Summary
In adrenalectomized rats the influence of salt loading or salt deprivation on the vasopressin and oxytocin content of the median eminence (ME) and the neural lobe (NL) was studied by means of various methods: (1) morphometric and microphotometric analysis of aldehyde fuchsin-stained sections of ME and NL; (2) immunohistochemical demonstration of neurophysin, oxytocin, and vasopressin in the ME and in the NL; (3) radioimmunological measurement of oxytocin and vasopressin in the ME and in the NL. Adrenalectomy in salt-substituted rats raised the vasopressin content of the outer layer of the ME (OLME) but had no influence on the amount of vasopressin in the inner layer of the ME and in the NL. Osmotic stimulation of adrenalectomized rats by hypertonic saline markedly diminished vasopressin and oxytocin in the inner layer of the ME and in the NL but did not, or only slightly reduced vasopressin in the OLME. Withdrawal of salt supplementation in adrenalectomized rats resulted in a decrease of plasma sodium and plasma volume. It did not change the vasopressin or oxytocin content of the inner layer of the ME and of the NL, but it was correlated with a decrease of vasopressin in the OLME. The present findings may suggest that vasopressin in the OLME is involved in salt and/or volume regulation by influencing the hypophysial-adrenal axis.
Similar content being viewed by others
References
Agus ZS, Goldberg M (1971) Role of antidiuretic hormone in the abnormal water diuresis of anterior hypopituitarism in man. J Clin Invest 50:1478–1489
Aizawa T, Yasuda N, Greer MA, Sawyer WH (1982) In vivo adrenocorticotropin-releasing activity of neurohypophyseal hormones and their analogs. Endocrinology 110:98–104
Antunes JL, Carmel PW, Zimmerman EA (1977) Projections from the paraventricular nucleus to the zona externa of the median eminence of the rhesus monkey: an immunohistochemical study. Brain Res 137:1–10
Balment RJ, Chester-Jones I, Henderson IW, Oliver JA (1976) Effects of adrenalectomy and hypophysectomy on water and electrolyte metabolism in male and female rats with inherited hypothalamic diabetes insipidus (Brattleboro strain). J Endocrinol 71:193–217
Baylis PH (1983) Posterior pituitary function in health and disease. Clin Endocinol Metab 12:747–770
Bentley PJ, Scott WN (1978) The actions of aldosterone. In: Chester-Jones I, Henderson IW (eds) General, comparative and clinical endocrinology of the adrenal cortex, Vol. 2, London-New York-San Francisco: Academic Press, pp 497–564
Bie P (1980) Osmoreceptors, vasopressin, and control of renal water excretion. Physiol Rev 60:961–1048
Bock R (1972) Morphometrische Untersuchungen zum histologischen Nachweis des Corticotropin-Releasing Factor im Infundibulum der Ratte. Z Anat Entwickl Gesch 137:1–19
Bock R, Jurna I (1977) Ipsilateral diminution of CRF-granules after unilateral hypothalamic lesions. Cell Tissue 185:215–229
Bock R, Forstner RV, Mühlen K aus der, Stöhr PhA (1969) Beiträge zur funktionellen Morphologie der Neurohypophyse. III. Über die Wirkung einer Corticoid-oder ACTH-Behand-lung auf das Auftreten “gomoripositiver” Granula in der Zona externa infundibuli von Ratten und Mäusen nach beidseitiger Adrenalektomie oder Hypophysektomie. Z Zellforsch 96:142–150
Bock R, Salland Th, Schwabedal PE (1976) Histochemical and immunohistochemical properties of the CRF-granules and other “Gomori-positive” substances of the rat. Histochemistry 46:81–105
Bock R, Detzer K, Leicht E, Röder R (1980) Functional difference between “classical” neurosecretory material and vasopressin-like substances of the outer layer of the median eminence. Cell Tissue Res 212:257–277
Bock R, Detzer K, Geiger A, Lang RE, Östermann E, Sinner G (1983) Effect of adrenalectomy and administration of hypertonic saline on the content of aldehyde fuchsin-positive neurosecretory material and posterior lobe hormones in the median eminence and the neural lobe of rats. Cell Tissue Res 228:127–138
Brimble MJ, Dyball REJ (1977) Characterization of the responses of oxytocin- and vasopressin-secreting neurones in the supraoptic nucleus to osmotic stimulation. J Physiol 271:253–271
Brimble MJ, Dyball REJ, Forsling ML (1978) Oxytocin release following osmotic activation of oxytocin neurones in the paraventricular and supraoptic nuclei. J Physiol 278:69–78
Brinkmann H, Bock R (1970) Quantitative Veränderungen “Go-mori-positiver” Substanzen in Infundibulum und Hypophysenhinterlappen der Ratte nach Adrenalektomie und Kochsalz-oder Durstbelastung. J Neurol Visc Relat 32:48–64
Brinkmann H, Bock R (1973) Influence of various corticoids on the augmentation of “Gomori-positive” granules in the median eminence of the rat following adrenalectomy. Naunyn-Schmiedeberg's Arch Pharmacol 280:49–62
Brinkmann H, Wittkowski W, Bock R (1975) Gomori-positive elementary granules in inner and outer layer of the infundibulum. Cell Tissue Res 163:503–508
Bumpus FM, Sen S, Bravo EL, Shainoff JR (1982) New regulators of aldosterone secretion. In: F Mantero, EG Bigheri, CRW Edwards, Endocrinology of hypertension, London-New York. Academic Press, pp 19–22
Burlet A, Chateau M, Czernichow P (1979) Infundibular localization of vasopressin, oxytocin and neurophysins in the rat; its relationships with corticotrope function. Brain Res 168:275–286
Burlet A, Tonon MCh, Tankosic P, Coy D, Vaudry H (1983) Comparative immunocytochemical localization of corticotropin releasing factor (CRF-41) and neurohypophysial peptides in the brain of Brattleboro and Long-Evans rats. Neuroendo-crinology 37:64–72
Conaglen JV, Donald RA, Espiner EA, Livesey JH, Nicholls MG (1984) The effect of ovine corticotropin-releasing factor on catecholamine, vasopressin, and aldosterone secretion in normal man. J Clin Endocrinol Metab 58:463–466
Davis JO (1975) Regulation of aldosterone secretion. In: Handbook of Physiology, section 7 (Endocrinology), Vol VI (Adrenal gland), Washington DC: American Physiological Society pp 77–106
DeBold CR, Sheldon WR, DeCherney G St, Jackson RV, Alexander AN, Vale W, Rivier J, Orth DN (1984) Arginine vasopressin potentiates adrenocorticotropin-release induced by ovine corticotropin-releasing factor. J Clin Invest 73:533–538
Dierickx K, Vandesande F, deMey J (1976) Identification, in the external region of the rat median eminence, of separate neurophysin-vasopressin and neurophysin-oxytocin containing nerve fibres. Cell Tissue Res 168:141–151
Dornhorst A, Carlson DE, Seif SM, Robinson AG, Zimmerman EA, Gann DS (1981) Control of release of adrenocorticotropin and vasopressin by the supraoptic and paraventricular nuclei. Endocrinology 108:1420–1424
Dubé D, Leclerc R, Pelletier G (1976) Electron microscopic immunohistochemical localization of vasopressin and neurophysin in the median eminence of normal and adrenalectomized rats. Am J Anat 147:103–108
Edwards CRW, Al-Dujaili AS, Boscaro M, Gow I, Williams BC (1982) Peptidergic and monoaminergic regulation of aldosterone secretion. In: F Mantero, EG Biglieri, CRW Edwards (eds) Endocrinology of hypertension, London-New York: Academic Press, pp 11–18
Friedman SM, Sreter FA, Nakashima M, Friedman CL (1962) Adrenal cortex and neurohypophyseal deficiency in salt and water homeostasis of rats. Am J Physiol 203:697–701
Gaunt R, Chart JJ (1962) Mineralocorticoid action of adrenocortical hormones. In: O Eichler, A Farah (eds) Handbuch der experimentellen Pharmakologie, Bd. XIV, Teil I, The adrenocortical hormones. Their origin, chemistry, physiology, and pharmacology. Part I (Subed. HW Deane), Berlin-Göttingen-Heidelberg: Springer, pp 514–569
George JM (1976) Vasopressin and oxytocin are depleted from rat hypothalamic nuclei after oral hypertonic saline. Science 193:146–148
Giguere V, Labrie F (1982) Vasopressin potentiates cyclic AMP accumulation and ACTH release induced by corticotropin-releasing factor (CRF) in rat anterior pituitary cells in culture. Endocrinology 111:1752–1754
Gill JR Jr, Gann DS, Bartter FC, Ambrose IM, Smith GW (1962) Restoration of water diuresis in addisonian patients by expansion of the volume of extracellular fluid. J Clin Invest 41:1078–1085
Gillies GE, Linton EA, Lowry PJ (1982) Corticotropin releasing activity of the CRF is potentiated several times by vasopressin. Nature 299:355–356
Ginsburg M (1954) The secretion of antidiuretic hormone in response to haemorrhage and the fate of vasopressin in adrenal-ectomized rats. J Endocrinol (Lond) 11:165–176
Green HH, Harrington AR, Valtin H (1970) On the role of anti-diuretic hormone in the inhibition of acute water diuresis in adrenal insufficiency and the effects of gluco- and mineralocorticoids in reversing the inhibition. J Clin Invest 49:1724–1736
Gregersen MI, Gibson JJ, Staed EA (1935) Plasma volume determination with dyes: errors in colorimetry use of blue dye T-1824. Am J Physiol 113:54–55
Großkopf R (1976) Verfahren für photometrische Messungen mit Fernseh-Bildanalysegeräten. Microscop Acta 60:61–69
Jones CW, Pickering BT (1969) The effects of water deprivation and sodium chloride inhibition on the hormone content of the neurohypophysis of the rat. J Physiol 203:449–458
Kiss JZ, Mezey E, Skirboll L (1984) Corticotropin-releasing factor-immunoreactive neurons of the paraventricular nucleus become vasopressin positive after adrenalectomy. Proc Natl Acad Sci USA 81:1854–1858
Kleeman CR, Czaczkes JW, Cutter R (1964) Mechanisms of impaired water excretion in adrenal and pituitary insufficiency. IV. Antidiuretic hormone in primary and secondary adrenal insufficiency. J Clin Invest 43:1641–1650
Lang RE, Rascher W, Unger Th, Ganten D (1981a) Reduced content of vasopressin in the brain of spontaneously hypertensive as compared to normotensive rats. Neurosci Lett 23:199–202
Lang RE, Rascher W, Heil J, Unger Th, Wiedemann G, Ganten D (1981b) Angiotensin stimulates oxytocin release. Life Sci 29:1425–1428
Laragh J, Selay JE (1973) The renin-angiotensin-aldosterone hormonal system and regulation of sodium, potassium, and blood pressure homeostasis. In: J Orloff, RW Berliner (eds) Handbook of Physiology section 8 (Renal Physiology), Washington DC: American Physiological Society, pp 831–908
Lee TC, Wal B van der, Wied D de (1968) Influence of the anterior pituitary on the aldosterone secretory response to dietary sodium restriction in the rat. J Endocrinol (Lond) 42:465–475
Livingstone A (1973) Ultrastructure of the rat neural lobe during recovery from hypertonic saline treatment. Z Zellforsch 137:361–374
Matsuoka H, Mulrow PJ, Franco-Saenz R, Li CH (1981b) Stimulation of aldosterone production by β-melanotropin. Nature 291:155–156
McCaa RE, Young DB, Guyten AC, McCaa CS (1974) Evidence for a role of an unidentified pituitary factor in regulation aldosterone secretion during altered sodium balance. Circ Res [Suppl] 1:34–35, 15–25
Merchenthaler I, Vigh S, Petrusz P, Schally AV (1982) Immunocytochemical localization of corticotropin-releasing factor (CRF) in the rat brain. Am J Anat 165:385–396
Moses AM (1963) Adrenal-neurohypophysial relationships in the dehydrated rat. Endocrinology 73:230–236
Müller W (1973) Das LEITZ-Textur-Analyse-System. LEITZ Mitt Wiss Techn [Suppl] 1:101–116
Olschowka JA, O'Donohue TL, Müller GP, Jacobowitz DM (1982) Hypothalamic and extrahypothalamic distribution of CRF-like immunoreactive neurons in the rat brain. Neuroendocrinology 35:305–308
Palkovits M, deJong W, deWied D (1974) Hypothalamic control of aldosterone production in sodium-deficient rats. Neuroendocrinology 14:297–309
Pelletier G, Leclerc R, Dubé D (1976) Immunohistochemical localization of hypothalamic hormones. J Histochem Cytochem 24:864–871
Recht LD, Hoffman DL, Haldar J, Silverman AJ, Zimmerman EA (1981) Vasopressin-concentrations in hypophysial portal plasma: Insiginificant reduction following removal of the posterior pituitary gland. Neuroendocrinology 33:88–90
Reid IA, Schwartz J, Ben L, Maselli J, Keil LC (1983) Interactions between vasopressin and the renin-angiotensin system. Prog Brain Res 60:475–491
Rhodes CH, Morell JI, Pfaff DW (1981) Changes in oxytocin content in the magnocellular neurons of the rat hypothalamus following water deprivation or estrogen treatment. Cell Tissue Res 216:47–55
Rivier C, Vale W (1983a) Interaction of corticotropin-releasing factor and arginine vasopressin on adrenocorticotropin secretion in vivo. Endocrinology 113:939–942
Rivier C, Vale W (1983b) Modulation of stress-induced ACTH release by corticotropin-releasing factor, catecholamines and vasopressin. Nature 305:325–327
Robertson GL (1977) The regulation of vasopressin function in health and disease. Recent Prog Horm Res 33:333–385
Robinson AG, Seif SM, Verbalis JG, Brownstein MJ (1983) Quantitation of changes in the content of neurohypophyseal peptides in hypothalamic nuclei after adrenalectomy. Neuroendocrinology 36:347–350
Roth KA, Weber E, Barchas JD (1982) Immunoreactive corticotropin releasing factor (CRF) and vasopressin are colocalized in a subpopulation of the immunoreactive vasopressin cells in the paraventricular nucleus of the hypothalamus. Life Sci 31:1857–1860
Sachs L (1968) Statistische Auswertungsmethoden. Berlin-Heidelberg-New York: Springer
Sawchenko PE, Swanson LW, Vale WW (1984a) Corticotropin-releasing factor: Co-expression within distinct subsets of oxytocin-, vasopressin-, and neurophysin-immunoreactive neurons in the hypothalamus of the male rat. J Neurosci 4:1118–1129
Sawchenko PE, Swanson LW, Vale WW (1984b) Co-expression of corticotropin-releasing factor and vasopressin immunoreactivity in parvocellular neurosecretory neurons of the adrenalectomized rat. Proc Natl Acad Sci USA 81:1883–1887
Schneider E, Blömer A, Bock R, Brinkmann H, Goslar HG (1974) Verhalten „Gomori-positiver” Granula im Infundibulum verschiedener Säugerspecies nach Adrenalektomie; zugleich ein Beitrag zur speciesdifferenten Enzymausstattung von Neurohypophyse und Ependym des III. Ventrikels. Acta Histochem 48:172–190
Schrier RW, Berl T, Anderson RJ (1979) Osmotic and nonosmotic control of vasopressin release. Am J Physiol 236:F321-F332
Schwabedal PE, Bock R, Winkler C (1975) Influence of adrenalectomy, total body x-irradiation and dexamethasone on the amount of CRF-granules and “classical” neurosecretory material in the rat neurohypophysis. Anat Embryol 148:267–278
Schwabedal PE, Partenheimer U, Bock R (1976) Influence of sodium chloride on the amount of CRF-granules and “classical” neurosecretory material (NSM) in the neurohypophysis of bilaterally adrenalectomized rats. Anat Embryol 149:307–313
Seybold V, Elde R, Hökfelt T (1981) Terminals of reserpine-sensitive vasopressin-neurophysin neurons in the external layer of the rat median eminence. Endocrinology 108:1803–1809
Share L (1974) Blood pressure, blood volume, and the release of vasopressin. In: Handbook of Physiology. Sect. 7 vol. IV, part I, Washington D. C. USA: American Physiological Society, pp 243–255
Share L, Travis RH (1970) Plasma vasopressin concentration in the adrenally insufficient dog. Endocrinology 86:196–201
Share L, Travis RH (1971) Interrelationships between the adrenal cortex and the posterior pituitary. Fed Proc 30:1378–1382
Silverman AJ (1976) Ultrastructural studies on the localization of neurohypophysial hormones and their carrier proteins. J Histochem Cytochem 24:816–827
Sladek CD (1983) Regulation of vasopressin release by neurotransmitters, neuropeptides and osmotic stimuli. Prog Brain Res 60:71–90
Sofroniew MV, Weindl A, Wetzstein R (1977) Immunoperoxidase staining of vasopressin in the rat median eminence following adrenalectomy and steroid substitution. Acta Endocrinol (K bh) [Suppl] 212:72
Sternberger LA, Hardy PH Jr, Cuculis JJ, Meyer HG (1970) The unlabeled antibody enzyme method of immunohistochemistry. Preparation and properties of soluble antigen-antibody complex (horseradish peroxidase-antihorseradish peroxidase) and its use in identification of spirochetes. J Histochem Cytochem 18:315–333
Stilman MA, Recht LD, Rosario SL, Seif SM, Robinson AG, Zimmerman EA (1977) The effects of adrenalectomy and gluco-corticoid replacement on vasopressin and vasopressin-neurophysin in the zona externa of the median eminence of the rat. Endocrinology 101:42–49
Streeten DHP, Souma M, Ross GS, Miller M, Lewis R (1981) Action of cortisol introduced into the supraoptic nucleus, on vasopressin and antidiuresis during hypertonic saline infusion in conscious rhesus monkeys. Acta Endorinol 98:195–204
Swanson LW, Sawchenko PE, Rivier J, Vale WW (1983) Organization of ovine corticotropin-releasing factor immunoreactive cells and fibers in the rat brain: an immunohistochemical study. Neuroendocrinology 36:165–186
Tramu G, Pillez E (1982) Localization immunohistochimique des terminaisons nerveuses à corticoliberine (GRF) dans l'eminence mediane du cobaye et du rat. CR Acad Sci (Paris) 294:107–114
Turkelson CM, Thomas CR, Arimura A, Chang D, Chang JK, Shimizu M (1982) In vitro potentiation of the activity of synthetic ovine corticotropin-releasing factor by arginine vasopressin. Peptides 1:111–113
Ufferman RC, Schrier W (1972) Importance of sodium intake and mineralocorticoid hormone in the impaired water excretion in adrenal insufficiency. J Clin Invest 51:1639–1646
Uhlich E, Weber P, Haslbeck R (1976) Angiotensin II and prostaglandin stimulated release of vasopressin-in vitro and in vivo experiments. In: W. Kaufmann, DK Krause, Central nervous control of Na+ balance-relations to the renin-angiotensin system, Stuttgart: Thieme, pp 64–69
Valiquette G (1980) Posterior pituitary hormones and neurophysins. In: M. Motta: The endocrine functions of the brain, pp 386–417. New York: Raven Press
Vandesande F, DeMey J, Dierickx K (1974) Identification of neurophysin producing cells. I. The origin of the neurophysin-like substance-containing nerve fibres of the external region of the median eminence of the rat. Cell Tissue Res 151:187–200
Vandesande F, Dierickx K, DeMey J (1977) The origin of the vasopressinergic and oxytocinergic fibres of the external region of the median eminence of the rat hypophysis. Cell Tissue Res 180:443–452
Wakerly JB, Poulain DA, Brown D (1978) Comparison of firing patterns in oxytocin- and vasopressin-releasing neurones during progressive dehydration. Brain Res 148:423–440
Watkins WB, Schwabedal P, Bock R (1974) Immunohistochemical demonstration of a CRF-associated neurophysin in the external zone of the rat median eminence. Cell Tissue Res 152:411–421
Yates FE, Russell SM, Dallman MF, Hedge GA, McCann SM, Dhariwal APS (1971) Potentiation by vasopressin of corticotrophin release induced by corticotrophin-releasing factor. Endocrinology 88:3–15
Zimmerman EA, Silverman AJ (1983) Vasopressin and adrenal cortical interactions. Prog Brain Res 60:493–504
Author information
Authors and Affiliations
Additional information
The study was supported by the Deutsche Forschungsgemeinschaft (Bo 392/6-51 and SFB 90, Cardiovasculäres System, A52). The morphometric measurements with the TAS plus were carried out at the Max-Planck-Institut für Psychiatrie, Munich, FRG. We are particularly indebted to Prof. G. W. Kreutzberg and Prof. P. Schubert for their help
Rights and permissions
About this article
Cite this article
Mink, D., Lang, R.E., Östermann, E. et al. Effect of salt loading and salt deprivation on the vasopressin and oxytocin content of the median eminence and the neural lobe in adrenalectomized rats. Cell Tissue Res. 246, 413–423 (1986). https://doi.org/10.1007/BF00215904
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00215904