과제정보
This work was supported by the Major Projects of the Ministry of Science and Technology of China (2021ZD0202300) and the National Natural Science Foundations of China (32070986, 32171005, 82160152).
참고문헌
- Zhang BB, Jin H, Bing YH, Zhang XY, Chu CP, Li YZ, Qiu DL. A nitric oxide-dependent presynaptic LTP at glutamatergic synapses of the PVN magnocellular neurosecretory cells in vitro in rats. Front Cell Neurosci. 2019;13:283.
- Csaki A, Kocsis K, Halasz B, Kiss J. Localization of glutamatergic/ aspartatergic neurons projecting to the hypothalamic paraventricular nucleus studied by retrograde transport of [3H]D-aspartate autoradiography. Neuroscience. 2000;101:637-655.
- van den Pol AN, Wuarin JP, Dudek FE. Glutamate, the dominant excitatory transmitter in neuroendocrine regulation. Science. 1990;250:1276-1278.
- Decavel C, Van den Pol AN. GABA: a dominant neurotransmitter in the hypothalamus. J Comp Neurol. 1990;302:1019-1037.
- Wuarin JP, Dudek FE. Patch-clamp analysis of spontaneous synaptic currents in supraoptic neuroendocrine cells of the rat hypothalamus. J Neurosci. 1993;13:2323-2331.
- Stern JE, Galarreta M, Foehring RC, Hestrin S, Armstrong WE. Differences in the properties of ionotropic glutamate synaptic currents in oxytocin and vasopressin neuroendocrine neurons. J Neurosci. 1999;19:3367-3375.
- Panatier A, Gentles SJ, Bourque CW, Oliet SH. Activity-dependent synaptic plasticity in the supraoptic nucleus of the rat hypothalamus. J Physiol. 2006;573:711-721.
- Salter EW, Sunstrum JK, Matovic S, Inoue W. Chronic stress dampens excitatory synaptic gain in the paraventricular nucleus of the hypothalamus. J Physiol. 2018;596:4157-4172.
- Matsuura T, Kawasaki M, Suzuki H, Fujitani T, Baba K, Nishimura H, Ikeda N, Yamanaka Y, Tsukamoto M, Yoshimi Y, Ohnishi H, Ueta Y, Sakai A. Nitric oxide synthase contributes to the maintenance of LTP in the oxytocin-mRFP1 neuron of the rat hypothalamus. J Neuroendocrinol. 2023;35:e13340.
- Maguire J. Stress-induced plasticity of GABAergic inhibition. Front Cell Neurosci. 2014;8:157.
- Stanton LM, Price AJ, Manning EE. Hypothalamic corticotrophin releasing hormone neurons in stress-induced psychopathology: revaluation of synaptic contributions. J Neuroendocrinol. 2023;35:e13268.
- Herman JP, Tasker JG. Paraventricular hypothalamic mechanisms of chronic stress adaptation. Front Endocrinol (Lausanne). 2016;7:137.
- Chappell PB, Smith MA, Kilts CD, Bissette G, Ritchie J, Anderson C, Nemeroff CB. Alterations in corticotropin-releasing factor-like immunoreactivity in discrete rat brain regions after acute and chronic stress. J Neurosci. 1986;6:2908-2914.
- Ma XM, Lightman SL, Aguilera G. Vasopressin and corticotropin-releasing hormone gene responses to novel stress in rats adapted to repeated restraint. Endocrinology. 1999;140:3623-3632.
- Bartsch JC, von Cramon M, Gruber D, Heinemann U, Behr J. Stress-induced enhanced long-term potentiation and reduced threshold for N-methyl-D-aspartate receptor- and β-adrenergic receptor-mediated synaptic plasticity in rodent ventral subiculum. Front Mol Neurosci. 2021;14:658465.
- Chay A, Zamparo I, Koschinski A, Zaccolo M, Blackwell KT. Control of βAR- and N-methyl-D-aspartate (NMDA) receptor-dependent cAMP dynamics in hippocampal neurons. PLoS Comput Biol. 2016;12:e1004735.
- Han SK, Chong W, Li LH, Lee IS, Murase K, Ryu PD. Noradrenaline excites and inhibits GABAergic transmission in parvocellular neurons of rat hypothalamic paraventricular nucleus. J Neurophysiol. 2002;87:2287-2296.
- Inoshita T, Hirano T. Norepinephrine facilitates induction of longterm depression through β-adrenergic receptor at parallel fiber-to-Purkinje cell synapses in the flocculus. Neuroscience. 2021;462:141-150.
- Cui LN, Sun N, Li BX, Wang LF, Zhang XY, Qiu DL, Chu CP. Noradrenaline inhibits complex spikes activity via the presynaptic PKA signaling pathway in mouse cerebellar slices. Neurosci Lett. 2020;729:135008.
- Wang JY, Weng WC, Wang TQ, Liu Y, Qiu DL, Wu MC, Chu CP. Noradrenaline depresses facial stimulation-evoked cerebellar MLI-PC synaptic transmission via α2-AR/PKA signaling cascade in vivo in mice. Sci Rep. 2023;13:15908.
- Yamaguchi N, Mimura K, Okada S. GABAB receptors in the hypothalamic paraventricular nucleus mediate β-adrenoceptor-induced elevations of plasma noradrenaline in rats. Eur J Pharmacol. 2019;848:88-95.
- Domingos-Souza G, Martinez D, Sinkler S, Heesch CM, Kline DD. Alpha adrenergic receptor signaling in the hypothalamic paraventricular nucleus is diminished by the chronic intermittent hypoxia model of sleep apnea. Exp Neurol. 2021;335:113517.
- Chu CP, Jin WZ, Bing YH, Jin QH, Kannan H, Qiu DL. Effects of stresscopin on rat hypothalamic paraventricular nucleus neurons in vitro. PLoS One. 2013;8:e53863.
- Tasker JG, Dudek FE. Electrophysiological properties of neurones in the region of the paraventricular nucleus in slices of rat hypothalamus. J Physiol. 1991;434:271-293.
- O'Dell TJ, Connor SA, Guglietta R, Nguyen PV. β-Adrenergic receptor signaling and modulation of long-term potentiation in the mammalian hippocampus. Learn Mem. 2015;22:461-471.
- Laing M, Bashir ZI. β-Adrenoceptors and synaptic plasticity in the perirhinal cortex. Neuroscience. 2014;273:163-173.
- O'Dell TJ, Connor SA, Gelinas JN, Nguyen PV. Viagra for your synapses: enhancement of hippocampal long-term potentiation by activation of beta-adrenergic receptors. Cell Signal. 2010;22:728-736.
- Wang M, Ramasamy VS, Kang HK, Jo J. Oleuropein promotes hippocampal LTP via intracellular calcium mobilization and Ca2+-permeable AMPA receptor surface recruitment. Neuropharmacology. 2020;176:108196.
- Park P, Georgiou J, Sanderson TM, Ko KH, Kang H, Kim JI, Bradley CA, Bortolotto ZA, Zhuo M, Kaang BK, Collingridge GL. PKA drives an increase in AMPA receptor unitary conductance during LTP in the hippocampus. Nat Commun. 2021;12:413.