| scholarly article | Q13442814 |
| P2093 | author name string | Bingbing Song | |
| Xueren Wang | |||
| Li-Jun Lao | |||
| Juan Carlos G. Marvizon | |||
| P2860 | cites work | Inhibition of hyperalgesia by ablation of lamina I spinal neurons expressing the substance P receptor | Q73763175 |
| Nerve growth factor- and neurotrophin-3-induced changes in nociceptive threshold and the release of substance P from the rat isolated spinal cord | Q73797605 | ||
| Time-course of the internalization and recycling of neurokinin 1 receptors in rat dorsal horn neurons | Q74430664 | ||
| Evidence for tonic activation of NK-1 receptors during the second phase of the formalin test in the Rat | Q78025269 | ||
| Spinal substance P receptor expression and internalization in acute, short-term, and long-term inflammatory pain states | Q78166434 | ||
| Altered nociception, analgesia and aggression in mice lacking the receptor for substance P | Q24322842 | ||
| Leucine aminopeptidase: bestatin inhibition and a model for enzyme-catalyzed peptide hydrolysis | Q24563697 | ||
| Receptors and antagonists for substance P and related peptides | Q28287568 | ||
| CB(1) receptor antagonist SR141716A increases capsaicin-evoked release of Substance P from the adult mouse spinal cord | Q28344830 | ||
| Primary afferent tachykinins are required to experience moderate to intense pain | Q28506575 | ||
| Deficits in visceral pain and hyperalgesia of mice with a disruption of the tachykinin NK1 receptor gene | Q31395644 | ||
| Role of central and peripheral tachykinin NK1 receptors in capsaicin-induced pain and hyperalgesia in mice. | Q31889264 | ||
| Novel approaches to targeting neuropeptide systems | Q34106722 | ||
| Repeated systemic administration of the mixed inhibitor of enkephalin-degrading enzymes, RB101, does not induce either antinociceptive tolerance or cross-tolerance with morphine | Q34295761 | ||
| Inhibition of the enkephalin-metabolizing enzymes by the first systemically active mixed inhibitor prodrug RB 101 induces potent analgesic responses in mice and rats | Q34377116 | ||
| Synaptic relationship between substance P and the substance P receptor: light and electron microscopic characterization of the mismatch between neuropeptides and their receptors | Q37558489 | ||
| Peptidases prevent mu-opioid receptor internalization in dorsal horn neurons by endogenously released opioids. | Q40263009 | ||
| Tachykinin receptors in the spinal cord | Q40940969 | ||
| Characterization of antisera specific to NK1, NK2, and NK3 neurokinin receptors and their utilization to localize receptors in the rat gastrointestinal tract. | Q41156993 | ||
| Substance P release in the dorsal horn assessed by receptor internalization: NMDA receptors counteract a tonic inhibition by GABA(B) receptors | Q41610524 | ||
| The dual nature of the tachykinin NK1 receptor. | Q41633157 | ||
| Internalization of mu-opioid receptors in rat spinal cord slices | Q41684135 | ||
| Spinal opioid analgesia: how critical is the regulation of substance P signaling? | Q41697764 | ||
| Effect of the tachykinin NK1 receptor antagonists, RP 67580 and SR 140333, on electrically-evoked substance P release from rat spinal cord | Q41790903 | ||
| Involvement of enzymatic degradation in the inactivation of tachykinin neurotransmitters in neonatal rat spinal cord | Q41809899 | ||
| Comparison of the effects of epithelium removal and of an enkephalinase inhibitor on the neurokinin-induced contractions of guinea-pig isolated trachea | Q42848928 | ||
| Presynaptic regulation of spinal cord tachykinin signaling via GABA(B) but not GABA(A) receptor activation | Q43557132 | ||
| Projection neurons in lamina I of rat spinal cord with the neurokinin 1 receptor are selectively innervated by substance p-containing afferents and respond to noxious stimulation. | Q43999186 | ||
| Amino acid-mediated EPSPs at primary afferent synapses with substantia gelatinosa neurones in the rat spinal cord | Q44134973 | ||
| Postsynaptic signaling via the [mu]-opioid receptor: responses of dorsal horn neurons to exogenous opioids and noxious stimulation. | Q44333978 | ||
| Effects of three peptidase inhibitors, amastatin, captopril and phosphoramidon, on the hydrolysis of [Met5]-enkephalin-Arg6-Phe7 and other opioid peptides | Q44348401 | ||
| Relationship between capsaicin-evoked substance P release and neurokinin 1 receptor internalization in the rat spinal cord. | Q44406479 | ||
| Differential contribution of substance P and neurokinin A to spinal cord neurokinin-1 receptor signaling in the rat. | Q45027502 | ||
| Studies on the effect of SCH-34826 and thiorphan on [Met5]enkephalin levels and release in rat spinal cord. | Q45934622 | ||
| Inflammation increases the distribution of dorsal horn neurons that internalize the neurokinin-1 receptor in response to noxious and non-noxious stimulation. | Q46304913 | ||
| NMDA-receptor regulation of substance P release from primary afferent nociceptors | Q46378238 | ||
| Thiorphan increases capsaicin-evoked release of substance P from slices of dorsal spinal cord of guinea pig. | Q46494871 | ||
| Neurokinin 1 receptor internalization in spinal cord slices induced by dorsal root stimulation is mediated by NMDA receptors. | Q46662825 | ||
| Effect of peptidase inhibition on the pattern of intraspinally released immunoreactive substance P detected with antibody microprobes | Q47569918 | ||
| Lack of physical dependence in mice after repeated systemic administration of the mixed inhibitor prodrug of enkephalin-degrading enzymes, RB101 | Q48407392 | ||
| Aminopeptidase P from rat brain. Purification and action on bioactive peptides | Q48719143 | ||
| Blind patch-clamp recordings from substantia gelatinosa neurons in adult rat spinal cord slices: pharmacological properties of synaptic currents. | Q51671347 | ||
| Bronchoconstrictor and hypotensive effects in relation to pharmacokinetics of tachykinins in the guinea-pig--evidence for extraneuronal cleavage of neuropeptide K to neurokinin A. | Q51787780 | ||
| C-fiber excitability in the cat. | Q54074721 | ||
| Inhibition of aminopeptidases N, A and W | Q56450176 | ||
| Enkephalin degradation in mouse brain studied by a new H.P.L.C. method: Further evidence for the involvement of carboxydipeptidase | Q66981908 | ||
| Excitability characteristics of the A- and C-fibers in a peripheral nerve | Q67435205 | ||
| Is substance P released from slices of the rat spinal cord inactivated by peptidase(s) distinct from both ‘enkephalinase’ and ‘angiotensin-converting enzyme’? | Q67689315 | ||
| Phosphoramidon potentiates mammalian tachykinin-induced biting, licking and scratching behaviour in mice | Q67689702 | ||
| Release of substance P from the cat spinal cord | Q69022182 | ||
| Peptidase inhibitors improve recovery of substance P and calcitonin gene-related peptide release from rat spinal cord slices | Q71570083 | ||
| The correlation between the distribution of the NK1 receptor and the actions of tachykinin agonists in the dorsal horn of the rat indicates that substance P does not have a functional role on substantia gelatinosa (lamina II) neurons | Q71662662 | ||
| Receptor endocytosis and dendrite reshaping in spinal neurons after somatosensory stimulation | Q71696623 | ||
| The spinal contribution of substance P to the generation and maintenance of inflammatory hyperalgesia in the rat | Q71733165 | ||
| Gamma-aminobutyric acidB, but not gamma-aminobutyric acidA receptor activation, inhibits electrically evoked substance P-like immunoreactivity release from the rat spinal cord in vitro | Q72094858 | ||
| Long-term potentiation and long-term depression of primary afferent neurotransmission in the rat spinal cord | Q72640836 | ||
| Action of peptidase inhibitors on methionine5-enkephalin-arginine6-phenylalanine7 (YGGFMRF) and methionine5-enkephalin (YGGFM) metabolism and on electroacupuncture antinociception | Q72739799 | ||
| Neurochemical and cellular reorganization of the spinal cord in a murine model of bone cancer pain | Q73263697 | ||
| Noxious cutaneous thermal stimuli induce a graded release of endogenous substance P in the spinal cord: imaging peptide action in vivo | Q73507903 | ||
| Low-frequency stimulation of afferent Adelta-fibers induces long-term depression at primary afferent synapses with substantia gelatinosa neurons in the rat | Q73542551 | ||
| Enzymatic inactivation of enkephalin neurotransmitters in the spinal cord of the neonatal rat | Q73544660 | ||
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | pharmacology | Q128406 |
| NK1 receptor antagonists | Q12744608 | ||
| P304 | page(s) | 1389-1398 | |
| P577 | publication date | 2003-11-17 | |
| P1433 | published in | British Journal of Pharmacology | Q919631 |
| P1476 | title | Effect of peptidases on the ability of exogenous and endogenous neurokinins to produce neurokinin 1 receptor internalization in the rat spinal cord | |
| P478 | volume | 140 |
| Q28578470 | Acute inflammation induces segmental, bilateral, supraspinally mediated opioid release in the rat spinal cord, as measured by mu-opioid receptor internalization |
| Q33803774 | Cannabinoid CB1 receptor facilitation of substance P release in the rat spinal cord, measured as neurokinin 1 receptor internalization |
| Q36155156 | Comparing analgesia and mu-opioid receptor internalization produced by intrathecal enkephalin: requirement for peptidase inhibition |
| Q35186509 | Inflammation enhances Y1 receptor signaling, neuropeptide Y-mediated inhibition of hyperalgesia, and substance P release from primary afferent neurons. |
| Q37998313 | Inhibiting the breakdown of endogenous opioids and cannabinoids to alleviate pain |
| Q44348612 | Inhibition by spinal mu- and delta-opioid agonists of afferent-evoked substance P release. |
| Q44349884 | Mechanisms of μ-opioid receptor inhibition of NMDA receptor-induced substance P release in the rat spinal cord |
| Q34536694 | N-methyl-D-aspartate receptors and large conductance calcium-sensitive potassium channels inhibit the release of opioid peptides that induce mu-opioid receptor internalization in the rat spinal cord |
| Q39576351 | NMDA receptors in primary afferents require phosphorylation by Src family kinases to induce substance P release in the rat spinal cord |
| Q34142913 | Src family kinases mediate the inhibition of substance P release in the rat spinal cord by μ-opioid receptors and GABA(B) receptors, but not α2 adrenergic receptors |
| Q41924456 | Substance P release and neurokinin 1 receptor activation in the rat spinal cord increase with the firing frequency of C-fibers. |
| Q26745801 | The involvement of TRPV1 in emesis and anti-emesis |
| Q37721910 | μ-Opioid receptor inhibition of substance P release from primary afferents disappears in neuropathic pain but not inflammatory pain |
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