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West Indian Medical Journal

versión impresa ISSN 0043-3144

West Indian med. j. vol.61 no.2 Mona mar. 2012

 

ORIGINAL ARTICLES

 

Elevated ferric, calcium and magnesium ions in the brain induce protein aggregation in brain mitochondria

 

El aumento de iones férricos, calcio y magnesio en el cerebro induce la agregación de proteínas en las mitocondrias del cerebro

 

 

T AlleyneI; N MohanI; A AdogwaII

IDepartment of Preclinical Sciences, School of Veterinary Medicine, Faculty of Medical Sciences, The University of the West Indies, St Augustine, Trinidad and Tobago
IISchool of Veterinary Medicine, Faculty of Medical Sciences, The University of the West Indies, St Augustine, Trinidad and Tobago

Correspondence

 

 


ABSTRACT

OBJECTIVE: Alzheimer s disease and Parkinson s disease are two of several neurodegenerative disorders that affect the elderly. Although their aetiology remains uncertain, studies suggest that elevated aluminium or other metal ions in the brain directly influence the development of the histological abnormalities normally associated with these diseases; other investigations suggest that metal-ion-induced-dysfunction of mitochondria might be a critical factor.
METHODS: In this study, the impact of elevated aluminum (Al3+), ferric (Fe3+), calcium (Ca2+) and magnesium (Mg2+) ions on brain histology and on the protein composition of brain mitochondria were evaluated. Rabbits were injected intra-cerebrally with 1.4% solutions of either aluminium chloride (AlCl3), ferric chloride (FeCl2), calcium chloride (CaCl2) or magnesium chloride (MgCl2) and sacrificed 10 days later.
RESULTS: Histological analysis revealed that Al3+ but not the other ions induced neurofibrillary degeneration within the midbrain and medulla. Alternatively, SDS-PAGE revealed that Fe3+, Ca2+ and Mg2+ but not Al3+ induced alterations to the distribution of brain mitochondrial proteins. Both Fe3+ and Ca2+ triggered decreased concentration of three low molecular weight proteins (~7-14 kd) but Ca precipitated their total absence. Both ions led to increased concentration of a high molecular weight protein (~ 110 kd). In contrast, Mg2+ led to the total absence of the protein of lowest molecular weight (~7 kd) and increased concentration of a ~36 kd protein.
CONCLUSION: These results suggest that elevation of some metal ions in the brain induces protein aggregation with the nature of the aggregation being highly ion dependent. The results also point toward major differences between the histopathological effect of Al3+ and other ions.

Keywords: Alzheimer's, metal ions, neurodegenerative disorder, protein aggregation


RESUMEN

OBJETIVO: La enfermedad de Alzheimer y la enfermedad de Parkinson son dos de los varios trastornos neurodegenerativos que afectan al anciano. Aunque su etiologia sigue siendo incierta, los estudios sugieren que el aumento de los iones de aluminio, influyen directamente sobre el desarrollo de las anormalidades histológicas asociadas normalmente con estas enfermedades. Otras investigaciones sugieren que la disfunción de las mitocondrias, inducida por iones metálicos, pudiera ser un factor critico.
MÉTODOS: Este estudio evalúa el impacto del aumento de los iones de aluminio (Al3+), los iones férricos (Fe3+), y los iones de calcio (Ca2+) y magnesio (Mg2+) sobre la histologia del cerebro y la composición proteica de las mitocondrias del cerebro. Un número de conejos recibieron inyecciones intracerebrales de soluciones al 1.4% de soluciones de cloruro de aluminio (AlCl3), cloruro ferroso (FeCl3), cloruro de calcio (CaCl2), o cloruro de magnesio (MgCl2), y fueron sacrificados después de 10 días.
RESULTADOS: El análisis histológico reveló que el Al3+ indujo una degeneración neurofibrilar dentro del mesencéfalo y la médula, Sin embargo, esto no ocurrió con los otros iones. Alternativamente, la técnica de electroforesis SDS-PAGE reveló que los iones Fe3+, Ca2+ y Mg2+, a diferencia del ión Al3+, inducían alteraciones de la distribución de las proteínas mitocondriales cerebrales. Tanto el Fe3+ como el Ca2+ desencadenaron una disminución de la concentración de tres proteínas de bajo peso molecular (~7-14 kd) pero Ca2+ precipitó su ausencia total. Ambos iones condujeron a un aumento de una proteína de peso molecular alto (~ 110 kd). En cambio, Mg2+ llevó a la ausencia total de la proteína de más bajo peso molecular (~7 kd) y al aumento de la concentración de una proteína de ~36 kd.
CONCLUSIÓN: Estos resultados parecen sugerir que la elevación de algunos iones de metal en el cerebro induce la agregación de la proteína, siendo la naturaleza de la agregación altamente dependiente de los iones. Los resultados también apuntan a grandes diferencias entre el efecto histopatológico del Al3+ y otros iones.

Palabras claves: Alzheimer, iones de metal, trastomo neurodegenerativo, agregación proteica


 

 

INTRODUCTION

In the last decade, Alzheimer's disease (AD) and Parkinson's disease (PD), two of the more common neurodegenerative disorders, have emerged as major causes of death and morbidity in the aged (1,2). At the pathological level, AD is characterized by the presence of neurofibrillary tangles and amyloid plaques (3, 4) while biochemically, the disease is characterized by decreased cytochrome c oxidase (COX) activity (5-7) and by increased activity of cathepsin D (8).

Whereas, there is consensus on what constitutes the pathological and biochemical characteristics of AD, there is no such consensus with regard to its aetiology. A number of studies have reported the presence of decreased magnesium [Mg2+] (9) but elevated aluminum (Al3+), ferric (Fe3+) and calcium (Ca2+) ions (10-12) in the brains of persons with AD. Presently, however, it is not clear whether these altered levels cause the disease or occur as a result of it (9, 13). Querfurth and Selkoe (14), using cultured cells, have demonstrated that the presence of Ca2+ ionophores can lead to increased production of amyloid beta peptides, while Emilsson et al (15) have reported the presence of altered Ca2+ signalling genes in AD patients. To add to the state of confusion, Murayama et al (16) have shown that neurofibrillary degeneration of the type seen in AD can be caused by interaction of aluminium ions with paired helical filament tau proteins.

Parkinson's disease is characterized pathologically by the presence of Lewy bodies and Lewy neurites in the brain (17, 18) but like AD, its aetiology is unresolved. A number of studies have detected elevated Fe3+ in the brain of patients with PD (19) while others have shown that Al3+ and other heavy metals increase the production of α-synuclein, the major constituent of Lewy bodies (20, 21).

In recent times, Bueler (22) has suggested that mitochondrial dysfunction might be playing a critical role in the pathogenesis of PD. Similarly, a number of studies have led to the conclusion that inhibitor-induced alterations to mitochondrial function may be a critical factor in the pathogenesis of AD (23).

In an attempt to get better insight into the role played by metal ions and mitochondria in the pathogenesis of neurodegenerative disorders, we decided to extend the rabbit studies of Klatzo et al (24). In their study, Klatzo et al (24) reported that the injection of aluminium salts into the cerebral region of the rabbit brain caused the animals to develop ataxia after about ten days. They further reported that by such time, the treatment had also induced neurofibrillary degeneration and other pathological changes similar to those seen in the brain of patients with AD. Our objective in this study was to determine if other valency two and three metal ions had similar effects on rabbits and what effects if any the injected metal ions had on brain mitochondrial protein composition. We injected aluminium chloride (AlCl3), ferric chloride (FeCl3), calcium chloride (CaCl2) and magnesium chloride (MgCl2) and compared their effects on the physical behaviour, brain histology as well as the difference spectra and protein composition of brain mitochondria.

 

SUBJECTS AND METHOD

New Zealand white rabbits were used throughout the study; only alert, active animals were employed. Six groups of rabbits, two controls and four experimental, were studied; groups comprised five rabbits each. All protocols were approved by The University of the West Indies (UWI), St Augustine, Ethics Committee.

Metal ion injection: Solutions of AlCl3, FeCl3, CaCl2 and MgCl2, each 1.4%, were prepared in 2.5% sodium phosphate buffer, pH 6.5. Using the method described by Klatzo et al (24), one each of the metal ions was injected into the cerebral hemisphere of a selected group of rabbits. Two groups of control animals were employed. For one group of controls, the animals were injected with the phosphate buffer minus the added metal ions; the second control group received no injections. All animals were sacrificed ten days after injections were performed and the brains removed. The left hemispheres of each brain were dissected and stored at -70ºC to be used for biochemical studies. Tissue from the brainstem region was harvested to be used for histological studies; the tissue was immersed in 10% buffered formal saline and stored for approximately one month before processing.

Histological analysis: Samples from the medulla and midbrain of the two groups of controls and four groups of metalion-injected rabbits were prepared for histological examination as described by Luna (25). The sections were stained with Mitchell's silver stain for viewing (26).

Biochemical Methods

Mitochondria were isolated from the brains of controls and treated animals by the method of Yonetani (27) and stored at -70ºC until needed. In the studies conducted, there was no pooling of tissue; the tissue from each rabbit was processed and studied independently. For each preparation of mitochondria, the difference spectra and protein composition were determined.

Difference spectra: Difference spectra, reduced minus oxidized, 400-630 nm, were recorded for mitochondria isolated from the six different groups of animals. Spectra were recorded in phosphate buffer 0.1 M, pH 7.4, containing 0.3% Tween 80 as previously described (28).

SDS-PAGE: Following solubilization of the mitochondrial membrane using a buffered solution of 2% sodium cholate, the mitochondrial proteins from the six groups were compared using SDS-PAGE. Subsequently, densitometric analysis of the stained gels was performed as described elsewhere (29).

 

RESULTS

The injection of sodium phosphate, FeCl3, CaCl2 or MgCl2 had no visible immediate or long-term effect on the behaviour of the rabbits. For those injected with the AlCl3 solution, however, while there was no immediate effect, the animals started to show signs of lethargy and ataxia in the hind legs by day nine, consistent with previous reports (24). Histological analysis of the midbrain revealed that the AlCl3-injected rabbits exhibited the presence of neurofibrillary tangle-like structures, at the level of the rostral colliculi as previously reported (24). Similar degeneration was found in large multipolar neurons of the midbrain, particularly those of the red nucleus, occulomotor nucleus and lateral vestibular nucleus, as well as neurons of the facial nucleus and in neurons of the medulla. However, none of the other ions led to the development of such histological changes (Figs. 1: A-E).

 

 

Unlike the case of rabbits raised on a Cu-cholesterol rich diet (30), the difference spectra of mitochondria isolated from the brain of the metal-ion injected animals appeared normal. All six groups of rabbits (the two control and four experimental) produced difference spectra that were typical, with the major peak centred around 434 nm and two smaller peaks centred at 550 nm and 604 nm, respectively (Fig. 2). For each spectrum, the ratio of the area under the curve of the major and minor peaks was calculated. The calculations detected no significant differences between the spectra produced by the different cohorts.

 

 

SDS-PAGE combined with densitometric analysis revealed that the protein composition of mitochondria isolated from the brains of rabbits injected with Al3+ was very similar if not identical to the controls (Figs. 3A and 3B). For mitochondria from the Fe3+ and Ca2+ injected animals, there was increased concentration of a high molecular weight protein (~ 110 kd) and decreased concentration of three low molecular weight proteins (~7-14 kd) [Figs. 3A and 3C]. In the case of Ca2+ , the three low molecular weight proteins appeared to be totally absent. For Mg2+, there was also decreased concentration of the three low molecular weight proteins but for this ion, there was total absence of the protein of lowest molecular weight (~7 kd). The Mg2+ results differed in one other important way. Whereas Fe3+ and Ca2+ led to increased concentration of a 110 kd protein, Mg2 led to increased concentration of a protein of ~36 kd (Figs. 3A and 3B).

 

 

DISCUSSION

Consistent with the reports of Klatzo et al (24), the present study showed that rabbits injected with AlCl3 into the cerebral hemisphere displayed lethargy and ataxia of the hind legs after about ten days. In addition, these rabbits also developed neurofibrillary degeneration within neurons of the midbrain and medulla (Fig. 1). The fact that none of the other salts injected (FeCl3, CaCl2 or MgCl2) exerted a similar effect indicates that the chloride ions, common to all four salts, did not contribute toward the development of the ataxia or neurodegeneration. The results further suggest that the alterations to the animals' state of physical health was most probably linked to the neurodegeneration and that both the physical ill health and the neurodegeneration were probably linked specifically to the presence of Al3+ ions in the brain; none of the other ions produced such effects, at least after ten days. It seems, therefore, that Fe3+, Ca2+ and Mg2+ either have no direct effect on the neurodegeneration of neurons or that if they do, they act much more slowly than Al3+.

In contrast to their lack of impact on the animals' mobility and neuropathology, the results of the SDS-PAGE in combination with densitometry showed that after ten days Fe3+, Ca2+ and Mg2+ had already induced changes to the protein composition of the brain mitochondria of the rabbits. Surprisingly, Al3+, which had a profound effect on the animals' neuropathology and physical activity, induced no changes to the protein composition of mitochondria. These results appear to suggest that elevated metal ions in the brain precipitate a range of changes with different metals inducing different initial effects. This conclusion is consistent with the finding of our earlier study which investigated the impact of these injected ions on brain COX activity. Then, it was found that all four ions led to decrease enzymatic activity but to differing extents (31). When the latter results are recalculated so that the ions are equimolar rather than being of equal percentage, the inhibition by Fe3+ is twice that of Mg2+ and three times that of Al3+ and Ca2+.

Returning to the impact of the injected ions on the structure of brain mitochondria, two of the metals, Fe3+ and Ca2+ appeared to induce similar kinds of changes, in which there was decreased concentration of three low molecular weight proteins (7-14 kd) and increased concentration of a protein with an approximate weight of 110 kd. However, whereas Fe3+ merely led to decreased protein concentration, Ca2+ led to the total disappearance of the three low molecular weight proteins (Fig. 2). This result appeared to suggest that Fe3+ and Ca2+ might be activating a common pathway, with the effects of Ca2+ being much more pronounced. Alternatively, since the method used in this study (24) employed percentages rather than molar concentrations, the difference in the extent of change induced by the two ions could be reflecting their difference in molar concentration; FeCl3, 0.086 mol L-1 compared to CaCl2, 0.126 mol L-1. The other ion studied, Mg2+, appeared to be acting in a way that was completely different to Fe3+ and Ca2+. In the case of Mg2+, there was decreased concentration of the low molecular weight proteins but only the protein of lowest molecular weight (~7 kd) disappeared totally while there was increased concentration of a 36 kd protein (Fig. 2).

Although there might be a small concentration effect, the overall picture emerging from this study is one of a complicated sequence of biochemical events, the outcomes of which are ion specific. It has long been established that there are at least three different types of amyloid beta plaques found in the brains of patients with AD (32-34). It has also been shown that formation of these plaques result from aggregation of fragments of amyloid precursor protein, abnormal neurites and other structures formed as a result of ion-induced (35, 36) or enzyme catalysed processes (37-39). Similarly, metal-ion-induced aggregation of a-synuclein has been linked to the pathogenesis of PD (21). Our present results appear to be suggesting that increases of certain metal ions in the brain also induce aggregation of some mitochondrial proteins, with the nature of the aggregation being highly dependent on the properties of the specific ion. These results are consistent with the findings from several studies which have shown that elevated Al3+, Fe3+ and Ca2+ in the brain are associated with mitochondrial dysfunction and that the latter plays a critical role in the aetiology of AD (23) and PD (22). Moreover, our earlier finding that these injected ions also lead to low brain COX activity (31) may have unearthed the link between mitochondrial dysfunction and AD. We have proposed that low COX activity could trigger the release of oxygen free radicals and that these free radicals could cause damage to cell organelles. We speculate that the aggregation of proteins reported here may be linked to increased oxidative stress which was precipitated by ion-induced low COX activity. Establishing the identity of the low molecular weight proteins involved in this aggregation process should provide some very useful information.

Finally, a number of studies (9, 40) have shown that decreased rather than increased Mg2+ in the brain is a factor in the pathogenesis of AD. Our finding that within mitochondria, elevated Mg2+ induces structural changes that are different to those promoted by Al3+, Fe3+ and Ca2+ is, therefore, noteworthy. Whereas low Mg2+ is likely to impair the activity of magnesium dependent enzymes, we have shown that elevated Mg2+ inhibits COX (31); it would seem therefore that either below normal levels or above normal levels of brain Mg2+ could be factors in the pathogenesis of AD. Equally noteworthy is the fact that over the ten-day period of the study, Al3+ induced neurodegeneration but no protein aggregation, while the other ions did the exact reverse; they induced protein aggregation but no neurodegeneration. This finding appears to set Al3+ apart from other ions.

 

REFERENCES

1. Kochanek KD, Murphy SL, Anderson RN, Scott C. Deaths: Final data for 2002. National Vital Statistics Report 2004; 53: 1-116.

2. McConnel C, Turner L. Medicine, ageing and human longevity: The economics and ethics of anti-ageing interventions. EMBO Reports 2005; 6 (S1): S59-S62.

3. Hampel H, Mitchell A, Blennow K, Frank RA, Brettschneider S, Weller L et al. Core biological marker candidates of Alzheimer's disease -perspectives for diagnosis, prediction of outcome and reflection of biological activity. J Neural Transm 2004; 111: 247-72.

4. Maccioni RB, Lavados M, Maccioni CB, Mendoza-Naranjo A. Biological markers of Alzheimer's disease and mild cognitive impairment. CurrAlz Res 2004; 1: 307-14.

5. Kish SJ, Bergeron C, Rajput A, Dozie S, Mastrogiacomo F, Chang LJ et al. Brain cytochrome oxidase in Alzheimer's disease. J Neurochem 1992; 59: 776-9.

6. Parker WD, Mahr N, Filley C, Parks J, Hughes D, Young D et al. Reduced platelet cytochrome c oxidase activity in Alzheimer's disease. Neurology 1994; 44: 1086-90.

7. Parker WDJ, Parks J. Cytochrome c oxidase in Alzheimer's disease brain: Purification and characterization. Neurology 1995; 45: 482-6.

8. Suzuki H, Takeda M, Nishimura T. Enzymatic characterization of cathepsin D in rabbit brains with experimental neurofibrillary changes. Biochem Mol Biol Int 1994; 32: 1033-9.

9. Glick JL. Dementias; the role of magnesium deficiency and an hypothesis concerning the pathogenesis of Alzheimer's disease. Med Hypothesis 1990; 31: 211-25.

10. Good PF, Perl DP, Bierer LM, Schmeidler J. Selective accumulation of aluminium and iron in the neurofibrillary tangles of Alzheimer's disease: a lasermicroprobe (LAMMA).AnnNeurol 1992; 31: 286-92.

11. Huang X, Moir R, Tanzi R, Bush A, Rogers J. Redox-active metals, oxidative stress and Alzheimer's disease pathology. Ann NY Acad Sci 2006; 1012: 153-63.

12. Ito E, Oka K, Etcheberrigaray R, Nelson TJ, McPhie DL, Tofel-Grehl B et al. Internal Ca2+ mobilization is altered in fibroblasts from patients with Alzheimer disease. Proc Natl Acad Sci USA 1994; 91: 534-8.

13. Ke Y, Qian ZM. Iron misregulation in the brain: a primary cause of neurodegenerative disorders. Lancet Neurol 2003; 2: 246-53.

14. Querfurth HW, Selkoe DJ. Calcium ionophore increases amyloid beta peptide production by cultured cells. Biochemistry 1994; 33: 4550-61.

15. Emilsson L, Saetre P, Jazin E. Alzheimer's disease: mRNA expression profiles of multiple patients show alterations of genes involved with calcium signalling. Neurobiol Dis 2006; 21: 618-25.

16. Murayama H, Shin RW, Higuchi J, Shibuya S, Muramoto T, Kitamoto T. Interaction of aluminum with PHFtau in Alzheimer's disease neurofibrillary degeneration evidenced by desferrioxamine-assisted chelating autoclave method. Am J Pathol 1999; 155: 877-85.

17. Forno LS. Neuropathology of Parkinson's disease. J Neuropathol Exp Neurol 1996; 55: 259-72.

18. Hughes AJ, Daniel SE, Lees AJ. Improved accuracy of clinical diagnosis of Lewy body Parkinson's disease. Neurology 2001; 57: 1497-9.

19. Oakley AE, Collingwood JF, Dobson J, Love G, Perrott HR, Edwardson JA et al. Individual dopaminergic neurons show raised iron levels in Parkinson's disease. Neurology 2007; 68: 1820-5.

20. Rybick BA, Johnson CC, Uman J, Gorell JM. Parkinson's disease mortality and the industrial use of heavy metals in Michigan. Mov Disord 1993; 8: 87-92.

21. Uversky VN, Li J, FinkAL. Metal-triggered structural transformations, aggregation, and fibrillation of human alpha-synuclein. A possible molecular link between Parkinson's disease and heavy metal exposure. J Biol Chem 2001; 276: 44284-96.

22. Bueler H. Impaired mitochondrial dynamics and function in the pathogenesis of Parkinson's disease. Exp Neurol 2009; 218: 235-46.

23. Farber S, Slack B, Blusztajn J. Acceleration of phosphatidylcholine synthesis and breakdown by inhibitors of mitochondrial function in neuronal cells: a model of the membrane defect of Alzheimer's disease. FASEB J 2000; 14: 2198-206.

24. Klatzo I, Wisniewski H, Streicher E. Experimental production of neurofibrillary degeneration: Light microscopic observations. J Neuropathol Exp Neurol 1965; 24: 187-99.

25. Luna LG, ed. Manual of histologic staining methods of the Armed Forces Institute of Pathology. 3rd Ed. New York: McGraw-Hill Book Company; 1968: 12-20.

26. Kiernan JA. Histological and Histochemical Methods: Theory and Practice. 3rd ed. Oxford: Butterworth Heinemann; 1999: 368-9.

27. Yonetani T. Studies on cytochrome oxidase. Improved preparation and some properties. J Biol Chem 1961; 236: 1680-8.

28. Alleyne T, Joseph J, Lalla A, Sampson V, Adogwa A. Cytochrome c oxidase isolated from the brain of Swayback-Diseased sheep displays unusual structure and uncharacteristic kinetics. Mol Chem Neuropathol 1998; 3: 233-47.

29. Sampson V, Alleyne T. Cytochrome c/cytochrome c oxidase interaction. Direct structural evidence for conformational changes during enzyme turnover. Eur J Biochem 2001; 268: 6534-44.

30. Mohan N, Alleyne T, Joseph J, Adogwa A. Low activity and poor membrane tethering for brain cytochrome c oxidase in cholesterol-copper Alzheimer's model. J Mol Neurosci 2009; 38: 273-9.

31. Alleyne T, Mohan N, Joseph J, Adogwa A. Unraveling the role of metal ions and low catalytic activity of cytochrome c oxidase in Azheimer's disease. J Mol Neurosci 2011; 43: 284-9.

32. Terry R, Gonatas NK, Weiss M. Ultra-structural studies inAlzheimer's presenile dementia. Am J Pathol 1964; 44: 269-97.

33. Wisniewski HM, Terry RD. Morphology of the aging brain, human and animal. Prog Brain Res 1973; 40: 167-86.

34. Krigman MR, Feldman RG, Bensch K. Alzheimer's presenile dementia. A histochemical and electron microscopic study. Lab Invest 1965; 14: 381-96.

35. Hensley K, Carney JM, Mattson MP, Aksenova M, Harris M, Wu JF et al. A model for beta-amyloid aggregation and neurotoxicity based on free radical generation by the peptide: relevance to Alzheimer disease. Proc NatlAcad Sci USA. 1994; 91: 3270-4.

36. Huang X, Atwood CS, Hartshorn MA, Multhaup G, Goldstein LE, Scarpa RC et al. The A beta peptide of Alzheimer's disease directly produces hydrogen peroxide through metal ion reduction. Biochemistry 1999; 38: 7609-16.

37. Allinson TM, Parkin ET, Turner AJ, Hooper NM. ADAMs family members as amyloid precursor protein alpha-secretases. J Neurosci Res 2003; 74: 342-52.

38. Vassar R, Bennett BD, Babu-Khan S, Kahn S, Mendiaz EA, Denis P et al. Beta-secretase cleavage of Alzheimer's amyloid precursor protein by the transmembrane aspartic protease BACE. Science 1999; 286: 735-41.

39. Wolfe MS, Xia W, Ostaszewski BL, Diehl TS, Kimberly WT, Selkoe DJ. Two transmembrane aspartates in presenilin-l required for pre-senilin endoproteolysis and gamma secretase activity. Nature 1999; 398: 513-17.

40. Andrasi E, Igaz S, Molnar Z, Mako S. Disturbances of magnesium concentrations in various brain areas in Alzheimer's disease. Magnes Res 2000; 13: 189-96.

 

 

Correspondence:
Dr T Alleyne
Biochemistry Unit, Faculty of Medical Sciences, The University of the West Indies
Eric Williams Medical Sciences Complex
Uriah Butler Highway, Champs Fleurs, Trinidad and Tobago.
E-mail: trevor.alleyne@gmail.com