International Journal of Fisheries and Aquatic Studies 2015; 3(2): 132-135
ISSN: 2347-5129
(ICV-Poland) Impact Value: 5.62
(GIF) Impact Factor: 0.352
IJFAS 2015; 3(2): 132-135
© 2015 IJFAS
www.fisheriesjournal.com
Received: 12-08-2015
Accepted: 13-09-2015
Palash Halder
Upazila Fisheries Officer,
Department of Fisheries,
Ministry of Fisheries and
Livestock, Bangladesh.
Hazrat Ali
WorldFish, Bangladesh & South
Asia Office, Dhaka, Bangladesh.
Temporal changes in body composition of striped catfish
(Pangasius hypophthalmus, Sauvage, 1878) during
starvation
Palash Halder, Hazrat Ali
Abstract
The present study was conducted to investigate the changes in body composition of Thai pangas
(Pangasius hypophthalmus) during food deprivation at Fish Physiology and Fish Nutrition Lab of Khulna
University, Khulna from 10 November to 7 December, 2007. Fish were starved for a 27 days in10 glass
tanks (50cm×30cm×30 cm) at 3 individual per tank. At the initial stage (1st day) of the experiment, the
water, protein, lipid and ash contents were 76.88±1.13%, 20.5±0.23%, 1.4±0.02% and 1.20±0.05%,
respectively whereas at the 27th day water, protein, lipid, and ash contents were 78.35±0.42%,
19.40±0.25%, 0.80±0.02% and 1.42±0.02%, respectively. The results revealed that lipid and protein
concentration of muscle was decreased with prolongation of deprivation, with a significant decline of
lipid concentration recorded after 6 days of deprivation (P≤.05). On the other hand, water and ash
concentration was increased during deprivation without any significant variation.
Keywords: Pangasius hypophthalmus, starvation, body composition, temporal change.
Correspondence
Palash Halder
Upazila Fisheries Officer,
Department of Fisheries,
Ministry of Fisheries and
Livestock, Bangladesh.
1. Introduction
The studies on fish starvation are important in order to understand of the growth biology of
fish in wild state [1]. Some of the fish species are subjected to a natural starvation period during
part of the year and have developed an ability to survive without food [2]. In these species
which have been studied the strategy to adapt to dietary deprivation varies considerably. Fish
use energy generated from the catabolism of body reserves to maintain routine metabolism
when deprived of food, either partially or completely [3, 4, 5, 6]; and the oxygen consumption rate
reduced tends to conserve body energy reserves [5, 7, 8, 9]. The deprived fish lose body mass and
body energy reserves with the prolongation of food deprivation [4, 10]. Some of the fish species
use muscle protein as a major energy source rather than stored glycogen which is maintained
by gluconeogenesis [11], but other conserve body protein at the expense of their fat and
glycogen stores [12, 13]. The body composition of fish is influenced by a number of factors such
as morphological, physiological and environmental and consequently there is a good indicator
of condition, which is often assessed from a measure of the deviation of the mass of an
individual fish species from average mass for length of population [14].
During starvation period the essential processes are maintained at the expense of accumulated
energy reserve which is results in the progressive depletion of body tissue [2]. The starvation
also indicated in tissue hydration [4, 15, 16]. This plays a role in the limitation of the loss or even
the maintenance of wet body weight during starvation period [2]. The finding of starvation
indicates the significant decrease in lipid contents of the carcass and viscera. Resulting
depletion of liver lipid stores, lipid contained in perivisceral adipose tissue is utilized along
with apaxial muscle glycogen. Lipid is stored in the liver, viscera, and muscles in the fish and
it is broken down early in starvation, and often constitutes the main energy source for
maintenance during over wintering starvation. The depletion of lipid during starvation has
been demonstrated in rainbow trout [17]. The metabolic rate of fishes might be decrease during
food restriction period [4] and the expenditure of energy during starvation of fish can be
reduced by decreased locomotion activity [18]. The effects of food deprivation on body
composition in a wide range of fish species have been studied; however the knowledge of the
time sequence of changes during food deprivation is still inadequate. Striped catfish or Thai
pangas (Pangasius hypophthalmus) is a warm-water omnivorous species, with a partial
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International Journal of Fisheries and Aquatic Studies
capacity for compensatory growth. However, there is a lack of
information on body composition during food deprivation.
Based on the current context, the present study was undertaken
to evaluate the temporal changes in body composition of Thai
pangas during food deprivation.
2. Materials and Methods
2.1 Sample collection
The experiment was carried out at Fish physiology and Fish
Nutrition Lab of Fisheries and Marine Resources Technology
Discipline of Khulna University, Khulna from 10 November to
7 December, 2007. Thai pangas used for the experiment were
collected from Khulna University Lake and were transported
live in plastic drum and were maintained in glass stock tanks
prior to experimentation. Fish were brought to the Laboratory
and acclimatized in the experimental 10 glass tanks
(50cm×30cm×30cm) at the rate of 3 fish per tank. Mean
temperature of the aquaria was (25+1 °C). All other
parameters of water quality like dissolved oxygen (D.O) and
pH were kept constant throughout the study. In the experiment,
Thai pangas (48.00±2.52 g) were deprived of food for 27 days,
during which proximate composition in muscle of the fish was
monitored at 3 days intervals. For measurement of body
composition during food deprivation, fish were randomly
sampled on days 0, 3, 6, 9, 12, 15, 18, 21, 24 and 27,
respectively.
2.2 Sample Preparation
Sample was taken randomly on each experiment day for the
determination of proximate composition. After collection, the
sample was washed thoroughly with the fresh tap water and
kept in a slanting position in a tray to remove the water. A
considerable amount of sample was taken for analysis. The
sample (muscle) was taken from a site near the dorsal fin. For
the proximate composition, each experiment was conducted
with three replications. Crude protein (Kjeldahl method), lipid
concentration and water content in muscle of fish were
determined according to AOAC procedures [19]. Data from the
experiment were entered into software package, (MS Excel
(Microsoft Corporation) and Statistical Package for Social
Science, SPSS (SPSS, Chicago, IL, USA) for statistical
analysis. A probability of less than 5% (P < 0.05) was
considered as significant in all instances.
3. Results and Discussion
The proximate body composition including protein, lipid, ash
and moisture of Thai pangas during deprivations are shown in
Table 1. The results indicated that the concentrations of lipid
and protein in muscle of fish body decreased, while water and
ash concentration were increased. Water content was inversely
correlated to either lipid concentration (r = -0.784, n= 30, P <
0.01) or protein concentration (r = -0.995, n = 30, P < 0.01).
Table 1: Effect of starvation on proximal body composition (% wet weight) of Thai pangas
Starvation period
(days)
Body composition parameter (%)
Protein content
(mean±SD)
Lipid content
(mean±SD)
Ash content
(mean±SD)
Moisture content
(mean±SD)
0
20.5±0.23
1.4±0.02
1.20±0.05
76.88±1.13
3
20.10±0.15
1.1±0.04
1.25±0.02
77.54±0.92
6
19.85±0.30
0.93±0.01
1.30±0.01
77.89±0.30
9
20.00±0.22
0.97±0.02
1.28±0.03
77.73±0.45
12
20.20±.0.35
0.95±0.02
1.30±0.03
77.55±0.65
15
20.00±0.31
0.93±0.01
1.32±0.02
77.73±0.14
18
19.95±0.10
0.90±0.02
1.35±0.01
77.79±0.32
21
19.75±0.26
0.87±0.01
1.35±0.02
78.00±0.26
24
19.50±0.34
0.85±0.01
1.40±0.01
78.22±0.52
27
19.40±0.25
0.80±0.02
1.42±0.02
78.35±0.42
3.1 Protein content
The protein concentration in the body of Thai pangas changed
from 20.5±0.23 to 19.40±0.25 from the first date to last date of
experiment (Table 1 and Fig. 1). There was no significant
difference (P≥0.05) found in the changes of protein
concentration. Among the experiment period drastic changes
in protein content was found with 12-24 days, where it varies
from 20.20±.0.35% to 19.50±0.34% afterwards it decrease
gradually with the prolongation of starvation. A gradual
decrease in protein content (% wet weight) which is largely
due to inverse relationship of protein with water in starving
fish is well documented [14]. A similar trend was observed in
grass carp in which no change in protein contents (% dry
weight) was found [1]. This is in confirmation with the results
that the effect of food deprivation on the use of reserved
protein, lipid or glycogen as a metabolic fuel seems to be
species-specific [10, 13].
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Fig 1: Protein content (% wet weight) in the muscle of Thai pangas
during 27-day food deprivation.
International Journal of Fisheries and Aquatic Studies
3.2 Lipid content
Lipid content of the starved fish varies significantly during
deprivation with the initial stage (P≤0.05). The Lipid content
changes from 1.4±0.02% to 0.80±0.02% from the first date to
last date of experiment (Table 1 and Fig. 2). Among the
experiment period drastic changes in lipid content was found
within 0-6 days, where it varies from 1.4±0.02% to
0.93±0.01% afterwards it decrease gradually with the
prolongation of starvation. So it is clear that lipids are the most
important energy provider for Thai pangas during the first
week of food deprivation. Similar findings are reported by
Wieser et al. [18] on juveniles of Lueciscus cephalus,
Chalcolburnus chalcoides mento, Scardinius erythropthalmus
and Ali et al. [1] for Ctenopharyngodon idella. Many
investigators found that the first effect of starvation is the
mobilization of lipids for example Cyprinus carpio [20],
Micropterus salmoides [21] and Anguilla anguilla [3].
Fig 2: Lipid content (% wet weight) in the muscle of Thai pangas during 27-day food deprivation
3.3 Water content
Water content of the starved fish during the experimental
period were increased gradually but not differ significantly
(P≥0.05).The water content were changed from 76.88±1.13%
to 78.35±0.42% from the first date to last date of experiment
(Table 1 and Fig.3). The results indicated a trend of increase in
water contents with increase in number of days of starvation.
Among the experiments period main changes in water content
was found with 12-27 days, where it was varied from
77.55±0.65% to 78.35±0.42%. An inverse relationship
between body lipid and water content occurs due to the
replacement of catabolized lipid by an equal volume of water.
A similar trend reported by Denton and Yousef [22]; Love [2]
and they mentioned that body weight is maintained by water
uptake to compensate for organic matter losses during
starvation. Numerous studies have been demonstrated a rise in
water content in several fish species during starvation [3, 4, 15]
and similar trends were found in the present study. The amount
of water is inversely related with the quantity of lipid in the
muscle of fish body and it was found that maximum quantity
of water was present in starved fish. A similar trend was
documented for Esox lucius (L.), Cirrhinus mrigala and
Ctenopharyngodon idella [1, 14].
starvation, it was changed from 1.20±0.05% to 1.42±0.02%
during the experimental period (Table 1 and Fig.4). Ash
content remained constant 18-21 days. A well-marked increase
was observed between 0-6 and 21-27 days of starvation which
was 1.20±0.05% to 1.30±0.01% and 1.35±0.02% to
1.42±0.02% gradually. A gradual increase in ash contents was
observed during starvation in the present study which was
similar for grass carp [1]. There was no significant change in
ash contents was found in the present study which was also
similar to the response of other species [1]. Herrera and Munoz
[23]
and Phillips and Livingstone [24] reported that total ash
content increased during starvation period for Sardina
pilchardus and Salvelinus fontinalis, respectively which was
conformity of the present study results. Although fatty and
non-fatty fish have different distribution of reserve lipid, both
respond to starvation in a similar way in that much of the lipid,
whether in liver or muscle drawn upon before the protein is
utilized, any reserve of carbohydrate are used first of all [2]. So
it is concluded that, Thai pangas utilize lipids as a major
energy source during the first week of deprivation and it is
further concluded that fish body tried its best through
physiological and biological means to buffer the effect of
starvation on its body composition. This biochemical strategy
to maintain body composition during periods of starvation may
be an adaptation to seasonal periods of fasting that many fish
experience as part of their natural life cycle [15].
Fig 3: Water content (% wet weight) in the muscle of Thai pangas
during 27-day food deprivation
3.4 Ash Content
A gradual increase in ash content was observed till 27 days of
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Fig 4: Ash content (% wet weight) in the muscle of Thai pangas
during 27-day food deprivation
International Journal of Fisheries and Aquatic Studies
4. Conclusion
The study assessed the body composition response with
relation to stress induced by different food deprivation
regimes. The present study results revealed that water and ash
concentration was increased while lipid and protein
concentration was decreased with the prolongation of
starvation. The results also indicated that Thai pangas utilize
body lipid as a major energy source during the first week of
food deprivation, and turn to utilize body proteins as an
alternative energy source when maximum body lipids are
exhausted. However, possible attempt has been made to throw
some light on the study of this species. Finally it can be
concluded that the findings of the present study could be
helpful to create greater interest among the fisheries scientist
of the country for intensive research on culture and proper
management of Thai pangas.
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