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Veterinary research communications1989; 13(6); 413-419; doi: 10.1007/BF00402561

Different gradients for neurotransmitter metabolites and protein in horse cerebrospinal fluid.

Abstract: The serotonin metabolite, 5-hydroxyindoleacetic acid (5-HIAA) and the dopamine metabolite, homovanillic acid (HVA) in the cerebrospinal fluid (CSF) of seven clinically normal horses were evaluated with reverse phase high pressure liquid chromatography and electrochemical detection. Comparisons of the neurotransmitter metabolite concentrations were made on CSF collected simultaneously from the atlanto-occipital and lumbosacral regions. There were significantly higher amounts of 5-HIAA and HVA in atlanto-occipital CSF than in lumbosacral CSF. Mean 5-HIAA concentrations in atlanto-occipital and lumbosacral CSF were 206.1 +/- 37.0 nmol/L and 68.5 +/- 12.6 nmol/L, respectively. The mean HVA concentration in atlanto-occipital CSF was 254.4 +/- 50.4 nmol/L. No HVA was detected in lumbosacral CSF. In contrast, significantly greater protein concentrations were present in lumbosacral CSF than in atlanto-occipital CSF. Lumbosacral and atlanto-occipital CSF contained 32.1 +/- 3.7 mg protein/dl and 25.0 +/- 1.3 mg protein/dl, respectively. Thus, between the atlanto-occipital and lumbosacral space of the horses, a rostrocaudal gradient existed for neurotransmitter metabolites and a caudorostral gradient existed for protein.
Publication Date: 1989-01-01 PubMed ID: 2483597DOI: 10.1007/BF00402561Google Scholar: Lookup
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Summary

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This study examines the concentration of serotonin and dopamine metabolites alongside protein levels in the cerebrospinal fluid (CSF) of horses. The researchers found higher levels of these metabolites in the CSF in the upper part of the spinal cord, compared to the lower part, which conversely, had higher protein concentrations.

Objective and Methodology:

  • The research aimed to understand the variation in concentration of two neurotransmitter metabolites, 5-hydroxyindoleacetic acid (5-HIAA) – a serotonin metabolite, and homovanillic acid (HVA) – a dopamine metabolite, in the cerebrospinal fluid of horses.
  • The researchers also wanted to examine how protein levels vary in different parts of the CSF. For this, they used seven healthy horses as their study sample.
  • The metabolite concentrations were evaluated using techniques known as reverse phase high pressure liquid chromatography and electrochemical detection.
  • The researchers analysed the CSF collected simultaneously from two regions of the spinal cord: atlanto-occipital (upper part) and lumbosacral (lower part).

Findings:

  • The findings showed higher amounts of 5-HIAA and HVA in the atlanto-occipital CSF compared to the lumbosacral CSF.
  • In terms of specific numbers, the mean concentration of 5-HIAA was 206.1 nmol/L in the atlanto-occipital CSF, while it was 68.5 nmol/L in lumbosacral CSF. The mean HVA concentration in the atlanto-occipital CSF was 254.4 nmol/L, but no HVA was detected in the lower part of the spinal cord.
  • On the other hand, significantly greater concentrations of protein were observed in the lumbosacral CSF than in the atlanto-occipital CSF. The mean protein level was 32.1 mg/dL in the lumbosacral CSF and 25.0 mg/dL in the atlanto-occipital CSF.

Conclusions:

  • The researchers concluded that there is a rostrocaudal gradient (from head to tail, or top to bottom) for neurotransmitter metabolites in the CSF, meaning the concentrations were higher in the upper part of the spinal cord.
  • Conversely, a caudorostral gradient (from tail to head, or bottom to top) existed for protein, as the concentrations were higher in the lower part of the spinal cord.

This study helps us understand how neurotransmitter metabolite and protein concentrations change along the spinal cord. This could prove vital in studying various neurological diseases in animals and potentially in humans.

Cite This Article

APA
Vaughn DM, Smyth GB. (1989). Different gradients for neurotransmitter metabolites and protein in horse cerebrospinal fluid. Vet Res Commun, 13(6), 413-419. https://doi.org/10.1007/BF00402561

Publication

ISSN: 0165-7380
NlmUniqueID: 8100520
Country: Switzerland
Language: English
Volume: 13
Issue: 6
Pages: 413-419

Researcher Affiliations

Vaughn, D M
  • Medicinal Biochemistry Laboratory, College of Veterinary Medicine, Auburn University, Alabama 36849-5525.
Smyth, G B

    MeSH Terms

    • Animals
    • Cerebrospinal Fluid Proteins / metabolism
    • Chromatography, High Pressure Liquid
    • Female
    • Homovanillic Acid / cerebrospinal fluid
    • Horses / cerebrospinal fluid
    • Hydroxyindoleacetic Acid / cerebrospinal fluid
    • Lumbosacral Region
    • Male
    • Neurotransmitter Agents / cerebrospinal fluid
    • Spinal Canal

    References

    This article includes 15 references
    1. Bailey CS, Higgins RJ. Comparison of total white blood cell count and total protein content of lumbar and cisternal cerebrospinal fluid of healthy dogs.. Am J Vet Res 1985 May;46(5):1162-5.
      pubmed: 4003891
    2. Bertilsson L. 5-Hydroxyindoleacetic acid in cerebrospinal fluid--methodological and clinical aspects.. Life Sci 1987 Aug 17;41(7):821-4.
      pubmed: 2441222doi: 10.1016/0024-3205(87)90171-8google scholar: lookup
    3. Stanley M, Traskman-Bendz L, Dorovini-Zis K. Correlations between aminergic metabolites simultaneously obtained from human CSF and brain.. Life Sci 1985 Oct 7;37(14):1279-86.
      pubmed: 2413327doi: 10.1016/0024-3205(85)90242-5google scholar: lookup
    4. Vaughn DM, Smyth GB, Whitmer WL, Satjawatcharaphong C. Analysis of equine cisterna magna cerebrospinal fluid for the presence of some monoamine neurotransmitters and transmitter metabolites.. Vet Res Commun 1989;13(3):237-49.
      pubmed: 2476887doi: 10.1007/BF00142050google scholar: lookup
    5. Roccatagliata G, Albano C, Cocito L, Maffini M. Interactions between central monoaminergic systems: dopamine-serotonin.. J Neurol Neurosurg Psychiatry 1979 Dec;42(12):1159-62.
      pubmed: 160445doi: 10.1136/jnnp.42.12.1159google scholar: lookup
    6. Vaughn DM, Coleman E, Simpson ST, Whitmer B, Satjawatcharaphong C. A rostrocaudal gradient for neurotransmitter metabolites and a caudorostral gradient for protein in canine cerebrospinal fluid.. Am J Vet Res 1988 Dec;49(12):2134-7.
      pubmed: 2467594
    7. Bulat M, Zivković B. Origin of 5-hydroxyindoleacetic acid in the spinl fluid.. Science 1971 Aug 20;173(3998):738-40.
      pubmed: 5109594doi: 10.1126/science.173.3998.738google scholar: lookup
    8. DAHLSTROEM A, FUXE K. EVIDENCE FOR THE EXISTENCE OF MONOAMINE-CONTAINING NEURONS IN THE CENTRAL NERVOUS SYSTEM. I. DEMONSTRATION OF MONOAMINES IN THE CELL BODIES OF BRAIN STEM NEURONS.. Acta Physiol Scand Suppl 1964;:SUPPL 232:1-55.
      pubmed: 14229500
    9. Agren H, Mefford IN, Rudorfer MV, Linnoila M, Potter WZ. Interacting neurotransmitter systems. A non-experimental approach to the 5HIAA-HVA correlation in human CSF.. J Psychiatr Res 1986;20(3):175-93.
      pubmed: 2430098doi: 10.1016/0022-3956(86)90002-6google scholar: lookup
    10. Kristensen F, Firth EC. Analysis of serum proteins and cerebrospinal fluid in clinically normal horses, using agarose electrophoresis.. Am J Vet Res 1977 Jul;38(7):1089-92.
      pubmed: 70183
    11. Mayhew IG, deLahunta A, Whitlock RH, Krook L, Tasker JB. Spinal cord disease in the horse.. Cornell Vet 1978 Jan;68 Suppl 6:1-207.
      pubmed: 618720
    12. Mayhew IG. Collection of cerebrospinal fluid from the horse.. Cornell Vet 1975 Oct;65(4):500-11.
      pubmed: 1192748
    13. Mayhew IG, Whitlock RH, Tasker JB. Equine cerebrospinal fluid: reference values of normal horses.. Am J Vet Res 1977 Aug;38(8):1271-4.
      pubmed: 911095
    14. Vaughn DM, Coleman E, Simpson ST, Satjawatcharaphong C. Analysis of neurotransmitter metabolite concentrations in canine cerebrospinal fluid.. Am J Vet Res 1988 Aug;49(8):1302-6.
      pubmed: 2459997
    15. Kirk GR, Neate S, McClure RC, Hutcheson DP. Electrophoretic pattern of equine cerebrospinal fluid.. Am J Vet Res 1974 Sep;35(9):1263-4.
      pubmed: 4138877

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