Short Communication · Volume 51, Issue 1, 21 January 2019 · Open Access
Effect of Diarrhea on Hematocrit and Serum Biochemical Profile in Foals
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Affiliations & Notes ⌄
- 1Department of Clinical Medicine and Surgery, University of Veterinary and Animal Sciences, Lahore 54600 2Department of Livestock and Dairy Development, Punjab 3University College of Veterinary and Animal Sciences, The Islamia University of Bahawalpur, Bahawalpur 63100 , * Corresponding author: sadaqat.ali@iub.edu.pk
Article Info ⌄
- Journal:
- Pakistan Journal of Zoology
- Published:
- 21 January 2019

Abstract
Materials and methods
This study was conducted at various public and private sector veterinary hospitals as well as equine stud farms in and around Lahore district, Pakistan. A total of 105 foals (n = 35 horse foals, n = 35 donkey foals and n = 35 mule foals) which were affected clinically with diarrhea regardless of the etiology and 12 apparently healthy foals (n = 4 horse foals, n = 4 donkey foals and n = 4 mule foals) were selected as control group for this study.
Peripheral blood was collected aseptically from puncture of jugular vein into 5 mL vacuum plain tubes and 5 mL vacuum tubes containing ethylene diamine tetraacetic acid (EDTA) separately. Plain tubes were kept undisturbed for 30 min to clot the blood samples. Plain tubes were centrifuged for 12 min at 3,000 rpm after incubation (37oC, 60 min). Serum was withdrawn into 1.5ml Eppendorf tubes and frozen at −80oC for later biochemical analysis. Tubes containing EDTA were used for determination of PCV using microhematocrit method. The serum samples were analyzed by atomic absorption spectrophotometer. Macro minerals (calcium, potassium and sodium) and trace elements (copper and iron), and ultra-trace elements (lithium) were estimated as described by Basaki et al. (2012), Tajik and Nazifi (2013) and Akhter et al. (2007) at Quality Operations Laboratory, UVAS, Lahore. The values were compared with references values.
Data obtained from comparative study of two groups (i.e. diarrheic and healthy foals) on hematocrit and serum biochemical profile were analyzed by student t-test using IBM® SPSS (Statistical Product and Service Solutions) Statistics® version 22.0. The probability (p) value less than 0.05 were considered significant.
Table I.- Effect of diarrhea on the average packed cell volume, serum macro minerals, trace and ultratrace elements in Foals.
| Parameter | Species | Diarrheic foals | Healthy foals |
| PCV (%) | Horse | 56.00 ± 4.40* | 40.75 ± 3.59 |
| Donkey | 57.00 ± 9.80* | 45.25 ± 0.95 | |
| Mule | 59.00 ± 3.90* | 42.00 ± 2.90 | |
| Sodium (mmol/L) | Horse | 109.1 ± 6.22* | 142.7 ± 5.17 |
| Donkey | 103.8 ± 6.50* | 139.2 ± 2.04 | |
| Mule | 102.1 ± 3.63* | 137.0 ± 2.61 | |
| Potassium (mmol/L) | Horse | 06.20 ± 0.73* | 03.73 ± 0.31 |
| Donkey | 06.30 ± 0.75* | 04.14 ± 0.15 | |
| Mule | 05.90 ± 0.65* | 03.53 ± 0.15 | |
| Calcium (mmol/L) | Horse | 02.20 ± 0.12* | 02.87 ± 0.26 |
| Donkey | 02.20 ± 0.11* | 02.79 ± 0.16 | |
| Mule | 02.20 ± 0.11* | 02.94 ± 0.21 | |
| Copper (µg/dL) | Horse | 70.00 ± 21.0* | 142 ± 17.00 |
| Donkey | 68.00 ± 13.0* | 135 ± 09.00 | |
| Mule | 59.00 ± 19.0* | 130 ± 05.00 | |
| Iron (µg/dL) | Horse | 102.0 ± 18.0* | 220 ± 27.00 |
| Donkey | 095.0 ± 13.0* | 205 ± 19.00 | |
| Mule | 098.0 ± 14.0* | 224 ± 14.00 | |
| Lithium (µg/dL) | Horse | 06.00 ± 1.00* | 14.0 ± 4.00 |
| Donkey | 05.00 ± 2.00* | 12.0 ± 2.00 | |
| Mule | 06.00 ± 1.00* | 12.0 ± 2.00 |
* Significant difference p < 0.05.
Results and discussion
PCV in all diarrheic foals of horses, donkey and mules was significantly higher (p-value<0.05) compared to their healthy counterparts. Average PCV (%) levels in diarrheic foals of horses, donkeys, and mules were revealed 56, 57, and 59, respectively (Table I). PCV was slightly higher in mule foals, followed by donkey and horse foals. Concentration of sodium, potassium, calcium, copper, iron and lithium were evaluated in the serum sample of diarrheic as well as control group of equine foals. Serum sodium, copper, iron and lithium levels in diarrheic foals of all species in the study were decreased significantly (p< 0.05) when matched with healthy ones. The serum potassium values were however significantly increased (p< 0.05) in all diarrheic foals comparing with healthy foals.
Increased PCV in all diarrheic foals compared to healthy foals was consistent with the findings of Frederick et al. (2009), who reported increased PCV in non-survivor compared to survivor diarrheic foals. A case of an adult horse with acute diarrhea having high PCV stated by Oliver and Stampfli (2006) also confirmed these results. PCV increases in diarrhea due to the loss of the water from plasma consequently cellular part of blood converts to major portion.
Keeping in view the control group, reduced serum sodium concentrations in all diarrheic foals were in agreement with previous studies ; , which disclosed hyponatremia in adult horses with acute diarrhea. Diarrhea leads to loss of isotonic fluid (hypovolemia). Excessive loss of gastrointestinal water, sodium, chloride, and bicarbonate diminish the extracellular portion of these electrolytes. Kidney response of fluid loss is to accelerate proximal tubule’s reabsorption sodium, chloride, bicarbonate and water. Normal plasma sodium to chloride (1.4:1) is decreased so it is called hyperchloremic metabolic acidosis. Sodium reabsorption results in sodium delivery at distal tubule for H+ exchange exacerbating the acidosis .
Higher serum potassium values in all three categories of diarrheic foals supported the results of case report about diarrhea in non-suckling horses . Grinberg et al. (2009) reported hyperkalemia in hospitalized foals affected with cryptosporidiosis are also in close agreement with this study. Contradictory to this, hypokalemia were reported by various authors ; ; . Underlying whole body potassium deficit might be the reason of hypokalemia in previous studies.
Consistent low serum calcium levels in all diarrheic foals during the study coincided with earlier work in which both total and ionized calcium levels were decreased in colic horses with diarrhea. Another study revealed lower total, ionized and adjusted ionized calcium levels in horses with diarrhea are also accorded with our results. Likewise, Dart et al. (1992) also described lower serum ionized calcium concentration in horses with surgical managed gastrointestinal disease. Previously, other studies also stated hypocalcemia in diarrheic calves ; ; . Possible reasons of hypocalcemia might be alterations in the levels of ionized calcium due to modifications in blood pH and plasma albumin levels, infection, inadequate food intake, and intravenous fluid therapy without calcium supplementation, and ileus .
Decreased serum concentration of copper and zinc in diarrheic people ; Arora et al., 2006) were congruent to hypocupremia of present study in diarrheic foals. Copper is required for hemoglobin formation, iron transport, and ceruloplasmin synthesis. Ceruloplasmin (ferroxidase) is a glycoprotein enzyme produced in the liver and essential in iron oxidation, permitting it to bind with the iron transport protein transferrin . Copper is generally thought to be readily absorbed in the upper gastrointestinal tract including stomach, duodenum and jejunum . Hypocupremia may be inherited and acquired copper deficiency. The causes of latter include dietary deficiency, protein deficiency, high amount of iron, zinc or ascorbic acid, diarrhea, inflammatory bowel disease, short bowel syndrome, stoma, fistula, and celiac disease in humans ; ; . So, it can be concluded that hypocupremia leads to serum iron deficiency consistent with findings of this study. Iron deficiency anemia were reported in children affected with acute gastroenteritis due to Entamoeba histolytica and Giardia lamblia in Gaza (Al-Laham et al., 2015), latter may be cause of diarrhea in our foals. Relation of iron deficiency anemia and celiac disease in was well described which included impaired duodenal mucosal uptake of iron due to reduced surface absorptive area, blood loss due to ulceration and neoplasia, immune-mediated hemolysis, and reduced expression of regulatory proteins involved in iron uptake .
Serum lithium levels in all diarrheic foals were decreased versus healthy foals. Unfortunately, there was no published work on diarrheic effect on lithium body reserves. Lithium is assimilated in the alimentary tract and expelled by urinary system entirely ; ; Shahzad et al., 2016). Lithium is distributed in total body water and does not bind to serum proteins ; Shahzad et al., 2016). Lithium competes with cations, especially Na+, K+, Mg++ and Ca++. It may also interact with ammonia groups (including biogenic amines) . It interacts with cyclic-AMP-mediated processes, notably in the kidney, thyroid, and CNS . It has effects on membranes (i.e., red cell membrane), neurotransmitter systems and serotonin synthesis ; . Lithium deficiency may likely be attributed to the lithium-poor nutrition and mothers of the diarrheic foals, not the diarrhea. It was reported in goats that lithium-poor nutrition decreased feed intake in growing youngones, lower birth weight of kids, lesser conception rate, increased abortion rates, delivery of more female kids, decreased milk production, life expectancy and serum enzyme activity (isocitric acid dehydrogenase, malate dehydrogenase, aldolase, and glutamine dehydrogenase), except stress indicator enzyme (creatinine kinase), and skin lesions (Anke et al., 1983, 1991; .
Conclusion
It can be concluded that diarrhea in foals lead to changes in blood hematocrit, serum minerals, trace elements and ultra-trace elements. With diarrhea there is an increase in PCV% and concentration of potassium, while the concentration of sodium, calcium, copper, iron and lithium decreased.
Acknowledgements
The authors are grateful to Higher Education Commission, Pakistan and Medicine Laboratory, University of Veterinary and Animal Sciences, Lahore for the provision of laboratory and technical assistance for the smooth run of this research study.
Statement of conflict of interest
Authors have declared no conflict of interest.
References
- Akhter, M.Z., Khan, A., Sarwar, M. and Javaid, A., 2007. Asian-Aust. J. Anim. Sci., 20: 393-398.
- Al-Laham, N.A., Elyazji, M.S., Al Haddad, R.J. and Ridwan, F.N., 2015. Annls. Med. Hlth. Sci. Res., 5: 292-298.
- Anke, M., Arnhold, W., Groppel, B., Krause, U., 1991. In: Lithium in biology and medicine (eds. G.H. Schrauzer and G.H. Klippel). VHC, pp. 149-167.
- Anke, M., Groppel, B., Kronemann, H., Grim, M., 1983. In: Spurenelement Symposium – Lithium (eds. M. Anke, W. Baumann, H. Braunlich and C. Bruckner). Universitat Leipzig, Universitat Jena, pp. 58-65.
- Arora, R., Kulshreshtha, S., Mohan, G., Singh, M. and Sharma, P., 2006. Biol. Trace Elem. Res., 114: 121-126. https://doi.org/10.1385/BTER:114:1:121[CrossRef]
- Basaki, M., Saeb, M., Nazifi, S. and Shamsaei, H.A., 2012. Biol. Trace Elem. Res., 148: 161-164. https://doi.org/10.1007/s12011-012-9360-6[CrossRef]
- Bunney, WE. and Mandell, A.J., 1979. In: Lithium: Controversies and unresolved issues (eds. T.B. Coopr, S. Gershon, N.S. Kline and M. Schou). Int. Congr. Ser. No. 478, Amsrerdam-Oxford-Princeton ExetMeic, pp. 984; pp. 673-674.
- Cabello, G., Michel, M.C., Foucher, C. and Lafarge, C., 1977. Annls. Rech. Vet., 8: 203-211.
- Carlson, G.P., 1979. Vet. Clin. North Am. Large Anim. Pract., 1: 313-329. https://doi.org/10.1016/S0196-9846(17)30187-8[CrossRef]
- Cohen, N., 1994. J. Am. Vet. Med. Assoc., 204: 1644-1651.
- Dart, A.J., Snyder, J.R., Spier, S.J. and Sullivan, K.E., 1992. J. Am. Vet. Med. Assoc., 201: 1244-1248.
- Ebstein, R.P. and Belmaker, R.H., 1979. Lithium and brain adenylate cyclas. Amsterdam: Experta Medica, pp. 703-729.
- Frederick, J., Giguere, S. and Sanchez, L,C., 2009. J. Vet. Intern. Med., 23: 1254-1260. https://doi.org/10.1111/j.1939-1676.2009.0383.x[CrossRef]
- Freeman, H.J., 2015. World J. Gastroenterl., 21: 9233.
- Gomez, D.E., Arroyo, L.G., Stampfli, H.R., Cruz, L.E. and Oliver, O.J., 2013. J. Vet. Intern. Med., 27: 548-553. https://doi.org/10.1111/jvim.12071[CrossRef]
- Grinberg, A., Pomroy, W.E., Carslak, H.B., Shi, Y., Gibson, I.R. and Drayton, B.M., 2009. N.Z. Vet. J., 57: 284-289. https://doi.org/10.1080/00480169.2009.58622[CrossRef]
- Groutides, C.P. and Michell, A.R., 1990. Br. Vet. J., 146: 205-210.
- Haq, I., Durrani, A.Z., Khan, M.S., Mushtaq, M.H., Ahmad, I., Khan, A. and Ali, M., 2018. Pakistan J. Zool., 50: 381-384. http://dx.doi.org/10.17582/journal.pjz/2018.50.1.sc5[Full text][CrossRef]
- Jain, N.C., 1993. Essentials of veterinary hematology. Lea and Febiger, Philadelphia, pp. 173-175.
- Kilic, E., Yazar, S. and Saraymen, R., 2003. Biol. Trace Elem. Res., 96: 153-158. https://doi.org/10.1385/BTER:96:1-3:153[CrossRef]
- Knottenbelt, D.K., Holdstock, N. and Madigan, J.E., 2005. In: Equine neonatology: Medicine and surgery. Elseiver, London, England, pp. 219.
- Kolk, J.V., Nachreiner, R.F., Refsal, K.R., Brouillet, D. and Wensing, T., 2002. Equine Vet. J., 34: 528-531. https://doi.org/10.2746/042516402776117692[CrossRef]
- Linakis, J.G., 2007. Toxicity, lithium. eMedicine, 8 January 2007. http://www.emedicine.com/EMERG/topic301.htm.
- Magdesian, K.G., 2005. Vet. Clin. N. Am. Equine Pract., 21: 295-312.
- Mandell, A.J. and Knapp, S., 1976. Neuropsyhopharakol, 9: 116-126.
- Michell, A.R., Brooks, H.W., White, D.G. and Wagstaff, A.J., 1992. Br. Vet. J., 148: 507-522. https://doi.org/10.1016/0007-1935(92)90006-M[CrossRef]
- Mueller, R., Anke, M. and Betz, L., 2010. In: Proceedings of the 30 Scientific symposium of industrial toxicology (eds. A. Fargasova, M. Jambrich, M. Jambrich, V. Koprda, V. Koprda and M. Melnik). Slovakia, pp. 376.
- Navarro, M., Monreal, L., Segura, D., Armengou, L. and Anor, S., 2005. J. Vet. Intern. Med., 19: 871-877. https://doi.org/10.1111/j.1939-1676.2005.tb02780.x[CrossRef]
- Netherwood, T., Wood, J.L., Townsend, H.G., Mumford, J.A. and Chanter, N., 1996. Epidemiol. Infect., 117: 375-383. https://doi.org/10.1017/S0950268800001564[CrossRef]
- Okusa, M.D. and Crystal, L.J., 1994. Am. J. Med., 97: 383-389. https://doi.org/10.1016/0002-9343(94)90308-5[CrossRef]
- Oliver, O.E. and Stampfli, H., 2006. Vet. Clin. N. Am. Equine Practic., 22: 73-84.
- Rodriguez, A., Soto, G., Torres, S., Venegas, G. and Castillo-Duran, C., 1985. Acta Pediat., 74: 770-774. https://doi.org/10.1111/j.1651-2227.1985.tb10029.x[CrossRef]
- Rosenthal, N.E. and Goodwin, F.K., 1982. Annu. Rev. Med., 33: 555-568. https://doi.org/10.1146/annurev.me.33.020182.003011[CrossRef]
- Rucker, R.B., Fascetti, A.J. and Keen, C.L., 2008. In: Clinical biochemistry of domestic animals. Elsevier Inc., pp. 663-693. https://doi.org/10.1016/B978-0-12-370491-7.00022-2[CrossRef]
- Sandstead, H.H., 1982. Am. J. clin. Nutr., 35: 809-814. https://doi.org/10.1093/ajcn/35.4.809[CrossRef]
- Schrauzer, G.N., 2002. J. Am. Coll. Nutr., 21: 14-21. https://doi.org/10.1080/07315724.2002.10719188[CrossRef]
- Shahzad, B., Mughal, M.N., Tanveer, M., Gupta, D. and Abbas, G., 2016. Environm Sci. Pollut. Res. Int., 24: 103-115.
- Spiegel, J.E. and Willenbucher, R.F., 1999. J. Parenter. Enteral. Nutr., 23: 169-172.
- Sternlieb, I., 1967. Gastroenterology, 52: 1038-1040.
- Tajik, J. and Nazifi, S., 2013. Pak. Vet. J., 33: 5-8.
- Wilson, E. and Green, R., 1986. J. Equine Vet. Sci., 6: 321-325. https://doi.org/10.1016/S0737-0806(86)80006-5[CrossRef]
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