|
Nigerian Journal of Physiological Sciences
Physiological Society of Nigeria
ISSN: 0794-859X
Vol. 24, Num. 1, 2009, pp. 59-61
|
Nigerian Journal Of Physiological Sciences, Vol. 24, No. 1, 2009, pp. 59-61
The Effect Of Potassium Bromate
On Some Haematological Parameters Of Wistar Rats
P. U. Achukwu, S. A. Ufelle,
E. O. Ukaejiofo, F. E. Ejezie1, D. N. Nwachukwu2, U. I.
Nwagha2, W. C. Nworie3, U. S. B. Anyaehie2
Department
of Medical Laboratory Sciences, Faculty of Health Sciences and Technology, College of Medicine, University of Nigeria, Enugu Campus. Nigeria, 1 Department of Medical
Biochemistry, College of Medicine, University of Nigeria Enugu Campus. Nigeria. 2 Department of Physiology, College of Medicine, University of Nigeria Enugu Campus. 3 Department of Haematology, Neuropsychiatric Hospital Enugu, Nigeria.
Code Number: np09009
Summary
Potassium
bromate used widely in foods has been associated with various complications in humans.
However there is paucity of literature on adverse effects on haematological parameters.
Thus we decided to carry out an experimental study to determine the effects of
potassium bromate on some blood indices using Wister rats. Twenty (20) male Wister
rats aged 2-3 months obtained from the department of Veterinary Medicine, University of Nigeria Nsukka were acclimatized for two weeks. They were divided into five
groups and fed with graded doses of potassium bromate solution for six weeks.
One of the groups served as the control. Pre and post administration blood
samples were collected and analyzed the same day using standard methods. The
results revealed significant decrease in the platelet count when compared with
the controls (P<0.05). There were no statistically significant differences
in the mean Cell haemoglobin concentration, haematocrit, and total leukocyte
counts between the test and control rats. Potassium bromate is injurious to
health if consumed continuously and in high quantity. It has been shown to
reduce platelet count in rats, and thus may cause thrombocytopenia in humans. It
is therefore imperative to take adequate measures to eliminate the use of
potassium bromate in the preparation of food products
Key words: Potassium
bromate, blood count, reduced platelet count.
Introduction
Potassium bromate is a white crystal, granules or
powder, which is colourless, odourless, and tasteless. It has no medicinal
value but is added to flour as a maturing agent, to dough, to fish paste as a
conditioner, and also to beer or cheese (Chipman 1988). It has also been used
as a constituent in cold wave hair solution (Ueno2000).
Potassium bromate is a substance that has a vapour
density of 5.8 (air=1) and density of 3.27 (gcm3) and when in
contact with combustible material may cause fire. It is incompatible with
organics, reducing agents, aluminum, and finely powdered metals (USEPA 1993).
When heated, it produces toxic fumes of bromine (RCC 1999). It has an infinite
solubility in water, and at drinking water pH, it should exist almost
exclusively in the ionic form (USEPA 1998a). The problem of potassium bromate
started with ozonation of drinking water to form bromate as a major by product
(WHO (1993). When research was done to confirm the safety of ozonated water,
it was found that potassium bromate causes renal cancer in rats when they drank
water with potassium bromate.Following this discoveries, many countries, Health
Organizations and Agencies started banning the use of potassium bromate (NAFDAC,
2003). Some of the countries where potassium bromate has been banned include United Kingdom in 1990 and Canada in 1994. Other countries where potassium bromate has been removed
from the list of permitted food additives are Belgium, Greece, Norway, Denmark, Spain, Portugal, Japan, and Switzerland (NAFDAC 2003). WHO also banned the
use of potassium bromate in 1993. In Nigeria, the National Agency for Food and
Drug Administration and Control in 2002, held consultative meeting with the Association
of Master Bakers in the various states of the country on the danger of use of
potassium bromate in bread and the need to stop its use. Despite the awareness
created by NAFDAC on the danger of using potassium bromate as flour enhancer,
many bakers still use the restricted substance (NAFDAC 2003).In Nigeria, there is no technology yet to detect food product containing potassium bromate or
the dangerous health hazard that potassium bromate may cause. However several
researches have been carried out in different parts of the world to prove that
potassium bromate is dangerous to health if consumed in food or water. It has
been shown to be nephrotoxic in both man and experimental animals (Uchida et
al 2006). Furthermore it induces renal cell tumors, mesotheliomas of the
peritoneum, and follicular cell tumors of the thyroid (Kurokawa et al.
1990).
It was discovered that potassium bromate which was
administered to male rats in drinking water resulted in combined incidence of
adenomas and carcinoma of the kidney (Kurokawa et al, 1986). Mice
appeared to be more sensitive than rats to the effect of potassium bromate
exposure (Kurokawa et al. 1986). At the kidney, the potassium bromate
induces renal oxidative stress which is known to cause renal failure,
methaemoglobinaemia and kidney cancer (De Angelo et al 1988, Parsons and
Chipman 2000). There has not been much reports on the effect of potassium
bromate on haematological indices, thus this research was designed to experimentally
investigate the effect of potassium bromate on some blood parameters using Wister
rats.
Materials
and Method
Twenty Wistar rats collected from Veterinary Medicine
Department of University of Nigeria were divided into five groups of four rats
each. The first four cages labeled (A-D) were administered with graded doses of
potassium bromate solution in the order of 30mg/kg, 50mg/kg, 70mg/kg, and
90mg/kg body weight respectively for six weeks. The fifth cage labeled (E)
served as the control and was administered with water only.Pre and post
administration of potassium bromate blood samples were collected into EDTA
anti-coagulant containers from twenty male albino Wister rats aged 2-3 months. QBC
Auto read Plus centrifugal system made by Becton Dickson was used for auto
analysis of venous blood collected into EDTA containers. We measured the
following parameters; total leucocyte count, haematocrit and mean cell haemoglobin
concentration .The blood film was read using standard methods (Davies and Lewis
2007).
Statistical
analysis. The results of the tests
were statistically analyzed using SPSS windows version 11 software. Results
were presented as mean and standard deviation. Student t-test was used to test
for significance. P values of ≤ 0.05 at 95% confidence intervalwere
considered as significant.
Results
There was a non significant increase in total white
cell count as shown in Table 1. The changes in the Mean Cell Haemoglobin
Concentration and Haematocrit were also not statistically significant
(P>0.05). The results are as shown in Tables, 2, and 3 respectively. The
post administration results of Platelet count showed a significantly decreased
value when compared with both the pre administration and the control result
(P<0.05). The blood film for pre administration blood samples for test and
control shows normocytic/normochromic red blood cells, leucocytes and platelet
appeared normal. The blood film for post administration blood samples for test
shows normocytic/normochromic red blood cells, platelets appeared inadequate.
There was with moderate lymphocytosis.
Discussion
From this study, it was observed that leucocytes and
platelet counts were decreased in rats administered with potassium bromate in
water. The decrease in the leucocyte count though not statistically significant
is in agreement with the work of Thompson and Westfall (1949), who reported a
decrease of leucocytes count from 15,500/mm3 to 9,600/mm3
in a two and half year old boy in a period of two months after swallowing a
half glass of neutralizer containing potassium bromate. Decreased leucocyte
count has also been reported due to consumption of chemicals like Bromate
(Hoffbrand et al. 2004).
Table
1: Mean Total Leukocyte Count(x109/L) ± SD
Group |
Pre-Administration |
Post Administration |
P-Values
|
A |
12.3 ± 0.30 |
12.0 ± 0.41 |
P>0.05 |
B |
10.9 ± 0.25 |
9.5 ± 0.93 |
P>0.05 |
C |
11.0 ± 0.30 |
10.4 ± 0.61 |
P>0.05 |
D |
12.7 ± 0.30 |
10.0 ± 0.58 |
P>0.05
|
E (Control) |
11.3 ± 0.62 |
11.5 ± 0.44 |
P>0.05 |
Table
2: Mean Haematocrit Values (%) ± SD
Group |
Pre-Administration |
Post Administration |
P-Values
|
A |
35 ±1.80 |
48 ± 1.87 |
P<0.05 |
B |
39 ±0.39 |
43 ± 1.87 |
P>0.05 |
C |
40 ±1.87 |
39 ± 1.22 |
P>0.05 |
D |
39.5 ±1.87 |
35 ± 1.41 |
P>0.05 |
E (Control) |
37.2 ±2.2 |
40.5 ± 0.61 |
P>0.05 |
Table
3: Mean Cell Haemoglobin Concentration (MCHC) Values (%) ± SD
Group
|
Pre-Administration |
Post
Administration |
P-Values
|
A |
33.4
± 1.30 |
33.8
± 0.78 |
P>0.05 |
B |
33.0
± 1.41 |
33.7
± 0.15 |
P>0.05 |
C |
33.0
± 1.00 |
33.3
± 0.18 |
P>0.05 |
D |
33.2
± 0.61 |
32.8
± 0.12 |
P>0.05 |
E
(Control) |
33.6
± 0.74 |
33.3
± 0.30 |
P>0.05 |
Table
4; Mean Platelet Count (x109/L) ±SD
Group
|
Pre-Administration |
Post
Administration |
P-Values
|
A |
353
± 15.30 |
150
± 11.37 |
P<0.05 |
B |
242
± 4.63 |
120
± 3.74 |
P<0.05 |
C |
313
± 17.16 |
170
± 6.16 |
P<0.05 |
D |
336
± 11.57 |
190
± 3.08 |
P<0.05 |
E
(Control) |
350
± 16.20 |
300
± 9.35 |
P>0.05 |
The platelet count showed
statistically significant decreased values in post administration rats when
compared with the control. These reductions in the leucocyte and platelet count
could be due to the DNA strand breakage in these cells induced by the oxidative
stress associated with potassium bromate, (Chipman et al. 1988, Sai et
al .2000, Parson and Chipman, 2000, Thompson and Westfall 1949).Furthermore,
there could have been bone marrow suppression with selective megakaryocyte
depression (Hoffbrand et al. 2004).On the other hand it could be that
potassium bromate has a direct damaging effect on the platelets. The blood
picture showed moderate lymphocytosis in rats administered with potassium
bromate,which could be due to the depletion of the intra cellular GSH by diethylmaleate
in lymphocytes, which decreases the amount of strand breakage induced by
potassium bromate (Parson and Chipman, 2000). There was no statistically
significant difference in the test and control samples of the MCHC and
haematocrit values. In the report of a two and half year boy who swallowed a
neutralizing solution containing potassium bromate, the only haematological
finding was a change in hemoglobin concentration from 11.4g/dl to 10.7g/dl in
a period of two months (Thompson and Westfall 1949). Furthermore, a study in mice
showed no change in blood parameters apart from transient reduction in red cell
count (Ginocchio et al,1979)
Potassium bromate (KBrO3) has many dangerous effects.
It exerts nephrotoxic and ototoxic effects in experimental animals as well as
in man. KBrO3 is a carcinogen inducing renal cell tumors, mesotheliomas and
thyroid follicular cell tumors in rats. It is highly probable that active
oxygen radicals are involved in these effects leading to DNA damage. We have
also noted its possible toxic effects on platelets. Further studies should be
encouraged in this regard. Furthermore; the effort to stop the use of potassium
bromate in preparation of foods should be intensified. NAFDAC should also focus
attention not only on bread, but on other bakery products in which flour is
used as a raw material. The physical properties of KBrO3 make it easy to be
taken or administered as a poison to human, thus its use and handling should be
highly regulated by the relevant authorities.
References
- Chipman, J.K., Davies, J.E., Parson, J.L.,
ONeill, G., and Fawell., J.K. (1988): DNA Oxidation by Potassium Bromate; a
Direct Mechanism or Link to Lipid Peroxidation? Toxicology. 126:93-102.
- De Angelo, A.B., George, M.H., Kilburn,
S.R., Moore, T.M. and Wolf, D.C. (1988). Carcinogenicity of Potassium Bromate
Administered in the Drinking Water of Male B6C3F Mice and F344/N Rats. Toxicol.
Pathol. 26:587-594.
- Hoffbrand, A.V., Petit, J.E. and Moss
P.A.H.(2004). Essential Haematology. (4th edn) Blackwell, Oxford. pp 252-253.
- Kurokawa, Y., Aoki, S., Matsushinna, Y.,
Takamura, N., Imazawa, T. and Hayeshi, Y. (1986a). Dose Response Studies on the
Carcinogenicity of Potassium Bromate in F344 Rats after long term Oral
Administration. J. Natl. Cancer Inst. 77: 977-982.
- Kurokawa, Y., Maekawa, A., Takahashi .and
M. ,Hayasi, Y. (1990).Toxicity and Carcinogenicity of Potassium Bromate; A New
Renal Carcinogen. Environ. Health Persp. 87:309-335.
- Ginocchio, A.V., Waite, V.,
Hardy, J., Fisher, N., Hutchinson, J.B. and Berry, R. (1979). Long-term
toxicity and carcinogenicity studies of the bread improver potassium bromate.
2. Studies in mice. Food Cosmet Toxicol, 17, 4147.
- Lewis, S.M.,Bain, B.J. and Bates, I. (eds)
(2007).In; Davies and Lewis Practical Haematology, Churchill
Livingstone, Edinburgh, United Kingdom. 10th Edition, pp 25-58.
- NAFDAC (2003): Consumer Safety Bulletin
Volume 2 No. ISSN: 1576-3594.
- Parsons, J.L. and Chipman, J.K.(2000).The
role of glutathione in DNA damage by potassium bromate in vitro. Mutagenesis.15(4):311-316.
- Ricca Chemical Company (RCC). (1999).
Material Safety Data Sheet. Section 1: Chemical Product and Company
Identification.
- Sai, K., Uchiyama, S., Ohno,Y., Hasegawa,
R and Kurokawa, Y. (1992).Generation of active oxygen species in Vitro by the
interaction of Potassium Bromate with rat kidney. Cell Carcinogenesis 13:333-339.
- Thompson, H.C. and Westfall, S.W.
(1949). Potassium Bromate Poisoning. Report of a case due to ingestion of a
Cold Wave Neutralizer. J. Paed, 34:362-364.
- Uchida, H. A., Sugiyama, H., Kanehisa, S.,
Harada, K., Fujiwara, K. and Ono, T.(2006). An elderly patient with severe acute
renal failure due to sodium bromate intoxication. Intern Med 45: 151-154.
- Ueno, H., Oishi, K., Sayato, Y. and
Nakamuro, K. (2000). Oxidative cell damage in kat-sod anay of oxyhalides as
inorganic disinfection by products and their occurrence by ozonation. Arch Environ.
Contam. Toxicol. 38:1-6.
- USEPA (1993): Final Draft for the
Drinking Water Criteria Document on Bromate. Prepared for the Health and
Ecological Criteria Division, Office of Science and Technology, Office of Water
by Clement International Corporation.
- USEPA (1998a). National Primary Drinking
Water Regulation: Disinfectants and Disinfection Byproducts: Final Rule
Federal Register 63 (241): 69389-69476.
- WHO (1993). Guidelines for Drinking
Water Quality, 2nd Edition volume 1. Recommendations Geneva, WHO, P.96.
Copyright © 2009 - Physiological Society Of Nigeria
|