2015
DOI: 10.1016/j.npep.2015.03.007
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Role of adrenomedullin in the cerebrospinal fluid-contacting nucleus in the modulation of immobilization stress

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Cited by 16 publications
(6 citation statements)
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References 45 publications
(50 reference statements)
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“…and neuron–body fluids pathways. Moreover, in previous studies, the distribution and change in the expression of substance P (Lu et al, 2011), acid-sensing ion channel 3 (ASIC 3 ) (Wang et al, 2014), transient receptor potential vanniloid-1 (TRPV 1 ) (Xu et al, 2011), Wnt 5a (Wang J. et al, 2015), extracellular signal-regulated kinase-5 (ERK 5 ) (Wang C. G. et al, 2015), mechanistic target of rapamycin (mTOR) and ERK 1/2 (Li et al, 2015), neurokinin-1 receptor (NK 1 R) (Zhang et al, 2017), and adrenomedullin (Wu et al, 2015), as well as dozens of neuroactive substances (including neurotransmitters, receptors, and ion channel proteins) in the CSF-contacting nucleus in morphine physical dependence (Lu et al, 2011), inflammatory pain (Wang et al, 2014), neuropathic pain (Xu et al, 2011; Li et al, 2015; Wang C. G. et al, 2015; Wang J. et al, 2015), visceral pain (Zhang et al, 2017) and stress (Wu et al, 2015). Studying the characteristics of the CSF-contacting nucleus and understanding the changes in the substances distributed in the nucleus will help elucidate the function of the nucleus and its relationship to physiological processes.…”
Section: Discussionmentioning
confidence: 99%
“…and neuron–body fluids pathways. Moreover, in previous studies, the distribution and change in the expression of substance P (Lu et al, 2011), acid-sensing ion channel 3 (ASIC 3 ) (Wang et al, 2014), transient receptor potential vanniloid-1 (TRPV 1 ) (Xu et al, 2011), Wnt 5a (Wang J. et al, 2015), extracellular signal-regulated kinase-5 (ERK 5 ) (Wang C. G. et al, 2015), mechanistic target of rapamycin (mTOR) and ERK 1/2 (Li et al, 2015), neurokinin-1 receptor (NK 1 R) (Zhang et al, 2017), and adrenomedullin (Wu et al, 2015), as well as dozens of neuroactive substances (including neurotransmitters, receptors, and ion channel proteins) in the CSF-contacting nucleus in morphine physical dependence (Lu et al, 2011), inflammatory pain (Wang et al, 2014), neuropathic pain (Xu et al, 2011; Li et al, 2015; Wang C. G. et al, 2015; Wang J. et al, 2015), visceral pain (Zhang et al, 2017) and stress (Wu et al, 2015). Studying the characteristics of the CSF-contacting nucleus and understanding the changes in the substances distributed in the nucleus will help elucidate the function of the nucleus and its relationship to physiological processes.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, our recent studies reveal that this nucleus receives the projections from the hypothalamus (Song et al, 2020b) and brainstem (Song et al, 2020a), which implies that the CSF-contacting nucleus participates in complex and diverse neural circuits modulating different behaviors. The relationships with some of the life activities such as pain (Liu et al, 2017), stress (Wu et al, 2015), and drug addiction (Lu et al, 2011) have been already reported.…”
Section: Introductionmentioning
confidence: 96%
“…8 This connection is not found in any known nerve or nucleus in the nervous system. The basic biological properties of the CSF-contacting nucleus, such as methods that can be used to specifically label it, 9 its location and stereotactic coordinates, 8 the distribution of receptors, neurotransmitters, and ion channels [10][11][12] and its relationship with morphine dependence and withdrawal, stress, sodium appetite, ion channels 10,[13][14][15] have been revealed. A model animal with the CSF-contacting nucleus eliminated has been successfully established.…”
Section: Introductionmentioning
confidence: 99%