PEER REVIEWED
Sickle cell anemia (sickle cell disease) is a potentially
lethal, lifelong, inherited disorder for which there is no cure. Palliative care can provide some relief from the symptoms,
but such treatment requires access and financial means. The penetrance of the
underlying genetic disorder, a mutation resulting in a single amino acid change
in the critical oxygen-carrying protein, hemoglobin, varies greatly among
populations. In certain tribal populations in India, and in regions of
sub-Saharan Africa (e.g. Nigeria) where malaria was, or is still widespread, as
many as 30% of individuals may be carriers of the trait, and up to 4% of the
population may actually have the disease. The high prevalence in these areas
relates to the ironic fact that those with the sickle cell trait are actually
more resistant to malaria than those without the mutation, so the selective
evolutionary pressure which might otherwise keep such a disease-causing
mutation at very low prevalence, is not operating in isolation. The following
short paper presents encouraging in-vitro results for the anti-sickling
properties of a local and commonly eaten Nigerian plant, a nut that also has
substantial nutritional value.
Abstract
Methanol and aqueous extracts of Cyperus esculentus
(tiger nut sedge), cultivated and sold in Nigeria, were investigated for
their comparative in-vitro effects on sickle cell hemoglobin (hemoglobin-S)
polymerization (gelation).
Three concentrations (100%, 50% and 20%) of the
extracts were used. Both extracts demonstrated pronounced anti-sickling
activity [through inhibition of hemoglobin-S (HbS) gelation]. The methanol
extract, however, showed more pronounced inhibition of HbS. For instance, at 10
mins incubation with the crude extracts, HbS gelation reduced from 100% to
48.21% and 82.14% for the methanol and aqueous extracts respectively. Proximate
analyses of C. esculentus seeds gave the following mean values in
percentages for the fresh (moist) and dry samples respectively: 3.94% and 7.94%
for protein; 16.19% and 41.39% for carbohydrate; 19.67% and 27.54% for lipids;
15.60% and 21.36% for fiber; 32.16% and 9.74% for moisture. The ash content of
the dry sample was 1.79%, while a value of 2.68% was obtained for the fresh
sample.
This nutritious nut/seed may thus prove very
beneficial to sickle cell subjects and could be harnessed in the nutritional
management of sickle disease.
Introduction
The Cyperaceae juss are monocotyledonous
plants which include up to 4,000 species worldwide (1,2). Members of the Cyperaceae
family include Cyperus dilalatus, C. rotundus, C. tuberosus,
C. papyrus, and C. esculentus. These are of little economic value with the
exception of C. papyrus, which is used in the manufacture of paper, and C.
esculentus, which is edible (3).
C. esculentus is the botanical name for
tiger nut sedge (Figure 1), also known as chufa (European sedge). It has
small, edible, nut-like tubers that are also called earth almond, ground almond
or rush nut. It is a member of the Cyperaceae family, which is cultivated
occasionally for its small edible tubers (2). In Africa, it is common in the northern
territories and among some Togo tribes in the West, where they use it chiefly
uncooked as a side dish. The nut is also produced and consumed in Cote d’Ivore
and Sierra Leone (1).
Tiger nut is widely known and consumed in Nigeria by
both adults and children. The nuts are either consumed raw or in the dried
form, mainly as a snack (1).
According to the Consego Regulator de chufa de
Valencia (4) in Valencia, Spain, the nutritional composition per 100 ml of
a classical Horchata de chufas (a traditional tiger-nut milk extract),
or Orxata de xutes in Valencian language, is as follows: energy content,
around 66 kcal; proteins, around 0.5 g; carbohydrates, over 10 g; starch, at
least 1.9 g; and fats, at least 2 g.
Work has yet to be done to ascertain the possible
effect (beneficial or otherwise) of these nuts on sickle cell disease or on
sickle cell subjects who may consume them .
Sickle cell disease is an inherited disorder of red
blood cells characterized by life-long anemia and recurrent painful episodes.
It is a potentially lethal disease, with several clinical manifestations
resulting from the homozygous expression of a mutant gene (5,6). For
hemoglobin-S (HbS) disease, the result is the substitution of the hydrophilic
amino acid glutamate at position-6 of the beta globin chain of hemoglobin with
the hydrophobic amino acid valine (7,6). The highest prevalence of the hemoglobinopathies
is found in black Africa, with sickle cell trait (HbAS) and sickle cell disease
(HbSS) predominating. They are also found in some Mediterranean countries such
as Greece, Italy and Israel, as well as in Saudi Arabia and India (8). The
prevalence of this gene disorder in Nigeria is between 20 and 25% (9,10).
The relationship between sickle cell disease (SCD) and
nutrition has been reviewed (11,12,13). However, SCD remains one of the major
chronic diseases in which the role of nutrition in its etiology has not been
systematically addressed. Several investigators have commented on the
abnormally low levels of certain micronutrients in sickle cell blood (14) and
that certain dietary constituents such as thiocyanate, phenylalanine and
ascorbic acid are definitely beneficial in ameliorating the symptoms (15,16).
This work explores the possible beneficial effect of C.
esculentus on HbSS subjects. C. esculentus is widely consumed in
southern Nigeria by SCD and healthy persons alike, and there are undocumented
and unverified claims of health improvements in SCD persons who consumed these
seeds regularly. The present study is an attempt to investigate the validity of
such claims.
Materials and Methods
C. esculentus samples were bought from nearby
markets in Port Harcourt, Nigeria, and used immediately following a taxonomical
confirmation by the department of plant science and biotechnology of the University
of Port Harcourt.
Sickle cell blood samples which were confirmed as HbSS
blood using standard haemoglobin electrophoresis were supplied by the haematology
department of the University of Port Harcourt Teaching Hospital. The blood
samples were stored in lithium-heparin bottles at 40C until use.
Permission to use the blood samples was granted by the bio-ethics committee of
the University of Port Harcourt.
For the hemoglobin polymerization experiment, the heparinized
blood was centrifuged at 1200 G for 10 min using an MSE minor centrifuge. The
blood plasma was removed with a Pasteur pipette and the resulting erythrocytes
were washed three times with isotonic saline (0.98% NaCl). The washed
erythrocytes were then suspended in a volume of isotonic saline equivalent to
the volume of the displaced plasma and frozen at 00C. The samples
were subsequently thawed to produce the hemolysates for the hemoglobin gelation
test. Three HbSS blood samples were used for the experiment.
All chemicals used were of at least analytical grade
and all were products of Sigma chemical company (St Louis, Missouri, USA).
C. esculentus Extracts
Methanol extract: The methanol extract was obtained by
finely homogenizing (grinding) the tiger nut (C. esculentus) to
homogeneity. Fifty grams of the product was dissolved in 100 ml of 60% methanol
(v/v), left to stand for a day at 40C, and then filtered with a
muslin cloth to obtain the methanol soluble extract (MSE). The extract
(filtrate) was then heated for 20 min at 600C using temperature
control to produce the methanol/water soluble (MWS) extract, which was used for
the anti-sickling experiment.
Aqueous (water) extract: Fifty grams of C. esculentus
was dissolved in 100 ml of distilled water and left to stand for a day at 40C.
The extract was subsequently filtered with a muslin cloth and used accordingly
for the anti-sickling experiment.
Samples for Proximate Analysis
Fresh and dry samples were ground separately with a
domestic electric grinder to a fineness that enabled them to pass through a 70
nm mesh sieve. The powdered samples (five each of the fresh and dry) were used
immediately for proximate analysis.
Experimental Procedures
Anti-sickling experiment
The hemoglobin gelation (polymerization) experiment
was based on the method described by Noguchi and Schechter (17). The underlying
principle is that hemoglobin-S (HbS) undergoes gelation when deprived of
oxygen; sodium metabisulphite was used as a reductant. Exactly 4.8 ml of 2%
sodium metabisulphite, 0.1 ml HbS hemolysate and 0.1 ml of isotonic saline
(0.98% NaCl) were rapidly mixed in a cuvette and the optical density
(absorbance) readings taken at 700 nm at one minute intervals for 10 minutes
using a spectrophotometer (Spectronic 20 DR; Nordson Engineering, Luneburg,
Germany); this served as the control experiment. For the test experiment, 0.1
ml of the test compound (C. esculentus in dilutions of 100%, 59%,
20%) was used in place of the 0.1 ml isotonic saline and the procedure repeated
as above. As a reference standard, 10 mL of the anti-sickling amino acid
phenylalanine (18) was used in place of the test compound and the test
conducted accordingly.
Proximate Analysis of Fresh and Dried C. esculentus
The recommended methods of the Association of Official
Analytical Chemists (19) were adopted for the determination of moisture, crude
protein, ash and crude fat (lipid). Crude protein (N x 6.25) was determined by
the Macro-Kjeldal method using 1.0 g samples. Ash was determined by the
incineration of a 1.0 g sample placed in a muffle furnace maintained at 5500C
for 6 hours (until ash was obtained). Crude lipid (ether extract) was
determined by exhaustively extracting 5.0 g of the sample with petroleum ether
by use of a Soxhlet apparatus.
The level of carbohydrate was obtained by the
difference method, that is, by subtracting the sum of the protein, fat (lipid)
and ash from the total dry matter. The calorific value was calculated by
multiplying the mean values of the crude protein, fat and carbohydrates by Atwater
factors of 4, 9 and 4 respectively, taking the sum of the products and expressing
the result in kilocalories according to the method of Edem, et al. (20).
Results and Discussion
Results of this study have established the seeds of C.
esculentus consumed in Southern Nigeria as very nutritious. The dry seeds
gave proximate values (%) of 7.94, 27.54, 41.39 and 21.36 for protein, lipid,
carbohydrate and fiber respectively (Table 1), while the fresh seeds gave
corresponding values (%) of 3.94, 19.67, 16.19 and 15.60 for protein, lipid,
carbohydrate and fiber respectively (Table 1). Compared to the proximate values
for some widely consumed nuts already reported in literature (Table 2), the
protein level of C. esculentus (both dry and fresh) is quite low and
within the range for hickory nut (3.60 g), chestnut (4.53 g), coconut (2.06 g) and
pine nut (6.81 g). Cyperus esculentus, however, gave relatively
high levels of fiber (21.36% and 15.60% for the dry and fresh samples) in
comparison with the amounts reported in Table 2 for some other nuts. The
existence of a causal relationship between the absence of fiber in a diet and
the incidence of a wide range of diseases in man, notably diabetes mellitus,
obesity and coronary heart disease, has long been reported (21,22,23). The
consumption of significant quantities of C. esculentus would therefore
not constitute a risk factor to such pathologic states.
The caloric value of C. esculentus (429.18
Kcal/100 g for dry sample) shows it could be a reliable source of energy and
can thus provide a large portion of the daily requirement of 2,500 to 3,000 Kcals
for adults if large quantities are consumed, as is usually the case in Southern
Nigeria.
Results of the hemoglobin-S (HbS) gelation experiment
(Table 3) revealed that both the methanol and aqueous extracts of C. esculentus
possess anti-sickling activity, with the methanol extract having a more
pronounced anti-HbS gelation activity (possibly as a result of some anti-sickling
liposoluble factor). This finding holds some relevance especially towards a
possible nutritionally-based therapeutic handling of sickle cell patients. The
use of indigenous plants in the management of diseases has been a common
practice over the years (24,25). It has also been suggested that the study and
understanding of ethnobotanical information, chemical constituents of a plant and
the therapeutic application of the plant-based medicine will help in
understanding the efficacy of the plant as a potent remedy, extending our
knowledge of the pharmacological activity, active principle, dosage and
administration (24,25). C. esculentus has, in this work, been
established as both nutritious and possessing anti-sickling activity, although
the active anti-sickling principles have yet to be elucidated.
Sickle cell disease (SCD) remains the one disease in
which the role of nutrition in its etiology has yet to be systematically
addressed (11,12,13). Considering the relative abundance and nutritional
quality of this seed plant (as confirmed in this work), it is suggested that
sickle cell (HbSS) patients might be helped in managing their condition by
consuming these seeds and/or their extracts. Further clinical work must now be
performed to establish the safety and efficacy of such a regime.
Acknowledgment
The authors are grateful to the hematology department
of University of Port Harcourt Teaching Hospital, Nigeria, for the provision of
HbSS blood samples, and to the bio-ethics committee of the same institution for
permitting the use of the blood samples.
(Click to enlarge)
Figure 1: Nigerian Cyperus esculentus plant
(Click to enlarge)
Figure 2: Nigerian Cyperus esculentus fresh nuts
(Click to enlarge)
Figure 3: Nigerian Cyperus esculentus dried nuts
Table
1: Proximate composition of fresh and dry nut samples of the tiger nut (Cyperus
esculentus)
|
Tiger Nut
|
Moisture (%)
|
Dry matter (%)
|
Ash (%)
|
Organic matter (%)
|
Protein (%)
|
Fats (%)
|
CHO (%)
|
Fiber (%)
|
Kcalories per 100g (mean)
|
Fresh
|
32.16
± 0.23
|
67.84
± 0.98
|
2.68
± 0.05
|
97.32
± 2.31
|
7.94
± 0.03
|
19.67
± 0.52
|
16.19
± 0.49
|
21.36
± 0.32
|
273.55
|
Dry
|
9.74
± 0.21
|
90.26
± 1.22
|
1.79
± 0.03
|
98.21
± 3.21
|
3.94
± 0.05
|
27.54
± 0.34
|
41.59
± 0.12
|
15.60
± 0.42
|
429.18
|
Table 2: Nutritional composition (grams/200 grams)
of some widely consumed nuts
|
Nuts/Qty
|
Carbohydrate
(g)
|
Protein
(g)
|
Fat
(g)
|
Fiber
(g)
|
Water
(g)
|
Calcium
(g)
|
Zinc
(g)
|
Iron
(g)
|
Copper
(g)
|
Calories
(Kcal)
|
Walnut
|
15.1
|
30.4
|
70.7
|
10.6
|
5.45
|
72.5
|
4.28
|
3.84
|
1.28
|
759
|
Brazil nut
|
17.0
|
20.1
|
92.7
|
12.5
|
4.68
|
24.6
|
6.42
|
4.76
|
2.48
|
919
|
Hazelnut
|
20.7
|
17.6
|
84.5
|
9.20
|
7.32
|
25.3
|
3.24
|
4.41
|
2.04
|
852
|
Hickory nut
|
5.17
|
3.6
|
18.3
|
0.92
|
0.76
|
17.0
|
1.22
|
0.60
|
0.21
|
187
|
Chestnut
(Roasted)
|
75.7
|
4.53
|
3.15
|
18.5
|
51.9
|
42.0
|
0.82
|
1.30
|
0.73
|
350
|
Coconut
(Grated/
fresh)
|
12.2
|
2.60
|
26.8
|
11.2
|
37.6
|
12.0
|
0.88
|
1.94
|
0.35
|
283
|
Peanut
(Dried)
|
23.6
|
37.5
|
71.8
|
12.7
|
9.71
|
85.0
|
4.78
|
4.72
|
1.46
|
827
|
Pine nut
|
4.03
|
6.81
|
14.4
|
0.50
|
1.90
|
7.39
|
1.21
|
2.61
|
0.29
|
146
|
Source: Nieman, 1990
Table 3: Effect of the water-soluble and
methanol extracts of Cyperus esculentus on human sickle cell haemoglobin
(HbS) gelation rate (∆Abs/700)*
|
Time
(Mins)
|
Control†
|
Phe
(10 mM)
|
Methanol Extract
|
Water Soluble Extract
|
100%
|
50%
|
20%
|
100%
|
50%
|
20%
|
1
|
0.00
± 0.00
|
0.00
± 0.00
|
0.00
± 0.00
|
0.00
± 0.00
|
0.00
± 0.00
|
0.00
± 0.00
|
0.00
± 0.00
|
0.00
± 0.00
|
2
|
0.38
± 0.03
|
0.09
± 0.01
|
0.11
± 0.00
|
0.17
± 0.01
|
0.19
± 0.02
|
0.22
± 0.03
|
0.25
± 0.00
|
0.28
± 0.01
|
3
|
0.48
± 0.03
|
0.18
± 0.02
|
0.23
± 0.03
|
0.30
± 0.02
|
0.32
± 0.01
|
0.36
± 0.01
|
0.38
± 0.03
|
0.42
± 0.03
|
4
|
0.61
± 0.02
|
0.22
± 0.02
|
0.33
± 0.02
|
0.39
± 0.02
|
0.40
± 0.00
|
0.41
± 0.03
|
0.44
± 0.01
|
0.48
± 0.01
|
5
|
0.74
± 0.05
|
0.26
± 0.03
|
0.36
± 0.03
|
0.41
± 0.01
|
0.46
± 0.02
|
0.48
± 0.05
|
0.50
± 0.03
|
0.54
± 0.01
|
6
|
0.85
± 0.04
|
0.30
± 0.01
|
0.47
± 0.02
|
0.48
± 0.03
|
0.51
± 0.03
|
0.56
± 0.02
|
0.59
± 0.02
|
0.62
± 0.03
|
7
|
0.90
± 0.04
|
0.34
± 0.02
|
0.50
± 0.03
|
0.55
± 0.02
|
0.61
± 0.03
|
0.64
± 0.04
|
0.70
± 0.03
|
0.74
± 0.02
|
8
|
0.99
± 0.05
|
0.44
± 0.03
|
0.54
± 0.02
|
0.60
± 0.02
|
0.62
± 0.02
|
0.69
± 0.03
|
0.73
± 0.03
|
0.76
± 0.00
|
9
|
1.02
± 0.04
|
0.46
± 0.02
|
0.54
± 0.02
|
0.65
± 0.01
|
0.70
± 0.01
|
0.75
± 0.03
|
0.79
± 0.04
|
0.86
± 0.04
|
10
|
1.12
± 0.04
|
0.66
± 0.04
|
0.54
± 0.01
|
0.71
± 0.02
|
0.84
± 0.03
|
0.92
± 0.01
|
0.98
± 0.02
|
1.00
± 0.04
|
* Results are means ±
SD of triplicate determinations.
† Control had saline (0.98%) in place of the extracts.
Table 3b: Effect of Cyperus esculentus
extracts on the relative gelation rate (%age) of sickle cell haemoglobin
(mean; n=10) after 10 mins incubation
|
Extract
|
Control*
|
Phe
(10 mM)
|
Methanol Extract
|
Water Extract
|
100%
|
50%
|
20%
|
100%
|
50%
|
20%
|
Gelation rate (%age)
|
100.00
|
58.93†
|
48.21†
|
72.32†
|
75.00†
|
82.14†
|
87.50†
|
89.29†
|
Decrease in gelation (%age)
|
0.00
|
41.07†
|
51.79†
|
27.68†
|
25.00†
|
17.86†
|
12.5†
|
10.71†
|
* Control had saline
(0.98%) in place of the extracts.
† Significantly different from control at 95% level (P≤ 0.05)
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