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Daily variation in plasma electrolyte and acid–base status in fasted horses over a 25 h period of rest

Published online by Cambridge University Press:  09 March 2007

Amanda Waller*
Affiliation:
Dept. of Human Biology and Nutritional Sciences, University of Guelph, Guelph, ON, Canada, N1G 2W1
Kerri Jo Smithurst
Affiliation:
Dept. of Human Biology and Nutritional Sciences, University of Guelph, Guelph, ON, Canada, N1G 2W1
Gayle L Ecker
Affiliation:
Equine Centre, University of Guelph, Guelph, ON, Canada, N1G 2W1
Ray Geor
Affiliation:
Dept. of Biomedical Sciences, University of Guelph, Guelph, ON, Canada, N1G 2W1
Michael I Lindinger
Affiliation:
Dept. of Human Biology and Nutritional Sciences, University of Guelph, Guelph, ON, Canada, N1G 2W1
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Abstract

Measurement and interpretation of acid–base status are important in clinical practice and among racing jurisdictions to determine if horses have been administered alkalinizing substances for the purpose of enhancing performance. The present study used the physicochemical approach to characterize the daily variation in plasma electrolytes and acid–base state that occurs in horses in the absence of feeding and exercise. Jugular venous blood was sampled every 1–2 h from two groups (n=4 and n=5) of Standardbred horses over a 25 h period where food and exercise were withheld. One group of horses was studied in October and one in December. The time course and magnitude of circadian responses differed between the two groups, suggesting that subtle differences in environment may manifest in acid–base status. Significant daily variation occurred in plasma weak acid concentration ([Atot]) and strong ion difference ([SID]), [Cl], [K+], [Na+] and [lactate], which contributed to significant changes in [H+] and TCO2. The night-time period was associated with a mild acidosis, marked by increases in plasma [H+] and decreases in TCO2, compared with the morning hours. The night-time acidosis resulted from an increased plasma [Atot] due to an increased plasma protein concentration ([PP]), and a decreased [SID] due to increases in [Cl] and decreases in [Na+]. An increased plasma [K+] during the night-time had a mild alkalotic effect. There were no differences in pCO2. It was concluded that many equine plasma electrolyte and acid–base parameters exhibit fluctuations in the absence of feeding and exercise, and it is likely that some of these changes are due to daily variation.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2006

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References

1Yashiki, K, Kusunose, R and Takagi, S (1995). Diurnal variations of blood constituents in young Thoroughbred horses. Journal of Equine Science 6: 9197.CrossRefGoogle Scholar
2Greppi, GF, Casini, L, Gatta, D, Orlandi, M and Pasquini, M (1996). Daily fluctuations of haematology and blood biochemistry in horses fed varying levels of protein. Equine Veterinary Journal 28: 350353.CrossRefGoogle ScholarPubMed
3Clarke, LL, Ganjam, VK, Fichtenbaum, B, Hatfield, D and Garner, HE (1988). Effect of feeding on rehin-angiotensin-aldosterone system of the horse. American Journal of Physiology: Regulatory, Integrative and Comparative Physiology 254: R524R530.Google ScholarPubMed
4Piccione, G, Assenza, A, Fazio, F, Guidice, E and Caola, G (2001). Different periodicities of some haematological parameters in exercise-loaded athletic horses and sedentary horses. Journal of Equine Science 12: 1723.CrossRefGoogle Scholar
5Slocombe, RF, Huntington, PJ, Lind, KL and Vine, JH (1995). Plasma CO2 and electrolytes: diurnal changes and effects of adrenaline, doxapram, rebreathing and transport. Equine Veterinary Journal Supplement 18: 331336.CrossRefGoogle Scholar
6Jansson, A and Dahlborn, K (1999). Effects of feeding frequency and voluntary salt intake on fluid and electrolyte regulation in athletic horses. Journal of the American Physiological Society 86: 16101616.Google ScholarPubMed
7Stewart, PA (1983). Modern quantitative acid–base chemistry. Canadian Journal of Physiology and Pharmacolgy 61: 14411461.Google ScholarPubMed
8Waller, A, Smithhurst, KJ, Ecker, GL, Geor, R and Lindinger, MI (2005). Cyclical plasma electrolyte and acid–base responses to meal feeding in horses over a 24 h period. Equine and Comparative Exercise Physiology 2: 159169.CrossRefGoogle Scholar
9Lindinger, MI (2004). Acid–base physiology during exercise and in response to training. In: Hinchcliff, KW, Kaneps, AJ & Geor, RJ. (eds), Equine Sports Medicine and Surgery: Basic and Clinical Sciences of the Athletic Horse. Elsevier: New York, pp. 586610.Google Scholar
10Constable, PD (1997). A simplified strong ion model for acid–base equilibria: application to horse plasma. Journal of Applied Physiology 83: 297311.CrossRefGoogle ScholarPubMed
11Lepage, OM, Descoteaux, L, Marcoux, M and Tremblay, A (1991). Circadian rhythms of osteocalcin in equine serum. Correlation with alkaline phosphatase, calcium, phosphate and total protein levels. Canadian Journal of Veterinary Research 55: 510.Google ScholarPubMed
12Wang, HY and Huang, RC (2004). Diurnal modulation of the Na +/K + -ATPase and spontaneous firing in the rat retinorecipient clock neurons. Journal of Neurophysiology 92: 22952301.CrossRefGoogle ScholarPubMed
13Kerr, MG and Snow, DH (1982). Alterations in haematocrit, plasma proteins and electrolytes in horses following the feeding of hay. The Veterinary Record 110: 538540.Google Scholar
14Feneberg, R, Sparber, M, Veldhuis, JD, Mehls, O, Ritz, E and Schaffer, F (1999). Synchronous fluctuations of blood insulin and lactate concentrations in humans. Journal of Clinical Endocrinology and Metabolism 84: 220227.Google ScholarPubMed
15Hagstrom, E, Arner, P, Ungerstedt, U and Bolinder, J (1990). Subcutaneous adipose tissue: a source of lactate production after glucose ingestion in humans. American Journal of Physiology 258: E888893.Google ScholarPubMed
16Dombrowski, G and Swiatek, KR (1991). Lactate genesis by rat liver and muscle during development. Journal of Pediatric Research 30: 331336.CrossRefGoogle ScholarPubMed
17Houpt, KA, Eggleston, K, Kunkle, K and Houpt, TR (2000). Effect of water restriction on equine behaviour and physiology. Equine Veterinary Journal 32: 341344.CrossRefGoogle ScholarPubMed
18Minematsu, S, Watanabe, M, Tsuchiya, N, Watanabe, M and Amagaya, S (1995). Diurnal variations in blood chemical items in Sprague-Dawley rats. Experimental Animals 44: 223232.CrossRefGoogle ScholarPubMed
19Talan, MI, Engel, BT and Kawate, R (1992). Overnight increases in haematocrit: additional evidence for a nocturnal fall in plasma volume. Acta Physiologica Scandinavica 144: 473476.CrossRefGoogle ScholarPubMed
20Kronfeld, DS, Ferrante, PL, Taylor, LE and Tiegs, W (1999). Partition of plasma hydrogen ion concentration changes during repeated sprints. Equine Veterinary Journal Supplement 30: 380383.CrossRefGoogle Scholar
21Waller, A and Lindinger, MI (2005). Physicochemical analysis of acid–base status during recovery from high intensity exercise in Standardbred racehorses. Equine and Comparative Exercise Physiology 2: 119127.CrossRefGoogle Scholar