Baghel D. S, Verma M, Paneri S, Mawase S. Evaluation of Oxidative Stress and Other Biochemical Markers in Female Subjects Suffering from Chronic Renal Failure and Chronic Renal Failure with Hypertension. Biomed Pharmacol J 2009;2(1)
Manuscript received on :February 12, 2009
Manuscript accepted on :April 04, 2009
Published online on: 14-11-2015
How to Cite    |   Publication History
Views Views: (Visited 141 times, 1 visits today)   Downloads PDF Downloads: 375

Drutpal Singh Baghel, Meena Verma, Sangeeta Paneri and Saroj Mawase

Department of Medical Biochemistry, M. G. M. Medical College, Indore (India).

Abstract

The current study was performed in the Department of Medical Biochemistry, M. G. M. Medical College, Indore (M.P.) to asses the trend of antioxidatnts and some important biochemical markers in female subjects suffering from chronic renal failure and chronic renal failure with hypertension. The blood samples were analyzed for sodium, potassium, protein, creatinine, urea, superoxide dismutase, glutathione reductase, glutathione peroxidase, catalase, and malondialdehyde. Highly singnificant (P<0.001) increased results were observed in case of serum postassium ions, creatinine, urea and plasma malondialdehyde. Serum sodium ions, protein, superoxide dismutase and haemolysate glutathione reductase, glutathione peroxidase and catalase were decreased highly significantly (p<0.001) in chronic renal failure and chronic renal failure with hypertension groups when compared with age matched female healthy control group.

Keywords

Chronic Renal Failure; Hypertension

Download this article as: 
Copy the following to cite this article:

Baghel D. S, Verma M, Paneri S, Mawase S. Evaluation of Oxidative Stress and Other Biochemical Markers in Female Subjects Suffering from Chronic Renal Failure and Chronic Renal Failure with Hypertension. Biomed Pharmacol J 2009;2(1)

Copy the following to cite this URL:

Baghel D. S, Verma M, Paneri S, Mawase S. Evaluation of Oxidative Stress and Other Biochemical Markers in Female Subjects Suffering from Chronic Renal Failure and Chronic Renal Failure with Hypertension. Biomed Pharmacol J 2009;2(1). Available from: http://biomedpharmajournal.org/?p=707

Introduction

Hypertension is an important public health challenge in the United States because of its high prevalence and concomitant increased in risk of cardiovascular-renal disease,1 and estimated that in the United State 50 millions have hypertension,2 and 20 millions have chronic renal fialure3. Kidneys are vital in pathogenesis of hypertension4. As a consequence the prevalance and incidence of hypertension also increases with age. The relationship beteween age and hypertension has been consistently demonstrated in cross-sectional survey as well as in longitudinal cohort studies conducted in western population5,6. Estimation of chronic kidney disease are also age dependent because chronic kidney disease wa present in about 8% of the framingham population, but inreased to 20% in elederly7. Chronic renal failure and chronic renal failure with hypertension in females are associated with the changes in biochemical markers in the form of sodium, potassium, protein, creatinine, urea, superoxide dismutase, glutathione reductase, glutathione peroxidase, catalase and malondialdehyde which are useful toof for the diagnosis of morbid groups. 

Materials and Methods

The clinical material for present study comprised 20 patients of chronic renal failure, 20 chronic renal failures with hypertension admitted in medicine ward M Y Hospital, M. G. M. Medical College, Indore and 20 ages matched female healthy control group. The age ranges was taken from 40 to 70 years. Blood samples were collected from the patients at the time of admission as well as from individuals of female healthy control group. Clinical investigations were performed in the Department of Medical Biochemistry, M. G. M. Medical College, Indore (M.P.). Serum protein, creatinine, urea and superoxide dismutase were estimated by biuret, jaffe’s, diacetyl monoxime and misra H P et al methods respectively. Plasma malondialdehyde and haemolysate glutathione reductase, glutathione peroxidase, and catalase, were estimated by Jean CD at al method (1983), Horn H D (1963), Hafeman D G method (1974) and Asror K Sinha method (1972) respectively. Serum electroyltes were estimated by using flame phtotometer. Obtained data were analyzed statistically by using student “t“ test.

Observation

Table 1: Mean ± S. D. values and significant test between female healthy control group v/s chronic renal failures.

S.

No.

Parameters Healthy control group

(20)

Chronic renal failure

(20)

P – values
Mean ± S. D. Mean ± S. D.
Electrolytes:
1 Sodium (mEq./L.) 142 ± 2.68 120.2 ± 4.43 P<0.001
2 Potassium (mEq./L.) 4.31 ± 0.46 6.6 ± 0.50 P<0.001
Biochemical:
3 Protein (mg/dl) 7.19 ± 0.17 6.36 ± 0.17 P<0.001
4 Creatinine (mg/dl) 0.76 ± 0.10 3.41 ± 1.31 P<0.001
5 Urea (mg/dl) 26.2 ± 5.30 57.65 ± 7.31 P<0.001
Antioxidants:
6 Superoxide dismutase (EU/mg protein/ml) 12.76 ± 1.33 8.76 ± 0.62 P<0.001
7 Glutathione reductase (EU/gm protein) 19.35 ± 0.57 16.37 ± 0.50 P<0.001
8 Glutathione peroxidase (EU/mg Hb%) 9.36 ± 1.06 6.71 ± 0.43 P<0.001
9 Catalase (EU/mg protein/ml) 5.8 ± 0.43 3.77 ± 0.39 P<0.001
Oxidant product:
10 Malondiadehyde (nano mol/ml) 3.2 ± 0.48 5.41 ± 0.95 P<0.001

P<0.001; (Highly significant)


Table 2: Mean ± S. D. values and significant test between female healthy control group v/s chronic renal failures with hypertension.

S.

No.

Parameters Healthy control group

(20)

Chronic renal failure

(20)

P – values
Mean ± S. D. Mean ± S. D.
Electrolytes:
1 Sodium (mEq./L.) 142 ± 2.68 111.65 ± 8.38 P<0.001
2 Potassium (mEq./L.) 4.31 ± 0.46 6.6 ± 0.56 P<0.001
Biochemical:
3 Protein (mg/dl) 7.47 ± 0.29 6.10 ± 0.19 P<0.001
4 Creatinine (mg/dl) 0.76 ± 0.10 4.76 ± 0.78 P<0.001
5 Urea (mg/dl) 26.2 ± 5.30 57 ± 6.62 P<0.001
Antioxidants:
6 Superoxide dismutase (EU/mg protein/ml) 12.76 ± 1.33 8.8 ± 0.37 P<0.001
7 Glutathione reductase (EU/gm protein) 19.35 ± 0.57 16.32 ± 0.62 P<0.001
8 Glutathione peroxidase (EU/mg Hb%) 9.36 ± 1.06 6.76 ± 0.34 P<0.001
9 Catalase (EU/mg protein/ml) 5.8 ± 0.43 3.79 ± 0.24 P<0.001
Oxidant product:
10 Malondiadehyde (nano mol/ml) 3.2 ± 0.48 5.8 ± 0.83 P<0.001

P<0.001; (Highly significant)

Results

Table number 1 and 2 are showing levels of biochemical markers in female chronic renal failure and chronic renal failure with hypertensive patients and age matched female healthy control group.

We observed, highly significance (p<0.001) increased biochemical markers values were found in the form of serum potassium ions, creatinine, urea and plasma malondialdehyde as compared to female healthy control group.

Other biochemical markers such as serum sodium ions, protein, superoxide dismutase, and haemolysate glutathione reductase, glutathione peroxidase catalase were decreased highly significantly (p<0.001) in female chronic renal failure and chronic renal failure with hypertensive patients when compared to age matched female healthy control group.

Discussion and Conclusion

Hypertension is a complex disorders resulting from the combined effects of genetic, environmental and demographic factrors8. Hypertension is more prevalent in women9. Epidemiological study have consistently identified an important and independent link between high blood pressure and impaired renal function10.

Hypertension is common in individuals with renal disease. The prevalence of hypertension varies with the causes of the underlying renal disease11. Hypertension is associated with higher prevalence of chronic renal disease12,13.

14Hypertension is an important presenting feature of renal disease and is probably the most important factor contributing to the progression of renal failure15. Increased oxidative stress and inflammation manifest in chronic renal failure16,17.

History of female chronic renal failure and chronic renal failure with hypertension, the serum creatinine, urea, potassium ions and plasma malondialdehye levels were found increased 18,19,20. In the present study, the results were found to be same i.e. hyperkalemia and increased creatinine, urea and plasma malondialdehye levels. Chronic renal failure and chronic renal failure with hypertension are characterized by decreased sodium ions, superoxide dismutase, glutathione reductase, glutathione peroxidase and catalase21. In the present study, all the above sated parameters in chronic renal failure and chronic renal failure with hypertensive patients were found to be decreased when compared with normal male healthy control age matched individuals. So it is concluded that chronic renal failure and chronic renal with hypertension are associated with increased in same of the parameters on one side and decreased in some others on the other hand.

References

  1. Jiang He, Paul K. Wghelton: Epidemiology and prevention of hypertension. Med Clin of N Am; Vol 81 (5): p-1077, (Sep. 1997).
  2. Chobaman A. V., Bakris G. L., Block H.R., et al: The seventh report of the Joint National Committee on prevention, detection, evaluation and treatment of high blood pressure, JAMA, 289, 2560-72 (2003).
  3. Coresh J., Astar B. C., Greene T., et al: Prevalence of chronic kidney disease and decreased kidney function in the adult US Population: Third National Health and Nutrition Examination Survey, Am J. Kidney Dis 41: 1-12 (2003).
  4. Burt V. L., Whelton P., Rocella E. J. et al: Prevalence of hypertension in the US adult Population; result from the third National Health and Nutrition Examination Survey; 1988 (99); Hypertension;1995; 25: 305-13.
  5. Joffres M. R., Homet P., Rabkins S.W., et al: Prevalence, control and awareness of high blood pressure among Canadian adults; Can Med Assoc. J.; 146; 1997-2005: 1992.
  6. Van Leer E. M., Scidell J. C., Kromhout D.: Levels and trends in blood pressure and Prevalence and treatment of hypertension in the Netherlands, 1987-1991; Am J. Prev. Med. 10’ 194-199, (1994).
  7. Culleton B. F., Larson M. G., Evans J. C., et al: Prevalence and Correlates of elevated serum Creatinine levels; Arch Intern Med; 159; 1785-99 (1999).
  8. Lifton R. P., Gharavi A. G., Geller D. S. Molecular mechanism of human hypertension, Cell 104: 545-556, (2001).
  9. Azizi, A. Ghanbarian, M. Madjid, M. Rahmani, Distribution of blood pressure and prevalence of hypertension in Tehran adult population, Tehran lipid and glucose study (TLGS), 1999-2000.
  10. Beegom R. et al. Diet, central obesity and prevalence of hypertension in the urban population of South India. International J. Cardiology, 51 (2): 183-191 (1995).
  11. Malhotra D., Schrier R. W, Bilateral Kidney disease and hypertension, In Luscher T. F., Kaplan N. M. (eds): Renovascular and Renal Paranchymatous Hypertension, Berlin, Springerverlay, PP 439-65 (1992).
  12. Nissenson A. R., Periera B. J., Collins A. J., et al., Prevalence and characteristics of individuals with chronic kidney disease in a large health maintenance organization, Am J. Kidney Dis., 37: 1177-83 (2001).
  13. Culleton B. F., Larson M. G., Evans J. C., et al., Prevalence and correlates of elevated serum creatinine lavels, Arch Intern. Med., 159: 1785-99 (1999).
  14. Coresh J., Wei G. L., MC. Quillan G., et al., Prevalence of high blood pressure and elevated serum creatinine level in the adult S. population, Third National Health and Nutrition Examination Survey (1988-1994), Arch. Inter. N. Med., 161: 1207-16 (2001).
  15. R. N., The rennin-angiotensin system, Med. Clin North Am., 71:5, (1987).
  16. Shipak M. G., Fried L. F., Crump C., et al., Elevations of inflammatory and pro coagulant biomarkers in elderly persons with renal insufficiency, Circulation, 107: 87-92 (2003).
  17. Oberg B. P., Mc. Menamin E., Lucas F. L., et al, Increased prevalence of oxidative stress and inflammation in patients with moderate to sever chronic kidney disease, Kidney Int., 65: 1009-16 (2004).
  18. Metheny N. Fluid and electrolyte balance, 4th Philadelphia, Pa: Lippincott Williams and Wilkins; (2000).
  19. Prices S. Wilson L. Pathophysiology; Clinical concept of disease process, 6th St. Louis Mo.; mosbyi; (2003).
  20. Kishore B. K., Gejyo F., Arokawa M., Malondialdehyde – A putative uremic toxin, IRCS Med. SCi., 11: 750-751 (1983).
  21. Sener Goksel, Paokaloglu Kubra, Satiroglu Henden, Alican Inci., Kacmaz Ayhan, Sckarcan Abdullah, L- canitine amellorates oxidative damage due to chronic renal failure in rats, Cardiol Pharma, 43 (5): 693-705 (2004).
Share Button
(Visited 141 times, 1 visits today)

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.