Acta Scientiarum. Biological Sciences
ISSN: 1679-9283
[email protected]
Universidade Estadual de Maringá
Brasil
Andreato, Leonardo Vidal; Esteves, João Victor Del Conti; Almeida, Felipe Natali; Ribeiro,
Tatiane Aparecida da Silva; Barrena, Helenton Cristhian; Peres, Sidney Barnabé; Moraes,
Solange Marta Franzói de
Use of the anabolic steroid nandrolone decanoate associated to strength training in Wistar
rats
Acta Scientiarum. Biological Sciences, vol. 35, núm. 2, abril-junio, 2013, pp. 283-291
Universidade Estadual de Maringá
Maringá, Brasil
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Doi: 10.4025/actascibiolsci.v35i2.15513
Use of the anabolic steroid nandrolone decanoate associated to
strength training in Wistar rats
Leonardo Vidal Andreato1,2*, João Victor Del Conti Esteves1,3, Felipe Natali Almeida1,3, Tatiane
Aparecida da Silva Ribeiro1, Helenton Cristhian Barrena1, Sidney Barnabé Peres1 and Solange
Marta Franzói de Moraes1
1
Laboratório de Fisiologia do Esforço, Departamento de Ciências Fisiológicas, Universidade Estadual de Maringá, Maringá, Paraná, Brasil.
Departamento de Esporte, Escola de Educação Física e Esporte, Universidade de São Paulo, São Paulo, São Paulo, Brasil. 3Instituto de
Ciências Biomédicas, Departamento de Fisiologia e Biofísica, Universidade de São Paulo, São Paulo, São Paulo, Brasil. *Autor para
correspondência. E-Mail:
[email protected]
2
ABSTRACT. Anabolic steroids have been constantly used among athletes and physically active
individuals. Adverse effects of such use are reported in the literature. However, little is known about the
effects of anabolic steroid use associated with strength training. Thus, this research aimed to identify
possible morphophysiological alterations in Wistar rats treated with the anabolic steroid nandrolone
decanoate and submitted to strength training. Twenty Wistar rats were divided in four groups: sedentary
control (SC), sedentary hormone (SH), trained control (TC) and trained hormone (TH). After the
experimental protocol period, animals were killed and body weight, adiposity, renal and hepatic injury
markers, plasmatic lipid profile, glycemia, and insulinemia were determined. The experimental conditions
strength training and nandrolone decanoate (isolated or associated) were positively correlated to a
reduction on visceral and subcutaneous adipose tissue. The association of strength training with
nandrolone decanoate was the most effective condition to increase muscle mass. Heart and kidneys
weights, aspartate aminotransferase (AST) and high density lipoprotein (HDL) concentration were also
negatively modified. The data demonstrated effects of anabolic steroids in body composition, with better
results when associated with strength training, but collateral effects were observed.
Keywords: anabolic steroids, nandrolone decanoate, strength training.
Uso do esteróide anabólico decanoato de nandrolona associado ao treinamento de força
em ratos Wistar
RESUMO. Os esteróides anabólicos são usados indiscriminadamente entre atletas e praticantes de
atividades físicas sendo que os efeitos adversos desse uso constam na literatura. Contudo, pouco se sabe dos
efeitos do uso de esteróides anabólicos associados ao treinamento de força. Assim, este estudo objetivou
identificar possíveis alterações morfofisiológicas em ratos Wistar tratados com decanoato de nandrolona e
submetidos ao treinamento de força. Para atingir tal propósito, vinte ratos Wistar foram divididos em
quatro grupos: sedentário controle (SC), sedentário hormônio (SH), treinado controle (TC) e treinado
hormônio (TH). Após o período experimental, foram analisados o peso corporal, a adiposidade, marcadores
de lesões hepáticas e renais, o perfil lipídico, a glicemia e a insulinemia. Foram observados efeitos do
treinamento de força e do uso de decanoato de nandrolona (isolados ou associados) nos tecidos adiposos
viscerais e subcutâneo. A associação de treinamento de força e uso de decanoato de nandrolona foi mais
efetiva para aumentar a massa muscular. Os pesos dos rins e coração, e concentrações de aspartato
aminotransferase (AST) e lipoproteína de alta densidade (HDL) foram negativamente modificados. Os
dados demonstram efeitos do esteróide anabólico sobre a composição corporal, com melhores resultados
obtidos com a associação ao treinamento de força, contudo efeitos colaterais foram observados.
Palavras-chave: anabolizantes, decanoato de nandrolona, treinamento de força.
Introduction
Steroid hormones are derived from cholesterol
and metabolic precursors produced by the adrenal
cortex and gonads (HÄKKINEN et al., 2001).
Belonging to this class of hormone is testosterone, a
molecule with anabolic and androgenic properties,
Acta Scientiarum. Biological Sciences
which has also been synthetically produced and used
for medical therapy (HANDELSMAN, 2001). From
a historical perspective, german soldiers in World
War II did the first non-medical use of anabolic
steroids in order to boost aggression (FULLER,
1993). It was later discovered that these substances
Maringá, v. 35, n. 2, p. 283-291, Apr.-June, 2013
284
could facilitate the growth of skeletal muscle in
laboratory animals, leading to the abusive use of
these compounds (NIDA, 2007).
Currently, the non-medical use of anabolic
steroids has reached alarming proportions, affecting
other population segments, as health club users and
even high school students (MAHARAJ et al., 2000;
YESALIS; BAHRKE, 2000). It is estimated that 3%
of young population in United States have already
used steroids, and about 3.5 million Americans were
users of anabolic steroids (EKLÖF et al., 2003). In
Brazil, the percentage of anabolic steroid users on
school is about 2% (VENÂNCIO et al., 2010).
The use of steroids usually occurs in
supraphysiological doses, and the dose used
associated or not to exercise, is approximately forty
times more than the baseline and twenty times the
therapeutic use (EVANS, 2004). This abuse has
resulted in liver (SCHUMACHER et al., 1999),
kidney (YOSHIDA et al., 1994), and coronary
problems (DO CARMO et al., 2011; FERRERA
et al., 1997), psychological disorders (COWART,
1987; SU et al., 1993), hair and clitoris growth,
menstrual disorders and male voice in women
(STRAUSS et al., 1985), and gynecomastia, acne
and baldness in men (PARKINSON; EVANS,
2006; HARTGENS; KUIPERS, 2004).
According to the National Institute on Drug
Abuse (NIDA, 2000), nandrolone is one of the most
used anabolic derivative of testosterone, because of
its moderate androgenic potential associated with
the good anabolic properties. Furthermore, the use
of nandrolone decanoate has been applied for
therapeutic purposes, and has been effective, for
example, to reduce loss of body mass and muscle in
HIV patients (SAHA et al., 2009), increase the
number of satellite cells per muscle fiber
(ALLOUH; ROSSER, 2010) and control of
refractory anemia (CHAWLA et al., 2009).
In contrast, the deleterious effects of nandrolone
decanoate improper use have also been found.
Shokri et al. (2010) reported that physical training
associated to the nandrolone decanoate utilization
for eight weeks has affected fertility of rats, as well as
generate testicular atrophy. Additionally, the use for
a long period (more than three months) of
nandrolone decanoate may affect the cardiovascular
system by decreasing the myocardial contractile
capacity (NORTON et al., 2000), as well as generate
increased left ventricular wall (WOODIWISS et al.,
2000) and ventricular morphological changes
(MEDEI et al., 2010). In addition, Fineschi et al.
(2011) showed that decanoate supplementation
Acta Scientiarum. Biological Sciences
Andreato et al.
associated to physical exercise, for 42 days caused
body weight gain and a raise in total cholesterol. In
addition to, they also observed a moderate increase
on heart weight, cardiac hypertrophy and evidence
of myocardial lesions.
However, animal model research that combined
exercise and anabolic steroids have adopted the
aerobic or anaerobic exercise on treadmill or water
(GEORGIEVA; BOYADJIEV, 2004). Using the
apparatus proposed by Tamaki et al. (1992), which
allows animals to reproduce the squat weight-lifting
training,
we
proposed
to
analyze
the
supraphysiological effects of nandrolone decanoate
use in association to strength training on body
composition, lipid and glucose homeostasis, liver
and renal injury markers and strength gain in adult
male rats.
Material and methods
Animals and experimental procedures
The sample consisted of 20 male 4-month-old
Wistar rats that were provided by the Central
Animal Facilities, State University of Maringá. They
were given a balanced diet and water ad libitum, kept
on light/dark cycle of 12/12h. The animals were
randomly divided into four groups: (1) sedentary
control (SC); (2) sedentary hormone, treated with
nandrolone decanoate (SH); (3) trained control
(TC); (4) trained hormone, treated with nandrolone
decanoate (TH).
The entire experimental protocol that involved
the use of animals was approved by the Ethics
Committee for Animal Research at the State
University of Maringá, and was conducted in
accordance with the institutional and national
guidelines for the care and use of animals
(028/2011).
Anabolic steroid
The SH and TH groups received intramuscular
nandrolone decanoate (Deca-Durabolin®; Organon
of Brazil LTDA, São Paulo State, Brazil) in a dose of
10 mg kg-1 week-1 (two applications 5 mg kg-1
week-1) during 4 weeks. The weekly dose used in
the study protocol was similar to that used in earlier
researches (NORTON et al., 2000; TRIFUNOVIC
et al., 1995; WOODIWISS et al., 2000), and it is
equivalent to the rates of abuse often applied by
athletes.
Strength exercise training
For the strength exercise protocol, a squat
apparatus was made and adapted from the model
proposed by Tamaki et al. (1992), which simulated
Maringá, v. 35, n. 2, p. 283-291, Apr.-June, 2013
Use of the anabolic steroid nandrolone decanoate in Wistar rats
the execution of the squat. The animals were
submitted to one week of adaptation to the
apparatus. Subsequently, after the stimulus, the
training load (1 maximum repetition - MR) was
used to the measure whether the rats could perform
the correct movement, defined as the minimum
load lifted. During the test, the rats performed no
more than five attempts in order to estimate the
maximum load completely suspended.
After determination of the maximum load, the
training load was set to 75% of 1MR. The 1MR was
measured fortnightly. The group TC and TH held
three sets of 10 repetitions with 1 minute of rest
between each set, three times a week for a period of
4 weeks.
Tissue harvesting procedures
After the experimental procedure, the animals
were anesthetized with sodium pentobarbital
(Hypinol® 3%, 4 mg 100 g-1 of body weight,
intraperitoneally), and laparotomy was carried out to
collect blood (4 mL) from the vena cava and to
remove the tissues (heart, kidney, spleen, liver,
seminal vesicles, adrenal gland, testicle, epididymal,
retroperitoneal, subcutaneous and brown adipose
tissues, and the soleus and gastrocnemius muscles)
that were weighed and stored in a freezer at -80ºC.
Biochemical analysis
The plasma was stored in eppendorf tubes and
frozen at -80ºC to subsequent analysis. The
determination of the plasma concentration of
triglycerides, total cholesterol, high density
lipoprotein
(HDL),
creatinine,
aspartate
aminotransferase (AST), alanine aminotransferase
(ALT) and glucose was conducted using the
colorimetric method (Gold Analiza®, Belo Horizonte,
Minas Gerais State, Brazil). Plasma insulin was
determined by radioimmunoassay (RIA).
Statistical analysis
Statistical evaluation of results was performed by
two-way analysis of variance with Newman-Keuls
multiple comparison as a post-test, prefixing the
level of significance at 5% (p < 0.05). Statistical tests
were performed using the Prism v.2.1 (GraphPad®,
USA) and Microsoft Excel® programs.
Results
Body mass, fat and fat free mass
Neither the administration of nandrolone
decanoate and/or resistance exercise training for a
period of 4 weeks resulted in significant differences
in body weight (Table 1).
Acta Scientiarum. Biological Sciences
285
Table 1. Body weight, initial and final fat weight (g), periepididymal,
retroperitoneal and subcutaneous tissue (g.100g-1 body weight) and
food intake (g.day-1 animal-1) of sedentary control (SC), sedentary
hormone (SH) trained control (TC) and trained hormone (TH)
groups. Values are represented as mean ± SEM.
Initial body weight (g)
Final body weight (g)
Retroperitoneal adipose
tissue
Periepididymal adipose
tissue
Subcutaneous adipose
tissue
Food consumption
SC
SH
TC
TH
411.5 ± 9.5 431.4 ±
406.6 ±
415.6 ±
16.8
17.8
21.0
450.2 ±
451.0 ±
432.6 ±
431.5 ±
11.5
24.2
21.1
22.6
2.07 ± 0.16 1.41 ±
1.46 ±
1.28 ±
0.23*
0.11*
0.20*
1.90 ± 0.13 1.31 ±
1.21 ±
1.34 ±
0.21*
0.15*
0.17*
2.01 ± 0.20 0.74 ±
0.61 ±
0.72 ±
0.07*
0.11*
0.10*
28.6 ± 2.2 26.0 ± 0.04 24.5 ± 0.8 27.9 ± 0.5
*p < 0.05 compared to SC group.
With regard to body adiposity, the effects of
strength training and administration of nandrolone
decanoate were observed on the visceral and
subcutaneous depots of adipose tissue. Significant
differences were seen between the groups SH, TC
and TH compared to the SC group (p < 0.05).
However, the association between strength training
and administration of nandrolone decanoate did not
cause an accumulative effect (Table 1). The food
consumption did not change between groups.
To identify the influence of the experimental
protocol on fat free mass, we analyzed two different
muscles: soleous (Figure 1A) and gastrocnemius
(Figure 1B). There were no influences on soleous
muscle mass (which features a large formation of
oxidative fibers) among the groups, except a
tendency in TH group (SC vs. TH, p = 0.069). In
relationship to gastrocnemius muscle mass (which
has a higher content of glycolytic fibers when
compared to soleus muscle), we observed a
pronounced effect of strength training, with the
trained groups (TC and TH groups) presenting an
increased gastrocnemius muscle mass in comparison
to the sedentary groups (SC and SH groups, p < 0.05).
The isolated action of nandrolone was not observed, as
noted by the absence of significant difference between
groups SC vs. SH and TC vs. TH.
Tissue weight
Table 2 presents the response of different tissues
to strength training and administration of
nandrolone decanoate. The TH group presented a
heart weight statistically higher than SC group
p < 0.05). In addition, the administration of
nandrolone decanoate led to an increase in kidney
mass, regardless of the realization of strength
training (SH and TH vs. SC and TC, p < 0.05). In
the absence of strength training, administration of
Maringá, v. 35, n. 2, p. 283-291, Apr.-June, 2013
286
Andreato et al.
Soleus muscle (mg 100 g-1 of body weight)
nandrolone decanoate caused a reduction in brown
adipose tissue (SH vs. SC, p < 0.05). The weight of
the remaining tissues did not present any
differences.
0.6
A
0.4
Table 3. Creatinine, aspartate aminotransferase (AST) and
alanine aminotransferase (ALT) of sedentary control rats
(SC), sedentary hormone (SH), trained control (TC) and
trained hormone (TH). Values are expressed as mean ± SEM.
0.2
0.0
Gastrocnemius muscle (mg 100 g-1 of body weight)
SC
8
after the administration of nandrolone decanoate,
there were no changes in creatinine plasma levels
(Table 3), which is a parameter used to identify
modifications in glomerular filtration. However,
when we determined the concentrations of
aspartate aminotransferase (AST) and alanine
aminotransferase (ALT) the SH group showed
higher levels of AST in comparison to the other
groups but no changes in ALT concentration
(Table 3).
SH
TC
TH
B
Creatinine
AST
ALT
SC
SH
TC
TH
1.09 ± 0.04
27.76 ± 1.10
33.99 ± 1.24
0.96 ± 0.06
35.85 ± 3.01*
42.03 ± 2.86
0.87 ± 0.03
24.25 ± 0.80
36.51 ± 0.83
1.07 ± 0.08
24.33 ± 1.90
39.97 ± 2.26
*p < 0.05 compared to other groups.
*
6
The plasma lipid profile was also measured in
our study (Table 4). There were no significant
differences in the levels of total cholesterol and
triglycerides, but there was a significant reduction
in HDL cholesterol in the SH group compared to
other groups.
*
4
2
0
SC
SH
TC
TH
Figure 1. (A) Soleus muscle weight (mg.100g-1 body weight)
and (B) gastrocnemius muscle (mg 100 g -1 body weight) of
sedentary control (SC), sedentary hormone (SH), trained
control (TC) and trained hormone (TH) groups. *p < 0.05
compared to group SC and SH. Values are represented as
mean ± SEM.
Table 2. Weight of different tissues (g 100 g-1 body weight) of
sedentary control (SC), sedentary hormone (SH), trained control
(TC) and trained hormone (TH) rats. Values are represented as
mean ± SEM.
SC
SH
TC
TH
0.37 ± 0.01
0.39 ± 0.01
0.40 ± 0.01 0.44 ± 0.01*
Heart
0.54 ± 0.02 0.67 ± 0.01# 0.57 ± 0.03 0.67 ± 0.03#
Kidney
0.15 ± 0.01
0.16 ± 0.01
0.15 ± 0.01
0.15 ± 0.01
Spleen
2.75 ± 0.15
2.82 ± 0.15
2.93 ± 0.05
2.92 ± 0.09
Liver
Seminal vesicle
0.53 ± 0.05
0.48± 0.07
0.49 ± 0.03
0.57 ± 0.02
Adrenal glands
0.013 ± 0.001 0.011 ± 0.001 0.013 ± 0.001 0.012 ± 0.001
Testicle
0.68 ± 0.02
0.72 ± 0.03
0.76 ± 0.03
0.72± 0.04
Brown adipose tissue 0.13 ± 0.01 0.05 ± 0.01* 0.11 ± 0.02 0.10 ± 0.01
*p < 0.05 compared to SC group; # p < 0.05 compared to SC and TC groups.
Markers of kidney and liver damage
The association between the use of anabolic
steroids with renal and hepatic lesions, led us to
perform the analysis of plasma markers to detect
any potential harmful effect of nandrolone
decanoate. Despite the increase in kidney mass
Acta Scientiarum. Biological Sciences
Lipid profile and glycemic control
Table 4. Plasma lipid profile of sedentary control (SC),
sedentary hormone (SH), trained control (TC) and trained
hormone (TH) rats. Values are expressed as mean ± SEM.
SC
Total cholesterol 73.30 ± 6.12
HDL cholesterol 49.60 ± 1.98
Triglycerides
56.80 ± 5.08
SH
TC
TH
57.38 ± 1.11 68.63 ± 1.73 64.26 ± 3.92
41.70 ± 1.45* 53.38 ± 3.44 51.70 ± 3.15
38.10 ± 9.24 58.25 ± 7.60 46.90 ± 12.74
*p < 0.05 compared to other groups.
Additionally, we also determined glucose
plasma levels. The TC group presented lower
blood glucose (Figure 2A). However, neither the
administration of anabolic steroid nor the
resistance physical training led to changes in
insulin levels (Figure 2B) and HOMA index
(Figure 2C).
Development of muscle strength
The development of muscular strength is
associated with an increase in muscle area and
steroid use (SCHROEDER et al., 2003). In order to
measure this muscular capacity we performed the
test of one maximum repetition throughout the
experimental protocol. During the 4 weeks of
strength training, there were no significant
differences in muscle strength gain (Figure 3)
between the trained groups (TC vs. TH).
Maringá, v. 35, n. 2, p. 283-291, Apr.-June, 2013
Use of the anabolic steroid nandrolone decanoate in Wistar rats
Glucose (mg dL-1)
200
A
Discussion
150
*
100
50
0.0
5
SC
SH
TC
TH
SC
SH
TC
TH
SC
SH
TC
TH
B
Insulinemy (ng mL-1)
4
3
2
1
0
50
C
HOMA index
40
30
20
10
0
Figure 2. (A) Glucose, (B) insulin and (C) HOMA index of
sedentary control rats (SC), sedentary hormone (SH), trained
control (TC) and trained hormone (TH). Values are expressed as
mean ± SEM. *p < 0.05 compared to SH.
60
Strength gain (%)
287
40
20
0
TC
TH
Figure 3. Gain muscle strength after 4 weeks of resistance
exercise training.
Values are represented as mean ± SEM.
Acta Scientiarum. Biological Sciences
The use of anabolic steroids is very common in
sports, whether in the professional or amateur
situations. Among the various anabolic steroids
available, nandrolone decanoate is presented as one
of the most used, although in experimental
procedures challenging to mimic the strength
training adopted by gym athletes. With the squat
apparatus utilized in our study, we tried to
reproduce the experimental protocol training to a
very common squat exercise performed in gyms.
Several studies have sought to study the
therapeutic action of nandrolone decanoate aiding in
the recovery of body weight of HIV infection
(GOLD et al., 2006; SARDAR et al., 2010), cachexia
(MUSCARITOLI et al., 2006) and hemodialysis
patients (JOHANSEN et al., 2006). In contrast, the
drug administration to rats or bodybuilders
(HARTGENS et al., 2001) with no history of preexisting condition that would lead to reduced body
weight, the effects of nandrolone decanoate on body
weight, apparently, are absent (FINESCHI et al.,
2011). The same was observed in our study, in
which body weight was not altered by
administration of nandrolone decanoate. This
influence was independent of the realization of
strength training. Some studies show a decrease in
body weight by the combination of exercise
associated to the use of nandrolone decanoate
(FINESCHI et al., 2011; ROCHA et al., 2007).
Regarding the adipose tissue, the administration
of nandrolone decanoate caused a significant
decrease in both visceral (epididymal and
retroperitoneal) and subcutaneous fat depots. This is
an interesting data since adipose tissue, in special
visceral depots, are associated to the development of
several metabolic diseases (WRONSKA, KMIEC,
2012). In this way, nandrolone decanoate and
exercise alone reflected the same adiposity changes,
with no addictive effects of their association. Is also
important to highlight that we used data from
visceral and subcutaneous fat depots due regional
differences previously reported (PALOU et al.,
2010; TCHOUKALOVA et al., 2010a and b;
WRONSKA, KMIEC, 2012).
In a recent study, Alsiö et al. (2009) observed a
dose-response effect of testosterone decanoate in
gene expression of β-3 adrenergic receptors in
visceral adipose tissue surrounding the adrenal gland
of rats, which suggestive of an increased lipolytic
activity in this tissue. Regarding the reduction of
subcutaneous tissue, a dose-response study revealed
that only when high doses (600 mg) were
Maringá, v. 35, n. 2, p. 283-291, Apr.-June, 2013
288
administered there were reductions in body fat
percentage of subjects, while lower doses (25 and 50
mg) led to an increase in fat mass (BHASIN et al.,
2001). However, the dose and time used in our
experiment led to reductions in both depots,
indicating that additional studies are necessary to
answer this question. In relationship to exercise and
adiposity reduction, its beneficial effects were
previously reported (ISMAIL et al., 2012).
Some studies have reported a more pronounced
gain in muscular strength with the association
between anabolic steroid with strength training
(BHASIN et al., 2001; SCHROEDER et al., 2003;
SCHROEDER et al., 2005), however we observed a
lack of significant differences on this parameter,
when comparing the groups TC and TH. We
believe that this lack of difference may be due to
differences in the drug action between the various
anabolic steroids used in previous studies and due to
the time involved in the experimental protocol, i.e.,
four weeks. We also observe an increase in the mass
of the gastrocnemius muscle in the groups who
performed strength training, regardless of the
administration of nandrolone decanoate was
identified. Nonetheless, we have not performed any
additional experimental that could help us to explain
the molecular mechanisms that may be involved in
the effects of using nandrolone decanoate in
combination or not with strength training on
muscle mass hypertrophy.
The effect of anabolic steroid use on the
cardiovascular system has been the reported by
several studies. In our work we observed that the
strength training associated to the administration of
nandrolone promoted an increased in heart weight.
Similar effects have been reported by Fineschi et al.
(2011), which described that nandrolone
supplementation associated with physical exercise,
for 42 days led to moderate increase in heart weight,
cardiac hypertrophy and evidence of myocardial
lesions. In a research that aimed to establish if a
single and high dose of nandrolone decanoate
(20 mg kg-1) could elicit anabolic effects on
morphological parameters the authors observed an
increase in heart weight after 10 days of steroid
administration (TYLICKI et al., 2007). Medei et al.
(2010) found cellular remodeling in both ventricles,
together with electrical changes in the left ventricle
towards the use of nandrolone decanoate super dose.
It has also been pointed out that the use of the drug
may generate an increase in left ventricular wall
(WOODIWISS et al., 2000). Finally, Silva et al.
(2010) observed ECG negative changes with 3
weeks of nandrolone use.
Acta Scientiarum. Biological Sciences
Andreato et al.
In relation to the weight of the kidneys, we
found differences in the two groups that were
treated with nandrolone. Hoseini et al. (2009)
showed that animals treated with nandrolone had
the kidney weight increased by about 30%. An
attention should be given to this fact, since the
outcomes of the use of anabolic steroids on kidney
function in physically healthy individuals remain
inconclusive.
No changes were found between groups with
respect to the weight of spleen, liver, seminal
vesicles, adrenal glands and testes. Nevertheless, the
steroid administration had a negative impact on liver
function, whereas in the SH group AST was found
significantly higher compared to the others. Since
elevated levels of serum transaminases aspartate
aminotransferase
(AST)
and
alanine
aminotransferase (ALT) may reflect secondary
hepatic dysfunction when excessive doses of
anabolic steroids are administered (PERTUSI et al.,
2001), our result indicates that decanoate
nandrolone use caused a negative effect on liver.
Corroborating our findings, Vieira et al. (2008)
showed that administration of nandrolone decanoate
leads to a dose-dependent increase of serum
aspartate aminotransferase (AST) and alanine
aminotransferase (ALT). In addition, the authors
demonstrate that administration of the drug in
higher doses in clinics can be potentially harmful to
the liver, leading to incipient fibrosis. It is noted that
the TH group did not achieve such high indicators
of liver injury. However, further analysis is needed
to prove a possible cytoprotective effect of strength
training.
In regard to glucose and lipid metabolism, our
results were partially similar to that obtained by
Venâncio et al. (2010). The authors reported a
reduction on the levels of LDL, total cholesterol,
HDL and triglycerides in individuals who have
undergone resistance training and made use of
steroids. Our data only observed a reduction in
HDL cholesterol in the SH group. In this sense, a
classic study conducted by Kirkland et al. (1987),
with 57 boys in four developmental stages of
puberty, through clinical examination, found that
the increase in testosterone at puberty resulted in a
decrease in HDL. However, when hypogonadism is
induced experimentally through the administration
of GnRH agonists or when the endogenous
production of testosterone is inhibited an increase in
HDL is elicited. Thus, we conclude that in most of
the cases the use of anabolic steroids is capable to
induce a decrease in HDL (DOBS et al., 2001).
Additionally, strength training seems to promote a
Maringá, v. 35, n. 2, p. 283-291, Apr.-June, 2013
Use of the anabolic steroid nandrolone decanoate in Wistar rats
liver protective effect by restoring ALT and AST
values back to a normal range in TH group.
The present work also evaluated the beneficial
effect of strength training on circulating levels of
glucose and insulin. The TC group presented a
lower fasting glycemia when compared to the others
groups. Exercise has been shown to positively
influence glucose homeostasis through increased
glucose transport system on muscle and reduction of
hormonal stimulus for production and release of
hepatic glucose (HENRIKSEN, 2002).
Conclusion
This research points out to positive effects of
administration of nandrolone decanoate, especially
associated to strength training on body composition
by act reducing visceral and subcutaneous adipose
tissue. However, due no changes in muscle mass
and strength, associate to changes in markers of
renal and hepatic injury and the increase in heart
weight, we forewarn the use of nandrolone
decanoate except when clinically prescribed.
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