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Endocrine changes in cerebrospinal fluid, pituitary effluent, and peripheral plasma of anesthetized ponies.

Abstract: To investigate the effects of inhalation and total IV anesthesia on pituitary-adrenal activity in ponies. Methods: 9 healthy ponies: 5 geldings and 4 mares. Methods: Catheters were placed in the cavernous sinus below the pituitary gland and in the subarachnoid space via the lumbosacral space. After 72 hours, administration of acepromazine was followed by induction of anesthesia with thiopentone and maintenance with halothane (halothane protocol), or for the IV protocol, anesthesia induction with detomidine and ketamine was followed by maintenance with IV infusion of a detomidine-ketamine-guaifenesin combination. Arterial blood pressure and gas tensions were measured throughout anesthesia. Peptide and catecholamine concentrations were measured in pituitary effluent, peripheral plasma, and CSF. Peripheral plasma cortisol, glucose, and lactate concentrations also were measured. Results: Intravenous anesthesia caused less cardiorespiratory depression than did halothane. ACTH, metenkephalin, arginine vasopressin, and norepinephrine pituitary effluent and peripheral plasma concentrations were higher during halothane anesthesia, with little change during intravenous anesthesia. Pituitary effluent plasma beta-endorphin and peripheral plasma cortisol concentrations increased during halothane anesthesia only. Dynorphin concentrations did not change in either group. Hyperglycemia developed during intravenous anesthesia only. Minimal changes occurred in CSF hormonal concentrations during anesthesia. Conclusions: The pituitary gland has a major role in maintaining circulating peptides during anesthesia. Compared with halothane, IV anesthesia appeared to suppress pituitary secretion.
Publication Date: 1997-07-01 PubMed ID: 9215455
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research investigates how different forms of anesthesia affect pituitary-adrenal activity in ponies. The results suggest that intravenous anesthesia suppresses pituitary secretion more than inhaled anesthesia and produces lesser cardiorespiratory depression.

Methodology

  • Nine healthy ponies – 5 geldings and 4 mares – were involved in the study.
  • Catheters were placed in two separate areas: the cavernous sinus below the pituitary gland and in the subarachnoid space via the lumbosacral space.
  • After 72 hours, two types of anaesthesia protocols were followed.
  • For inhaled anesthesia, acepromazine was followed by induction of anesthesia with thiopentone and then maintenance with halothane. This is referred to as the halothane protocol.
  • For the IV protocol, anesthesia was induced with detomidine and ketamine, followed by maintenance with an IV infusion of a detomidine-ketamine-guaifenesin combination.
  • Several health parameters like arterial blood pressure and gas tensions were measured throughout the anesthesia process. Peptide and catecholamine concentrations in different sources, such as pituitary effluent, peripheral plasma, and CSF, along with peripheral plasma cortisol, glucose, and lactate concentrations, were also measured.

Results

  • It was observed that intravenous anesthesia caused less cardiorespiratory depression than halothane.
  • ACTH, metenkephalin, arginine vasopressin, and norepinephrine concentrations in pituitary effluent and peripheral plasma were higher during halothane anesthesia, and did not change much during intravenous anesthesia.
  • Dynorphin concentrations did not change in either type of anesthesia.
  • Only halothane anesthesia led to increased pituitary effluent plasma beta-endorphin and peripheral plasma cortisol concentrations.
  • Hyperglycemia developed only during intravenous anesthesia, and minimal changes were observed in CSF hormonal concentrations during anesthesia.

Conclusion

  • The research concluded that the pituitary gland plays a major role in maintaining circulating peptides during anesthesia.
  • Compared to halothane, intravenous anesthesia appears to suppress pituitary secretion more effectively, offering potential benefits in managing endocrine changes during anesthesia.

Cite This Article

APA
Luna SP, Taylor PM, Bloomfield M. (1997). Endocrine changes in cerebrospinal fluid, pituitary effluent, and peripheral plasma of anesthetized ponies. Am J Vet Res, 58(7), 765-770.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 58
Issue: 7
Pages: 765-770

Researcher Affiliations

Luna, S P
  • Animal Health Trust, Newmarket, United Kingdom.
Taylor, P M
    Bloomfield, M

      MeSH Terms

      • Adrenocorticotropic Hormone / blood
      • Adrenocorticotropic Hormone / cerebrospinal fluid
      • Adrenocorticotropic Hormone / metabolism
      • Anesthesia, Inhalation / veterinary
      • Anesthesia, Intravenous / veterinary
      • Animals
      • Arginine Vasopressin / blood
      • Arginine Vasopressin / cerebrospinal fluid
      • Arginine Vasopressin / metabolism
      • Female
      • Halothane
      • Horses / blood
      • Horses / cerebrospinal fluid
      • Horses / physiology
      • Hydrocortisone / blood
      • Hydrocortisone / cerebrospinal fluid
      • Hydrocortisone / metabolism
      • Male
      • Pituitary Gland / metabolism
      • beta-Endorphin / blood
      • beta-Endorphin / cerebrospinal fluid
      • beta-Endorphin / metabolism

      Citations

      This article has been cited 2 times.
      1. Aoki M, Wakuno A, Kushiro A, Mae N, Kakizaki M, Nagata SI, Ohta M. Evaluation of total intravenous anesthesia with propofol-guaifenesin-medetomidine and alfaxalone-guaifenesin-medetomidine in Thoroughbred horses undergoing castration.. J Vet Med Sci 2017 Dec 22;79(12):2011-2018.
        doi: 10.1292/jvms.16-0658pubmed: 29057764google scholar: lookup
      2. Nóbrega Neto PI, Luna SP, Queiroz-Williams P, Mama KR, Steffey EP, Carregaro AB. Cardiorespiratory and antinociceptive effects of two different doses of lidocaine administered to horses during a constant intravenous infusion of xylazine and ketamine.. BMC Vet Res 2013 Oct 9;9:199.
        doi: 10.1186/1746-6148-9-199pubmed: 24103634google scholar: lookup