By Berta Scharrer (auth.), Prof. Dr. Berta Scharrer, Priv. Doz. Dr. Horst-Werner Korf, Prof. Dr. Hans-Georg Hartwig (eds.)
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J Comp NeuroI179:677-697 Fritsch G (1890) Die elektrischen Fische. Zweite Abteilung: Die Torpedineen. von Veit & Co, Leipzig Luine VN, Rostene W, Rhodes J and McEwen BS (1984) Activation of choline acetyltransferase by vasoactive intestinal peptide. J Neurochem 42:1131-1134 Ohsawa K, Dowe GHC, Morris SJ, Whittaker VP (1979) The lipid and protein content of cholinergic synaptic vesicles from the electric organ of Torpedo marmorata purified to constant composition: implications for vesicle structure.
References Agnati LF, Fuxe K, Yu ZY, Harfstrans A, Okret S, Wikstrom AC, Goldstein M, Zoli M, Vale W, Gustafsson JA (1985) Morphometrical analysis of the distribution of corticotropin releasing factor, glucocorticoid receptor and phenylethanolamine-N-methyltransferase immunoreactive structures in the paraventricular hypothalamic nucleus of the rat. Neurosci Lett 54:147-152 Alonso G, Assenmacher I (1979) The smooth endoplasmic reticulum in neurohypophysial axons of the rat. Possible involvement in transport, storage and release of neurosecretory material.
1983) A VP concentration in the a3rdV CSF was several times higher than in plasma. 5. 1. After 24 h of dehydration ANG II concentrations increased by approximately 100 % in both compartments. 90 min after the animals had been given free access to water, normal osmolalities and AVP levels were measured in plasma and CSF samples. 3. ANG II significantly decreased in the CSF but remained unchanged in the plasma, an observation corresponding to the time course of plasma renin activity after rehydration (Thrasher et al.