Stress Responses and Alteration in Membrane-Bound Phosphatase Activities in Wistar Rats Treated with Adrenaline: The role of Senna occidentalis Extract

doi.org/10.26538/tjnpr/v5i12.14

Authors

  • Hassan Fatima Department of Plant Sciences, Institute for Agricultural Research, Ahmadu Bello University, Zaria, Nigeria
  • Owolabi A. Olumuyiwa Department of Biochemistry, Ahmadu Bello University, Zaria, Nigeria
  • Anigo M. Kola Department of Biochemistry, Ahmadu Bello University, Zaria, Nigeria
  • Ibrahim Sani Department of Biochemistry, Ahmadu Bello University, Zaria, Nigeria
  • Umar I. Alhaji Department of Biochemistry, Ahmadu Bello University, Zaria, Nigeria

Keywords:

Stress, Adrenaline, S. occidentalis, Na -K -ATPase, Ca2 - Mg2 - ATPase

Abstract

The cardiotoxic effect of Adrenaline has been recounted in several studies but its effect on membrane-bound phosphatase has not been known yet. The study assessed the biochemical changes and the alterations in membrane-bound phosphatase activities after the administration of adrenaline in Wistar rats. Adult rats were treated with Adrenaline (Adr) 2 mg/kg body weight and its effect on creatine kinase-MB, lactate dehydrogenase (LDH) and electrolyte levels (Na+ , K+ , Ionized Ca, Total Ca, Mg2+, PO4) were evaluated. Other parameters investigated include the activities of sodium/potassium adenosine triphosphate (Na+-K+-ATPase), calcium and magnesium dependent adenosine triphosphate (Ca2+ - Mg2+ - ATPase). An impairment in the activities of sodium/potassium adenosine triphosphate (Na+-K+-ATPase), calcium and magnesium dependent adenosine triphosphate (Ca2+ - Mg2+ - ATPase) in the vascular tissues of adrenaline treated rats was recorded. Administration of propranolol and Coffee Senna (S. occidentalis) extract was able to reverse the changes in a dose-dependent manner. The result also revealed a significant rise (P˂0.05) in the levels of serum creatine kinase-MB and lactate dehydrogenase (LDH) after adrenaline treatment, a significant decrease in serum electrolytes (sodium, calcium, magnesium, phosphate ions), and an insignificant decrease in the levels ofpotassium ions compared to controls. The changes  could be an outcome of the alteration in transmembrane transport mechanisms.

References

König U, Visser EK, Hall C. Indicators of stress in equitation. Appl Anim Behav Sci [Internet]. 2017; 190(2):43-56.

Ramírez-alvarado ED, López-luna A, Alejandra B, Martínez S, Flores- JA, Torre D, Ortega-Hernández Z , Moreno-Longoria J, Hugo S. Rol Of Cortisol In Cellular Stress. Int J Pharm Sci Invent. 2020; 9(I):30-36.

Daian MR, Petroianu A, Alberti LR. Current Knowledge on Psychic Stress in Surgical Procedures. Open J Biol Sci. 2016; 1:007-13.

Esler M. Mental stress and human cardiovascular disease. Neurosci Biobehav Rev [Internet]. 2017; 74:269-276.

Du J, Li M, Huang Q, Liu W, Li W qun, Li Y jian, Gong Z Cheng. The critical role of microRNAs in stress response: Therapeutic prospect and limitation. Pharmacol Res. 2019; 142:294-302.

Rossnerova A, Izzotti A, Pulliero A, Bast A, Rattan SIS, Rossner P. The molecular mechanisms of adaptive response related to environmental stress. Int J Mol Sci. 2020; 21(19):1-15.

Kelly RR, Mcdonald LT, Jensen NR, Sidles SJ, Amanda LC. Impacts of Psychological Stress on Osteoporosis : Clinical Implications and Treatment Interactions. Front Psychiatry. 2019; 10(200):1-21.

Verberne AJM, Korim WS, Sabetghadam A, Llewellyn-Smith IJ. Adrenaline : insights into its metabolic roles in hypoglycaemia and diabetes. Br J Pharmacol. 2016; 173:1425-1437.

Dao TT, Sehgal P, Tung TT, Vuust J, Nielsen J, Palmgren M, et al. Demethoxycurcumin Is A Potent Inhibitor of P-Type ATPases from Diverse Kingdoms of Life. PLOS. 2016; 11(9):1-19.

Ghosh B and Lepore ASGM. Understanding the Dysfunction of Na+/K+-ATPase in Rapid-Onset Dystonia Parkinsonism and Amyotrophic Lateral Sclerosis. In: Chakraborti S., Dhalla N. (eds) Regulation of Membrane Na+-K+ ATPase. Adv Biochem Heal Dis [Internet]. 2016; 15:145-157.

Clausen MV, Hilbers F, Poulsen H. The structure and function of the Na,K-ATPase isoforms in health and disease. Front Physiol. 2017; 8:1-16.

Pivovarov AS, Calahorro F, Walker RJ. Na +/ K + ‑ pump and neurotransmitter membrane receptors. Invertebr Neurosci [Internet]. 2019; 19(1):1-16.

Pirkmajer S and Chibalin AV. Na, K-ATPase regulation in skeletal muscle. Am J Endocrinol Metab. 2016; 311(1):E1–31.

Primeau JO, Armanious GP, Fisher MLE, Young HS. The SarcoEndoplasmic Reticulum Calcium ATPase. In: Harris J., Boekema E. (eds) Membrane Protein Complexes: Structure and Function. Subcell Biochem. 2018; 87:229-258.

Goico A, Chandrasekaran M, Herrera CJ. Novel developments in stress cardiomyopathy : From pathophysiology to prognosis. Int J Cardiol [Internet]. 2016; 223:1053-1058.

Patergnani S, Danese A, Bouhamida E, Aguiari G, Previati M, Pinton P, Giorgi C . Various Aspects of Calcium Signaling in the Regulation of Apoptosis, Autophagy, Cell Proliferation, and Cancer _ Enhanced Reader. Int J Mol Sci. 2020; 21(8323):1-27.

Chami M and Checler F. Alterations of the Endoplasmic Reticulum (ER) Calcium Signaling Molecular Components in Alzheimer’s Disease _ Enhanced Reader. Cells. 2020; 9(2577):1-23.

Tadini-Buoninsegni F, Smeazzetto S, Gualdani R, Moncelli MR. Drug interactions with the Ca2+-ATPase from Sarco(Endo)plasmic reticulum (SERCA). Front Mol Biosci. 2018; 5(APR):1-8.

Themistocleous SC, Yiallouris A, Tsioutis C, Zaravinos A, Johnson EO, Patrikios I. Clinical significance of P ‑ class pumps in cancer ( Review ). Oncol Lett. 2021; 22(658):1-18.

Yadav JP, Arya V, Yadav S, Panghal M, Kumar S, Dhankhar S. Fitoterapia Cassia occidentalis L .: A review on its ethnobotany , phytochemical and pharmacological profile. Fitoterapia [Internet]. 2010; 81(4):223-230.

Vasić V, Momić T, Petković M, Krstić D. Na+,K+-ATPase as the target enzyme for organic and inorganic compounds. Sensors. 2008; 8(12):8321-8360.

Olapade AA and Ajayi OA. Effect of roasting regime on phytochemical properties of Senna occidentalis seeds. Int J Food Stud. 2016; 5(2):203-211.

Lorke D. A New Approach to Practical Acute Toxicity Testing. Arch Toxicol. 1983; 54:275-276.

Radaković M, Borozan S, Djelić N, Ivanović S, Miladinović DĆ, Ristanić M, Spremo-Potparevic B, Stanimirovic Z. Nitrosooxidative stress, acute phase response, and cytogenetic damage in wistar rats treated with adrenaline. Oxid Med Cell Longev. 2018; 2018(1805354):1-12.

Olatunji LA and Soladoye AO. Effect of increased calcium intake on cardiac and vascular Na +-K+-ATPase activity in oral contraceptive-treated female Sprague-Dawley rats. Indian J Exp Biol. 2006; 44(11):875–879.

Davis PW. Inhibition of renal Na+, K+-activated adenosine triphosphatase activity by ethacrynic acid. Biochem Pharmacol. 1970; 19(6):1983-1989.

Ali F, Ali S, Naqvi S, Bismillah M, Wajid N. ScienceDirect Comparative analysis of biochemical parameters in diabetic and non-diabetic acute myocardial infarction patients. Indian Heart J [Internet]. 2016; 68(3):325-331.

Ballentine R and Burford D. Determination of Metals ( Na , K , Mg , Ca , Mn , Fe , Co , Cu , Zn ). Meth Enzymol. 1957; 3:1002-1035.

SL B. Sodium-potassium activated adenosine triphosphatase and cation transport. Membr Ion Transp EE Bittar, ed London Intersci Publ Ltd,. 1970. 257-263 p.

Fiske CH and Subbarow Y. The colorimetric determination of phosphorus. J Biol Chem. 1925; 66:375-400.

Hjerten S and Pan H. Agarose suspension electrophoresis. The. Biochim Biophys Acta,. 1983; 728:281-288.

Daly JA and Ertingshausen G. Direct method for determining inorganic phosphate in serum with the ―CentrifiChem‖. Clin Chem. 1972; 18(3):263-265.

Ohnishi T, Suzuki T, Suzuki Y, Ozawa K. A comparative study of plasma membrane Mg2+-ATPase activities in normal, regenerating and malignant cells. Biochim Biophys Acta. 1982; 684(1):67-74.

Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951; 193:265-275.

Nshinyabakobeje S. Using SAS PC with WINDOWS 95, 98,2000, and WINDOWS NT. Vol. 302/602, Biometry & Statistics 302/602, 2002; 1-59p.

Shkurashivska S and Ersteniuk H. The effect of adrenaline on the mineral and trace element status in rats. Open Life Sci. 2019; 14(1):158-164.

Dhalla NS. Formation of Aminochrome Leads to Cardiac Dysfunction and Sudden Cardiac Death. Circ Res. 2018; 123:409-411.

Van Belle H, Verheyen W, Ver Donck K, Janssen PAJ, Robertson JIS. Prevention of Catecholamine-Induced Cardiac Damage and Death with a Nucleoside Transport Inhibitor. J Cardiovasc Pharmacol. 1992; 20:173-178.

Kostov K and Halacheva L. Role of Magnesium Deficiency in Promoting Atherosclerosis , Endothelial Dysfunction , and Arterial Stiffening as Risk Factors for Hypertension. Int J Mol Sci. 2018; 19(1724):1-23.

Whang R, Flink EB, Dyckner T, Wester PO, Aikawa JK, Ryan MP. Magnesium Depletion as a Cause of Refractory Potassium Repletion. Arch Intern Med. 1985; 145(9):1686-1689.

Abraham AS, Rosenman D, Meshulam Z, Zion M, Eylath U. Serum, lymphocyte, and erythrocyte potassium, magnesium, and calcium concentrations and their relation to tachyarrhythmias in patients with acute myocardial infarction. Am J Med. 1986; 81(6):983–988.

Urso C, Canino B, Brucculeri S, Firenze A, Caimi G. Analysis of electrolyte abnormalities and the mechanisms leading to arrhythmias in heart failure . A literature review. Clin Ther. 2016; 167(4):e85-91.

Kodavanti PRS, Cameroo JA, Yallapragada PR, Desaiah D. Effect of Chlordecone ( Kepone @) on Calcium Transport Mechanisms in Rat Heart Sarcoplasmic Reticulum. Pharmacol Toxcol. 1990; 67: 227-234.

Hulting J. In hospital Ventricular Fibrillation and its Relation to Serum Potassium. Acta Med Scand Suppl. 1981; 647:109-116.

Kritmetapak K and Kumar R. Phosphate as a Signaling Molecule. Calcif Tissue Int. 2019; 108:16-31.

Ljunghall S, Joborn H, Rastad J, Åkerstrom G. Plasma Potassium and Phosphate Concentrations—Influence by Adrenaline Infusion, β‐blockade and Physical Exercise. Acta Med Scand. 1987; 221(1):83-93.

Megapanou E, Florentin M, Milionis H, Elisaf M, Liamis G. Drug ‑ Induced Hypophosphatemia : Current Insights. Drug Saf [Internet]. 2020; 43(3):107-210.

Yogeeta SK, Gnanapragasam A, Senthilkumar S, Subhashini R, Devaki T. Synergistic salubrious effect of ferulic acid and ascorbic acid on membrane-bound phosphatases and lysosomal hydrolases during experimental myocardial infarction in rats. Life Sci. 2006; 80(3):258-263.

Vasić VM, Ĉolović MB, Krstić DZ. Mechanism of Na+/K+-ATPase and Mg2+-ATPase inhibition by metal ions and complexes. Hem Ind. 2009; 63(5A):499-509.

Auer J, Weber T, Berent R, Lamm G, Eber B. Serum potassium level and risk of postoperative atrial fibrillation in patients undergoing cardiac surgery. J Am Coll Cardiol. 2004; 44(4):938-939.

Hazarika A and Sarkar SN. Effect of isoproturon pretreatment on the biochemical toxicodynamics of anilofos in male rats. Toxicol 01;165(2–3):87-95.

Krug LM and Berk BC. Na+,K+-adenosine triphosphatase

regulation in hypertrophied vascular smooth muscle cells.

Hypertens. 1992; 20(2):144-150.

Makynen H, Kahonen M, Arvola P, Wuorela H, Vapaatalo H,

Porsti I. Dietary calcium and magnesium supplements in

spontaneously hypertensive rats and isolated arterial reactivity.

Br J Pharmacol. 1995; 115(8):1455-1462.

Downloads

Published

2021-12-01

How to Cite

Fatima, H., A. Olumuyiwa, O., M. Kola, A., Sani, I., & I. Alhaji, U. (2021). Stress Responses and Alteration in Membrane-Bound Phosphatase Activities in Wistar Rats Treated with Adrenaline: The role of Senna occidentalis Extract: doi.org/10.26538/tjnpr/v5i12.14. Tropical Journal of Natural Product Research (TJNPR), 5(12), 2127–2132. Retrieved from https://tjnpr.org/index.php/home/article/view/259