TY - JOUR
T1 - Serotonergic afferents to the dorsal raphe nucleus
T2 - Evidence from HRP and synaptosomal uptake studies
AU - Mosko, Sarah S.
AU - Haubrich, Dean
AU - Jacobs, Barry L.
N1 - Funding Information:
This research was supported by Grants MH 23433 and MH 13445 from the National Institute of Mental Health, and the Spencer Foundation. We would like to thank Pfizer, Inc. (PCPA) and Lakeside Laboratories (DMI) for their generous gift of drugs. We thank Dr. Gary S. Lynch for generously donating his time and facilities in making the HRP portion of this paper possible and Thomas J. Chippendale for his assistance in the uptake studies.
Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 1977/1/7
Y1 - 1977/1/7
N2 - Afferent connections of the serotonin (5-HT)-containing dorsal raphe nucleus were investigated in the rat utilizing the horseradish peroxidase (HRP) retrograde cell labeling technique. Small quantities (0.1-0.5 μl) of HRP solutionswere infused into the dorsal raphe, and the brains were examined 19-72 h later for retrograde transport of the enzyme. Intrinsic connections within the dorsal raphe nucleus were revealed by this mapping technique, as was an input to the dorsal raphe from another serotonergic cell group, the median raphe nucleus. Little evidence was found for projections from other, more remote, brain sites. A serotonergic innervation of the dorsal raphe was also demonstrated by the presence of high affinity uptake of [3H]5-HT (Km = 0.17 μM) into synaptosomal suspensions of the dorsal raphe nucleus. Synpatosomal uptake of [3H]5-HT was blocked by selective destruction of serotonergic axon terminals induced by the intra-ventricular injection of 200 μg of 5,7-dihydroxytryptamine following desipramine HCl pretreatment, but not by destruction of catecholaminergic axon terminals induced by intraventricularly injected 6-hydroxydopamine (2 × 250 μg). The uptake of [3H]-5-HT by synaptosomes of the dorsal raphe was comparable to that of striatal and hypothalamic synaptosomes, and markedly greater than that of synaptosomes from the cerebellum or nearby dorsal central gray or midbrain reticular formation, indicating the presence of a relatively dense serotonergic innervation. These data together indicate that neurons in the dorsal raphe nucleus receive a prominent serotonergic input that is derived, at least in part, from other neurons within the dorsal nucleus and from a neighboring raphe nucleus.
AB - Afferent connections of the serotonin (5-HT)-containing dorsal raphe nucleus were investigated in the rat utilizing the horseradish peroxidase (HRP) retrograde cell labeling technique. Small quantities (0.1-0.5 μl) of HRP solutionswere infused into the dorsal raphe, and the brains were examined 19-72 h later for retrograde transport of the enzyme. Intrinsic connections within the dorsal raphe nucleus were revealed by this mapping technique, as was an input to the dorsal raphe from another serotonergic cell group, the median raphe nucleus. Little evidence was found for projections from other, more remote, brain sites. A serotonergic innervation of the dorsal raphe was also demonstrated by the presence of high affinity uptake of [3H]5-HT (Km = 0.17 μM) into synaptosomal suspensions of the dorsal raphe nucleus. Synpatosomal uptake of [3H]5-HT was blocked by selective destruction of serotonergic axon terminals induced by the intra-ventricular injection of 200 μg of 5,7-dihydroxytryptamine following desipramine HCl pretreatment, but not by destruction of catecholaminergic axon terminals induced by intraventricularly injected 6-hydroxydopamine (2 × 250 μg). The uptake of [3H]-5-HT by synaptosomes of the dorsal raphe was comparable to that of striatal and hypothalamic synaptosomes, and markedly greater than that of synaptosomes from the cerebellum or nearby dorsal central gray or midbrain reticular formation, indicating the presence of a relatively dense serotonergic innervation. These data together indicate that neurons in the dorsal raphe nucleus receive a prominent serotonergic input that is derived, at least in part, from other neurons within the dorsal nucleus and from a neighboring raphe nucleus.
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U2 - 10.1016/0006-8993(77)90311-0
DO - 10.1016/0006-8993(77)90311-0
M3 - Article
C2 - 830388
AN - SCOPUS:0017324580
SN - 0006-8993
VL - 119
SP - 269
EP - 290
JO - Brain Research
JF - Brain Research
IS - 2
ER -