- Short paper
- Open Access
Elevated CSF histamine levels in multiple sclerosis patients
© Kallweit et al.; licensee BioMed Central Ltd. 2013
- Received: 3 December 2012
- Accepted: 22 April 2013
- Published: 9 May 2013
Histamine is an ubiquitous inflammatory mediator of numerous physiological processes. Histamine and its receptors have been implicated in multiple sclerosis (MS) disease pathogenesis. We prospectively enrolled 36 MS patients and 19 age and gender-matched healthy volunteers for cerebrospinal fluid (CSF) histamine analysis.
CSF histamine levels in MS patient samples were significantly higher (median: 35.6 pg/ml) than in controls (median: 5.5 pg/ml; Beta = 0.525, p < 0.001). In addition, histamine increased with age (Pearson’s correlation, p < 0.003).
Histamine may be an important factor for both the initiation and maintenance of chronic inflammatory diseases of the central nervous system. Our observation encourages a deeper investigation of the role of histamine in MS.
- Multiple sclerosis
- Histamine receptors
- Granulocyte-macrophage colony-stimulating factor
- Chronic inflammatory diseases
Multiple sclerosis (MS) is a complex autoimmune disease with inflammation and demyelination within the central nervous system (CNS). Histamine and its receptors have been implicated in MS disease pathogenesis . Histamine is an ubiquitous inflammatory mediator of numerous physiological processes including local immune responses and allergic reactions, and it plays an important role in neurotransmission. The functions of histamine are mediated through 4 G-protein coupled receptors (H1-H4 receptors). Histamine and histamine receptors play a regulatory role in experimental allergic encephalomyelitis (EAE), the animal model of MS [1–3]. Rodent experiments revealed that histamine increases the permeability of the blood brain barrier, promoting CNS inflammation [1, 4, 5]. The cytokine granulocyte-macrophage colony-stimulating factor (GM-CSF) in auto-reactive T helper cells is mandatory to induce and sustain EAE in mice . GM-CSF stimulates granulocytes and macrophages, and both secrete histamine. A small study by Tuomisto et al. , reported on higher CSF histamine level by about 60% both in patients with remitting and progressive type of MS than in controls. Based on this observation and previous studies in EAE, we hypothesized that histamine might play a role in MS. Thus, we aimed at testing whether histamine is elevated in the CSF of MS patients.
We prospectively enrolled consecutive 36 MS patients (mean (±SD) age, 51 ± 10 years; 64% female; 24 patients with secondary progressive disease, 12 relapsing-remitting, RRMS) of Caucasian origin treated in the MS center of the University Hospital Zurich and 19 age and gender-matched healthy volunteers: age 46 ± 10 years (mean ±SD); 37% female. In all patients, the diagnosis of MS was made according to the McDonald diagnostic criteria 2005 . We enrolled all types of MS. Lumbar puncture was performed for diagnostic purposes. In 19 patients, LP was performed for diagnosis of MS and in 17 secondary progressive MS (SPMS) patients for evaluation of treatment effects of first-time intrathecal baclofen (N = 7) or triamcinolone acetonid (N = 10) application. In the controls, cerebrospinal fluid (CSF) was ascertained during spinal anesthesia. Subjects with signs of neurological or sleep-wake disorders were not included as controls. Patients and controls suffering from any allergic disease were not included into this study. All patients and healthy controls gave informed written consent. The study was approved by the local ethics committee.
Routine CSF analysis included oligoclonal bands and IgG index. For histamine analysis, after assessment of CSF, samples were immediately centrifuged, put on dry ice and stored at −80°C until assay. Storage was between 6 and 24 months (patients and controls). As far as we examined, histamine contents in biological samples stored at −80°C did not change over 2 years. Samples were separated by high-performance liquid chromatography (HPLC), thereafter histamine was post-labeled by O-phthalaldehyde and detected by fluorometric analysis . HPLC has been used for the measurement of histamine in CSF in other neurological disorders .
Statistical analyses were performed with SPSS 19.0. Group data are described by median. For the comparison of parametric data, we Student’s t-tests, and for non-parametric data, Whitney U-test was used. For correlation analyses in parametric data, we used Pearson’s correlation. To control for effects of sex, age and different types of MS on histamine concentrations, we ran multivariate logistic regression analyses.
This study confirmed results by Tuomisto  and our hypothesis that histamine levels are increased in MS patients. Histamine functions are not only limited to allergic functions but are extended to other processes related to neurology, immunology, or oncology . Until now, no CNS disease entity has been associated directly with brain histamine dysfunction, but different histamine receptors [H(3), H(4)] are recognized as drug targets for (e.g.) sleep-wake disorders, Parkinson’s disease, and neuroimmunopharmacology .
Histamine in CSF originates from mast cells and histaminergic neurons of the tuberomammillary nucleus of the posterior basal hypothalamus . The GM-CSF-mediated stimulation of granulocytes and macrophages may be one possible underlying mechanism for elevated histamine levels in MS. Thus histamine may be an important factor for both the initiation and maintenance of chronic inflammatory diseases of the central nervous system such as MS. This interpretation remains theoretical until data from other patient groups with acute and chronic inflammatory and non-inflammatory diseases of the CNS confirm our results.
Limitations of our study include the small study size and the large intra-group variability of histamine levels. We did not measure histamine levels in blood. Although peripheral histamine hardly enters into CNS through blood brain barrier [14, 15], we cannot completely exclude the possibility that histamine concentrations in CSF are not only controlled in brain, but also derive from blood. Furthermore, we cannot exclude DMT effects on histamine levels.
This observation encourages a deeper investigation of the role of GM-CSF, granulocytes, macrophages and histamine in MS. Further, histamine may be investigated as diagnostic marker for MS and other inflammatory CNS diseases.
- Jadidi-Niaragh F, Mirshafiey A: Histamine and histamine receptors in pathogenesis and treatment of multiple sclerosis. Neuropharmacology. 2010, 59: 180-189. 10.1016/j.neuropharm.2010.05.005.PubMedView ArticleGoogle Scholar
- Orr EL, Stanley NC: Brain and spinal cord levels of histamine in Lewis rats with acute experimental autoimmune encephalomyelitis. J Neurochem. 1989, 53: 111-118. 10.1111/j.1471-4159.1989.tb07301.x.PubMedView ArticleGoogle Scholar
- Emerson MR, Orentas DM, Lynch SG, LeVine SM: Activation of histamine H2 receptors ameliorates experimental allergic encephalomyelitis. Neuroreport. 2002, 13: 1407-1410. 10.1097/00001756-200208070-00012.PubMedView ArticleGoogle Scholar
- Lu C, Diehl SA, Noubade R: Endothelial histamine H1 receptor signaling reduces blood–brain barrier permeability and susceptibility to autoimmune encephalomyelitis. Proc Natl Acad Sci U S A. 2010, 107: 18967-18972. 10.1073/pnas.1008816107.PubMed CentralPubMedView ArticleGoogle Scholar
- Stanley NC, Jackson FL, Orr EL: Attenuation of experimental autoimmune encephalomyelitis by compound 48/80 in Lewis rats. J Neuroimmunol. 1990, 29: 223-228. 10.1016/0165-5728(90)90165-J.PubMedView ArticleGoogle Scholar
- Codarri L, Gyülvészi G, Tosevski V: RORγt drives production of the cytokinpg/mle GM-CSF in helper T cells, which is essential for the effector phase of autoimmune neuroinflammation. Nat Immunol. 2011, 12: 560-567. 10.1038/ni.2027.PubMedView ArticleGoogle Scholar
- Tuomisto L, Kilpelainen H, Riekkinen P: Histamine and histamine-N-methyltransferase in the CSF of patients with multiple sclerosis. Agents Actions. 1983, 13: 255-257. 10.1007/BF01967346.PubMedView ArticleGoogle Scholar
- Polman CH, Reingold SC, Edan G: Diagnostic criteria for multiple sclerosis: 2005 revisions to the “McDonald Criteria”. Ann Neurol. 2005, 58: 840-846. 10.1002/ana.20703.PubMedView ArticleGoogle Scholar
- Nagatsu T: Application of high-performance liquid chromatography to the study of biogenic amine-related enzymes. J Chromatogr. 1991, 566: 287-307.PubMedView ArticleGoogle Scholar
- Bassetti CL, Baumann CR, Dauvilliers Y, Croyal M, Robert P, Schwartz JC: Cerebrospinal fluid histamine levels are decreased in patients with narcolepsy and excessive daytime sleepiness of other origin. J Sleep Res. 2010, 19: 620-623. 10.1111/j.1365-2869.2010.00819.x.PubMedView ArticleGoogle Scholar
- Ohtsu H: Pathophysiologic role of histamine: evidence clarified by histidine decarboxylase gene knockout mice. Int Arch Allergy Immunol. 2012, 158 (Suppl 1): 2-6.PubMedView ArticleGoogle Scholar
- Tiligada E, Kyriakidis K, Chazot PL, Passani MB: Histamine pharmacology and new CNS drug targets. CNS Neurosci Ther. 2011, 17: 620-628. 10.1111/j.1755-5949.2010.00212.x.PubMedView ArticleGoogle Scholar
- Watanabe T, Taguchi Y, Shiosaka S: Distribution of the histaminergic neuron system in the central nervous system of rats; a fluorescent immunohistochemical analysis with histidine decarboxylase as a marker. Brain Res. 1984, 295: 13-25. 10.1016/0006-8993(84)90811-4.PubMedView ArticleGoogle Scholar
- Theoharides TC, Konstantinidou AD: Corticotropin-releasing hormone and the blood–brain-barrier. Front Biosci. 2007, 12: 1615-1628. 10.2741/2174.PubMedView ArticleGoogle Scholar
- Haas HL, Sergeeva OA, Selbach O: Histamine in the Nervous System. Physiol Rev. 2008, 88: 1183-1241. 10.1152/physrev.00043.2007.PubMedView ArticleGoogle Scholar
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