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Research in veterinary science1977; 23(2); 146-152;

Phenylalanine inhibited p-nitrophenyl phosphatase activity in the serum as an indication of intestinal cellular disruption in the horse.

Abstract: Examination of tissues obtained from thoroughbred horses showed that the 'intestinal' phosphatase activity could be differentiated from other phosphatases by analysis at a pH of 9-5 and inhibition with 15 mM L-phenylalanine. A simple method for the measurement of 'intestinal' phosphatase in heparinised plasma or serum is described. Application of the technique to serum or plasma from normal and diseased horses indicates that the increase in the activity of 'intestinal' phosphatase is associated with cases showing clinical, biochemical and haematological evidence of intestinal damage.
Publication Date: 1977-09-01 PubMed ID: 22115
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  • Journal Article

Summary

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This research examines how phenylalanine, an amino acid, affects the activity of a specific type of enzyme in horse serum, suggesting potential for diagnosing intestinal damage in horses.

Background on Enzymes and Phenylalanine

  • The study pertains to enzymes called ‘intestinal’ phosphatases, deemed to be different from other kinds of phosphatases based on their chemical behavior in a pH of 9.5 and with exposure to Phenylalanine.
  • Phenylalanine is an amino acid, usually found in proteins. It’s important for the body to function and is usually acquired from foods we eat. In the present study, it has been used as an inhibitor for the ‘intestinal’ phosphatase activity.

Method and Technique

  • The researchers describe a simple method to measure the activity of the ‘intestinal’ phosphatase in heparinised plasma or serum. Heparinised refers to plasma or serum that has been treated with the anticoagulant, heparin, to prevent blood clotting.
  • The described method provides a tool to analyze and trace the activity of this specific enzyme in the horse’s body, vital for investigating and diagnosing physiological conditions in horses.

Clinical Implications

  • The researchers tested their diagnostic technique on both healthy and diseased horses. They found that an increase in the activity of the ‘intestinal’ phosphatase was associated with horses exhibiting clinical, biochemical, and haematological signs of intestinal damage.
  • This finding illustrates a correlation between the specific enzyme activity and instances of intestinal damage, making it a potentially useful diagnostic tool for veterinarians in detecting intestinal diseases in horses.

Cite This Article

APA
Blackmore DJ, Palmer A. (1977). Phenylalanine inhibited p-nitrophenyl phosphatase activity in the serum as an indication of intestinal cellular disruption in the horse. Res Vet Sci, 23(2), 146-152.

Publication

ISSN: 0034-5288
NlmUniqueID: 0401300
Country: England
Language: English
Volume: 23
Issue: 2
Pages: 146-152

Researcher Affiliations

Blackmore, D J
    Palmer, A

      MeSH Terms

      • 4-Nitrophenylphosphatase / antagonists & inhibitors
      • 4-Nitrophenylphosphatase / blood
      • 4-Nitrophenylphosphatase / isolation & purification
      • Animals
      • Female
      • Horse Diseases / enzymology
      • Horses / blood
      • Hydrogen-Ion Concentration
      • Intestinal Diseases / enzymology
      • Intestinal Diseases / veterinary
      • Intestines / enzymology
      • Methods
      • Phenylalanine / pharmacology
      • Phosphoric Monoester Hydrolases / blood

      Citations

      This article has been cited 3 times.
      1. Trueman KF, Lumsden JH, McSherry BJ. Examination of the origin of increased equine serum alkaline phosphatase concentrations. Can Vet J 1983 Apr;24(4):108-11.
        pubmed: 17422242
      2. Ellison RS, Jacobs RM. The isoelectric focusing properties of serum alkaline phosphatase in disease and following prednisolone and phenylbutazone administration in the horse. Can J Vet Res 1990 Jan;54(1):126-31.
        pubmed: 2306661
      3. Ellison RS, Jacobs RM. An attempt to determine the tissue origin of equine serum alkaline phosphatase by isoelectric focusing. Can J Vet Res 1990 Jan;54(1):119-25.
        pubmed: 2306660