The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Distribution and regulation of aromatase activity in the rat hypothalamus and limbic system
Abstract
Conversion of androgen to estrogen in the rat brain is catalyzed by aromatase enzymes. The maximum concentrations of these enzymes are found within the hypothalamus and amygdala, where they appear to play an important role in the process by which androgens affect both behavior and neuroendocrine function. In the present study, we measured the levels of aromatase activity (AA) in 20 nuclei and brain regions of the adult rat brain. Individual nuclei were microdissected from 600-micron frozen sections. Tissues from 3 animals were pooled, and AA was measured by an in vitro radiometric assay that quantifies the stereospecific production of 3H2O from [1 beta-3H]androstenedione as an index of estrogen formation. We report that AA is heterogeneously distributed within the rat brain. The greatest amounts of activity were found in the bed nucleus (n.) of the stria terminalis (700 protein fmol/h . mg) and in the medial (MA) and cortical amygdala (400-600 fmol/h . mg protein) of the male. There was an evident rostral-caudal and medial-lateral gradient in AA throughout the diencephalon. Activity was high in the periventricular preoptic n. and medial preoptic n.; intermediate in the suprachiasmatic preoptic n., anterior hypothalamus, periventricular anterior hypothalamus, and ventromedial n.; and low in the arcuate n.-median eminence, lateral preoptic n., supraoptic n., dorsomedial n., and lateral hypothalamus. Regions devoid of measurable AA included the medial and lateral septum, caudate-putamen, hippocampus, and parietal cortex. In the female, AA was greatest in the MA and cortical amygdala. We found that AA in the MA, stria terminalis n., suprachiasmatic preoptic n., periventricular preoptic in., medial preoptic n., anterior hypothalamus, and ventromedial n. was significantly greater (P less than 0.05) in males than in females. Orchidectomy reduced AA to levels seen in females, and administration of testosterone to castrated males restored AA in these areas. No significant sex differences were observed in any other hypothalamic or amygdaloid nuclei, although AA was increased by testosterone treatment in the periventricular anterior hypothalamus, arcuate n.-median eminence, and lateral hypothalamus. Our results provide a quantitative profile of AA in specific hypothalamic and limbic nuclei of the rat brain as well as information on the control of AA within these discrete regions.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“It catalyzes the rate-limiting final step in estrogen (E) production, the hydroxylation of androstenedione to estrone and of T to E 2 (Fig. 1).”
From A new era in ovulation induction (2006) · cites this paper as [23]
Citations
Cites
PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT
Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 316,394
Statistical principles in experimental design.
Winer, B. J. (1962) · McGraw-Hill Book Company · doi:10.1037/11774-000 · Cited by 27,137
Atlas of estradiol‐concentrating cells in the central nervous system of the female rat
Pfaff, D. W., & Keiner, M. (1973) · The Journal of Comparative Neurology · doi:10.1002/cne.901510204 · Cited by 1,494
Isolated removal of hypothalamic or other brain nuclei of the rat
Palkovits, M. (1973) · Brain Research · doi:10.1016/0006-8993(73)90290-4 · Cited by 1,431
Sexual differentiation of the brain
McEwen, B. S. (1981) · Nature · doi:10.1038/291610a0 · Cited by 899
The Formation of Estrogens by Central Neuroendocrine Tissues
NAFTOLIN, F., RYAN, K. J., DAVIES, I. J., REDDY, V. V., FLORES, F., PETRO, Z., KUHN, M., WHITE, R. J., TAKAOKA, Y., & WOLIN, L. (1975) · Proceedings of the 1974 Laurentian Hormone Conference · doi:10.1016/b978-0-12-571131-9.50012-8 · Cited by 793
Beatty, W. W. (1979) · Hormones and Behavior · doi:10.1016/0018-506x(79)90017-5 · Cited by 631
Estrogen‐Neurons and estrogen‐neuron systems in the periventricular brain
Stumpf, W. E. (1970) · American Journal of Anatomy · doi:10.1002/aja.1001290209 · Cited by 305
Progestin receptor levels in rat hypothalamic and limbic nuclei
Parsons, B., Rainbow, T. C., MacLusky, N. J., & McEwen, B. (1982) · Journal of Neuroscience · doi:10.1523/jneurosci.02-10-01446.1982 · Cited by 250
Regulation of Brain Aromatase Activity in Rats*
Roselli, C. E., Ellinwood, W. E., & Resko, J. A. (1984) · Endocrinology · doi:10.1210/endo-114-1-192 · Cited by 233
Cited by
Sorted by citations
Items 101–200 of 414
Wood, R. I., Brabec, R. K., Swann, J. M., & Newman, S. W. (1992) · Brain Research · doi:10.1016/0006-8993(92)91536-n · Cited by 99
Distribution of aromatase-immunoreactive cells in the mouse forebrain
Balthazart, J., Foidart, A., Surlemont, C., & Harada, N. (1991) · Cell and Tissue Research · doi:10.1007/bf00318401 · Cited by 100
Harada, N., Yamada, K., Foidart, A., & Balthazart, J. (1992) · Molecular Brain Research · doi:10.1016/0169-328x(92)90146-3 · Cited by 98
Roles for Oestrogen Receptor β in Adult Brain Function
Handa, R. J., Ogawa, S., Wang, J. M., & Herbison, A. E. (2012) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2011.02206.x · Cited by 97
Harada, N., Abe-Dohmae, S., Loeffen, R., Foidart, A., & Balthazart, J. (1993) · Brain Research · doi:10.1016/0006-8993(93)90825-8 · Cited by 97
Sex Differences in the Effect of Puberty on Hippocampal Morphology
Satterthwaite, T. D., Vandekar, S., Wolf, D. H., Ruparel, K., Roalf, D. R., Jackson, C. T., Elliott, M. A., Bilker, W. B., Calkins, M. E., Prabhakaran, K., et al. (2013) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2013.12.002 · Cited by 102
Handa, R. J., Weiser, M. J., & Zuloaga, D. G. (2009) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2009.01840.x · Cited by 96
Aromatase distribution in the monkey temporal neocortex and hippocampus
Yagüe, J. G., Wang, A. C., Janssen, W. G. M., Hof, P. R., García‐Segura, L. M., Azcoitia, Í., & Morrison, J. H. (2008) · Brain Research · doi:10.1016/j.brainres.2008.02.061 · Cited by 97
Sex differences in lipid metabolism and metabolic disease risk
Sugiyama, M. G., & Agellon, L. B. (2012) · Biochemistry and Cell Biology · doi:10.1139/o11-067 · Cited by 98
Steroid Metabolism and the Activation of Social Behavior
Balthazart, J. (1989) · Advances in comparative and environmental physiology · doi:10.1007/978-3-642-73827-2_3 · Cited by 95
Trainor, B. C., Bird, I. M., Alday, N. A., Schlinger, B. A., & Marler, C. A. (2003) · Neuroendocrinology · doi:10.1159/000071704 · Cited by 147
Steroidogenic Enzymes in the Brain: Morphological Aspects
Pelletier, G. (2010) · Progress in brain research · doi:10.1016/s0079-6123(08)81011-4 · Cited by 101
Vockel, A., Pröve, E., & Balthazart, J. (1990) · Journal of Neurobiology · doi:10.1002/neu.480210514 · Cited by 93
Comprehensive Pharmacology and Clinical Efficacy of Aromatase Inhibitors
Njar, V. C. O., & Brodie, A. M. H. (1999) · Drugs · doi:10.2165/00003495-199958020-00003 · Cited by 92
Sun, T., Zhao, Y., Mangelsdorf, D. J., & Simpson, E. R. (1998) · Endocrinology · doi:10.1210/endo.139.4.5959 · Cited by 91
Quantitative Analysis of Long-Form Aromatase mRNA in the Male and Female Rat Brain
Tabatadze, N., Sato, S. M., & Woolley, C. S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0100628 · Cited by 89
Multiple mechanisms control brain aromatase activity at the genomic and non-genomic level
Balthazart, J., Baillien, M., Charlier, T. D., Cornil, C. A., & Ball, G. F. (2003) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/s0960-0760(03)00346-7 · Cited by 89
Aromatase inhibitors in advanced breast cancer: mechanism of action and clinical implications
Brodie, A. M. H., & Njar, V. C. O. (1998) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/s0960-0760(98)00022-3 · Cited by 88
Regulation of Steroid Hydroxylase Gene Expression Is Multifactorial in Nature
Waterman, M. R., & Simpson, E. R. (1989) · Elsevier eBooks · doi:10.1016/b978-0-12-571145-6.50016-9 · Cited by 86
Estrogen synthesis in the hippocampus
Fester, L., Prange‐Kiel, J., Jarry, H., & Rune, G. M. (2011) · Cell and Tissue Research · doi:10.1007/s00441-011-1221-7 · Cited by 88
Sex differences in the neural circuit that mediates female sexual receptivity
Flanagan-Cato, L. (2011) · Frontiers in neuroendocrinology (Print) · doi:10.1016/j.yfrne.2011.02.008 · Cited by 86
Gomez, D. M., & Newman, S. W. (1991) · The Anatomical Record · doi:10.1002/ar.1092310412 · Cited by 87
Lagranha, C. J., Silva, T. L. A., Silva, S. C. A., Braz, G. R. F., da Silva, A. I., Fernandes, M. P., & Sellitti, D. F. (2017) · Life Sciences · doi:10.1016/j.lfs.2017.11.043 · Cited by 88
Shinoda, K., Nagano, M., & Osawa, Y. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903430109 · Cited by 85
Simerly, R. B., & Swanson, L. W. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.7.2087 · Cited by 85
Testosterone in the brain: Neuroimaging findings and the potential role for neuropsychopharmacology
Höfer, P., Lanzenberger, R. R., & Kasper, S. F. (2012) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2012.04.013 · Cited by 88
Foidart, A., Harada, N., & Balthazart, J. (1995) · Cell and Tissue Research · doi:10.1007/bf00318360 · Cited by 83
Aromatase activity in human osteoblast-like osteosarcoma cell
Tanaka, S., Haji, M., Nishi, Y., Yanase, T., Takayanagi, R., & Nawata, H. (1993) · Calcified Tissue International · doi:10.1007/bf00308318 · Cited by 80
Progesterone modulation of androgen-dependent sexual behavior in male rats
Witt, D. M., Young, L. J., & Crews, D. (1995) · Physiology & Behavior · doi:10.1016/0031-9384(94)00247-3 · Cited by 79
Pillerová, M., Borbélyová, V., Hodosy, J., RILJAK, V., Renczés, E., Frick, K. M., & Tóthová, Ľ. (2021) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2021.100926 · Cited by 79
Zwain, I. H., Yen, S. S. C., & Cheng, C. Y. (1997) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/s0304-4165(96)00115-8 · Cited by 78
Montagnese, C. M., Poulain, D. A., & Theodosis, D. T. (1990) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1990.tb00855.x · Cited by 77
A novel variant of the putative demethylase gene, s-JMJD1C, is a coactivator of the AR
Wolf, S. S., Patchev, V. K., & Obendorf, M. (2007) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2007.01.017 · Cited by 76
Sex Differences in Androgen-regulated Expression of Cytochrome P450 Aromatase in the Rat Brain
Roselli, C. E., & Resko, J. A. (1997) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/s0960-0760(97)80034-9 · Cited by 76
The development of brain sex differences: a multisignaling process
Segovia, S., Guillamón, A., del Cerro, M. C. R., Ortega, E., Pérez-Laso, C., Zafra, M. R., & Beyer, C. (1999) · Behavioural Brain Research · doi:10.1016/s0166-4328(99)00083-2 · Cited by 75
Matochik, J. A., Sipos, M. L., Nyby, J., & Barfield, R. J. (1994) · Behavioural Brain Research · doi:10.1016/0166-4328(94)90141-4 · Cited by 73
Regional distribution of 5α-reductase type 2 in the adult rat brain: An immunohistochemical analysis
Castelli, M. P., Casti, A., Casu, A., Frau, R., Bortolato, M., Spiga, S., & Ennas, M. G. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.06.008 · Cited by 73
Karolczak‐Bayatti, M., Küppers, E., & Beyer, C. (1998) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1998.00200.x · Cited by 72
Beyer, C., Green, S. J., & Hutchison, J. B. (1994) · Endocrinology · doi:10.1210/endo.135.3.8070366 · Cited by 74
Shinoda, K., Mori, S., Ohtsuki, T., & Osawa, Y. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903220306 · Cited by 71
Pfaus, J. G., Jones, S. L., Flanagan‐Cato, L. M., & Blaustein, J. D. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397175-3.00050-8 · Cited by 73
Jenkins, C. M., Michael, D., Mahendroo, M., & Simpson, E. R. (1993) · Molecular and Cellular Endocrinology · doi:10.1016/0303-7207(93)90227-b · Cited by 71
Dehydroepiandrosterone Increases Hippocampal Spine Synapse Density in Ovariectomized Female Rats
Hajszán, T., MacLusky, N. J., & Léránth, C. (2003) · Endocrinology · doi:10.1210/en.2003-1252 · Cited by 71
Roselli, C. E., Stadelman, H. L., HORTON, L. E., & Resko, J. A. (1987) · Endocrinology · doi:10.1210/endo-120-1-97 · Cited by 71
Bryan, K. J., Mudd, J. C., Richardson, S. L., Chang, J., Lee, H., Zhu, X., Smith, M. A., & Casadesús, G. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06502.x · Cited by 73
Testosterone Regulates Aromatase Activity in Discrete Brain Areas of Male Rhesus Macaques1
Roselli, C. E., & Resko, J. A. (1989) · Biology of Reproduction · doi:10.1095/biolreprod40.5.929 · Cited by 70
Turillazzi, E., Neri, M., Cerretani, D., Cantatore, S., Frati, P., Moltoni, L., Busardò, F. P., Pomara, C., Riezzo, I., & Fineschi, V. (2016) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12748 · Cited by 78
Foidart, A., Harada, N., & Balthazart, J. (1994) · Brain Research · doi:10.1016/0006-8993(94)90958-x · Cited by 69
Beyer, C., Green, S. J., Barker, P. J., Huskisson, N. S., & Hutchinson, J. B. (1994) · Brain Research · doi:10.1016/0006-8993(94)90651-3 · Cited by 69
The distribution and regulation of aromatase activity in the central nervous system
Roselli, C. E., & Resko, J. A. (1987) · Steroids · doi:10.1016/0039-128x(87)90034-1 · Cited by 68
Regulation of Placenta-specific Expression of the Aromatase Cytochrome P-450 Gene
Yamada, K., Harada, N., Honda, S., & Takagi, Y. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.42.25064 · Cited by 68
Shinoda, K., Nagano, M., & Osawa, Y. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903290102 · Cited by 67
A GCM Motif Protein Is Involved in Placenta-specific Expression of Human Aromatase Gene
Yamada, K., Ogawa, H., Honda, S., Harada, N., & Okazaki, T. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.45.32279 · Cited by 67
Hinshelwood, M. M., Corbin, C. J., Tsang, P. C. W., & Simpson, E. R. (1993) · Endocrinology · doi:10.1210/en.133.5.1971 · Cited by 67
Progesterone and sexual behavior in males
Witt, D. M., Young, L. J., & Crews, D. (1994) · Psychoneuroendocrinology · doi:10.1016/0306-4530(94)90040-x · Cited by 66
Warner, M. N., Strömstedt, M., Möller, L., & Gustafsson, J.-Α. (1989) · Endocrinology · doi:10.1210/endo-124-6-2699 · Cited by 65
Age-Dependent Effects of Testosterone in Experimental Stroke
Cheng, J., Hu, W., Toung, T. J. K., Zhang, Z., Parker, S. M., Roselli, C. E., & Hurn, P. D. (2008) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2008.138 · Cited by 64
Evrard, H. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00930.2005 · Cited by 64
Chambers, K. C., Thornton, J. E., & Roselli, C. E. (1991) · Neurobiology of Aging · doi:10.1016/0197-4580(91)90050-t · Cited by 64
Alternative promotion of aromatase P-450 expression in the human placenta
Kilgore, M. W., Means, G., Mendelson, C. R., & Simpson, E. R. (1992) · Molecular and Cellular Endocrinology · doi:10.1016/0303-7207(92)90202-h · Cited by 63
Roselli, C. E., & Klosterman, S. A. (1998) · Endocrinology · doi:10.1210/endo.139.7.6101 · Cited by 110
Neuroestrogens Rapidly Regulate Sexual Motivation But Not Performance
Seredynski, A. L., Balthazart, J., Christophe, V., Ball, G. F., & Cornil, C. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2557-12.2013 · Cited by 62
Tsuruo, Y., Ishimura, K., Fujita, H., & Osawa, Y. (1994) · Cell and Tissue Research · doi:10.1007/bf00305775 · Cited by 62
Saldanha, C. J., Tuerk, M. J., Kim, Y., Fernandes, A. O., Arnold, A. P., & Schlinger, B. A. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20000807)423:4 · Cited by 245
Sex Differences and Steroid Control of Testosterone‐Metabolizing Enzyme Activity in the Quail Brain
Balthazart, J., Schumacher, M., & Evrard, L. (1990) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1990.tb00464.x · Cited by 61
Morris, J. A., Jordan, C. L., Dugger, B. N., & Breedlove, S. M. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20558 · Cited by 65
Zhao, C., Fujinaga, R., Tanaka, M., Yanai, A., Nakahama, K., & Shinoda, K. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21193 · Cited by 60
Agarwal, V. R., Ashanullah, C. I., Simpson, E. R., & Bulun, S. E. (1997) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.82.1.3655 · Cited by 63
Chai, J., Blaha, V., Meguid, M. M., Laviano, A., Yang, Z., & Varma, M. (1999) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1999.276.5.r1366 · Cited by 60
Neuroanatomical Distribution of Aromatase MRNA in the Rat Brain: Indications of Regional Regulation
Wagner, C. K., & Morrell, J. I. (1997) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/s0960-0760(97)80028-3 · Cited by 60
Dubois-Dauphin, M., Barberis, C., & de Bilbao, F. (1996) · Brain Research · doi:10.1016/s0006-8993(96)01019-0 · Cited by 57
Bender, R. A., Zhou, L., Wilkars, W., Fester, L., Lanowski, J.-S., Paysen, D., Konig, A., & Rune, G. M. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq047 · Cited by 58
Aromatase inhibitors: possible future applications
Karaer, Ö., Oruç, S., & Koyuncu, F. M. (2004) · Acta Obstetricia Et Gynecologica Scandinavica · doi:10.1111/j.0001-6349.2004.00562.x · Cited by 59
Balthazart, J., Foidart, A., Surlemont, C., Harada, N., & Naftolin, F. N. (1992) · Brain Research · doi:10.1016/0006-8993(92)90828-w · Cited by 59
Sex neurosteroids: Hormones made by the brain for the brain
Fester, L., & Rune, G. M. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135849 · Cited by 60
Aromatase expression in the normal and epileptic human hippocampus.
Yague, J. G., Azcoitia, Í., DeFelipe, J., Garcia-Segura, L., & Muñoz, A. (2010) · Brain Research · doi:10.1016/j.brainres.2009.09.111 · Cited by 62
Spatial memory performance in androgen insensitive male rats
JONES, B., & WATSON, N. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2005.03.023 · Cited by 57
The alternative exons 1 of the mouse aromatase cytochrome P-450 gene
Honda, S., Harada, N., & Takagi, Y. (1996) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/0167-4781(95)00200-6 · Cited by 57
Cornil, C. A. (2017) · Journal of Comparative Physiology A · doi:10.1007/s00359-017-1224-2 · Cited by 56
Endocrine Correlates of Partner Preference Behavior in Rams1
Resko, J. A., Perkins, A. E., Roselli, C. E., Fitzgerald, J. A., Choate, J. V. A., & STORMSHAK, F. (1996) · Biology of Reproduction · doi:10.1095/biolreprod55.1.120 · Cited by 55
Circulating gonadal steroid hormones regulate estrogen receptor mRNA in the male rat forebrain
Lisciotto, C. A., & Morrell, J. I. (1993) · Molecular Brain Research · doi:10.1016/0169-328x(93)90112-3 · Cited by 55
Aste, N., Panzica, G., Viglietti‐Panzica, C., Harada, N., & Balthazart, J. (1998) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(97)10023-0 · Cited by 55
Charlier, T. D., Po, K., Newman, A. E. M., Shah, A. H., Saldanha, C. J., & Soma, K. K. (2010) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2010.02.002 · Cited by 54
Revisiting the flip side: Long-term depression of synaptic efficacy in the hippocampus
Pinar, C., Fontaine, C. J., Triviño-Paredes, J., Lottenberg, C. P., Gil‐Mohapel, J., & Christie, B. R. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.06.001 · Cited by 60
Rubin, G., Duong, J., Clyne, C. D., Speed, C. J., Murata, Y., Gong, C., & Simpson, E. R. (2002) · Endocrinology · doi:10.1210/endo.143.8.8932 · Cited by 54
Aromatase activity in cultured brain cells: difference between neurons and glia
Negri‐Cesi, P., Melcangi, R. C., Celotti, F., & Martini, L. (1992) · Brain Research · doi:10.1016/0006-8993(92)91294-o · Cited by 54
Rani, S., Raheja, K., Luxami, V., & Paul, K. (2021) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2021.105017 · Cited by 53
Blair, J. A., McGee, H., Bhatta, S., Palm, R. F., & Casadesús, G. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00045 · Cited by 55
Molecular and cellular physiology of aromatase in the brain and retina
Callard, G. V., Drygas, M. E., & Gélinas, D. (1993) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/0960-0760(93)90257-w · Cited by 52
Immunohistochemical localization of cytochrome P-450 in the rat brain
Köhler, C., Eriksson, L. G., Hansson, T., Warner, M. N., & Åke-Gustafsson, J. (1988) · Neuroscience Letters · doi:10.1016/0304-3940(88)90392-8 · Cited by 52
Sexually Dimorphic Effects of Aromatase on Neurobehavioral Responses
Shay, D. A., Vieira‐Potter, V. J., & Rosenfeld, C. S. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00374 · Cited by 55
Neuroendocrine and Behavioral Development during Puberty: A Tale of Two Axes
Romeo, R. D. (2005) · Vitamins and hormones · doi:10.1016/s0083-6729(05)71001-3 · Cited by 51
Local modulation of steroid action: rapid control of enzymatic activity
Charlier, T. D., Cornil, C. A., Patte‐Mensah, C., Meyer, L., Mensah‐Nyagan, A. G., & Balthazart, J. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00083 · Cited by 49
Gintzler, A. R., & Liu, N. (2012) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2012.09.004 · Cited by 49
Role of Estrogen Receptor-β in Regulation of Vasopressin and Oxytocin Releasein Vitro
Somponpun, S. J., & Sladek, C. D. (2002) · Endocrinology · doi:10.1210/endo.143.8.8946 · Cited by 49
Shi, Z., & Brooks, V. L. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.284638 · Cited by 48
von Ziegler, N. I., Schlumpf, M., & LICHTENSTEIGER, W. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90186-m · Cited by 48
Northcutt, K. V., Wang, Z., & Lonstein, J. S. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21148 · Cited by 46
Koss, W. A., & Frick, K. M. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2019.01.002 · Cited by 47
Imaging of aromatase distribution in rat and rhesus monkey brains with [11C]vorozole
Takahashi, K., Bergström, M., Frändberg, P., Vesström, E.-L., Watanabe, Y., & Långström, B. (2006) · Nuclear Medicine and Biology · doi:10.1016/j.nucmedbio.2006.03.009 · Cited by 47
Metadata
- Authors
- ROSELLI, C. E., HORTON, L. E., & RESKO, J. A.
- Affiliations
- Oregon National Primate Research Center (US)
- ORCID
- ROSELLI, CHARLES E.
- Venue
- Endocrinology
- Publisher
- The Endocrine Society
- Published
- 1985-12
- Volume
- 117
- Issue
- 6
- Pages
- 2471-2477
- ISSN
- 0013-7227 (ISSN-L)
- 1945-7170
- OpenAlex
- W2078288264
- Cited by
- 415
- References
- 27
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 4 · 2023: 1 · 2022: 3 · 2021: 6 · 2020: 6 · 2019: 3 · 2018: 6 · 2017: 7 · 2016: 8 · 2015: 12 · 2014: 14 · 2013: 8 · 2012: 14
- FWCI
- 5.11
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Endocrinology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Center for Research Resources (RR-00163.)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD18196)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Estrogen and related hormone effects
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
- Health Sciences › Medicine › Reproductive Medicine › Hypothalamic control of reproductive hormones
- Keywords
- aromatase activity, hypothalamus, amygdala, bed nucleus of the stria terminalis, medial amygdala, preoptic area, sex differences, testosterone, orchiectomy, androgen metabolism, neuroendocrine regulation, diencephalon, medial preoptic nucleus, ventromedial hypothalamus, arcuate nucleus, median eminence
- MeSH terms
- Androstenedione, Animals, Aromatase, Female, Freezing, Hypothalamus, Limbic System, Male, Orchiectomy, Time Factors, Tissue Distribution, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review