- Open Access
Hyperalgesic activity of kisspeptin in mice
- Simona Spampinato†1, 2,
- Angela Trabucco†3,
- Antonella Biasiotta4,
- Francesca Biagioni3,
- Giorgio Cruccu4,
- Agata Copani5,
- William H Colledge6,
- Maria Angela Sortino1,
- Ferdinando Nicoletti3, 7Email author and
- Santina Chiechio3, 5
© Spampinato et al; licensee BioMed Central Ltd. 2011
- Received: 1 June 2011
- Accepted: 23 November 2011
- Published: 23 November 2011
Kisspeptin is a neuropeptide known for its role in the hypothalamic regulation of the reproductive axis. Following the recent description of kisspeptin and its 7-TM receptor, GPR54, in the dorsal root ganglia and dorsal horns of the spinal cord, we examined the role of kisspeptin in the regulation of pain sensitivity in mice.
Immunofluorescent staining in the mouse skin showed the presence of GPR54 receptors in PGP9.5-positive sensory fibers. Intraplantar injection of kisspeptin (1 or 3 nmol/5 μl) induced a small nocifensive response in naive mice, and lowered thermal pain threshold in the hot plate test. Both intraplantar and intrathecal (0.5 or 1 nmol/3 μl) injection of kisspeptin caused hyperalgesia in the first and second phases of the formalin test, whereas the GPR54 antagonist, p234 (0.1 or 1 nmol), caused a robust analgesia. Intraplantar injection of kisspeptin combined with formalin enhanced TRPV1 phosphorylation at Ser800 at the injection site, and increased ERK1/2 phosphorylation in the ipsilateral dorsal horn as compared to naive mice and mice treated with formalin alone.
These data demonstrate for the first time that kisspeptin regulates pain sensitivity in rodents and suggest that peripheral GPR54 receptors could be targeted by novel drugs in the treatment of inflammatory pain.
- inflammatory pain
- nociceptive sensitization
Kisspeptin is a 54-amino acid peptide originally discovered for its activity as metastasis-suppressor . It is encoded by the Kiss1 gene as a 145-amino acid precursor protein and cleaved to a 54-amino acid protein as well as into shorter products (kisspeptin-10,-13,-14) known to play a critical role in the neuroendocrine regulation of reproduction [2–5].
Loss-of-function mutations of GPR54 cause a non-Kallman variant of hypogonadotropic/hypogonadism in humans (i.e. hypogonadotropic/hypogonadism without anosmia) [2, 9]. Interestingly, the expression of kisspeptin and GPR54 is not restricted to the hypothalamus. Relatively high levels of kisspeptin and GPR54 are found in forebrain regions, such as the hippocampus and amygdala, as well as in the periacqueductal grey . The investigation of the extrahypothalamic functions of kisspeptin is still at its infancy. Treatment with kainic acid increases kisspeptin mRNA levels in the hippocampus, and kisspeptin enhances the amplitude of excitatory postsynaptic currents in granule cells of the hippocampal dentate gyrus [6, 7]. This suggests a potential role for kisspeptin in the regulation of synaptic plasticity in the CNS. Recent findings have shown an intense kisspeptin and GPR54 immunostaining in dorsal root ganglia (DRG) neurons and in lamina I and II of the dorsal horns of the spinal cord [11, 12]. The transcripts of kisspeptin and GPR54 are up-regulated in DRG and dorsal horn neurons in the complete Freund adjuvant (CFA) model of chronic inflammatory pain , suggesting that kisspeptin may play a role in mechanisms of nociceptive sensitization. However, how precisely kisspeptin regulates pain sensitivity is obscure at present.
We now report that peripheral or intrathecal injection of kisspeptin causes hyperalgesia and induces biochemical changes that are consistent with mechanisms of peripheral and central nociceptive sensitization.
Adult male CD1 mice (Charles River, Calco, CO, Italy), 129S6/Sv/Ev wild-type, and 129S6/Sv/Ev Gpr54- knock-out mice  aged between 8 and 9 weeks were used in these experiments. Mice were housed 10 animals per cage with food and water ad libitum in standard 12/12 h light/dark cycle, for a period of 2 weeks before testing.
All experiments were carried out according to the recommendations of Institutional Animal Care and Use Committee (IACUC). All efforts were made to minimize animal suffering and to reduce the number of animals used.
Kisspeptin (Calbiochem Merck KGaA, Darmstadt, Germany) was dissolved in 5% DMSO and injected intrathecally (3 μl) or subcutaneously (5 μl) into the plantar surface of the right hind paw using a 10 μl luertip-syringe (Hamilton) fitted with a 30-gauge needle. p234 (Sigma-Aldrich, St. Louis, MO) was dissolved in phosphate buffered saline (PBS) and injected in a volume of 3 μl for intrathecal administration or 5 μl for intraplantar administration.
Hot plate test
The hot plate test (Ugo Basile, Italy) was used to asses thermal sensitivity. CD1 mice were placed onto the hot plate at the temperature of 55 ± 0.1°C. Paw withdrawal thresholds were determined in the hind paws of ipsilateral hind limb. Animals were kept on the plate until the first sign of ipsilateral paw lift or lick was recorded as basal withdrawal latency (pre-drug latency). A maximum cut-off paw withdrawal latency of 20 seconds was chosen to prevent tissue damage (cut-off time). Post-dose thresholds were taken at 5, 15, 30, and 60 minutes after drug administration (post-drug latency). For each animal, results were expressed as the percentage maximum possible effect (%MPE) calculated using the following formula: [(post-drug latency - pre-drug latency)/(cut-off time - pre-drug latency)] × 100.
Inflammatory pain was assessed using the formalin test. Ten μl of a 5% formalin solution was injected subcutaneously into the plantar surface of the right hind paw of CD1 mice. After the injection, mice were immediately placed in a plexiglas box (20 × 15 × 15 cm) surrounded by mirrors to allow the observation of nociceptive responses that include licking, lifting and shaking of the injected paw. Tests were performed between 08:00 h and 12:00 h to minimize variability. Mice were observed for 1 hour. Formalin scores were separated into two phases, phase I (0-10 min) and phase II (15-45 min). The mean behavioural score was calculated in blocks of 5 min for each of the two phases. A mean response was then calculated for each phase.
CD1 mice that received intraplantar injection of kisspeptin or vehicle were placed in a cage immediately after the injection, and the duration of hind paw lifting and licking during the first 5 minutes were measured.
All behavioral tests were analyzed by observers blind to the treatment of the animals.
Animals were euthanized with chloral hydrate (320 mg/kg i.p.). 2.5-mm punch skin biopsies from the plantar surface of the hind paws were performed and fixed in Zamboni fixative (2% paraformaldehide, 15% picric acid saturated aqueous solution, 0.1 M phosphate buffer pH 7.4) for 24 hours. Biopsies were cryoprotected with 20% sucrose in PBS overnight at 4°C. Sections of 10 μm were cut at the cryostat and mounted on glass slides for immunohistochemical analysis.
Immunohistochemistry procedures were performed as previously described . Double immunofluorescence was performed in skin biopsies from CD1 male mice incubating sections overnight with polyclonal rabbit anti-human PGP 9.5 (1:1000; AbD Serotec, Kidlington, UK) and goat polyclonal anti-GPR54 (1:20; Santa Cruz Biotechnology, Santa Cruz, CA) and then for 1 h with secondary fluorescein anti-rabbit (1:100; Vector Laboratories, Burlingame, CA) and Cy3 anti-goat (1:400; Chemicon, Billerica, MA) antibodies. Control staining was performed without the primary antibodies.
Immunostaining was performed in skin biopsies from male 129S6/Sv/Ev wild-type and 129S6/Sv/Ev Gpr54- knock-out mice  to test the specificity of the anti-GPR54 antibody. Tissue sections were incubated overnight with goat polyclonal anti-GPR54 (1:20; Santa Cruz Biotechnology, Santa Cruz, CA) and then for 1 h with secondary biotin-coupled anti-goat (1:100; Vector Laboratories, Burlingame, CA). SG (SG substrate kit; Vector Laboratories, Burlingame, CA, USA) chromogen was used for detection.
CD1 mice (n = 5 per group) were used. 3 min after kisspeptin (3 nmol) or vehicle (DMSO) were co-injected with formalin in the right hind paw and lumbar spinal cords were removed and fixed in formalin (4%) overnight, transferred in 70% ethanol and included in paraffin. Ten serial sections were cut and used for immunohistochemical analysis. Deparaffinized sections were treated with 10 mmol/L citrate buffer, pH 6.0, and heated by microwave for 10 minutes for antigen unmasking. Sections were soaked in 3% hydrogen peroxide to block endogenous peroxidase activity. Tissue sections were incubated overnight with monoclonal rabbit antibody anti-phospho-p44/42 (Erk1/2) (Thr202/Tyr204) (D13.14.4E)XP™ (1:200; Cell Signaling Technology, Denver, MA, USA) and then for 1 h with secondary biotin-coupled anti-rabbit (1:200; Vector Laboratories). 3,3-Diaminobenzidine tetrachloride was used for detection. Control staining was performed without the primary antibodies.
Densitometric analysis of p-ERK immunoreactivity
Intensity of p-ERK immunoreactivity was quantified by measuring the optical densities of the outer laminae of the dorsal horn in the stained sections relative to the background (ventral horn). Images were acquired using a computer-based microdensitometer (NIH Image Software, Bethesda, MD, USA). Values were the mean of measurements made on ten sections (10 μm) sampled 1 into a 3 series spanning the extent of the L4-L5 spinal cord.
Western blot analysis
CD1 Mice were sacrificed 3 min following treatment and skin lysates of all groups were processed in western blot. Skin homogenates were obtained as previously described . Ten μg of total protein were separated by 10% SDS-polyacrylamide gel electrophoresis and electrophoretically transferred onto protein-sensitive nitrocellulose membranes (Criterion blotter; Bio-Rad Laboratories, Hercules, CA). The membranes were blocked in Odyssey blocker (LI-COR Biosciences, Lincoln, NE) for 1 h, and the following primary antibodies were used: anti-TRPV1 (phospho S800) polyclonal antibody (1:400, Abnova, Aachen, Germany); anti-actin monoclonal antibody (1:1000, Sigma). Secondary antibodies were: goat anti-rabbit (IRD800CW) and goat anti-mouse (Alexa 680, LI-COR, Bioscience) antibodies. Proteins were detected with the Odyssey Infrared Fluorescence Imaging System (LI-COR).
These data offer the first demonstration that kisspeptin, a peptide known for its role in the regulation of the hypothalamic-pituitary-gonadal axis, lowers pain threshold and enhances nocifensive behavior in mice. Immunohistochemical analysis showed the presence of the kisspeptin receptor, GPR54, in peripheral sensory fibers, a finding that is consistent with the detection of GPR54 mRNA and protein in DRG neurons [11, 12]. The lack of staining in GPR54 KO mice indicates that GPR54 is present in peripheral nociceptors explaining the hyperalgesia caused by intraplantar injection of kisspeptin in the hot plate and formalin test. We wish to highlight that intraplantar kisspeptin induced only a small nocifensive response on its own, suggesting that a main action of kisspeptin is to amplify pain sensitivity in response to noxious stimuli. Intraplantar injection of the GPR54 antagonist, p234, caused a robust analgesia in the formalin test, suggesting that endogenous kisspeptin acts extracellularly to activate GPR54 receptors during inflammatory pain. Kisspeptin is present in DRG neurons, where it co-localizes with isolectin B4 and calcitonin gene-related peptide, and its expression is up-regulated by chronic inflammatory pain . It is likely that kisspeptin is released from peripheral nociceptors in response to noxious stimuli, therefore behaving as an autocrine/paracrine factor to promote peripheral nociceptive sensitization. Whether other cells can produce and secrete kisspeptin during inflammation is unknown at present. Phosphorylation of the TRPV1 ion channel is a key event in mechanisms of peripheral nociceptive sensitization [20–22]. The TRPV1 receptor can be phosphorylated by multiple protein kinases, including protein kinase A, protein kinase C (PKC), calcium/calmodulin-dependent protein kinase II, and SRC [23–34]. In, particular, PKC phosphorylates TRPV1 at Ser-502 and Ser-800, thus amplifying ion channel activity [31, 35–37]. Intraplantar kisspeptin caused a robust increase in (Ser800)-TRPV1 phosphorylation, an effect that was likely mediated by the activation of the GPR54 receptor, with ensuing stimulation of inositol phospholipid hydrolysis, diacylglycerol formation, and PKC activation [2, 8]. Thus, kisspeptin might act similarly to other hyperalgesic molecules that activate Gq-coupled receptors and phosphorylate TRPV1 channels in peripheral nociceptors, such as bradykinin, group-I mGlu receptor agonists, P2Y2 receptor agonists, EP1 receptor, and prokineticin [28, 38–48].
Hyperalgesia by kisspeptin and analgesia by p234 were also seen in the second phase of the formalin test, which reflects the development of central nociceptive sensitization in the dorsal horns of the spinal cord [17, 18]. Central nociceptive sensitization is mediated by a series of mechanisms that ultimately lead to an enhancement of excitatory transmission at the synapses between primary afferent fibers and second order sensory neurons in the dorsal horns of the spinal cord . The relevance of the MAPK pathway in the development of central sensitization has been highlighted in a recent review . Intraplantar injection of formalin is known to induce a rapid phosphorylation of ERK1/2 in the spinal cord, which has been causally related to the increase in nocifensive behavior seen in the second phase of the formalin test . Pharmacological activation of mGlu1 and mGlu5 receptors, which also couple to the Gq protein just like GPR54 , can also enhance ERK1/2 phosphorylation in the spinal cord . Activation of GPR54 by kisspeptin has been shown to stimulate the ERK/MAPK pathway both in recombinant expression systems and hypothalamic explants [52, 53]. Intraplantar injection of kisspeptin markedly amplified ERK1/2 phosphorylation induced by formalin in the ipsilateral dorsal horn, evidence that nicely supports the behavioral data obtained with kisspeptin in the second phase of the formalin test. Interestingly, kisspeptin retained the hyperalgesic activity (and p234 the analgesic activity) when injected by the intrathecal route. Thus, it is likely that the modulation of pain sensitivity by GPR54 extends beyond peripheral nociceptors. Effects of kisspeptin on different receptors cannot be excluded. In particular it has been reported that kisspeptin can also bind neuropeptide FF (NPFF) receptors . However in our hands intrathecal injection of kisspeptin lowers pain threshold, whereas intrathecal injection of NPFF is known to cause analgesia , thus the effect of kisspeptin in the spinal cord is likely mediated by the activation of the GPR54 receptor excluding an interaction of kisspeptin with NPFF receptors.
The presence of GPR54 receptor in the amygdala  may suggest that kisspeptin acts also at higher brain centers that control the affective components of pain and contributes to the top-down regulation of pain threshold.
In conclusion, our data disclose a new aspect in the physiology of kisspeptin and suggest that peripheral GPR54 receptor antagonists (lacking potential hypothalamic side effects) can be developed as new drugs for the treatment of inflammatory pain. In addition, it will be interesting to explore whether individuals with hypogonadotropic hypogonadism due to inactivating mutations of GPR54 show alterations in the sensitivity to pain.
Supported by University of Catania Research Grant to SC and by Italian Ministry of Health Grant RF-2009-1474272 to SC.
- Lee JH, Miele ME, Hicks DJ, Phillips KK, Trent JM, Weissman BE, Welch DR: KiSS-1, a novel human malignant melanoma metastasis-suppressor gene. J Natl Cancer Inst 1996, 88: 1731–1737. 10.1093/jnci/88.23.1731PubMedView ArticleGoogle Scholar
- Seminara SB: Mechanisms of Disease: the first kiss-a crucial role for kisspeptin-1 and its receptor, G-protein-coupled receptor 54, in puberty and reproduction. Nat Clin Pract Endocrinol Metab 2006, 2: 328–334. 10.1038/ncpendmet0139PubMedView ArticleGoogle Scholar
- Kauffman AS, Clifton DK, Steiner RA: Emerging ideas about kisspeptin- GPR54 signaling in the neuroendocrine regulation of reproduction. Trends Neurosci 2007, 30: 504–511. 10.1016/j.tins.2007.08.001PubMedView ArticleGoogle Scholar
- Colledge WH: Kisspeptins and GnRH neuronal signalling. Trends Endocrinol Metab 2009, 20: 115–21. 10.1016/j.tem.2008.10.005PubMedView ArticleGoogle Scholar
- Lehman MN, Coolen LM, Goodman RL: Minireview: kisspeptin/neurokinin B/dynorphin (KNDy) cells of the arcuate nucleus: a central node in the control of gonadotropin-releasing hormone secretion. Endocrinology 2010, 151: 3479–3489. 10.1210/en.2010-0022PubMed CentralPubMedView ArticleGoogle Scholar
- Arai AC, Orwig N: Factors that regulate KiSS1 gene expression in the hippocampus. Brain Res 2008, 1243: 10–8.PubMedView ArticleGoogle Scholar
- Arai AC: The role of kisspeptin and GPR54 in the hippocampus. Peptides 2009, 30: 16–25. 10.1016/j.peptides.2008.07.023PubMedView ArticleGoogle Scholar
- Gottsch ML, Clifton DK, Steiner RA: Kisspepeptin-GPR54 signaling in the neuroendocrine reproductive axis. Mol Cell Endocrinol 2006, 254–255: 91–6.PubMedView ArticleGoogle Scholar
- de Roux N, Genin E, Carel JC, Matsuda F, Chaussain JL, Milgrom E: Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Proc Natl Acad Sci USA 2003, 100: 10972–10976. 10.1073/pnas.1834399100PubMed CentralPubMedView ArticleGoogle Scholar
- Oakley AE, Clifton DK, Steiner RA: Kisspeptin signaling in the brain. Endocr Rev 2009, 30: 713–743. 10.1210/er.2009-0005PubMed CentralPubMedView ArticleGoogle Scholar
- Dun SL, Brailoiu GC, Parsons A, Yang J, Zeng Q, Chen X, Chang JK, Dun NJ: Metastin-like immunoreactivity in the rat medulla oblongata and spinal cord. Neurosci Lett 2003, 335: 197–201. 10.1016/S0304-3940(02)01191-6PubMedView ArticleGoogle Scholar
- Mi WL, Mao-Ying QL, Liu Q, Wang XW, Li X, Wang YQ, Wu GC: The distribution of kisspeptin and its receptor GPR54 in rat dorsal root ganglion and up-regulation of its expression after CFA injection. Brain Res Bull 2009, 78: 254–260. 10.1016/j.brainresbull.2008.12.003PubMedView ArticleGoogle Scholar
- Seminara SB, Messager S, Chatzidaki EE, Thresher RR, Acierno JS, Shagoury JK, Bo-Abbas Y, Kuohung W, Schwinof KM, Hendrick AG, Zahn D, Dixon J, Kaiser UB, Slaugenhaupt SA, Gusella JF, O'Rahilly S, Carlton MB, Crowley WF, Aparicio SA, Colledge WH: The GPR54 gene as a regulator of puberty. N Engl J Med 2003, 349: 1614–1627. 10.1056/NEJMoa035322PubMedView ArticleGoogle Scholar
- McCarthy BG, Hsieh ST, Stocks A, Hauer P, Macko C, Cornblath DR, Griffin JW, McArthur JC: Cutaneous innervation in sensory neuropathies: evaluation by skin biopsy. Neurology 1995, 45: 1848–1855.PubMedView ArticleGoogle Scholar
- Jin L, Miyamoto O, Toyoshima T, Kobayashi R, Murakami TH, Itano T: Localization of calbindin-D28k in normal and incised mouse skin: immunohistochemical and immunoblot analysis. Arch Dermatol Res 1997, 289: 578–84. 10.1007/s004030050243PubMedView ArticleGoogle Scholar
- Pheng V, Uenoyama Y, Homma T, Inamoto Y, Takase K, Yoshizawa-Kumagaye K, Isaka S, Watanabe TX, Ohkura S, Tomikawa J, Maeda K, Tsukamura H: Potencies of centrally- or peripherally-injected full-length kisspeptin or its C-terminal decapeptide on LH release in intact male rats. J Reprod Dev 2009, 55: 378–82. 10.1262/jrd.20240PubMedView ArticleGoogle Scholar
- Coderre TJ, Melzack R: The contribution of excitatory amino acids to central sensitization and persistent nociception after formalin-induced tissue injury. J Neurosci 1992, 12: 3665–3670.PubMedGoogle Scholar
- Tjølsen A, Berge OG, Hunskaar S, Rosland JH, Hole K: The formalin test: an evaluation of the method. Pain 1992, 51: 5–17. 10.1016/0304-3959(92)90003-TPubMedView ArticleGoogle Scholar
- Roseweir AK, Kauffman AS, Smith JT, Guerriero KA, Morgan K, Pielecka-Fortuna J, Pineda R, Gottsch ML, Tena-Sempere M, Moenter SM, Terasawa E, Clarke IJ, Steiner RA, Millar RP: Discovery of potent kisspeptin antagonists delineate physiological mechanisms of gonadotropin regulation. J Neurosci 2009, 29: 3920–9. 10.1523/JNEUROSCI.5740-08.2009PubMed CentralPubMedView ArticleGoogle Scholar
- Hucho T, Levine JD: Signaling pathways in sensitization: toward a nociceptor cell biology. Neuron 2007, 55: 365–76. 10.1016/j.neuron.2007.07.008PubMedView ArticleGoogle Scholar
- Stucky CL, Dubin AE, Jeske NA, Malin SA, McKemy DD, Story GM: Roles of transient receptor potential channels in pain. Brain Res Rev 2009, 60: 2–23. 10.1016/j.brainresrev.2008.12.018PubMed CentralPubMedView ArticleGoogle Scholar
- Studer M, McNaughton PA: Modulation of single-channel properties of TRPV1 by phosphorylation. J Physiol 2010, 588: 3743–3756. 10.1113/jphysiol.2010.190611PubMed CentralPubMedView ArticleGoogle Scholar
- Tominaga M, Caterina MJ, Malmberg AB, Rosen TA, Gilbert H, Skinner K, Raumann BE, Basbaum AI, Julius D: The cloned capsaicin receptor integrates multiple pain-producing stimuli. Neuron 1998, 21: 531–543. 10.1016/S0896-6273(00)80564-4PubMedView ArticleGoogle Scholar
- Tominaga M, Wada M, Masu M: Potentiation of capsaicin receptor activity by metabotropic ATP receptors as a possible mechanism for ATP-evoked pain and hyperalgesia. Proc Natl Acad Sci USA 2001, 98: 6951–6956. 10.1073/pnas.111025298PubMed CentralPubMedView ArticleGoogle Scholar
- Premkumar LS, Ahern GP: Induction of vanilloid receptor channel activity by protein kinase C. Nature 2000, 408: 985–990. 10.1038/35050121PubMedView ArticleGoogle Scholar
- De Petrocellis L, Harrison S, Bisogno T, Tognetto M, Brandi I, Smith GD, Creminon C, Davis JB, Geppetti P, Di Marzo V: The vanilloid receptor (VR1)-mediated effects of anandamide are potently enhanced by the cAMP-dependent protein kinase. J Neurochem 2001, 77: 1660–1663. 10.1046/j.1471-4159.2001.00406.xPubMedView ArticleGoogle Scholar
- Bhave G, Zhu W, Wang H, Brasier DJ, Oxford GS, Gereau RW: cAMP-dependent protein kinase regulates desensitization of the capsaicin receptor (VR1) by direct phosphorylation. Neuron 2002, 35: 721–731. 10.1016/S0896-6273(02)00802-4PubMedView ArticleGoogle Scholar
- Hu HJ, Bhave G, Gereau RW: Prostaglandin and protein kinase A-dependent modulation of vanilloid receptor function by metabotropic glutamate receptor5: potential mechanism for thermal hyperalgesia. J Neurosci 2002, 22: 7444–7452.PubMedGoogle Scholar
- Rathee PK, Distler C, Obreja O, Neuhuber W, Wang GK, Wang SY, Nau C, Kress M: PKA/AKAP/VR-1 module: A common link of Gs-mediated signaling to thermal hyperalgesia. J Neurosci 2002, 22: 4740–4745.PubMedGoogle Scholar
- Sugiura T, Tominaga M, Katsuya H, Mizumura K: Bradykinin lowers the threshold temperature for heat activation of vanilloid receptor1. J Neurophysiol 2002, 88: 544–548.PubMedGoogle Scholar
- Bhave G, Hu HJ, Glauner KS, Zhu W, Wang H, Brasier DJ, Oxford GS, Gereau RW: Protein kinase C phosphorylation sensitizes but does not activate the capsaicin receptor transient receptor potential vanilloid 1 (TRPV1). Proc Natl Acad Sci USA 2003, 100: 12480–12485. 10.1073/pnas.2032100100PubMed CentralPubMedView ArticleGoogle Scholar
- Dai Y, Moriyama T, Higashi T, Togashi K, Kobayashi K, Yamanaka H, Tominaga M, Noguchi K: Proteinase-activated receptor 2-mediated potentiation of transient receptor potential vanilloid subfamily 1 activity reveals a mechanism for proteinase-induced inflammatory pain. J Neurosci 2004, 24: 4293–4299. 10.1523/JNEUROSCI.0454-04.2004PubMedView ArticleGoogle Scholar
- Jung J, Shin JS, Lee SY, Hwang SW, Koo J, Cho H, Oh U: Phosphorylation of vanilloid receptor1 by Ca2+/calmodulin-dependent kinase II regulates its vanilloid binding. J Biol Chem 2004, 279: 7048–7054.PubMedView ArticleGoogle Scholar
- Jin X, Morsy N, Winston J, Pasricha PJ, Garrett K, Akbarali HI: Modulation of TRPV1 by nonreceptor tyrosine kinase, c-Src kinase. Am J Physiol Cell Physiol 2004, 287: C558–563. 10.1152/ajpcell.00113.2004PubMedView ArticleGoogle Scholar
- Numazaki M, Tominaga T, Toyooka H, Tominaga M: Direct phosphorylation of capsaicin receptor VR1 by protein kinase C epsilon and identification of two target serine residues. J Biol Chem 2002, 277: 13375–13378. 10.1074/jbc.C200104200PubMedView ArticleGoogle Scholar
- Numazaki M, Tominaga M: Nociception and TRP channels. Curr Drug Targets CNS Neurol Disord 2004, 3: 479–485. 10.2174/1568007043336789PubMedView ArticleGoogle Scholar
- Mandadi S, Tominaga T, Numazaki M, Murayama N, Saito N, Armati PJ, Roufogalis BD, Tominaga M: Increased sensitivity of desensitized TRPV1 by PMA occurs through PKCepsilon-mediated phosphorylation at S800. Pain 2006, 123: 106–116. 10.1016/j.pain.2006.02.016PubMedView ArticleGoogle Scholar
- Bhave G, Karim F, Carlton SM, Gereau RW: Peripheral group I metabotropic glutamate receptors modulate nociception in mice. Nat Neurosci 2001, 4: 417–23. 10.1038/86075PubMedView ArticleGoogle Scholar
- Hu HJ, Alter BJ, Carrasquillo Y, Qiu CS, Gereau RW: Metabotropic glutamate receptor 5 modulates nociceptive plasticity via extracellular signal-regulated kinase-Kv4.2 signaling in spinal cord dorsal horn neurons. J Neurosci 2007, 27: 13181–91. 10.1523/JNEUROSCI.0269-07.2007PubMedView ArticleGoogle Scholar
- Moriyama T, Iida T, Kobayashi K, Higashi T, Fukuoka T, Tsumura H, Leon C, Suzuki N, Inoue K, Gachet C, Noguchi K, Tominaga M: Possible involvement of P2Y2 metabotropic receptors in ATP-induced transient receptor potential vanilloid receptor 1-mediated thermal hypersensitivity. J Neurosci 2003, 23: 6058–6062.PubMedGoogle Scholar
- Ferreira J, da Silva GL, Calixto JB: Contribution of vanilloid receptors to the overt nociception induced by B2 kinin receptor activation in mice. Br J Pharmacol 2004, 141: 787–94. 10.1038/sj.bjp.0705546PubMed CentralPubMedView ArticleGoogle Scholar
- Vellani V, Colucci M, Lattanzi R, Giannini E, Negri L, Melchiorri P, McNaughton PA: Sensitization of transient receptor potential vanilloid 1 by the prokineticin receptor agonist Bv8. J Neurosci 2006, 26: 5109–5116. 10.1523/JNEUROSCI.3870-05.2006PubMedView ArticleGoogle Scholar
- Negri L, Lattanzi R, Giannini E, Colucci M, Margheriti F, Melchiorri P, Vellani V, Tian H, De Felice M, Porreca F: Impaired nociception and inflammatory pain sensation in mice lacking the prokineticin receptor PKR1: focus on interaction between PKR1 and the capsaicin receptor TRPV1 in pain behavior. J Neurosci 2006, 26: 6716–27. 10.1523/JNEUROSCI.5403-05.2006PubMedView ArticleGoogle Scholar
- Malin SA, Davis BM, Koerber HR, Reynolds IJ, Albers KM, Molliver DC: Thermal nociception and TRPV1 function are attenuated in mice lacking the nucleotide receptor P2Y2. Pain 2008, 138: 484–96. 10.1016/j.pain.2008.01.026PubMed CentralPubMedView ArticleGoogle Scholar
- Kim YH, Park CK, Back SK, Lee CJ, Hwang SJ, Bae YC, Na HS, Kim JS, Jung SJ, Oh SB: Membrane-delimited coupling of TRPV1 and mGluR5 on presynaptic terminals of nociceptive neurons. J Neurosci 2009, 29: 10000–10009. 10.1523/JNEUROSCI.5030-08.2009PubMedView ArticleGoogle Scholar
- Mizumura K, Sugiura T, Katanosaka K, Banik RK, Kozaki Y: Excitation and sensitization of nociceptors by bradykinin: what do we know? Exp Brain Res 2009, 196: 53–65. 10.1007/s00221-009-1814-5PubMedView ArticleGoogle Scholar
- Moriyama T, Higashi T, Togashi K, Iida T, Segi E, Sugimoto Y, Tominaga T, Narumiya S, Tominaga M: Sensitization of TRPV1 by EP1 and IP reveals peripheral nociceptive mechanism of prostaglandins. Mol Pain 2005, 1: 3. 10.1186/1744-8069-1-3PubMed CentralPubMedView ArticleGoogle Scholar
- Ji RR, Gereau RW, Malcangio M, Strichartz GR: MAP kinase and pain. Brain Res Rev 2009, 60: 135–148. 10.1016/j.brainresrev.2008.12.011PubMed CentralPubMedView ArticleGoogle Scholar
- Karim F, Bhave G, Gereau RW: Metabotropic glutamate receptors on peripheral sensory neuron terminals as targets for the development of novel analgesics. Mol Psychiatry 2001, 6: 615–617. 10.1038/sj.mp.4000961PubMedView ArticleGoogle Scholar
- Nicoletti F, Bockaert J, Collingridge GL, Conn PJ, Ferraguti F, Schoepp DD, Wroblewski JT, Pin JP: Metabotropic glutamate receptors: From the workbench to the bedside. Neuropharmacology 2011, 60: 1017–41. 10.1016/j.neuropharm.2010.10.022PubMed CentralPubMedView ArticleGoogle Scholar
- Karim F, Wang CC, Gereau RW: Metabotropic glutamate receptor subtypes 1 and 5 are activators of extracellular signal-regulated kinase signaling required for inflammatory pain in mice. J Neurosci 2001, 1–21: 3771–3779.Google Scholar
- Kotani M, Detheux M, Vandenbogaerde A, Communi D, Vanderwinden JM, Le Poul E, Brézillon S, Tyldesley R, Suarez-Huerta N, Vandeput F, Blanpain C, Schiffmann SN, Vassart G, Parmentier M: The metastasis suppressor gene KiSS-1 encodes kisspeptins, the natural ligands of the orphan G protein-coupled receptor GPR54. J Biol Chem 2001, 276: 34631–34636. 10.1074/jbc.M104847200PubMedView ArticleGoogle Scholar
- Castellano JM, Navarro VM, Fernández-Fernández R, Castaño JP, Malagón MM, Aguilar E, Dieguez C, Magni P, Pinilla L, Tena-Sempere M: Ontogeny and mechanisms of action for the stimulatory effect of kisspeptin on gonadotropin-releasing hormone system of the rat. Mol Cell Endocrinol 2006, 257–258: 75–83.PubMedView ArticleGoogle Scholar
- Oishi S, Misu R, Tomita K, Setsuda S, Masuda R, Ohno H, Naniwa Y, Ieda N, Inoue N, Ohkura S, Uenoyama Y, Tsukamura H, Maeda K, Hirasawa A, Tsujimoto G, Fujii N: Activation of Neuropeptide FF Receptors by Kisspeptin Receptor Ligands. ACS Med Chem Lett 2011, 2: 53–57. 10.1021/ml1002053PubMed CentralPubMedView ArticleGoogle Scholar
- Roumy M, Zajac JM: Neuropeptide FF, pain and analgesia. Eur J Pharmacol 1998, 345: 1–11. 10.1016/S0014-2999(97)01604-XPubMedView ArticleGoogle Scholar
- Lee DK, Nguyen T, O'Neill GP, Cheng R, Liu Y, Howard AD, Coulombe N, Tan CP, Tang-Nguyen AT, George SR, O'Dowd BF: Discovery of a receptor related to the galanin receptors. FEBS Lett 1999,446(1):103–7. 10.1016/S0014-5793(99)00009-5PubMedView ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.