Differences in adrenocortical secretory and gene expression responses to stimulation in vitro by ACTH or prolactin between high- and low-avoidance Hatano rats

References

• Asai S, Ohta R, Shirota M, Watanabe G, Taya K. Differential responses of the hypothalamo–pituitary–adrenocortical axis to acute restraint stress in Hatano high- and low-avoidance rats. J Endocrinol 2004; 181: 515–520
   PubMedGoogle Scholar
• Asai S, Ohta R, Fujikawa T, Sakai RR, Shirota M, Ogata M, Watanabe G, Taya K. Gastric ulceration and expression of prolactin receptor in the brain in Hatano high- and low-avoidance rats. Endocrine 2006; 30: 161–166
   PubMedGoogle Scholar
• Chang LL, Lo MJ, Kan SF, Huang WJ, Chen JJ, Kau MM, Wang JL, Lin H, Tsai SC, Chiao YC, Yeh JY, Wun WS, Wang PS. Direct effects of prolactin on corticosterone release by zona fasciculata-reticularis cells from male rats. J Cell Biochem 1999; 73: 563–572
   PubMedGoogle Scholar
• Chang LL, Wun WS, Lin YL, Wang PS. Effects of S-petasin on cyclic AMP production and enzyme activity of P450scc in rat zona fasciculata-reticularis cells. Eur J Pharmacol 2004; 489: 29–37
   PubMedGoogle Scholar
• Cherradi N, Rossier MF, Vallotton MB, Timberg R, Friedberg I, Orly J, Wang XJ, Stocco DM, Capponi AM. Submitochondrial distribution of three key steroidogenic proteins (steroidogenic acute regulatory protein and cytochrome p450scc and 3beta-HSD isomerase enzymes) upon stimulation by intracellular calcium in adrenal glomerulosa cells. J Biol Chem 1997; 272: 7899–7907
   PubMedGoogle Scholar
• Ducret T, Boudina S, Sorin B, Vacher AM, Gourdou I, Liguoro D, Guerin J, Bresson-Bepoldin L, Vacher P. Effects of prolactin on intracellular calcium concentration and cell proliferation in human glioma cells. Glia 2002; 38: 200–214
   PubMed Web of Science ®Google Scholar
• Gallo-Payet N, Payet MD. Mechanism of action of ACTH: Beyond cAMP. Microsc Res Tech 2003; 61: 275–287
   PubMed Web of Science ®Google Scholar
• Gallo-Payet N, Côte M, Chorvatova A, Guillon G, Payet MD. Cyclic AMP-independent effects of ACTH on glomerulosa cells of the rat adrenal cortex. J Steroid Biochem Mol Biol 1999; 69: 335–342
   PubMedGoogle Scholar
• Glasow A, Haidan A, Gillespie J, Kelly PA, Chrousos GP, Bornstein SR. Differential expression of prolactin receptor (PRLR) in normal and tumorous adrenal tissues: Separation of cellular endocrine compartments by laser capture microdissection (LCM). Endocr Res 1998; 24: 857–862
   PubMed Web of Science ®Google Scholar
• Gomez F, Lahmame A, de Kloet ER, Armario A. Hypothalamic–pituitary–adrenal response to chronic stress in five inbred rat strains: Differential responses are mainly located at the adrenocortical level. Neuroendocrinology 1996; 63: 327–337
   PubMed Web of Science ®Google Scholar
• Jaroenporn S, Nagaoka K, Ohta R, Watanabe G, Taya K. Direct effects of prolactin on adrenal steroid release in male Hatano high-avoidance (HAA) rats may be mediated through Janus kinase 2 (Jak2) activity. J Reprod Dev 2007; 53: 887–893
   PubMedGoogle Scholar
• Kaminska B, Ciereszko RE, Opalka M, Dusza L. Prolactin signaling in porcine adrenocortical cells: Involvement of protein kinases. Domest Anim Endocrinol 2002; 23: 475–491
   PubMed Web of Science ®Google Scholar
• Kanesaka T, Taya K, Sasamoto S. Radioimmunoassay of corticosterone using 125I-labeled radioligand. J Reprod Dev 1992; 38: 85–89
   Google Scholar
• Kan SF, Kau MM, Low-Tone Ho L, Wang PS. Inhibitory effects of bromocriptine on corticosterone secretion in male rats. Eur J Pharmacol 2003; 468: 141–149
   PubMedGoogle Scholar
• Kau MM, Lo MJ, Tsai SC, Chen JJ, Pu HF, Chien EJ, Chang LL, Wang PS. Effects of prolactin on aldosterone secretion in rat zona glomerulosa cells. J Cell Biochem 1999; 72: 286–293
   PubMedGoogle Scholar
• Kosti O, Raven PW, Renshaw D, Hinson JP. Intra-adrenal mechanisms in the response to chronic stress: Investigation in a rat model of emotionality. J Endocrinol 2006; 189: 211–218
   PubMedGoogle Scholar
• Lo MJ, Wang PS. Involvement of cAMP but not PKA in the increase of corticosterone secretion in rat zona fasciculata-reticularis cells by aging. J Cell Biochem 2002; 85: 35–41
   PubMedGoogle Scholar
• Lo MJ, Wang PS. Relative and combined effects of estradiol and prolactin on corticosterone secretion in ovariectomized rats. Chin J Physiol 2003; 46: 103–109
   PubMedGoogle Scholar
• Lo MJ, Kau MM, Chen YH, Tsai SC, Chiao YC, Chen JJ, Liaw C, Lu CC, Lee BP, Chen SC, Fang VS, Ho LT, Wang PS. Acute effects of thyroid hormones on the production of adrenal cAMP and corticosterone in male rats. Am J Physiol 1998; 74: E238–E245
   Google Scholar
• Lo MJ, Kau MM, Cho WL, Wang PS. Aging effects on the secretion of corticosterone in male rats. J Investig Med 2000; 48: 335–342
   PubMedGoogle Scholar
• Lo MJ, Kau MM, Wang PS. Effect of aging on the corticosterone secretion in diestrous rats. J Cell Biochem 2006; 97: 351–358
   PubMedGoogle Scholar
• Manna PR, Tena-Sempere M, Huhtaniemi IT. Molecular mechanisms of thyroid hormone-stimulated steroidogenesis in mouse leydig tumor cells. Involvement of the steroidogenic acute regulatory (StAR) protein. J Biol Chem 1999; 274: 5909–5918
   PubMed Web of Science ®Google Scholar
• Mountjoy KG, Robbins LS, Mortrud MT, Cone RD. The cloning of a family of genes that encode the melanocortin receptors. Science 1992; 257: 1248–1251
   PubMed Web of Science ®Google Scholar
• Ogle TF, Kitay JI. Interactions of prolactin and adrenocorticotropin in the regulation of adrenocortical secretions in female rats. Endocrinology 1979; 104: 40–44
   PubMed Web of Science ®Google Scholar
• Ohta R, Matsumoto A, Hashimoto Y, Nagao T, Mizutani M. Behavioral characteristics of rats selectively bred for high and low avoidance shuttlebox response. Congenit Anom 1995; 35: 223–229
   Google Scholar
• Ohta R, Shirota M, Adachi T, Tohei A, Taya K. Plasma ACTH levels during early, two-way avoidance acquisition in high- and low-avoidance rats (Hatano strains). Behav Genet 1999; 29: 137–144
   PubMedGoogle Scholar
• Opalka M, Kaminska B, Doboszynska T, Dusza L. The morphometric parameters of adrenal cortex in sows: In normal condition and after prolactin infusion. Folia Morphol (Warsz) 2001; 60: 317–322
   PubMedGoogle Scholar
• Prevarskaya NB, Skryma RN, Vacher P, Daniel N, Djiane J, Dufy B. Role of tyrosine phosphorylation in potassium channel activation. Functional association with prolactin receptor and JAK2 tyrosine kinase. J Biol Chem 1995; 270: 24292–24299
   PubMedGoogle Scholar
• Reincke M, Beuschlein F, Menig G, Hofmockel G, Arlt W, Lehmann R, Karl M, Allolio B. Localization and expression of adrenocorticotropic hormone receptor mRNA in normal and neoplastic human adrenal cortex. J Endocrinol 1998; 156: 415–423
   PubMedGoogle Scholar
• Sewer MB, Waterman MR. ACTH modulation of transcription factors responsible for steroid hydroxylase gene expression in the adrenal cortex. Microsc Res Tech 2003; 61: 300–307, Review
   PubMed Web of Science ®Google Scholar
• Silva EJ, Felicio LF, Nasello AG, Zaidan-Dagli M, Anselmo-Franci JA. Prolactin induces adrenal hypertrophy. Braz J Med Biol Res 2004; 37: 193–199
   PubMed Web of Science ®Google Scholar
• Slawik M, Reisch N, Zwermann O, Maser-Gluth C, Stahl M, Klink A, Reincke M, Beuschlein F. Characterization of an adrenocorticotropin (ACTH) receptor promoter polymorphism leading to decreased adrenal responsiveness to ACTH. J Clin Endocrinol Metab 2004; 89: 3131–3137
   PubMedGoogle Scholar
• Sorin B, Goupille O, Vacher AM, Paly J, Djiane J, Vacher P. Distinct cytoplasmic regions of the prolactin receptor are required for prolactin-induced calcium entry. J Biol Chem 1998; 273: 28461–28469
   PubMedGoogle Scholar
• Sorin B, Vacher AM, Djiane J, Vacher P. Role of protein kinases in the prolactin-induced intracellular calcium rise in Chinese hamster ovary cells expressing the prolactin receptor. J Neuroendocrinol 2000; 12: 910–918
   PubMedGoogle Scholar
• Taya K, Watanabe G, Sasamoto S. Radioimmunoassay for progesterone testosterone and estradiol-17β using 125I-iodohistamine radioligands. Jpn J Anim Reprod 1985; 31: 186–197
   Google Scholar
• Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, De Paepe A, Speleman F. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol 2002; 3, RESEARCH0034
   PubMed Web of Science ®Google Scholar
• Waterman MR, Bischof LJ. Mechanisms of ACTH (cAMP)-dependent transcription of adrenal steroid hydroxylases. Endocr Res 1996; 22: 615–620
   PubMed Web of Science ®Google Scholar
• Yamazaki T, Kimoto T, Higuchi K, Ohta Y, Kawato S, Kominami S. Calcium ion as a second messenger for o-nitrophenylsulfenyl-adrenocorticotropin (NPS-ACTH) and ACTH in bovine adrenal steroidogenesis. Endocrinology 1998; 139: 4765–4771
   PubMedGoogle Scholar
• Yamazaki T, Kawasaki H, Takamasa A, Yoshitomi T, Kominami S. Ca2+ signal stimulates the expression of steroidogenic acute regulatory protein and steroidogenesis in bovine adrenal fasciculata-reticularis cells. Life Sci 2006; 78: 2923–2930
   PubMedGoogle Scholar