GH.

redox; growth hormone-releasing factor; disulfide bonds





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