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Absence of histamine-induced itch in the African naked mole-rat and "rescue" by Substance P
© Smith et al; licensee BioMed Central Ltd. 2010
Received: 17 February 2010
Accepted: 24 May 2010
Published: 24 May 2010
Recent research has proposed a pathway in which sensory neurons expressing the capsaicin activated ion channel TRPV1 are required for histamine-induced itch and subsequent scratching behavior. We examined histamine-induced itch in the African naked mole-rat (Heterocephalus glaber) and found that although naked mole-rats display innate scratching behavior, histamine was unable to evoke increased scratching as is observed in most mouse strains. Using calcium imaging, we examined the histamine sensitivity of naked mole-rat dorsal root ganglia (DRG) neurons and identified a population of small diameter neurons activated by histamine, the majority of which are also capsaicin-sensitive. This suggested that naked mole-rat sensory neurons are activated by histamine, but that spinal dorsal horn processing of sensory information is not the same as in other rodents. We have previously shown that naked mole-rats naturally lack substance P (SP) in cutaneous C-fibers, but that the neurokinin-1 receptor is expressed in the superficial spinal cord. This led us to investigate if SP deficiency plays a role in the lack of histamine-induced scratching in this species. After intrathecal administration of SP into the spinal cord we observed robust scratching behavior in response to histamine injection. Our data therefore support a model in which TRPV1-expressing sensory neurons are important for histamine-induced itch. In addition, we demonstrate a requirement for active, SP-induced post-synaptic drive to enable histamine sensitive afferents to drive itch-related behavior in the naked mole-rat. These results illustrate that it is altered dorsal horn connectivity of nociceptors that underlies the lack of itch and pain-related behavior in the naked mole-rat.
Itch is an unpleasant sensation that evokes a craving to scratch and is characteristic of many inflammatory skin disorders . Human microneurography studies have identified a subset of mechano-insensitive C-fibers that are strongly activated by histamine and may generate itch . At the molecular level, pharmacological experiments have demonstrated a role for H1-receptors (H1R) in histamine-induced scratching in rodents and humans [3, 4]. There is also a key role for the capsaicin receptor TRPV1 as TRPV1-/- knockout mice exhibit decreased histamine-induced scratching [5, 6]. Centrally, dorsal spinal cord neurons expressing the gastrin-releasing peptide receptor are required for a wide range of pruritogens to evoke itch [7, 8]. The neuropeptide substance P (SP) is also implicated in central transmission of itch: intrathecal SP administration evokes scratching  and also enhances morphine-evoked scratching . In contrast, deleting the preprotachykinin A gene encoding SP, does not reduce serotonin-evoked scratching behavior , thus SP does not mediate all scratching behaviors.
We have previously shown that African naked mole-rats (Heterocephalus glaber) do not express SP in small diameter dorsal root ganglia (DRG) neurons  and display no nocifensive behavior in response to capsaicin or acid . Intrathecal administration of SP "rescued" a nocifensive licking behavior in response to capsaicin, but did not alter the lack of response to acid, demonstrating that naked mole-rats, uniquely among Mammalia, do not sense acid as a noxious stimulus .
Additional file 1: Naked mole-rats display low-level spontaneous scratching with the hind paws, similar to mice. (MOV 776 KB)
Additional file 2: In addition to scratching, naked mole-rats display bouts of vigorous back rubbing against the cage wall after combined intrathecal application of SP and intracutaneous histamine. Presumably the back rubbing is an attempt to scratch its back. (MOV 3 MB)
We have previously hypothesized that capsaicin fails to evoke nocifensive behavior in naked mole-rats because unlike in the mouse, where C-fibers predominantly terminate in the superficial "pain-signaling" laminae of the spinal cord dorsal horn, naked mole-rat C-fibers terminate in superficial and deeper laminae equally . Reintroduction of SP, via intrathecal administration, "rescued" behavioral sensitivity to capsaicin. We propose that addition of SP activates superficially located neurons expressing neurokinin-1 receptors and thus increases the excitatory drive into the superficial laminae, which overrides the simultaneous activation of deep dorsal horn neurons, which is unique to the naked-mole-rat.
In this study we find that SP is also able to "rescue" histamine-mediated scratching behavior, as well as inducing a vigorous back-rubbing behavior. This "rescue" suggests that naked mole-rat primary afferent neurons are normally activated by histamine, which our calcium imaging results confirm (Fig. 2). We suggest therefore that peripheral activation of naked mole-rat C-fibers by histamine usually leads to both superficial and deeper spinal laminae being activated and that SP administration allows for information travelling via superficial pathways, known to be involved in itch processing , to dominate, thus leading to the expression of scratching behavior. Because of the observation that SP administration enables histamine pruritogenicity in naked mole-rats, we suggest that a portion of the same C-fiber population that is responsible for transmitting capsaicin "pain" information may also transmit histamine "itch" information. Consequently, these results also support the model that TRPV1 expressing neurons are required for histamine-mediated scratching [5, 6].
Our data are also supportive of a role for SP in scratching behavior. Like others, we found that SP administration induces scratching , in addition to the "rescuing" of histamine-induced scratching behavior in naked mole-rats. However, it should be noted that histamine is relatively non-pruritinogenic in certain laboratory rodent strains, which endogenously express SP (ddY mice  and Sprague-Dawley rats ). Therefore, the importance of SP in mediating histamine-mediated scratching could very well be species/strain dependent, but clearly plays a key role in the naked mole-rat.
We can only speculate as to why naked mole-rats have evolved insensitivity to the pruritogenic effects of histamine. One possible explanation is that histamine-insensitivity is a result of sensory nervous system adaptations, which have evolved under selection pressure unrelated to itch. In the wild, naked mole-rats live in large colonies underground, which results in unusually high levels of carbon dioxide and ammonia . Carbon dioxide can be converted into carbonic acid, which activates C-fiber nociceptors causing pain [22–24] and the ability to detect acid as a noxious stimulus is evolutionarily conserved amongst both invertebrates and vertebrates . Therefore, the finding that naked mole-rats do not demonstrate any nocifensive response to acid suggests that the sensory nervous system of naked mole-rats (and their ancestors) has evolved under the selection pressure of noxiously high levels of environmental carbon dioxide with the result that acid is no longer detected as noxious . A lack of behavioral avoidance to ammonia  and loss of neuropeptides in cutaneous C-fibers  are also adaptations that may well have evolved in response to the unusual atmosphere that ancestors of the naked mole-rat experienced in order to alter how noxious stimuli are processed by the nervous system. Although this is only one possible explanation for how these unusual features of the naked mole-rat sensory nervous system have evolved, the histamine-insensitivity documented in this study may have arisen as a by-product of this evolutionary process. Indeed, the lack of histamine sensitivity is likely to be related to the lack of behavioral sensitivity to capsaicin that we have already documented and which is probably explained by the unusual connectivity of capsaicin-sensitive C-fibers in this species.
In summary, we show that the African naked mole-rat lacks histamine-mediated itch-related behavior, even though capsaicin-sensitive C-fibers are commonly histamine-sensitive in this species. However, histamine-induced scratching can be "rescued" after intrathecal SP administration. Our data support the theory that a population of TRPV1-positive C-fibers mediate histamine-induced itch and that it is the unique connectivity of these neurons in the spinal cord of naked mole-rats that underlies the absence of itch.
Materials and methods
In this study we tested 2-3 month-old, male C57BL6 mice (mean body weight = 21.7 g) and 6-18 month-old naked mole-rats (mean body weight = 20.0 g). The maximum life span of naked mole-rats approaches 30 years and those used here were considered to be young adults. Animal protocols were approved by the University of Illinois at Chicago Institutional Animal Care and Use Committee or German federal authorities (State of Berlin) as appropriate.
Histamine and scratching behavior
Histamine (Sigma) dissolved in physiological saline was administered by intracutaneous injection between the shoulder blades. Histamine concentrations and injection volumes were generally based on those reported by Green, et al. . Doses ranged from 10 μg/animal (0.65 mM) to 4.6 mg/animal (300 mM), delivered in a volume of 50 μl; doses encompassing those shown to be effective across a variety of mouse strains . After injection of histamine, we observed an animal for 20 minutes, during which time we counted bouts of scratching, which is referred to in the text as bouts/20 minutes. A bout of scratching was defined as the animal lifting a hind paw from the cage floor, scratching at the injection site with the paw, and returning the paw to the floor. Animals were tested in their home cages. Statistical comparisons between the mean scratching bouts evoked by different histamine doses were made using Student's T test.
Intrathecal application of SP
Animals were briefly anesthetized (~1-2 min) with isoflurane (2% in 2 L/min O2). Substance P, dissolved in physiological saline (100 μM in a 20 μl volume) was administered intrathecally between vertebrae L4 and L5. After recovery from anesthesia (~5 min later), histamine was applied and scratching behaviors recorded. The observer, counting the bouts of scratching, was blind to the whether saline or SP was administered intrathecally and to whether saline or histamine was administered intracutaneously. Statistical comparisons between the means were made using Student's T test.
DRG neurons from all spinal levels were prepared from naked mole-rat as described previously  and plated on to poly-L-lysine (200 mg/ml) and laminin (20 μg/ml) coated glass coverslips. Neurons were maintained in DMEM (Life Technologies) containing 10% heat-inactivated horse serum (Biochrom), 20 mM glutamine, 0.8% glucose, 100 U penicillin and 100 mg/ml streptomycin (Life Technologies) and incubated at 37°C in 5% CO2. Standard Fura-2 ratiometric calcium imaging was conducted to measure responses to histamine (100 μM, 60 seconds) and capsaicin (1 μM, 5 seconds). At the end of each experiment KCl (40 mM, 10 seconds) was administered to verify that cells were healthy neurons. In some experiments ruthenium red (10 μM, 10) was added to the histamine solution. An inverted microscope (Zeiss Observer A1) equipped with MetaFluor photonics imaging system, including a Polychromator V, and a CoolSNAP ES camera (Visitron) was used for cell imaging. Cell soma diameters were measured and the mean values for different groups are given ± the standard error of the mean (S.E.M.). Differences between groups, in terms of diameter and the magnitude of calcium responses, were assessed using Students T-test,
This work was supported by the Alexander von Humboldt Foundation (EStJS) and NSF grant 0744979 (TJP). We thank Jeffrey Ruttencutter and Catherine Barone for assistance in some of the experiments and Heike Thränhardt for technical support.
- Ikoma A, Steinhoff M, Stander S, Yosipovitch G, Schmelz M: The neurobiology of itch. Nature reviews 2006, 7: 535–47. 10.1038/nrn1950PubMedView ArticleGoogle Scholar
- Schmelz M, Schmidt R, Bickel A, Handwerker HO, Torebjork HE: Specific C-Receptors for Itch in Human Skin. J Neurosci 1997, 17: 8003–8008.PubMedGoogle Scholar
- Bell JK, McQueen DS, Rees JL: Involvement of histamine H4 and H1 receptors in scratching induced by histamine receptor agonists in Balb C mice. British journal of pharmacology 2004, 142: 374–80. 10.1038/sj.bjp.0705754PubMed CentralPubMedView ArticleGoogle Scholar
- Hagermark O, Strandberg K, Gronneberg R: Effects of histamine receptor antagonists on histamine-induced responses in human skin. Acta dermato-venereologica 1979, 59: 297–300.PubMedGoogle Scholar
- Shim W, Tak M, Lee M, Kim M, Kim M, Koo J, Lee C, Kim M, Oh U: TRPV1 Mediates Histamine-Induced Itching via the Activation of Phospholipase A2 and 12-Lipoxygenase. J Neurosci 2007, 27: 2331–2337. 10.1523/JNEUROSCI.4643-06.2007PubMedView ArticleGoogle Scholar
- Imamachi N, Park GH, Lee H, Anderson DJ, Simon MI, Basbaum AI, Han S: TRPV1-expressing primary afferents generate behavioral responses to pruritogens via multiple mechanisms. Proceedings of the National Academy of Sciences 2009, 106: 11330–11335. 10.1073/pnas.0905605106View ArticleGoogle Scholar
- Sun YG, Chen ZF: A gastrin-releasing peptide receptor mediates the itch sensation in the spinal cord. Nature 2007, 448: 700–3. 10.1038/nature06029PubMedView ArticleGoogle Scholar
- Sun YG, Zhao ZQ, Meng XL, Yin J, Liu XY, Chen ZF: Cellular basis of itch sensation. Science (New York, N.Y) 2009, 325: 1531–4.View ArticleGoogle Scholar
- Bossut D, Frenk H, Mayer DJ: Is substance P a primary afferent neurotransmitter for nociceptive input? II. Spinalization does not reduce and intrathecal morphine potentiates behavioral responses to substance P. Brain research 1988, 455: 232–9. 10.1016/0006-8993(88)90081-9PubMedView ArticleGoogle Scholar
- Sakurada T, Wako K, Sakurada C, Manome Y, Tan-no K, Sakurada S, Kisara K: Spinally-mediated behavioural responses evoked by intrathecal high-dose morphine: possible involvement of substance P in the mouse spinal cord. Brain research 1996, 724: 213–21. 10.1016/0006-8993(96)00319-8PubMedView ArticleGoogle Scholar
- Cuellar JM, Jinks SL, Simons CT, Carstens E: Deletion of the preprotachykinin A gene in mice does not reduce scratching behavior elicited by intradermal serotonin. Neuroscience letters 2003, 339: 72–6. 10.1016/S0304-3940(02)01458-1PubMedView ArticleGoogle Scholar
- Park TJ, Comer C, Carol A, Lu Y, Hong HS, Rice FL: Somatosensory organization and behavior in naked mole-rats: II. Peripheral structures, innervation, and selective lack of neuropeptides associated with thermoregulation and pain. The Journal of comparative neurology 2003, 465: 104–20. 10.1002/cne.10824PubMedView ArticleGoogle Scholar
- Park TJ, Lu Y, Juttner R, Smith ES, Hu J, Brand A, Wetzel C, Milenkovic N, Erdmann B, Heppenstall PA, Laurito CE, Wilson SP, Lewin GR: Selective inflammatory pain insensitivity in the African naked mole-rat (Heterocephalus glaber). PLoS biology 2008, 6: e13. 10.1371/journal.pbio.0060013PubMed CentralPubMedView ArticleGoogle Scholar
- Smith ES, Lewin GR: Nociceptors: a phylogenetic view. Journal of comparative physiology 2009, 195: 1089–1106. 10.1007/s00359-009-0482-zPubMed CentralPubMedView ArticleGoogle Scholar
- Green AD, Young KK, Lehto SG, Smith SB, Mogil JS: Influence of genotype, dose and sex on pruritogen-induced scratching behavior in the mouse. Pain 2006, 124: 50–8. 10.1016/j.pain.2006.03.023PubMedView ArticleGoogle Scholar
- Namer B, Carr R, Johanek LM, Schmelz M, Handwerker HO, Ringkamp M: Separate Peripheral Pathways for Pruritus in Man. J Neurophysiol 2008, 100: 2062–2069. 10.1152/jn.90482.2008PubMed CentralPubMedView ArticleGoogle Scholar
- Fasmer OB, Berge OG, Hole K: Similar behavioural effects of 5-hydroxytryptamine and substance P injected intrathecally in mice. Neuropharmacology 1983, 22: 485–7. 10.1016/0028-3908(83)90167-3PubMedView ArticleGoogle Scholar
- Carstens EE, Carstens MI, Simons CT, Jinks SL: Dorsal horn neurons expressing NK-1 receptors mediate scratching in rats. Neuroreport 2010, 21: 303–308. 10.1097/WNR.0b013e328337310aPubMed CentralPubMedView ArticleGoogle Scholar
- Kuraishi Y, Nagasawa T, Hayashi K, Satoh M: Scratching behavior induced by pruritogenic but not algesiogenic agents in mice. European journal of pharmacology 1995, 275: 229–33. 10.1016/0014-2999(94)00780-BPubMedView ArticleGoogle Scholar
- Thomsen JS, Petersen MB, Benfeldt E, Jensen SB, Serup J: Scratch induction in the rat by intradermal serotonin: a model for pruritus. Acta Derm Venereol 2001, 81: 250–254. 10.1080/00015550152572868PubMedView ArticleGoogle Scholar
- Bennett NC, Faulkes CG: African mole-rats: ecology and eusociality. Cambridge: Cambridge University Press; 2000.Google Scholar
- Anton F, Euchner I, Handwerker HO: Psychophysical examination of pain induced by defined CO2 pulses applied to the nasal mucosa. Pain 1992, 49: 53–60. 10.1016/0304-3959(92)90187-GPubMedView ArticleGoogle Scholar
- Anton F, Peppel P, Euchner I, Handwerker HO: Controlled noxious chemical stimulation: responses of rat trigeminal brainstem neurones to CO2 pulses applied to the nasal mucosa. Neuroscience letters 1991, 123: 208–11. 10.1016/0304-3940(91)90932-JPubMedView ArticleGoogle Scholar
- Steen KH, Reeh PW, Anton F, Handwerker HO: Protons selectively induce lasting excitation and sensitization to mechanical stimulation of nociceptors in rat skin, in vitro. J Neurosci 1992, 12: 86–95.PubMedGoogle Scholar
- LaVinka PC, Brand A, Landau VJ, Wirtshafter D, Park TJ: Extreme tolerance to ammonia fumes in African naked mole-rats: animals that naturally lack neuropeptides from trigeminal chemosensory nerve fibers. Journal of comparative physiology 2009, 195: 419–27. 10.1007/s00359-009-0420-0PubMedView ArticleGoogle Scholar
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