Igboh N. M, Chigbu N. C, Agomuo E. N, Audu A. U, Onwubiko D, Emuchey C. I, Okaraonye C. C, Onyesom I. Role of Alcoholic Root Concoctions on Haematological and Renohepatic Function Markers Among HIV Patients in Some Rural Communities in Eastern Nigeria. Biomed. Pharmacol. J.2009;2(1)
Manuscript received on :December 20, 2008
Manuscript accepted on :January 28, 2009
Published online on: 10-11-2015
How to Cite    |   Publication History
Views  Views: 
Visited 106 times, 1 visit(s) today
 
Downloads  PDF Downloads: 
444

N. M. Igboh¹, N. C. Chigbu1, E. N. Agomuo², A. U. Audu³, D. Onwubiko¹, C. I. Emuchey¹, Okaraonye C. C4 and Onyesom I5

¹College of Medicine and Health Sciences, Abia State University Uturu Nigeria. ²Department of Biochemistry, Faculty of Science, Imo State University , Owerri Nigeria. ³Godwin Hospital , Off Sacred Heart, Faulks Road, Aba, Abia State, Nigeria. 4Department of Pharmacology, College of Medicine, Abia State University,Nigeria. 5Deparment of Medical Biochemistry, Delta State University, Abraka Nigeria. Correspondence Author E-mail: drngomi @ yahoo.co.uk

Abstract

The spread of HIV is taking a frightening dimension among the rural people in Nigeria . Even in a situation, where some of these individuals exhibit suggestive symptoms of HIV infection or have been diagnosed HIV positive, instead of seeking for adequate medical care will rather take various alcoholic root extracts thereby, prolonging the time they would have used to seek appropriate medical care. We therefore carried out the normal routine HIV tests on the individuals who took such alcoholic root extracts before seeking for medical care and individuals that had not taken such extracts before coming to the hospital, focusing precisely on haematological indices, renal and liver function tests. Blood sample was collected from two hundred individuals involving 96 males and 104 females who took such alcoholic root extracts in Aba metropolis for more than six months before coming to the hospital. One hundred HIV positive patients who did not take such alcoholic extracts served as control. The haematological parameters monitored include total white blood cell counts (WBC), lymphocytes (L) neutrophil (N) counts, packed cell volume (PCV) and Hemoglobin (Hb) level. Biochemical parameters estimated were the concentrations of urea and creatinine. Serum aspartate transaminase (AST) and alanine transaminase (ALT) were also assayed. In addition, total bilirubin was also determined. As compared with patients who never took alcoholic root extracts, the patients that took such extracts before coming to the hospital when the symptoms manifested were severe, exhibited significant decrease in CD4, WBC and lymphocyte counts (P < 0.05). There was a slight increase in neutrophil number in those that used the alcoholic extracts compared with their HIV positive counterpart that never took such extracts. Observed in the same group was a significant reduction in Hb and PCV (P < 0.05). The activities of AST and ALT were also elevated in these individuals, same with total bilirubin. However, the concentrations of urea and creatinine were significantly different within the two groups (P < 0.05) but the concentrations obtained were within the normal range. The study tend to suggest that taking these alcoholic root extracts  and delay in seeking appropriate medical care may accelerate the progression of HIV to AIDS.

Keywords

Bilirubin; HIV; AIDS; Alcohol; CD4

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

Igboh N. M, Chigbu N. C, Agomuo E. N, Audu A. U, Onwubiko D, Emuchey C. I, Okaraonye C. C, Onyesom I. Role of Alcoholic Root Concoctions on Haematological and Renohepatic Function Markers Among HIV Patients in Some Rural Communities in Eastern Nigeria. Biomed. Pharmacol. J.2009;2(1)

Copy the following to cite this URL:

Igboh N. M, Chigbu N. C, Agomuo E. N, Audu A. U, Onwubiko D, Emuchey C. I, Okaraonye C. C, Onyesom I. Role of Alcoholic Root Concoctions on Haematological and Renohepatic Function Markers Among HIV Patients in Some Rural Communities in Eastern Nigeria. Biomed. Pharmacol. J.2009;2(1). Available from: http://biomedpharmajournal.org/?p=544

Introduction

HIV and AIDS pandemic has torn the social, economic and political fabric of several societies to shreds. Africa stands as the worst affected continent accounting for over three quarters of the 42 million cases world wide(Achebe, 2004). Nigeria contributes significantly to these Africa figures.  Current estimate places the rate of spread of HIV in Nigeria at one person per minute. Heterosexual transmission of HIV is primarily the mode of spread in Nigeria (Achebe, 2004).

In most of the developing world, sexually active youths (15 – 24 yrs), are the most vulnerable to HIV infections. Several factors contribute to the spread of HIV infections in Nigeria. Some of these include high prevalence of untreated sexually transmitted infections (STIs), low condom use, poverty, illiteracy and the dismal quality of the health system. Some others include stigmatization and ignorance of HIV risk among vulnerable groups (Achebe, 2004).

By progressively destroying the immune system, HIV weakens the body’s ability to fight diseases, making it prone to opportunistic infections. Infections, which are rarely seen in those with normal immune system but pose a deadly threat to HIV patients. One of these infections is tuberculosis (TB), an ancient infection that is enjoying resurgence as the leading cause of death from a single pathogen. The spread of TB may be due to inadequate medical treatment. TB is said to play a mutual role in the progression of HIV infection to AIDS.

Incidentally, the spread of HIV is taking a frightening dimension among the rural people in Nigeria . The factors responsible are essentially illiteracy and ignorance of the existence of HIV infection. Even in situation where some of these individuals exhibit suggestive clinical signs of HIV infection or have been diagnosed HIV positive, instead of seeking adequate medical care, will rather attribute their failing health to either witchcraft or unknown medical conditions. Some will secretly seek help from a herbalist who will promise to cure them by giving them various alcoholic root extracts.

Unfortunately, previous studies have revealed that alcohol potentiates hepatocyte damage (Igboh et al., 2006; Guerri and Griolia, 1980; Chiapotto et al., 1995). The study of Latvala et al., (2004) implicates alcohol to cause destruction of blood cells, subsequently leading to weak immune system and anaemia in alcoholics. Various animal and human studies have demonstrated other deleterious effects of alcohol on various organs of the body (Igboh and Braide, 2003; Niemele, 2004). Other studies indicated equally that alcohol mainly potentiates hepatocyte damage through its microsomal metabolism via cytochrome P450, especially (CYP450 2E1) which results in a significant release of free radicals particularly reactive oxygen species (ROS). These in turn deplete reduced glutathione (GSH) and other defense systems necessary to combat oxidative stress and also protect the liver (Lieber, 1997; Lieber, 2000a and b). Other studies have implicated the ROS generated from alcohol metabolism to cause many diseases other than liver disease; these include autoimmune disease e.g. rheumatoid disease, haemachromatosis, atherosclerosis and cardiovascular disease (Lieber, 1997 Lieber, 2000, Griending and FitzGerald, 2003). It was based on the findings of these deleterious effects of alcohol, that promoted the investigators to become interested in carrying out routine HIV test on patients that had taken alcoholic root extracts before coming to the hospital to seek appropriate medical care and others that had not, focusing precisely on haematological indices, renal and liver function tests.

Materials and Methods

Subject/Samples: Blood samples was collected from two hundred individuals with suggestive HIV symptoms (96 males and 104 females) who took local alcoholic root extracts for more than six months before coming to the hospital. One hundred HIV positive patients who did not take such alcoholic extracts served as control. These groups of patients were tested with Immuno Comb 1& 2 (Organics Ltd Yavne 706 50, Isreal).  HIV – kit and confirmed HIV-1-infected using ELISA Kits (SUDS HIV 1& 2 Murex) diagnostic method. About 7ml of venous blood was collected from each subject. Two milliter pant of the blood specimen was put into a clean universal container containing EDTA anticoagulant for haemoglobin, packed cell volume estimation, total and differential white cell count and the CD4+ T cells. The remaining 5ml of blood was allowed to clot and the serum used to assess the concentration of urea and creatinine to ascertain their renal status. Serum aspartate transaminase (AST) and alanine transaminase (ALT), in addition to total bilirubin were analysed to assess their liver functions.

Sample analysis: The Coulter Manual CD4 count kit of (Beckman Coulter, PN 4 2 36245-D) was used to identify and enumerate the CD4+T cells.

For Hb, the cyanomethaemoglobin method of Fairbanks (1982) was used. While the method of Dacie and Lewis, (1991) was used. For PCV, lymphocyte, neutrophile, and total WBC count. The methods of Wybenga et al. (1971), Owen et al. (1954) were employed in determining urea and creatinine concentrations. The activities of AST and ALT were determined using Reitmen and Frankel, (1957) method.  Total bilirubin was determined using MacDonald (1965) method.

Statistics: The statistical analysis used was the one-way analysis of variance, ANOVA. This was used for haematological parameters, while the Student’s T test was used in evaluating other parameters (Obi, 1986).

Results

The values obtained are shown on Tables 1 and 2. Table 1 summarized the haematological parameters, while Table 2 highlights the changes in serum urea, creatinine, bilirubin and liver enzymes (AST and ALT) activities. The data were obtained from HIV patients who did not take local alcoholic root extract before presenting themselves for proper medical examination.

Table 1: Haematological parameters of HIV patients who took alcoholic  root extracts and HIV patients who did not.

  CD4+ (C/mm3) Total Lymphocyte Neutrophiles PCV (%) Hb
    WBC (x109L) (C/mm3) (C/mm3)   (g/100ml)
HIV patients’ 229.4±48.9 6.2±1.5 49.2± 22.8 35.9 ± 6.2 40.9±7.0 9.9 ±2.5
A(n=100) (Did
not take extract)
HIV patients’ 104.4±38.4* 4.8±0.9* 29.8 ±15.3* 36.1± 16.8 22.0±1.8* 8.2 ±1.5 *
B(n=200)
(Took extracts)

* Significant difference at P < 0.05

Data are expressed as Mean + SD for ‘n’ subjects

 

Table 2: Values of some biochemical parameters in HIV positive subjects who did or did not take the alcoholic root extracts.

Urea Creatinine AST (U/L) ALT (U/L) Total
  (mmol/L) (mg/100ml)     bilirubin (mg/dL)
HIV patients’
A(n=100) (Did not 4.0 ± 2.0 0.6 ± 0.7 31.6 ± 5.0 23.1 ± 1.8 0.22± 0.3
take extracts)
HIV patients’
B(n=200) (took 6.3 ± 3.3* 1.0 ± 1.8* 78.0± 22.9* 37.4±12.0* 0.40 ± 7.1*
root extracts)

* Significant difference at P < 0.05

values are Mean + SD for ‘n’ patients.

 

As compared with patients who did not take alcoholic root extracts, those who took alcoholic  root extracts before coming to the hospital when the symptoms manifested were severe exhibited significant decrease in CD4, WBC and  lymphocyte counts  (P < 0.05 Table1). There was a slight increase in neutrophil number in those HIV patients that used the alcoholic extracts compared with their HIV positive counterpart who did not. Observed in the same group was a significant reduction in Hb and PCV (P < 0.05). Under biochemical parameters monitored, the activities of AST and ALT were also elevated in these individuals, same with total bilirubin. However, the concentrations of urea and creatinine were significantly different within the two groups (P < 0.05 Table 2).

The result equally revealed a significant increase in the level of total bilirubin in HIV patients who took alcoholic extracts compared with HIV patients who did not take alcoholic root extracts.

Discussion

The remarkable decline in CD4+, WBC, lymphocyte and neutrophil in patients took alcoholic extract and delayed before attending hospital seems to be the combined effects of the HIV and generation of much free radicals particularly (reactive oxygen species (ROS) through the microsomal metabolism of alcohol via cytochrome P450. Ordinarily, those with Human Immuno deficiency virus generate a lot of ROS (Igboh, et al., 2006). And alcohol metabolism also results in generation of much ROS. Normally, ROS react directly with cellular lipids, proteins and DNA causing cellular damage and death of cells (Davies, 1995 Hensley, et al., 2000; Hemnani and Parihar, 1998). Although ROS can only manifest their effects when cellular antioxidant defenses are over whelmed (Igboh, et al., 2006). Depletion of these antioxidants like glutathione, vitamin C and E will therefore render the blood cells very fragile, thus leading to accelerated destruction of the blood cells particularly the white blood cells (Plit et al., 1998; Van Antwerpen, et al., 1994; Van Antwerpen, et al., 1995, Van Antwerpen, et al., 1995; Ayalogu et al., 2001). The low CD4+, total WBC, lymphocyte and neutrophil counts, including PCV and Hb are indicative of massive destruction of blood cells which can lead to anaemia, weak immune system and hence, enhance susceptibility to various infections associated with HIV infections.

The elevation of AST in HIV positive patients who took root alcoholic extracts was not surprising considering that AST is elevated in conditions as in hemolytic anaemia due to destruction of red blood cells, cardiac and muscular dysfunctions. The destruction of blood cells may be one of the factors responsible for the high activity of AST in the plasma. Evaluation of ALT appears to reflect hepatic disease and it is more specific for hepatic disease than AST, because of the biochemical location of the enzymes. Although the activities of any of the enzymes (ALT or AST) may be elevated in extra hepatic disease, however, the elevation of ALT may reflect some inflammatory disease or injury to the liver.

The ratio of AST to ALT is also helpful in diagnosing hepatic function. An AST: ALT ratio of more than 2 : 1 is characteristic of patients with alcoholic liver disease. From the results [(control- AST 31.6 and ALT 23.1), (test – AST 78.0 and ALT 37.4)]. The ratio of AST/ALT for control is 1.4:1 and 2.1: 1 for HIV patients that took alcoholic root extracts. These points to the possible effect of alcohol in these individuals.

To further confirm hepatocellular status, the determined serum total bilirubin levels suggest hepatocellular dysfunction.

The study suggest that taking local alcoholic root extracts  and delay in seeking appropriate  medical care may cause rapid deterioration and accelerate the progression of HIV to AIDS.

Acknowledgement

The authors remain grateful to Miss Patience E. Agwu who handled the secretarial aspect of this work.

 References

  1. Achebe, C. C. (2004).  AIDS: A disease of mass destruction and assault to our shared humanity. Mary Slessor J Med 4(1): 1 -172.
  2. Ayalogu, E. O., Igboh, N. M and Dede, E. B. (2001).   Biochemical changes in the serum and liver of albino rats exposed to petroleum sample (gasoline, kerosene and petroleum) Apple. Sci. Environ. Mgt 5(1): 97-100.
  3. CHiapotto, E., Biasi, F., Scavazza, A., Camandola, S., Aragno, M., Tamagno, E. O., Dianzan, M. U. and Poli, G., (1995). Acetaldehyde involvement in ethanol induced potentiation of rats hepatocyte damage due to the carcinogen 1, 2 – dibromethanol. Alcohol Alcohol., 30(6): 72. 1 – 8.
  4. Dacie J. V. and Lewis S. M. (1991). Practical Haematology, Churchhill Livingstone Edinburgh.
  5. Davies K. J.(1995). Oxidative stress: the paradox of aerobic life. Biochem Soc. Symp. 61: 1 – 31.
  6. Fairbanks V. G. (1982). Haemaglobin derivatives and myoglobin. In Fundamentals of Clinical Chemistry N. W. Tietz, (Ed) Saunders Company, London, Pp. 34 – 54.
  7. Griendling K. K and FitzGerald G. A., Oxidative stress and cardiaovascular injury. Basic mechanism and in vivo monitoring of ROS. Circul Alcohol 108: 1912-1916 (2003).
  8. Guerri, C. and Grisolia, S., Changes in glutathione in acute and chronic alcohol intoxication, USA J Pharmacol Biochem 13: 53 -61 (1980).
  9. Hemnani, T, Parihar, M C., Reactive oxygen species and oxidative DNA damage. Indian J. Physiol. Pharmacol.  42: 440-452 (1998).
  10. Hensley, K, Robinson K. A, Gabbita S. P, Salsmans and Floyd R. A., Reactive oxygen species, cell signaling and cell injury. Free Radic. Biol. Med.  28, 1456-1463 (2000).
  11. Igboh, N. M. and Braide, S. A., Effect of alcohol and paracetamol  on hepatic glutathione concentration on albino rats. J Med Invest Pract   4: 8 –11 (2003).
  12. Igboh, N. M, Agomuo E. N. and Amadi, B. A., Effects of alcohol and paracetamol of albino rats Int’L J Nat. Appl Sci 2(1): 16-18 (2006).
  13. Latvala, J, Parkkilia, S., and Niemela, O., Excess alcohol consumption is common in patients with cytopenia: studies in blood and bone marrow cells. Clin Exp Res 28(4): 619-624(2004).
  14. Lieber, C. S., Role of oxidative stress and antioxidant therapy in alcoholic and non-alcoholics liver diseases. Pharmacology 38: 601-628 (1997)..
  15. Lieber, C. S., Alcohol: Its metabolism and interaction with nutrients Rev. Nut 20: 395- 430 (2000).
  16. Lieber C. S., Alcoholism liver disease: new insights in pathogenesis lead to new treatments. Hepatol Suppli 32: 113-128 (2000).
  17. Mac Donald, R. P., Standard methods in clinical chemistry. S. Meite (Ed) Vol. 5, Academic press, New York (1965).
  18. Niemela, O., Alcoholics macrocytosis: is there a role for acetalehyde and adducts? (Review). Addict Biol  9(1): 3 -10 (2004).
  19. Obi, I. U., Statistical Methods of Detecting Differences Between Treatment Means. Snaap Press (Nig) Ltd. Enugu, Nigeria (1986).
  20. Plit, M. L., Thereon, A. J. H., Van Renburg C. E. J. Pendel S. and Anderson R., Influence of antimicrobial chemotherapy and smoking status on the plasma concentrations of vitamin C. Vitamin E, Beta-carotene, acute phase reactants, iron and lipid peroxides in patients with pulmonary tuberculosis. Int’L J. Tubercul Lung Dis 2: 1-7 (1998).
  21. Reitmen, S. and Frankel, S (1956). Colormetic assay of alanine and aspartate aminotransferase.  Am J Clin Pathal
  22. Van Antwerpen, V. L., Theron, A. J. Richards G. A., Anderson R., Plasma Vitamin C and smoking. J smoking Related Dis  5: 167-170 (1994).
  23. Van Antwerpen V. L., Theron, J. Richards, G. A., Van der Merwe, C. A., Viljoen E., Van der Walt R. Anderson R., Plasma levels of beta-carotene are inversely correlated with circulating leucocyte and neutrophil counts in young male cigarette smokers. Inflammation 19: 405-414 (1995).
  24. Van Antwerpen, V. L., Theron, A. J. Richards G. A., Steenkemp, K. J., Van der Merwe C. A., Van der Walt R., and Anderson R.N., Vitamin E, Pulmonary functions and phagocyte-mediated oxidative stress in smokers and non-smokers. Free Radic Biol Med, 18: 935- 941 (1995).
  25. Wybenga D. R. Digiorgio, J. and Pileggi, V. J., Determination of Urea. Clin Chem. 17: 891-894 (1971).
Share Button
Visited 106 times, 1 visit(s) today

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