• google scholor
  • Views: 2559

  • PDF Downloads: 25

Serum 4-Hydroxy-2-Nonenal and Induced Nitric Oxide Synthase in Hypertension Patient

Alaa H. Jawad 1* , Ali Hammed 1 , Hadeel Adil 1 , Zyad Al-Qaisi 2 , Amamer Redwan 3 and Emad Yousif 3

1Department of Chemistry, Baghdad, Iraq, College of Science, Al-Nahrain University, Baghdad, Iraq .

2Department of Chemistry, Baghdad, Iraq, College of Science, University of Al-Mustansiriyah, Baghdad, Iraq .

3Department of Chemistry, Bani Walid, Libya, Faculty of Science, Bani Walid University, Bani Walid, Libya .

DOI: http://dx.doi.org/10.13005/OJPS02.01.05

Hypertension (HT) And related diseases such as chronic kidney disease(CKD) share in that one of the main reasons for them is to increase the oxidative stress, which in turn increases the severity of the disease and exacerbation of symptoms. Reactive molecules produced from oxidative stress, in addition to causing tissue damage by oxidation of biomolecules like DNA, lipids, proteins and sugars; they are lead to the formation of mediators with potent inflammatory effect. The objective of this study was to investigate some markers of oxidative stress in hypertension (HT) and HT with CKD patients in addition to some biochemical parameters related to these diseases. This study involved 84 male subjects aged between (25-65) year equally divided into three groups, first and second one belong to HT and HT with CKD patients respectively from Al-yarmouk Teaching hospital, while the third one for apparently healthy 28 subjects considered as control group. For each subject in the three groups these markers and parameters were evaluated; 4-hydroxy-2-nonenl(4HNE), induced nitric oxide synthase(iNOS), albumin, urea, creatinine ,total serum protein. The results were compared to control; There was a significantly higher (p<0.01) in 4HNE, and iNOS levels in both HT and HT with CKD patients, while serum albumin and Total serum protein shows significantly (p<0.01) lower levels in both groups. The elevation levels of oxidative stress markers may be due to oxidative damage of tissues that caused by these inflammatory diseases. Was concluded that there was a positive relation between oxidation results from these diseases and their developments and suggest increase need to intake of antioxidants as precaution in front of these disease.


Hypertension; antioxidants; 4-Hydroxy-2-nonenal

Copy the following to cite this article:

Jawad A. H, Hammed A, Adil H, Al-Qaisi Z, Redwan A, Yousif E. Serum 4-Hydroxy-2-Nonenal and Induced Nitric Oxide Synthase in Hypertension Patient. Orient J Phys Sciences 2017;2(1).

DOI:http://dx.doi.org/10.13005/OJPS02.01.05

Copy the following to cite this URL:

Jawad A. H, Hammed A, Adil H, Al-Qaisi Z, Redwan A, Yousif E. Serum 4-Hydroxy-2-Nonenal and Induced Nitric Oxide Synthase in Hypertension Patient. Orient J Phys Sciences 2017;2(1). Available from: https://bit.ly/3ognz7R


Download article (pdf)
Citation Manager


Introduction

Blood pressure is a measure of the force exercised circulation on the walls of the major arteries. hypertension is a chronic medical case which in the blood pressure in the arteries is elevated. Macrophages had been supposed to be the source of the most reactive oxygen species in the vessel's wall, However, it has become clear that  all the cells in the vessel wall produce ROS in different quantities and in response to diverse stimuli. Cardiovascular disease  is a pathological condition interrelated with cardiac valves, Oxidative stress promotes vascular smooth muscle cell proliferation and hypertrophy and collagen deposition, which leading to thickening in the vascular media and narrowing of the vascular cavity.  It has been shown that mechanical stretch to vessel wall induces ROS release. This suggests the possibility that high blood pressure itself causes raises to ROS independent of renin angiotensin system activity .  In addition, increased oxidative stress causes tissue damage by different mechanisms including promoting lipid peroxidation, DNA damage, and protein modification. . Reactive oxygen species (ROS) are highly reactive intermediates of the oxygen metabolism, which are constantly being generated and destroyed. ROS may originate from both exogenous and endogenous sources. Exogenous sources include environmental agents(like, UV or heat exposure), ionizing radiation, therapeutic agents, and tobacco smoke. Endogenous sources include mitochondria, peroxisome and inflammatory cell activation.  When there is an imbalance between the generation of ROS and the antioxidant defense system so that the latter be­comes overwhelmed, oxidative stress occurs . Oxidants and free radicals are inevitably produced during most physiological and metabolical processes, and the human body has defensive antioxidant mechanisms, these mechanisms vary according to the cell and tissue type and they may act antagonistically or synergistically. Oxidative stress leads to many pathophysiological conditions in the body. including neurodegenerative diseases like Parkinson's disease and Alzheimer's disease, gene mutations and cancers, chronic fatigue syndrome, heart and blood vessel Disturbance, atherosclerosis, heart, congestive heart attack and inflammatory diseases. In physiological conditions, low level ROS play a role in the protection the organism, while high levels of ROS may cause damage to the structures of the cell, nucleic acids, lipids, proteins or DNA damage .4-hydroxy-2-nonenal (4HNE), a high toxicity product of lipid peroxidation, is an inhibitor of mitochondrial respiration. 4HNE It exerts its influence on respiration by inhibiting α-ketoglutaratedehydrogenase(KGDH) . .  a study by  Teresa S.et al   recorded a significant increase in 4HNE values in hypertension patients  and Juliane Cruz Campos et al  2015  observed an increase in 4HNE  with hypertension and kidney disease Nitric oxide synthases (NOSs) are a family of enzymes catalyzing the production of nitric oxide (NO) from L-arginine. NO is an important cellular signaling molecule. Albumin represents the most abundant protein in the circulatory system with a significant antioxidant activity ,the antioxidant activity of albumin result from  its ability to bind bilirubin, homocysteine and lipids .The results of the present study showed that the levels of albumin was significantly decrease (p<0.01) in diagnosed hypertension  patients which is  agree with (Oda E) in hypertension .

History of the study

In this study found positive correlation between obesity and disease, this finding was agree with (Ahmed A. et al 2013)[1]  and (Shugar L et al 2008) [2]  who found a significant increase in BMI in hypertensive patients .Obese patients are more ready to be hypertensive than lean patients, and weight gain is typically associated with increases in arterial pressure.

Findings of the present study  in hypertension  patient is also found by (Kamelija Z. et al 2015) [3]  ,(Ethan J. et al2013) [4]  , and (Teresa Sousa et al 2012) [5]  .

There is significantly elevated (p<0.01) in diagnosed hypertension patient and oxidative stress and  this agree with (Mariso P. et al 2014)  [6]  .

The accumulation of 4-HNE-adducts is very high in the intimal aorta, mainly in older patients with high atherosclerosis grade. These data were expected since oxidized LDL and lipids accumulate in the intima in the early lesions and in the lipid core of advanced atherosclerotic lesions(Negre-Salvayre A et al 2010) [7]   .

These data confirm that 4-HNE is a main marker of oxidative stress and LDL oxidation which could contribute to the evolution of the lesions via its ability to modify proteins and generate cell dysfunction also found by(Subbotin V.M et al 2012 )[8]  .

The recently found  effect of 4-HNE suggests a role for this aldehyde in the development of vasa vasorum and micro capillaries in atherosclerotic plaque also found by( Mulligan-Kehoe M.J. 2014) [9]  .

It has been demonstrated that increased intracellular generation of ROS plays an important role in chronic inflammatory responses to arterial diseases ,  so this causes damage to the membrane polyunsaturated fatty acids leading to the generation of 4HNE cause elevation in 4HNE in these patients and this also found by(Antonio Ayala et al 2014) [10]  .

The results show a significant difference between hypertension patient and control group (p<0.01). these results were agreed with (Caroline J. Smith et al2011) [11]  who found a significant difference in iNOS levels in hypertensive patient. Also (Y Álvarez et al2009) [12]   found an elevation  in  NO synthesis might be associated with elevations of vascular resistance and, thus with hypertension.

The increased in iNOS in hypertensive subjects as compared to the control group which may be due to the increased generation of ROS in certain type of white blood cells which contribute in reduction bioavailability of nitric oxide and thus to the endothelial dysfunction and this agree with(Marian Valko et al 2007) [13]  .

(Rubbo H et al 1995 ) [14]  found that NO can then react with superoxide anion, produce highly reactive peroxynitrite, and cause oxidative damage to cellular components.

The results of the present study showed that the levels of albumin was significantly decrease (p<0.01) in diagnosed hypertension and hypertension with kidney  patients which is  agreed with (Oda E et al 2012) [15]  in hypertension and (Vandana M. et al 2005) [16]   in hypertension with kidney disease.

(Liu M., Chan C. P et al 2012 ) [17]   found that Plasma albumin levels are known to be decreased in inflammatory conditions, including infection, trauma, and surgery  .

In this study found increase in level of urea with hypertension and this also found by(Rakhee Y. et al2014) [18]  in hypertension and with  (Noor ul Amin et al2014) [19]  in hypertension with kidney disease.

(Harvey R. et al 2011) [20]   found In the heart failure and hypertension the blood flow decrease so less blood is delivered to the kidney; consequently, less urea is filtered.

(Hasan E  et al 2010) [21]   found that a reduction in renal blood flow leads to a decrease of glomular filtration, this is lead to a decrease distal tubular flow rate which lead to increase of urea reabsorption and decreased secretion which may be the reason for elevated serum urea concentration.

(Lisa M. Walker.et al 2001) [22]  Found that urea level increase with increase oxidative stress (4HNE) in hypertension.

There is a relation between creatinine which is antioxidant and hypertension and this also found by (Isra’a H. AL – Hamdani et al 2010 ) [23]  .

The elevation of serum creatinine concentration may be attributed to the decrease in creatinine clearance due to the decrease in the GFR  and this agree with(Pragna P et al 2015) [24]  .

There is a negative correlation between oxidative stress(4HNE) and creatinine in hypertension patient and control group was observed in this study which agreed with (Hiroyuki Kobori.et al2008) [25]   who found a negative correlation between 4HNE and creatinine.

The results showed a significant in TSP levels in patients groups when compared to control group and this agree with(Koenig W.et al1991) and(Marisol Peña S. et al2014) [26]   .     

There is a positive correlation between 4HNE and Protein  in hypertension patients group)  was observed in this study and this agreed with(Carlos K. et al2008) [27],[28],[29].

Conclusions

Oxidative stress in its markers and parameters is the main chemical manifestation of hypertension and cardiovascular diseases and related diseases in patients of this study. This conclusion was obvious in high significant difference between serum 4HNE, iNOS and albumin in patients of both HT and HT with CKD. urea, creatinine, protein field in achieve this results.

The association between albumine and 4Hydroxy-2-nonenal(4HNE) leads to conclude that low serum levels of albumine is very risky due to high probability of its oxidation which is exacerbate the diseases of underlying study. Also the association between 4HNE and iNOS leads to conclude the deep effect of cells from membrane to the nucleus by oxidative species.

Acknowledgements

The authors would like to thank Al-Nahrain University and Al-Yarmouk teaching hospital for the financial

supports and research facilities.

References

  1. Ahmad A., Singhal U., Mohd M., and Islam N et al.,The Role of the Endogenous Antioxidant Enzymes and Malondialdehyde in Essentia   Hypertension,  J Clinical Diagnostic Research, 7, 987-990,(2013).
  2. Shuger S., Xuemei S., Timothy S., and Rebecca A et al., Body Mass Index as a Predictor of Hypertension Incidence Among Initially Healthy Normotensive Women, American J of Hypertension, 21(6) , 613-619,(2008).
  3. Kamelija Zarkovic ., Pauline Larroque-Cardoso ., and Mélanie Pucelle et al . , Elastin aging and lipid oxidation products in human aorta, Redox Biology,4, 109–117,(2015).                                                                               
  4. Ethan J. Anderson., Lalage A. Katunga., and Monte S. Willis., Mitochondria as a Source and Target of Lipid Peroxidation Products in Healthy and Diseased Heart, Clin Exp Pharmacol Physiol, 39(2),1440-1681,(2013).
  5. Sousa, T., Oliveira, S., and Afonso, J et al., Role of H(2) o(2) in Hypertension Renin-Angiotensin System Activation and Renal Medullary Disfunction Caused by Angiotensin II, Br J Pharmacol, 166(8),2386-401,(2012).
  6. Marisol Peña-Sánchez., Sergio González-García., and Gretel Riverón-Forment et al., Association of Serum Antioxidant Enzymes and Nervous Tissue Markers in Hypertensive Patients, World Journal of Cardiovascular Diseases,4,160-168,(2014).
  7. Negre-Salvayre A., Auge N.,and Ayala V., Pathological aspects of lipid peroxidation, Free Radic, 44(10),1125–1171,(2010).
  8. Subbotin V.M., Neovascularization of coronary tunica intima (DIT) is the cause of coronary atherosclerosis. Lipoproteins invade coronary intima via neovascularization from adventitial vasa vasorum, but not from the arterial lumen: a hypothesis, Theor. Biol. Med., 9,11,(2012).     
  9. Mulligan-Kehoe M.J. , and  Simons M., Vasa vasorum in normal and diseased arteries,Circulation,129(24),2557–2566,(2014).
  10. Antonio Ayala., Mario F. Muñoz., and Sandro Argüelles., Lipid Peroxidation: Production, Metabolism, and Signaling Mechanisms of Malondialdehyde and 4-Hydroxy-2-Nonenal.Oxidative Medicine and Cellular Longevity, 31 pages,(2014).
  11. Caroline J. Smith., Lakshmi Santhanam., and Rebecca S. Bruning et al., Upregulation of Inducible Nitric Oxide Synthase Contributes to Attenuated Cutaneous Vasodilation in Essential Hypertensive Humans, 58,935-942,(2011).
  12. Y Álvarez., A M Briones., and R Hernanz et al ., Role of NADPH oxidase and iNOS in vasoconstrictor responses of vessels from hypertensive and normotensive rats, British Journal of Pharmacology,153,  Issue 5,  926–935 ,(2009).                       
  13. Marian Valko ., Dieter Leibfritz ., and Jan Moncol a et al., Free radicals and antioxidants in normal physiological functions and human disease, The International Journal of Biochemistry & Cell Biology, 39 , 44–84,(2007).                                                
  14. Rubbo H., Parthasarathy S., and Barnes S et al.,Nitric oxide inhibition of lipoxygenase-dependent liposome and lowdensity lipoprotein oxidation: termination of radical chain propagation reactions and formation of nitrogen-containing oxidized lipid derivatives, Arch Biochem Biophys, 324,15–25,(1995).
  15. Oda E et al., Decreased serum albumin predicts hypertension in a Japanese health screening population ,intern Med, 53(7), 655-660,(2012).                                       
  16. Vandana Menon., T.O.M. Greene., and Xuelei Wang et al ., C-reactive protein and albumin as predictors of all-cause and cardiovascular mortality inchronic kidney disease, Kidney International, 68 , 766–772,(2005).
  17. Liu M., Chan C. P.,  and Yan BP et al., Albumin levels predict survival in patients with heart
  18. failure and preserved ejection fraction , Eurpain J Heart Failure, 14(1),39-44,(2012).Rakhee Y., Jai P., Sunil K., Manoj K., Evaluation of blood urea, creatinine and uric acid as markers of kidney functions in hypertensive patients: a prospective study, Ind J of Basic and Applied Med. R., 3(2), 682-689,(2014).
  19. Harvey R., Ferrier D et al., Lippincott’s Illustrated  Reviews  Biochemistry, 5th ed., Walter Kluwer, Philadelphia,(2011). 
  20. Hasan E et al., Estimation of Serum Uric Acid, Urea and Creatinine in Essential Hypertensive Patients.Tikrit Me,. J., 16(1), 152-159,(2011).                                 .              
  21. Lisa M. Walker., J. Lyndal York., and Syed Z. Imam et al.,  Oxidative Stress and Reactive Nitrogen Species Generation during Renal Ischemia, toxecologlcal sciences 63, 143–148,(2001).                                                                                          
  22. Isra’a H. AL – Hamdani., Estimation of Serum Uric Acid, Urea and Creatinine in Essential Hypertensive Patients, Tikrit Medical Journal , 16(1),152-158 ,(2010).                                                                                                   
  23. Pragna P., Donald J.D., Hypertension-Related Congestive Heart Failure in West Africa: A Framework for Global Blood Pressure Control,  J Clin Hypertens (Greenwich)., 16, 8 pages,(2015).
  24. Hiroyuki Kobori.,Akemi Katsurada., and Yuri Ozawa et al., Enhanced Intrarenal Oxidative Stress and Angiotensinogen in IgA Nephropathy Patients, Biochem Biophys Res Commun, 358(1), 156–163,(2008).
  25. KoenigW., SundM, ErnstE., and KeilU et al ., Association between plasma viscosity and blood pressure. Results from the MONICA-project Augsburg, Am J Hypertens,4(6),529-36,(1991).          
  26. Marisol Peña-Sánchez., Sergio González-García., and Gretel Riverón-Forment et al., Association of Serum Antioxidant Enzymes and Nervous Tissue Markers in Hypertensive Patients, World Journal of Cardiovascular Diseases, 4, 160-168,(2014).                 
  27. Carlos Kusano and Bucalen Ferrari et al., Total Antioxidant Capacity: a biomarker in biomedical and nutritional studies, Journal of Cell and Molecular Biology 7(1), 1-15 ,(2008).
  28. Jawad A., Hammed A., Adil H., Hasan A., Al-Qaisi Z., Redwan A., and Yousif  E., Study the Level and the Fluctuation of Induced Nitric Oxide Synthase in Iraqi Patients with Hypertension, 4(3), 189-193, (2017).
  29. Jawad A., Ibrahim A., Hammed A., Al-Qaisi Z., Redwan A. and Yousif E., 4-Hydroxy-2-nonenal Statues in Hypertension, Patients, Preprints, doi:10.20944/preprints201703.0037.v1, (2017).
     
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.