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The Role of Adrenal Nerves in the Regulation of Adrenocortical Functionsa
Abstract
There is now convincing evidence for the distribution of several nerve plexuses in the outer zone of the adrenal cortex. At the ultrastructural level, the close proximity of nerve boutons to cortical cells establishes the anatomical substrate for a direct neural effect on adrenal cortical cell functions. Of those neurotransmitters and neuropeptides identified to date, catecholamine, VIP, and NPY appear to be most prevalent. Importantly, the amounts of morphologically identifiable catecholamine, VIP and NPY are differentially sensitive to alteration of several physiological conditions. Furthermore, the VIP plexus appears to be intrinsic to the adrenal while the catecholamine and NPY nerve fibers enter the adrenal along blood vessels. Together, these results suggest that these multiple nerve plexuses might exert control on several adrenocortical cellular processes in addition to the regulation of adrenal blood flow. Compensatory adrenal growth, a rapid proliferative response to unilateral adrenalectomy, was previously shown to be neurally mediated. The role of the catecholamine innervation in the mediation of this process has now been demonstrated. The elimination of the sympathetic nervous system by neonatal sympathectomy inhibited the proliferative response as measured by DNA synthesis. In vivo administration of beta-adrenergic receptor blockers did not inhibit the compensatory growth response. Furthermore, the beta-adrenergic agonist isoproterenol, inhibited the rate of DNA synthesis both in vivo and in vitro. The direct action of the beta-adrenergic agonist on the adrenocortical cell DNA synthesis rate suggests that the catecholaminergic nerves tonically inhibit cell proliferation associated with compensatory growth and that the release from the beta-adrenergic inhibition is necessary for compensatory growth. Whether inhibition of the beta-adrenergic innervation is the trigger for compensatory growth or whether it is permissive to the action of a still unidentified mitogenic substance, is not yet known. The direct role of VIP and catecholamines in the regulation of steroidogenesis has been investigated in vitro using the perifused capsule-glomerulosa preparation which is representative of a normal outer zone of the adrenal and is the site of the neural plexuses and identified receptors. Both VIP and isoproterenol stimulate steroidogenesis and specifically cause a greater increase in secretion of aldosterone than corticosterone. Although the concentrations of VIP and isoproterenol required to stimulate steroidogenesis are greater than reported circulating levels, release from resident nerves could provide high local concentrations.(ABSTRACT TRUNCATED AT 400 WORDS)
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“significant evidence now points to a neural SCN-adrenal gland connection, via the autonomic nervous system and independent from the HPA axis activation [19, 20]: this multisynaptic pathway from the SCN to the adrenal gland is able to transmit light information to the adrenal glands, modulating corticosterone release without changes in ACTH secretion [21].”
From Impact of Sleep and Its Disturbances on Hypothalamo-Pituitary-Adrenal Axis Activity (2010) · cites this paper as [20]
Citations
Cites
Hökfelt, T. G. M., Elfvin, L.-G., Schultzberg, M., Goldstein, M., & Nilsson, G. (1977) · Brain Research · doi:10.1016/0006-8993(77)90704-1 · Cited by 351
Varndell, I. M., Polak, J. M., Allen, J. M., Terenghi, G., & Bloom, S. R. (1984) · Endocrinology · doi:10.1210/endo-114-4-1460 · Cited by 198
Linnoila, R. I., DiAugustine, R. P., Hervonen, A., & Miller, R. J. (1980) · Neuroscience · doi:10.1016/0306-4522(80)90141-4 · Cited by 179
Angiotensin II regulates its receptor sites in the adrenal glomerulosa zone
Hauger, R. L., Aguilera, G., & Catt, K. J. (1978) · Nature · doi:10.1038/271176a0 · Cited by 123
The distribution of vasoactive intestinal peptide in the rat adrenal cortex and medulla
Holzwarth, M. A. (1984) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(84)90041-9 · Cited by 120
Self-citationControl of Adrenocortical Growth in Vivo
Dallman, M. F. (1984) · Endocrine Research · doi:10.1080/07435808409036499 · Cited by 117
Leboulenger, F., Leroux, P., Delarue, C., Tonon, M., Charnay, Y., Dubois, P. M., Coy, D. H., & Vaudry, H. (1983) · Life Sciences · doi:10.1016/0024-3205(83)90083-8 · Cited by 108
Aguilera, G., & Catt, K. J. (1986) · Endocrinology · doi:10.1210/endo-118-1-112 · Cited by 101
THE NEURAL REGULATION OF COMPENSATORY ADRENAL GROWTH*
Dallman, M. F., Engeland, W. C., & McBride, M. H. (1977) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1977.tb41869.x · Cited by 90
Somatostatin modulates effects of angiotensin II in adrenal glomerulosa zone
Aguilera, G., Harwood, J. P., & Catt, K. J. (1981) · Nature · doi:10.1038/292262a0 · Cited by 82
Research works printed but not linked: 4
- Whitfield J. F., 1980, Handbk Exp. Pharmacol., 267
- Gill G., 1979, Cold Spring Harbor Conference on Cell Proliferation, 6, 701
- Birnbaum R. S., 1980, Endocrinology, 106, 1270
- Aguilera G., 1980, Circul. Res., 46, 118
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Carrasco, G. A., & Van de Kar, L. D. (2003) · European Journal of Pharmacology · doi:10.1016/s0014-2999(03)01285-8 · Cited by 914
Intraadrenal interactions in the regulation of adrenocortical steroidogenesis.
Ehrhart-Bornstein, M., Hinson, J. P., Bornstein, S. R., Scherbaum, W. A., & Vinson, G. P. (1998) · Endocrine Reviews · doi:10.1210/edrv.19.2.0326 · Cited by 600
Impact of Sleep and Its Disturbances on Hypothalamo-Pituitary-Adrenal Axis Activity
Balbo, M., Leproult, R., & Van Cauter, E. (2010) · International Journal of Endocrinology · doi:10.1155/2010/759234 · Cited by 408
“In addition, significant evidence now points to a neural SCN-adrenal gland connection, via the autonomic nervous system and independent from the HPA axis activation [19, 20]: this multisynaptic pathway from the SCN to the adrenal gland is able to transmit light information to the adrenal glands, modulating corticoster…”
BackgroundDifferential control of sympathetic outflow
Morrison, S. F. (2001) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2001.281.3.r683 · Cited by 381
Resistance Exercise Overtraining and Overreaching
Fry, A. C., & Kraemer, W. J. (1997) · Sports Medicine · doi:10.2165/00007256-199723020-00004 · Cited by 286
Murphy, B. E. P. (1991) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/0960-0760(91)90312-s · Cited by 247
Adrenocorticotropin insensitivity syndromes
Clark, A. J. L., & Weber, A. (1998) · Endocrine Reviews · doi:10.1210/edrv.19.6.0351 · Cited by 234
Prüß, H., Tedeschi, A., Thiriot, A., Lynch, L., Loughhead, S. M., Stutte, S., Mazo, I. B., Kopp, M. A., Brommer, B., Blex, C., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4643 · Cited by 184
Pituitary-adrenal-gonadal responses to high-intensity resistance exercise overtraining
Fry, A. C., Kraemer, W. J., & Ramsey, L. (1998) · Journal of Applied Physiology · doi:10.1152/jappl.1998.85.6.2352 · Cited by 167
Gazarian, M., Cowell, C., Bonney, M., & Grigor, W. G. (1994) · European Journal of Pediatrics · doi:10.1007/bf01972967 · Cited by 140
Bornstein, S. R., Ehrhart‐Bornstein, M., Usadel, H., B�ckmann, M., & Scherbaum, W. A. (1991) · Cell and Tissue Research · doi:10.1007/bf00318133 · Cited by 113
Diagnosing overtraining in athletes using the two-bout exercise protocol
MEEUSEN, R. R., Nederhof, E., Buyse, L., Roelands, B., Schutter, G. D., & Piacentini, M. F. (2008) · British Journal of Sports Medicine · doi:10.1136/bjsm.2008.049981 · Cited by 112
The innervation of the mammalian adrenal gland.
Parker, T. L., Kesse, W., Mohamed, A., & Afework, M. (1993) · Europe PMC (PubMed Central) · Cited by 112
Sex-dependent alteration in cortisol response to endogenous adrenocorticotropin
Roelfsema, F., van den Berg, G., Frölich, M. A., Veldhuis, P. P., van Eijk, A., Buurman, M. M., & Etman, B. (1993) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.77.1.8392084 · Cited by 110
The Neuroendocrinology of the Adrenal Cortex
Vinson, G. P., Hinson, J. P., & Tóth, I. E. (1994) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1994.tb00578.x · Cited by 107
Allgrove syndrome: an autosomal recessive syndrome of ACTH insensitivity, achalasia and alacrima
Moore, P. S. J., Couch, R., PERRY, Y. S., Shuckett, E. P., & Winter, J. S. D. (1991) · Clinical Endocrinology · doi:10.1111/j.1365-2265.1991.tb00279.x · Cited by 101
Gerendai, I., & Halász, B. (1997) · Frontiers in Neuroendocrinology · doi:10.1006/frne.1997.0154 · Cited by 100
Autonomic control of adrenal function.
Edwards, A. V., & Jones, C. T. (1993) · PubMed · Cited by 100
Functional Zonation of the Adult Mammalian Adrenal Cortex
Vinson, G. P. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00238 · Cited by 108
Acute hormonal responses to heavy resistance exercise in strength athletes versus nonathletes
Ahtiainen, J. P., Pakarinen, A., Kraemer, W. J., & Hakkinen, K. (2004) · Canadian Journal of Applied Physiology · doi:10.1139/h04-034 · Cited by 97
Adrenocortical zonation and ACTH
Vinson, G. P. (2003) · Microscopy Research and Technique · doi:10.1002/jemt.10331 · Cited by 91
Role of Tachykinins in the Regulation of the Hypothalamo–Pituitary–Adrenal Axis
Nussdorfer, G. G., & Malendowicz, L. K. (1998) · Peptides · doi:10.1016/s0196-9781(98)00017-5 · Cited by 77
Vasoactive Intestinal Peptide Stimulates Adrenal Aldosterone and Corticosterone Secretion*
Cunningham, L. A., & Holzwarth, M. A. (1988) · Endocrinology · doi:10.1210/endo-122-5-2090 · Cited by 77
Self-citationDijkstra, I., Binnekade, R., & Tilders, F. J. H. (1996) · Endocrinology · doi:10.1210/endo.137.2.8593800 · Cited by 75
Sympathoadrenal regulation of adrenocortical steroidogenesis
Ehrhart-Bornstem, M., Bornstein, S. R., González-Hernández, J. A., Holst, J. J., Waterman, M. R., & Scherbaum, W. A. (1995) · Endocrine Research · doi:10.3109/07435809509030417 · Cited by 62
Effects of complex experience on somatic growth and organ development in rats
Black, J., Sirevaag, A. M., Wallace, C. S., Savin, M. H., & Greenough, W. T. (1989) · Developmental Psychobiology · doi:10.1002/dev.420220707 · Cited by 59
Food and the circadian activity of the hypothalamic-pituitary-adrenal axis
Leal, A. M. O., & Moreira, A. C. (1997) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x1997001200003 · Cited by 60
Hennessy, M. B., Harvey, A. T., Schiml, P. A., & Lucot, J. B. (1989) · Physiology & Behavior · doi:10.1016/0031-9384(89)90101-7 · Cited by 52
Hermann, G. E., Beck, F. M., Tovar, C. A., Malarkey, W. B., Allen, C. M., & Sheridan, J. F. (1994) · Journal of Neuroimmunology · doi:10.1016/0165-5728(94)90027-2 · Cited by 52
Development and function of the fetal adrenal
Pignatti, E., du Toit, T., & Flück, C. E. (2022) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-022-09756-3 · Cited by 51
Hinson, J. P., Vinson, G. P., Kapas, S., & Teja, R. (1991) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/0960-0760(91)90205-j · Cited by 50
Psychobiological Consequences of Social Relationshipsa
Levine, S., Lyons, D. M., & Schatzberg, A. F. (1997) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1997.tb51922.x · Cited by 50
Afework, M., Tomlinson, A., & Burnstock, G. (1994) · Cell and Tissue Research · doi:10.1007/bf00354792 · Cited by 48
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Bernet, F., Bernard, J., Laborie, C., Montel, V., Maubert, E., & Dupouy, J. (1994) · Neuroscience Letters · doi:10.1016/0304-3940(94)90852-4 · Cited by 42
Gwosdow, A. R., O'Connell, N. A., Spencer, J. A., Kumar, M., Agarwal, R., Bode, H., & Abou‐Samra, A. (1992) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1992.263.3.e461 · Cited by 42
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Self-citationMartin, Duclos, Aguerre, Mormède, P., Manier, & Chaouloff (2000) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.2000.00683.x · Cited by 38
Hinson, J. P., Cameron, L. A., Purbrick, A., & Kapas, S. (1994) · Regulatory Peptides · doi:10.1016/0167-0115(94)90135-x · Cited by 36
Leboulenger, F., Vaglini, L., Conlon, J. M., Homo-Delarche, F., Wang, Y., Kerdelhué, B., Pelletier, G., & Vaudry, H. (1993) · Endocrinology · doi:10.1210/endo.133.5.7691584 · Cited by 35
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Pignatelli, D., Ferreira, J. G. G., Vendeira, P., Magalhães, M., & Vinson, G. P. (2002) · Endocrine Research · doi:10.1081/erc-120016987 · Cited by 34
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Hinson, J. P., Purbrick, A., Cameron, L. A., & Kapas, S. (1994) · Neuropeptides · doi:10.1016/0143-4179(94)90024-8 · Cited by 33
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Holst, J. J., Ehrhart‐Bornstein, M., Messell, T., Poulsen, S. S., & Harling, H. (1991) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1991.261.1.e31 · Cited by 29
Basile, D. P., & Holzwarth, M. A. (1994) · Endocrinology · doi:10.1210/endo.134.6.8194474 · Cited by 28
Self-citationKostka, T., Patricot, M. C., Mathian, B., Lacour, J.-R., & Bonnefoy, M. (2003) · Aging Clinical and Experimental Research · doi:10.1007/bf03324489 · Cited by 32
Townsend, S. F., Dallman, M. F., & Miller, W. L. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)45678-5 · Cited by 28
Mendoza, S. P., Hennessy, M. B., & Lyons, D. M. (1992) · Psychobiology · doi:10.3758/bf03332064 · Cited by 27
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Dubrovsky, B. O. (1993) · PubMed Central · Cited by 26
Bodart, V., Babinski, K., Ong, H., & Léan, A. D. (1997) · Endocrinology · doi:10.1210/endo.138.2.4915 · Cited by 25
CARLSSON, S., Skarphedinsson, J. O., Jennische, E., Delle, M., & Thorén, P. (1990) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1990.tb09025.x · Cited by 25
Charlton, B. G., McGadey, J., Russell, D., & Neal, D. E. (1992) · Europe PMC (PubMed Central) · Cited by 24
Mazzocchi, G., Malendowicz, L., Macchi, C., Gottardo, G., & Nussdorfer, G. G. (1996) · Neuropeptides · doi:10.1016/s0143-4179(96)90050-5 · Cited by 24
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Cao, W.-H., & Morrison, S. F. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02964-4 · Cited by 24
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Walker, C., & McCormick, C. M. (2009) · Elsevier eBooks · doi:10.1016/b978-008088783-8.00061-9 · Cited by 23
Heym, C., Braun, B., Shuyi, Y., Klimaschewski, L. P., & Colombo‐Benkmann, M. (1995) · Histochemistry and Cell Biology · doi:10.1007/bf01835156 · Cited by 22
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Heym, C., Braun, B., Klimaschewski, L. P., & Kummer, W. (1994) · Cell and Tissue Research · doi:10.1007/bf00300702 · Cited by 22
Tsujimoto, S., Okumura, Y., Kamei, C., & Tasaka, K. (1993) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1993.tb13646.x · Cited by 21
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Apostolakis, E. M., Longo, L. D., Veldhuis, J. D., & Yellon, S. M. (1992) · Endocrinology · doi:10.1210/endo.130.5.1315248 · Cited by 21
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Walker, C., Welberg, L., & Plotsky, P. M. (2002) · Elsevier eBooks · doi:10.1016/b978-012532104-4/50074-3 · Cited by 21
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Makara, G. B., Varga, J. M., Barna, I., Pintér, O., Klausz, B., & Zelena, D. (2012) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-012-9842-2 · Cited by 20
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Self-citationDorovini‐Zis, K., & Zis, A. P. (1991) · Journal of Neural Transmission · doi:10.1007/bf01249111 · Cited by 19
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Spagnolo, E. V., Mondello, C., Cardia, L., Minutoli, L., Puzzolo, D., Asmundo, A., Macaione, V., Alibrandi, A., Malta, C., Baldino, G., et al. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20123065 · Cited by 15
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Suárez, M. M., Molina, S., Rivarola, M. A., & Perassi, N. I. (2002) · Life Sciences · doi:10.1016/s0024-3205(02)01830-1 · Cited by 12
Suárez, M. M., Maglianesi, M. A., & Perassi, N. I. (1998) · Physiology & Behavior · doi:10.1016/s0031-9384(98)00028-6 · Cited by 12
Belloni, A. S., Neri, G., Andreis, P. G., Musajo, F. G., Boscaro, M., Mazzocchi, G., & Nussdorfer, G. G. (1991) · Cell and Tissue Research · doi:10.1007/bf00318136 · Cited by 12
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Metadata
- Authors
- HOLZWARTH, M. A., CUNNINGHAM, L. A., & KLEITMAN, N.
- Affiliations
- University of Illinois Urbana-Champaign (US)
- Corresponding author
- KLEITMAN, N.
- Venue
- Annals of the New York Academy of Sciences
- Publisher
- Wiley
- Published
- 1987-12
- Volume
- 512
- Issue
- 1
- Pages
- 449-464
- ISSN
- 0077-8923 (ISSN-L)
- 1749-6632
- OpenAlex
- W1977107439
- Cited by
- 129
- References
- 26
- Citations by year
- 2024: 1 · 2023: 1 · 2022: 2 · 2019: 2 · 2017: 2 · 2016: 1 · 2014: 2 · 2012: 2
- FWCI
- 1.09
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annals of the New York Academy of Sciences (publishedVersion)
- PubMed (publishedVersion)
- Funders
- School of Medicine, Emory University
- National Institute of General Medical Sciences (5T32GM07)
- National Center for Research Resources (S-O7RR7030)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Keywords
- adrenocortical function, catecholamine innervation, vasoactive intestinal peptide, neuropeptide Y, steroidogenesis, aldosterone secretion, adrenalectomy, beta-adrenergic receptors, isoproterenol, adrenal blood flow, zona glomerulosa, adrenal innervation, DNA synthesis
- MeSH terms
- Adrenal Cortex, Adrenalectomy, Aldosterone, Animals, Animals, Newborn, Autonomic Nervous System, Cell Division, Corticosterone, DNA Replication, Guanethidine, Hydroxydopamines, Kinetics, Male, Rats, Inbred Strains, Sympathectomy, Chemical, Oxidopamine, Rats, In Vitro Techniques
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