The DOI matches its Crossref record.
The milk-ejection reflex of the rat: a 20-to 40-fold acceleration in the firing of paraventricular neurones during oxytocin release
Abstract
SUMMARY Antidromically-identified paraventricular (PV) neurones were studied in the anaesthetized rat during milk ejection (ME) evoked by the natural stimulus provided by the suckling young. An intermittent pattern of ME was observed, though the ME interval was slightly longer (10–20 min) in the doe during unit recording than in unoperated or conscious animals (5–15 min). PV neurones displayed a steady background of spike discharge in both the non-lactating rat and lactating rat during suckling. The firing rates ranged from 0 to 9·4 spikes/s and were exponentially distributed with 32% of the units firing at <1 spike/s. Phasic patterns of discharge were seen in 18% of the units. Fifty-eight per cent of the PV units displayed a stereotyped and explosive acceleration in spike activity some 15–20 s before the rise in intramammary pressure at ME. The peak firing rate during this brief (2–4 s) response was in the range of 24–84 spikes/s. A prominent after-inhibition was then displayed by these responsive units, though this second component of the response was variable in duration (7–56 s). The electrical activity of the remaining units, including all the cells with phasic discharge, was not correlated with ME. There was no apparent change in the intensity of the suckling stimulus at the time of PV activation, i.e. 15–20 s before ME. Secondly, the activity of the PV neurones was not influenced by the rise in the intramammary pressure and the increased sucking of the pups at the time of ME. Simulation of an individual ME was obtained with both 1 mu. exogenous oxytocin, i.v., and electrical stimulation of the neurohypophysis (50 pulses/s for 4 s). The latencies to ME ranged from 7–14 s and 11–23 s, respectively. In conclusion, an explosive increase in the electrical activity of PV neurones precipitates the release of oxytocin at ME.
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
“Oxytocin is a mammalian neurohormone composed of nine amino acids, known for its peripheral effects on parturition and lactation (5–7), as well as its central neuromodulatory effects on social behaviors such as affiliative, aggressive, and parental behaviors (8, 9).”
From Oxytocin during Development: Possible Organizational Effects on Behavior (2015) · cites this paper as [6]
Citations
Cited by
Sorted by citations
The oxytocin receptor: from intracellular signaling to behavior
Jurek, B., & Neumann, I. D. (2018) · Physiological Reviews · doi:10.1152/physrev.00031.2017 · Cited by 999
Electrophysiology of hypothalamic magnocellular neurones secreting oxytocin and vasopressin
Poulain, D. A., & Wakerley, J. B. (1982) · Neuroscience · doi:10.1016/0306-4522(82)90044-6 · Cited by 816
Self-citationNelson, E. E., & Panksepp, J. (1998) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(97)00052-3 · Cited by 688
“There is clear evidence that oxytocin is released from the posterior pituitary of female mammals during vaginal stimulation (100) nursing (207), and parturition (64), all of which occur during social interactions.”
BackgroundPain modulation by release of the endogenous cannabinoid anandamide
Walker, J. M., Huang, S. M., Strangman, N. M., Tsou, K., & Sañudo-Peña, M. C. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.21.12198 · Cited by 486
Pfaff, D. W., & Sakuma, Y. (1979) · The Journal of Physiology · doi:10.1113/jphysiol.1979.sp012690 · Cited by 461
Metabolic Mapping of Functional Activity in the Hypothalamo-Neurohypophysial System of the Rat
Schwartz, W. J., Smith, C. B., Davidsen, L., Savaki, H., Sokoloff, L., Mata, M., Fink, D. J., & Gainer, H. (1979) · Science · doi:10.1126/science.462184 · Cited by 454
Small-Conductance Ca2+-Activated K+Channels: Form and Function
Adelman, J. P., Maylie, J., & Sah, P. (2011) · Annual Review of Physiology · doi:10.1146/annurev-physiol-020911-153336 · Cited by 454
Dendrites of hypothalamic magnocellular neurons release neurohypophysial peptides by exocytosis
Pow, D. V., & Morris, J. F. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90091-2 · Cited by 446
Hatton, G. I. (1990) · Progress in Neurobiology · doi:10.1016/0301-0082(90)90017-b · Cited by 439
Renaud, L. P., & Bourquet, C. W. (1991) · Progress in Neurobiology · doi:10.1016/0301-0082(91)90020-2 · Cited by 348
Dendritic Release of Vasopressin and Oxytocin
Ludwig (1998) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1998.00279.x · Cited by 342
Physiological pathways regulating the activity of magnocellular neurosecretory cells
Leng, G., Brown, C. H., & Russell, J. A. (1999) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00072-0 · Cited by 312
Cazalis, M., Dayanithi, G., & Nordmann, J. J. (1985) · The Journal of Physiology · doi:10.1113/jphysiol.1985.sp015887 · Cited by 299
The neurobiology of preovulatory and estradiol-induced gonadotropin-releasing hormone surges
Christian, C. A., & Moenter, S. M. (2010) · Endocrine Reviews · doi:10.1210/er.2009-0023 · Cited by 300
The magnocellular oxytocin system, the fount of maternity: Adaptations in pregnancy
Russell, J. A., Leng, G., & Douglas, A. J. (2003) · Frontiers in Neuroendocrinology · doi:10.1016/s0091-3022(02)00104-8 · Cited by 295
Brimble, M. J., & Dyball, R. E. J. (1977) · The Journal of Physiology · doi:10.1113/jphysiol.1977.sp011999 · Cited by 283
Evolution of oxytocin pathways in the brain of vertebrates
Knobloch, H. S., & Grinevich, V. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00031 · Cited by 259
“This assumption was confirmed experimentally with 30 Hz optical stimulation, resembling the bursting activity of OT neurons during suckling (Wakerley and Lincoln, 1973; Poulain and Wakerley, 1982) and inducing axonal OT release in various brain regions (Knobloch et al., 2012, 2014)5.”
MethodCell Biology of Synaptic Plasticity
Cotman, C. W., & Nieto‐Sampedro, M. (1984) · Science · doi:10.1126/science.6382610 · Cited by 275
LINCOLN, D. W., & Wakerley, J. B. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010722 · Cited by 252
Self-citationElectrophysiological differentiation of oxytocin-and vasopressin-secreting neurones
Poulain, D. A., Wakerley, J. B., & Dyball, R. E. J. (1977) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1977.0046 · Cited by 243
Self-citationMorphological and electrophysiological classification of hypothalamic supraoptic neurons
Armstrong, W. E. (1995) · Progress in Neurobiology · doi:10.1016/0301-0082(95)80005-s · Cited by 246
Wakerley, J. B., Poulain, D. A., & Brown, D. A. (1978) · Brain Research · doi:10.1016/0006-8993(78)90730-8 · Cited by 229
Self-citationTol, H. H. M. V., Bolwerk, E., LlU, B., & Burbach, J. P. H. (1988) · Endocrinology · doi:10.1210/endo-122-3-945 · Cited by 226
Release of oxytocin within the supraoptic nucleus during the milk ejection reflex in rats
Moos, F., Poulain, D. A., Rodriguez, F., Guern�, Y., Vincent, J. D., & Richard, P. (1989) · Experimental Brain Research · doi:10.1007/bf00248916 · Cited by 221
“A bursting activity (periodic high frequency bursts of action potentials) is evoked both by suckling during the milk ejection reflex (Wakerley and Lincoln 1973) and during foetus expulsion during parturition (Summerlee 1981).”
BackgroundOpiate inhibition of peptide release from the neurohumoral terminals of hypothalamic neurones
Clarke, G., Wood, P., Merrick, L., & Lincoln, D. W. (1979) · Nature · doi:10.1038/282746a0 · Cited by 219
Diurnal and estradiol-dependent changes in gonadotropin-releasing hormone neuron firing activity
Christian, C. A., Mobley, J. L., & Moenter, S. M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504270102 · Cited by 218
An Allostatic Theory of Oxytocin
Quintana, D. S., & Guastella, A. J. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.03.008 · Cited by 223
“, pulsatile secretion during lactation [105] versus continuous secretion for natriuresis [106]), as well as the widespread delivery of oxytocin in the brain and periphery, have important implications for the coordination of physiology and behavior.”
Hatton, G. I., Perlmutter, L. S., Salm, A. K., & Tweedle, C. D. (1984) · Peptides · doi:10.1016/0196-9781(84)90271-7 · Cited by 214
Freund‐Mercier, M. J., & Richard, P. (1984) · The Journal of Physiology · doi:10.1113/jphysiol.1984.sp015302 · Cited by 212
Optimizing Release From Peptide Hormone Secretory Nerve Terminals
Bicknell, R. J. (1988) · Journal of Experimental Biology · doi:10.1242/jeb.139.1.51 · Cited by 207
Emergent Synchronous Bursting of Oxytocin Neuronal Network
Rossoni, E., Feng, J., Tirozzi, B., Brown, D., Leng, G., & Moos, F. (2008) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000123 · Cited by 207
“These features [8,9] led to the belief that bursting reflects mechanisms intrinsic to oxytocin cells, but these mechanisms have proved elusive.”
BackgroundResultCells of origin of the spinohypothalamic tract in the rat
Burstein, R., Cliffer, K. D., & Giesler, G. J. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902910302 · Cited by 206
Hussy, N., Deleuze, C., Desarménien, M. G., & Moos, F. (2000) · Progress in Neurobiology · doi:10.1016/s0301-0082(99)00071-4 · Cited by 207
Burst Discharge in Mammalian Neuroendocrine Cells Involves an Intrinsic Regenerative Mechanism
Andrew, R. D., & Dudek, F. E. (1983) · Science · doi:10.1126/science.6879204 · Cited by 198
Hrabovszky, E., Kalló, I., Hajszán, T., Shughrue, P. J., Merchenthaler, I. J., & Liposits, Z. (1998) · Endocrinology · doi:10.1210/endo.139.5.6024 · Cited by 193
Dye Transfer Through Gap Junctions Between Neuroendocrine Cells of Rat Hypothalamus
Andrew, R. D., MacVicar, B. A., Dudek, F. E., & Hatton, G. I. (1981) · Science · doi:10.1126/science.7466393 · Cited by 181
Control of pulsatile insulin secretion in man
Matthews, D. R., Lang, D. A., Burnett, M. A., & Turner, R. C. (1983) · Diabetologia · doi:10.1007/bf00282705 · Cited by 175
“They have been described with leuteinising hormone [26], arginine vasopressin [27], oxytocin [28], gonadotrophin releasing hormone [29], ACTH, corticosteroids and human growth hormone [30].”
MethodTheodosis, D. T., Poulain, D. A., & Vincent, J. D. (1981) · Neuroscience · doi:10.1016/0306-4522(81)90173-1 · Cited by 176
Brown, C. H., Bains, J. S., Ludwig, M., & Stern, J. E. (2013) · Journal of Neuroendocrinology · doi:10.1111/jne.12051 · Cited by 179
Belin, V., & Moos, F. (1986) · The Journal of Physiology · doi:10.1113/jphysiol.1986.sp016192 · Cited by 163
Brimble, M. J., Dyball, R. E. J., & Forsling, M. L. (1978) · The Journal of Physiology · doi:10.1113/jphysiol.1978.sp012293 · Cited by 162
Hatton, G. I., & Tweedle, C. D. (1982) · Brain Research Bulletin · doi:10.1016/0361-9230(82)90046-6 · Cited by 157
Summerlee, A. J. S. (1981) · The Journal of Physiology · doi:10.1113/jphysiol.1981.sp013967 · Cited by 154
Oxytocin and vasopressin gene expression during gestation and lactation
Zingg, H. H., & Lefebvre, D. L. (1988) · Molecular Brain Research · doi:10.1016/0169-328x(88)90011-3 · Cited by 151
Satô, A., Sato, Y., & Schmidt, R. F. (1997) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/bfb0046598 · Cited by 155
LINCOLN, D. W., & Wakerley, J. B. (1975) · The Journal of Physiology · doi:10.1113/jphysiol.1975.sp011064 · Cited by 148
Self-citationNorman, T. C. (1976) · International review of cytology · doi:10.1016/s0074-7696(08)60990-0 · Cited by 142
NMDA receptor‐mediated rhythmic bursting activity in rat supraoptic nucleus neurones in vitro.
Hu, B., & Bourque, C. W. (1992) · The Journal of Physiology · doi:10.1113/jphysiol.1992.sp019440 · Cited by 140
Neuroendocrine control of milk ejection
LINCOLN, D. W., & Paisley, A. C. (1982) · Reproduction · doi:10.1530/jrf.0.0650571 · Cited by 136
“About 50% of neurones in both the supraoptic and paraventricular nuclei display an explosive acceleration in activity for 2-4 sec, at about 10—12 sec before the rise in intramammary pressure at milk ejection (Wakerley & Lincoln, 1973; Lincoln & Wakerley, 1974, 1975).”
BackgroundSelf-citationLambert, R. C., Moos, F., & Richard, P. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90046-i · Cited by 132
Stern, J. E., & Armstrong, W. E. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-03-00841.1998 · Cited by 130
Castel, M., Gainer, H., & Dellmann, H. ‐. (1984) · International review of cytology · doi:10.1016/s0074-7696(08)62760-6 · Cited by 129
Allopregnanolone in the brain: Protecting pregnancy and birth outcomes
Brunton, P. J., Russell, J. A., & Hirst, J. J. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.08.005 · Cited by 122
“Each burst of electrical activity, every few minutes during suckling, leads to secretion of a pulse of oxytocin from the posterior pituitary gland, which then stimulates a sharp increase in intramammary pressure that causes milk transfer into the mouths of the suckling young (Wakerley and Lincoln, 1973).”
BackgroundThe maternal brain: an organ with peripartal plasticity
Hillerer, K. M., Jacobs, V. R., Fischer, T., & Aigner, L. (2014) · Neural Plasticity · doi:10.1155/2014/574159 · Cited by 120
Intraterminal recordings from the rat neurohypophysis in vitro.
Bourque, C. W. (1990) · The Journal of Physiology · doi:10.1113/jphysiol.1990.sp017943 · Cited by 116
Lincoln, D. W., Fraser, H. M., Lincoln, G. A., Martin, G. B., & McNeilly, A. S. (1985) · Elsevier eBooks · doi:10.1016/b978-0-12-571141-8.50013-5 · Cited by 117
Self-citationIntrinsic inhibition in magnocellular neuroendocrine cells of rat hypothalamus.
Andrew, R. D., & Dudek, F. E. (1984) · The Journal of Physiology · doi:10.1113/jphysiol.1984.sp015330 · Cited by 117
The milk ejection reflex in the pig
Ellendorff, F., Forsling, M. L., & Poulain, D. A. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014470 · Cited by 116
Neural circuitry for maternal oxytocin release induced by infant cries
Valtcheva, S., Issa, H. A., Bair-Marshall, C. J., Martin, K. A., Jung, K., Zhang, Y., Kwon, H.-B., & Froemke, R. C. (2023) · Nature · doi:10.1038/s41586-023-06540-4 · Cited by 115
Monroe, J. G., & Cambier, J. C. (1983) · The Journal of Experimental Medicine · doi:10.1084/jem.157.6.2073 · Cited by 112
Neuroendocrine Regulation of Lactation and Milk Production
Crowley, W. R. (2014) · Comprehensive physiology · doi:10.1002/cphy.c140029 · Cited by 135
Lyons, D. J., Horjales-Araújo, E., & Broberger, C. (2010) · Neuron · doi:10.1016/j.neuron.2009.12.024 · Cited by 105
Activity of phasic neurosecretory cells during haemorrhage
Wakerley, J. B., POULAIN, D. A., Dyball, R. E. J., & Cross, B. (1975) · Nature · doi:10.1038/258082a0 · Cited by 105
Self-citationStern, J. E., & Armstrong, W. E. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-16-04861.1996 · Cited by 104
“On the other hand, OT neurons during lactation display a synchronized, brief (2–4 sec), high-frequency (40–80 Hz) burst of activity preceding each milk ejection (Wakerley and Lincoln, 1973).”
BackgroundExcitatory effect of dopamine on oxytocin and vasopressin reflex releases in the rat
Moos, F., & Richard, P. (1982) · Brain Research · doi:10.1016/0006-8993(82)91061-7 · Cited by 104
A REVIEW ON NEUROSECRETORY GRANULES: THEIR CONTENTS AND MECHANISMS OF RELEASE
Dreifuss, J. J. (1975) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1975.tb34185.x · Cited by 103
Monroe, J. G., & Cambier, J. C. (1983) · The Journal of Experimental Medicine · doi:10.1084/jem.158.5.1589 · Cited by 101
“In other somatic cell systems (6-9), plasma membrane depolarization has been demonstrated to be important for activation and entry into cell cycle, and has further been postulated to be an initial and critical event in these processes.”
Sleep: A prerequisite for reflex milk ejection in the rat
LINCOLN, D. W., Hentzen, K., Hin, T., van der Schoot, P., Clarke, G., & Summerlee, A. J. S. (1980) · Experimental Brain Research · doi:10.1007/bf00236736 · Cited by 98
“Each milk ejection, in both anaesthetized (Wakerley and Lincoln, 1973) and conscious rats (Summerlee et al.”
BackgroundSelf-citationPittman, Q. J., Hatton, J. D., & Bloom, F. E. (1980) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.77.9.5527 · Cited by 94
Gibbens, G. L. D., & Chard, T. (1976) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(76)90283-0 · Cited by 89
Leng, G., Pineda, R., Sabatier, N., & Ludwig, M. (2015) · Journal of Endocrinology · doi:10.1530/joe-15-0087 · Cited by 85
The role of central adrenergic receptors in the reflex release of oxytocin
Tribollet, E., Clarke, G., Dreifuss, J.-J., & LINCOLN, D. W. (1978) · Brain Research · doi:10.1016/0006-8993(78)90177-4 · Cited by 85
Self-citationWakerley, J. B. (2006) · Elsevier eBooks · doi:10.1016/b978-012515400-0/50064-6 · Cited by 84
Self-citationOxytocinSynthesis, Secretion, and Reproductive Functions
BURBACH, J., YOUNG, L., & RUSSELL, J. (2006) · Knobil and Neill's Physiology of Reproduction · doi:10.1016/b978-012515400-0/50063-4 · Cited by 113
Akaishi, T., Negoro, H., & Kobayasi, S. (1980) · Brain Research · doi:10.1016/0006-8993(80)90048-7 · Cited by 82
GABA‐induced facilitation of the periodic bursting activity of oxytocin neurones in suckled rats.
Moos, F. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020949 · Cited by 79
Excitation of phasically firing hypothalamic supraoptic neurones by carotid occlusion in rats.
Dreifuss, J.-J., Harris, M. C., & Tribollet, E. (1976) · The Journal of Physiology · doi:10.1113/jphysiol.1976.sp011372 · Cited by 80
Oxytocin enhances myoepithelial cell differentiation and proliferation in the mouse mammary gland.
Sapino, A., Macrì, L., Tonda, L., et al. (1993) · Endocrinology · doi:10.1210/endo.133.2.8344220 · Cited by 79
Excitatory effects of intraventricular injections of oxytocin on the milk ejection reflex in the rat
Freund‐Mercier, M. J., & Richard, P. (1981) · Neuroscience Letters · doi:10.1016/0304-3940(81)90039-2 · Cited by 79
Oxytocin during Development: Possible Organizational Effects on Behavior
Miller, T. V., & Caldwell, H. K. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00076 · Cited by 79
Opioid modulation of magnocellular neurosecretory cell activity
Brown, C. H., Russell, J. A., & Leng, G. (2000) · Neuroscience Research · doi:10.1016/s0168-0102(99)00121-2 · Cited by 79
“A typical milk-ejection burst contains approximately 100 spikes and lasts 1–2 s (Wakerley and Lincoln, 1973; Lincoln and Wakerley, 1974; Wakerley and Ingram, 1993), releasing a bolus of about 1 mU (2 pmoles) of oxytocin into the circulation.”
BackgroundAHP's, HAP's and DAP's: How Potassium Currents Regulate the Excitability of Rat Supraoptic Neurones
Roper, P., Callaway, J. C., Shevchenko, T., Teruyama, R., & Armstrong, W. E. (2003) · Journal of Computational Neuroscience · doi:10.1023/a:1027424128972 · Cited by 76
Brèthes, D., Dayanithi, G., Letellier, L., et al. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.5.1439 · Cited by 76
Phasic bursting activity of rat paraventricular neurones in the absence of synaptic transmission
Hatton, G. I. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014231 · Cited by 76
Bioulac, B. H., Gaffori, O., Harris, M., et al. (1978) · Brain Research · doi:10.1016/0006-8993(78)91064-8 · Cited by 76
Organization of Mammalian Neuroendocrine System
Swanson, L. W. (1986) · Comprehensive physiology · doi:10.1002/cphy.cp010406 · Cited by 78
Poulain, D., Ellendorff, F., & Vincent, J. D. (1980) · Neuroscience · doi:10.1016/0306-4522(80)90113-x · Cited by 72
Stern, J. E., & Armstrong, W. E. (1997) · The Journal of Physiology · doi:10.1113/jphysiol.1997.sp022036 · Cited by 71
Wainwright, A., Rutter, A. R., Seabrook, G. R., Reilly, K., & Oliver, K. R. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20100 · Cited by 70
“This activity can be manifest as phasic burst and continuous firing and results in considerable release of OXT or VP (Wakerley and Lincoln, 1973; Lincoln and Wakerley, 36 A. WAINWRIGHT ET AL.”
BackgroundMontagnese, C. M., Poulain, D. A., Vincent, J., & Theodosis, D. T. (1988) · Brain Research Bulletin · doi:10.1016/0361-9230(88)90078-0 · Cited by 68
Sabatier, N., Richard, P., & Dayanithi, G. (1997) · The Journal of Physiology · doi:10.1111/j.1469-7793.1997.253bh.x · Cited by 66
Cobbett, P. J., & Hatton, G. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-12-03034.1984 · Cited by 67
“This showed that the incidence and percentage of somasomatic coupling were not changed, a somewhat surprising result since ultrastructural changes during dehydration have been described previously for the PVN (Gregory et al., 1980) and, to a much greater extent, for the SON ( Tweedle and Hatton, 1976, 1977 ).”
BackgroundOxytocin: Parallel Processing in the Social Brain?
Dölen, G. (2015) · Journal of Neuroendocrinology · doi:10.1111/jne.12284 · Cited by 65
Galanin Inhibits Continuous and Phasic Firing in Rat Hypothalamic Magnocellular Neurosecretory Cells
Papas, S., & Bourque, C. W. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-16-06048.1997 · Cited by 66
“Oxytocin, in turn, is well known for its role in promoting uterine contractions (Summerlee, 1981) and milk ejection (Wakerley and Lincoln, 1973).”
BackgroundStern, J. E., Galarreta, M., Foehring, R. C., Hestrin, S., & Armstrong, W. E. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-09-03367.1999 · Cited by 65
“During lactation, OT neurons display a periodic bursting activity synchronized among the whole population of neurons, resulting in a pulsatile release of the hormone into the circulation (Wakerley and Lincoln, 1973).”
BackgroundLeng, G., & Shibuki, K. (1987) · The Journal of Physiology · doi:10.1113/jphysiol.1987.sp016771 · Cited by 66
Lin, S., Miyata, S., Matsunaga, W., Kawarabayashi, T., Nakashima, T., & Kiyohara, T. (1998) · Brain Research · doi:10.1016/s0006-8993(97)01484-4 · Cited by 62
Onset of Bursting in Oxytocin Cells in Suckled Rats
Brown, D., & Moos, F. (1997) · The Journal of Physiology · doi:10.1111/j.1469-7793.1997.625bg.x · Cited by 64
“It is now well established that in lactating rats during suckling, oxytocin cells develop brief and intense accelerations of firing rate every 5—15 min, the ‘milk ejection bursts’ reported by Wakerley & Lincoln (1973).”
BackgroundToward a radically embodied neuroscience of attachment and relationships
Beckes, L., IJzerman, H., & Tops, M. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00266 · Cited by 72
Neural mechanisms underlying the milk ejection burst and reflex
Hatton, G. I., & WANG, Y. (2008) · Progress in brain research · doi:10.1016/s0079-6123(08)00414-7 · Cited by 61
“consisting of transient (2–6 s) high-frequency (16–80Hz) discharges of action potentials that recur every 2–15min of continuous suckling (Wakerley and Lincoln, 1973; Summerlee and Lincoln, 1981).”
Background
Metadata
- Authors
- WAKERLEY, J. B., & LINCOLN, D. W.
- Venue
- Journal of Endocrinology
- Publisher
- Bioscientifica
- Published
- 1973-06-01
- Volume
- 57
- Issue
- 3
- Pages
- 477-493
- ISSN
- 0022-0795 (ISSN-L)
- 1479-6805
- OpenAlex
- W2053881206
- Cited by
- 327
- References
- 0
- Citations by year
- 2026: 4 · 2025: 3 · 2024: 4 · 2023: 5 · 2022: 10 · 2021: 4 · 2020: 3 · 2019: 1 · 2018: 5 · 2017: 1 · 2016: 6 · 2015: 10 · 2014: 11 · 2013: 2 · 2012: 2
- FWCI
- 28.43
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Endocrinology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
- Health Sciences › Medicine › Reproductive Medicine › Hypothalamic control of reproductive hormones
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Keywords
- milk ejection reflex, oxytocin release, neuronal firing rate, suckling stimulus, intramammary pressure, lactation
- MeSH terms
- Action Potentials, Ethanol, Animals, Female, Hypothalamus, Lactation, Mammary Glands, Animal, Microelectrodes, Micromanipulation, Neurons, Oxytocin, Pituitary Gland, Pregnancy, Pressure, Reflex, Sucking Behavior, Urethane, 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