Terazosin-induced alterations in catalase expression and lipid peroxidation in the rat seminal vesicles

Summary Previous studies have shown that alpha1‐adrenergic receptor antagonists may alter seminal vesicle contractility and impair fertility in male rats. This study was designed to investigate the effects of terazosin on the catalase expression in the seminal vesicles and the lipid peroxidation of...

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Published inAndrologia Vol. 45; no. 2; pp. 128 - 134
Main Authors Mitropoulos, D., Patris, E., Deliconstantinos, G., Kyroudi-Voulgari, A., Anastasiou, I., Perea, D.
Format Journal Article
LanguageEnglish
Published Germany Blackwell Publishing Ltd 01.04.2013
John Wiley & Sons, Inc
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Online AccessGet full text
ISSN0303-4569
1439-0272
1439-0272
DOI10.1111/j.1439-0272.2012.01324.x

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Abstract Summary Previous studies have shown that alpha1‐adrenergic receptor antagonists may alter seminal vesicle contractility and impair fertility in male rats. This study was designed to investigate the effects of terazosin on the catalase expression in the seminal vesicles and the lipid peroxidation of the seminal fluid in normal adult rats. Wistar rats were treated with terazosin (1.2 mg kg−1 body weight, given orally every second day) for 120 days. Catalase expression was assessed immunohistochemically in tissue sections of the seminal vesicles, and lipid peroxidation was estimated by measuring the malondialdehyde (MDA) levels in the seminal vesicles' fluid. The seminal vesicles in terazosin‐treated rats were particularly distended in comparison with those of controls, and their secreting epithelium was suppressed. Cytoplasmic catalase expression in the secreting epithelial cells (% of cells) was increased in terazosin‐treated specimens in comparison with controls (76.1 ± 17.1 versus 51.3 ± 25.1, P = 0.005). MDA levels (μm) were also higher in samples from treated subjects in comparison with controls (2.67 ± 1.19 versus 1.39 ± 0.19, P = 0.01). Although the direct effect of terazosin treatment on the seminal vesicles is that of impaired contractility, an indirect effect is that on fertility by increasing lipid peroxidation in the seminal fluid and/or through degrading of hydrogen peroxide that is essential for sperm capacitation.
AbstractList Summary Previous studies have shown that alpha1-adrenergic receptor antagonists may alter seminal vesicle contractility and impair fertility in male rats. This study was designed to investigate the effects of terazosin on the catalase expression in the seminal vesicles and the lipid peroxidation of the seminal fluid in normal adult rats. Wistar rats were treated with terazosin (1.2 mg kg-1 body weight, given orally every second day) for 120 days. Catalase expression was assessed immunohistochemically in tissue sections of the seminal vesicles, and lipid peroxidation was estimated by measuring the malondialdehyde (MDA) levels in the seminal vesicles' fluid. The seminal vesicles in terazosin-treated rats were particularly distended in comparison with those of controls, and their secreting epithelium was suppressed. Cytoplasmic catalase expression in the secreting epithelial cells (% of cells) was increased in terazosin-treated specimens in comparison with controls (76.1 ± 17.1 versus 51.3 ± 25.1, P = 0.005). MDA levels (µm) were also higher in samples from treated subjects in comparison with controls (2.67 ± 1.19 versus 1.39 ± 0.19, P = 0.01). Although the direct effect of terazosin treatment on the seminal vesicles is that of impaired contractility, an indirect effect is that on fertility by increasing lipid peroxidation in the seminal fluid and/or through degrading of hydrogen peroxide that is essential for sperm capacitation. [PUBLICATION ABSTRACT]
Summary Previous studies have shown that alpha1‐adrenergic receptor antagonists may alter seminal vesicle contractility and impair fertility in male rats. This study was designed to investigate the effects of terazosin on the catalase expression in the seminal vesicles and the lipid peroxidation of the seminal fluid in normal adult rats. Wistar rats were treated with terazosin (1.2 mg kg−1 body weight, given orally every second day) for 120 days. Catalase expression was assessed immunohistochemically in tissue sections of the seminal vesicles, and lipid peroxidation was estimated by measuring the malondialdehyde (MDA) levels in the seminal vesicles' fluid. The seminal vesicles in terazosin‐treated rats were particularly distended in comparison with those of controls, and their secreting epithelium was suppressed. Cytoplasmic catalase expression in the secreting epithelial cells (% of cells) was increased in terazosin‐treated specimens in comparison with controls (76.1 ± 17.1 versus 51.3 ± 25.1, P = 0.005). MDA levels (μm) were also higher in samples from treated subjects in comparison with controls (2.67 ± 1.19 versus 1.39 ± 0.19, P = 0.01). Although the direct effect of terazosin treatment on the seminal vesicles is that of impaired contractility, an indirect effect is that on fertility by increasing lipid peroxidation in the seminal fluid and/or through degrading of hydrogen peroxide that is essential for sperm capacitation.
Previous studies have shown that alpha1-adrenergic receptor antagonists may alter seminal vesicle contractility and impair fertility in male rats. This study was designed to investigate the effects of terazosin on the catalase expression in the seminal vesicles and the lipid peroxidation of the seminal fluid in normal adult rats. Wistar rats were treated with terazosin (1.2 mg kg(-1) body weight, given orally every second day) for 120 days. Catalase expression was assessed immunohistochemically in tissue sections of the seminal vesicles, and lipid peroxidation was estimated by measuring the malondialdehyde (MDA) levels in the seminal vesicles' fluid. The seminal vesicles in terazosin-treated rats were particularly distended in comparison with those of controls, and their secreting epithelium was suppressed. Cytoplasmic catalase expression in the secreting epithelial cells (% of cells) was increased in terazosin-treated specimens in comparison with controls (76.1 ± 17.1 versus 51.3 ± 25.1, P = 0.005). MDA levels (μm) were also higher in samples from treated subjects in comparison with controls (2.67 ± 1.19 versus 1.39 ± 0.19, P = 0.01). Although the direct effect of terazosin treatment on the seminal vesicles is that of impaired contractility, an indirect effect is that on fertility by increasing lipid peroxidation in the seminal fluid and/or through degrading of hydrogen peroxide that is essential for sperm capacitation.Previous studies have shown that alpha1-adrenergic receptor antagonists may alter seminal vesicle contractility and impair fertility in male rats. This study was designed to investigate the effects of terazosin on the catalase expression in the seminal vesicles and the lipid peroxidation of the seminal fluid in normal adult rats. Wistar rats were treated with terazosin (1.2 mg kg(-1) body weight, given orally every second day) for 120 days. Catalase expression was assessed immunohistochemically in tissue sections of the seminal vesicles, and lipid peroxidation was estimated by measuring the malondialdehyde (MDA) levels in the seminal vesicles' fluid. The seminal vesicles in terazosin-treated rats were particularly distended in comparison with those of controls, and their secreting epithelium was suppressed. Cytoplasmic catalase expression in the secreting epithelial cells (% of cells) was increased in terazosin-treated specimens in comparison with controls (76.1 ± 17.1 versus 51.3 ± 25.1, P = 0.005). MDA levels (μm) were also higher in samples from treated subjects in comparison with controls (2.67 ± 1.19 versus 1.39 ± 0.19, P = 0.01). Although the direct effect of terazosin treatment on the seminal vesicles is that of impaired contractility, an indirect effect is that on fertility by increasing lipid peroxidation in the seminal fluid and/or through degrading of hydrogen peroxide that is essential for sperm capacitation.
Previous studies have shown that alpha1-adrenergic receptor antagonists may alter seminal vesicle contractility and impair fertility in male rats. This study was designed to investigate the effects of terazosin on the catalase expression in the seminal vesicles and the lipid peroxidation of the seminal fluid in normal adult rats. Wistar rats were treated with terazosin (1.2 mg kg(-1) body weight, given orally every second day) for 120 days. Catalase expression was assessed immunohistochemically in tissue sections of the seminal vesicles, and lipid peroxidation was estimated by measuring the malondialdehyde (MDA) levels in the seminal vesicles' fluid. The seminal vesicles in terazosin-treated rats were particularly distended in comparison with those of controls, and their secreting epithelium was suppressed. Cytoplasmic catalase expression in the secreting epithelial cells (% of cells) was increased in terazosin-treated specimens in comparison with controls (76.1 ± 17.1 versus 51.3 ± 25.1, P = 0.005). MDA levels (μm) were also higher in samples from treated subjects in comparison with controls (2.67 ± 1.19 versus 1.39 ± 0.19, P = 0.01). Although the direct effect of terazosin treatment on the seminal vesicles is that of impaired contractility, an indirect effect is that on fertility by increasing lipid peroxidation in the seminal fluid and/or through degrading of hydrogen peroxide that is essential for sperm capacitation.
Author Patris, E.
Kyroudi-Voulgari, A.
Mitropoulos, D.
Deliconstantinos, G.
Anastasiou, I.
Perea, D.
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  email: Dr Dionisios Mitropoulos, Department of Urology, University of Athens Medical School, Agiou Thoma 17, Athens 11527, Greece.Tel.: + 30 210 770 1141;Fax:  + 30 210 770 1141;, dmp@otenet.gr
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  surname: Perea
  fullname: Perea, D.
  organization: Department of Experimental Surgery & Surgical Research, University of Athens Medical School, Athens, Greece
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Kawabe K , Yoshida M , Homma Y , Silodosin Clinical Study Group (2006) Silodosin, a new alpha1A-adrenoceptorselective antagonist for treating benign prostatic hyperplasia: results of a phase III randomized, placebo-controlled, doubleblind study in Japanese men. BJU Int 98:1019-1024.
Zini A , Schlegel PN (1996) Catalase mRNA expression in the adult male rat reproductive tract. J Androl 17:473-480.
Sofikitis N , Takahashi C , Nakamura I , Kadowaki H , Okazaki T , Shimamoto T , Miyagawa I (1990) The role of rat copulatory plug for fertilization. Acta Eur Fertil 21:155-158.
Halliwell B , Chirico S (1993) Lipid peroxidation: its mechanism, measurement and significance. Am J Clin Nutr 57(Suppl):715S-725S.
Li K , Shang X , Chen Y (2004) High-performance liquid chromatographic detection of lipid peroxidation in human seminal plasma and its application to male infertility. Clin Chim Acta 346:199-203.
Giuliano F (2006) Impact of medical treatments for benign prostatic hyperplasia on sexual function. BJU Int 97(Suppl 2):34-38.
Ratnasooriya WD , Wadsworth RM (1990) Impairment of fertility of male rats with prazosin. Contraception 41:441-447.
Beyer C , Contreras JL , Larsson K , Olmedo M , Morali G (1982) Patterns of motor and seminal vesicle activities during copulation in the male rat. Phys Behav 29:495-500.
Sanbe A , Tanaka Y , Fujiwara Y , Tsumura H , Yamauchi J , Cotecchia S , Koike K , Tsujimoto G , Tanoue A (2007) Alpha1-Adrenoceptors are required for normal male sexual function. Br J Pharmacol 152:332-340.
Silva MA , Megale A , Avellar MC , Porto CS (1999) Expression and pharmacological characterization of alpha1-adrenoceptors in rat seminal vesicle. Eur J Pharmacol 381:141-149.
Ratnasooriya WD , Ananda UVDS , Ratnasooriya CP (1992) Effect of terazosin, a selective-adrenoceptor antagonist on fertility of male rats. Med Sci Res 20:133-135.
Giuliano F , Bernabe J , Droupy S , Alexandre L , Allard J (2004) A comparison of the effects of tamsulosin and alfuzosin on neurally evoked increases in bladder neck and seminal vesicle pressure in rats. BJU Int 93:605-608.
Meilhac O , Zhou M , Santanam N , Parthasarathy S (2000) Lipid peroxides induce expression of catalase in cultured endothelial cells. J Lipid Res 41:1205-1213.
Peitz B (1988) Effects of seminal vesicle fluid components on sperm motility in the house mouse. J Reprod Fertil 83:169-176.
Snyder DL , Pollard M , Wostmann BS , Luckert P (1990) Life span, morphology and pathology of diet-restricted germ-free and conventional Lobund-Wistar rats. J Gerontol 45:B52-B58.
Mendes FR , Hamamura M , Queiróz DB , Porto CS , Avellar MC (2004) Effects of androgen manipulation on alpha1-adrenoceptor subtypes in the rat seminal vesicle. Life Sci 75:1449-1463.
Debruyne FM (2000) Alpha blockers: are all created equal? Urology 56(Suppl 1):20-22.
Hisasue S , Furuya R , Itoh N , Kobayashi K , Furuya S , Tsukamoto T (2006) Ejaculatory disorder caused by alpha-1 adrenoceptor antagonists is not retrograde ejaculation but a loss of seminal emission. Int J Urol 13:1311-1316.
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2006; 97
2004; 346
1996; 17
1996; 729
2006; 13
1993; 61
2006; 98
2000; 44
2000; 41
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1994; 26
1992; 15
2008; 587
2001; 88
2003; 554
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1987; 15
1990; 41
1993; 57
2004; 75
1990; 21
1990; 45
1982; 29
2004; 93
2004; 71
1997; 11
1997; 54
2000; 56
2002; 124
1999; 381
1997; 122
2007; 152
2003; 24
1986
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1981; 18
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1989; 38
Ratnasooriya (10.1111/j.1439-0272.2012.01324.x-BIB0026|and1324-cit-0026) 1994; 26
Ratnasooriya (10.1111/j.1439-0272.2012.01324.x-BIB0027|and1324-cit-0027) 1992; 20
Sanbe (10.1111/j.1439-0272.2012.01324.x-BIB0028|and1324-cit-0028) 2007; 152
Meilhac (10.1111/j.1439-0272.2012.01324.x-BIB0019|and1324-cit-0019) 2000; 41
Ratnasooriya (10.1111/j.1439-0272.2012.01324.x-BIB0025|and1324-cit-0025) 1990; 41
Shima (10.1111/j.1439-0272.2012.01324.x-BIB0031|and1324-cit-0031) 1993; 61
Sofikitis (10.1111/j.1439-0272.2012.01324.x-BIB0034|and1324-cit-0034) 1990; 21
Giuliano (10.1111/j.1439-0272.2012.01324.x-BIB0008|and1324-cit-0008) 2006; 97
Ratnasooriya (10.1111/j.1439-0272.2012.01324.x-BIB0024|and1324-cit-0024) 1987; 15
Yono (10.1111/j.1439-0272.2012.01324.x-BIB0037|and1324-cit-0037) 2008; 587
Peitz (10.1111/j.1439-0272.2012.01324.x-BIB0023|and1324-cit-0023) 1988; 83
Silva (10.1111/j.1439-0272.2012.01324.x-BIB0032|and1324-cit-0032) 1999; 381
Yu (10.1111/j.1439-0272.2012.01324.x-BIB0038|and1324-cit-0038) 2003; 554
Beyer (10.1111/j.1439-0272.2012.01324.x-BIB0002|and1324-cit-0002) 1982; 29
Bohlen (10.1111/j.1439-0272.2012.01324.x-BIB0003|and1324-cit-0003) 2000; 44
Mendes (10.1111/j.1439-0272.2012.01324.x-BIB0020|and1324-cit-0020) 2004; 75
Griveau (10.1111/j.1439-0272.2012.01324.x-BIB0011|and1324-cit-0011) 1994; 17
Zini (10.1111/j.1439-0272.2012.01324.x-BIB0039|and1324-cit-0039) 1996; 17
Cabell (10.1111/j.1439-0272.2012.01324.x-BIB0004|and1324-cit-0004) 1997; 54
Londero (10.1111/j.1439-0272.2012.01324.x-BIB0017|and1324-cit-0017) 1996; 729
Sharif (10.1111/j.1439-0272.2012.01324.x-BIB0030|and1324-cit-0030) 1990; 341
Moriyama (10.1111/j.1439-0272.2012.01324.x-BIB0022|and1324-cit-0022) 1997; 122
Kawabe (10.1111/j.1439-0272.2012.01324.x-BIB0014|and1324-cit-0014) 2006; 98
Grisham (10.1111/j.1439-0272.2012.01324.x-BIB0010|and1324-cit-0010) 1986
Markus (10.1111/j.1439-0272.2012.01324.x-BIB0018|and1324-cit-0018) 1997; 17
Halliwell (10.1111/j.1439-0272.2012.01324.x-BIB0012|and1324-cit-0012) 1993; 57
Metafora (10.1111/j.1439-0272.2012.01324.x-BIB0021|and1324-cit-0021) 1989; 38
Chen (10.1111/j.1439-0272.2012.01324.x-BIB0006|and1324-cit-0006) 2003; 24
Snyder (10.1111/j.1439-0272.2012.01324.x-BIB0033|and1324-cit-0033) 1990; 45
Chen (10.1111/j.1439-0272.2012.01324.x-BIB0005|and1324-cit-0005) 2002; 124
Solomon (10.1111/j.1439-0272.2012.01324.x-BIB0036|and1324-cit-0036) 1997; 11
Agarwal (10.1111/j.1439-0272.2012.01324.x-BIB0001|and1324-cit-0001) 2003; 79
Li (10.1111/j.1439-0272.2012.01324.x-BIB0016|and1324-cit-0016) 2004; 346
Kedia (10.1111/j.1439-0272.2012.01324.x-BIB0015|and1324-cit-0015) 1981; 18
Zubkova (10.1111/j.1439-0272.2012.01324.x-BIB0040|and1324-cit-0040) 2004; 71
Debruyne (10.1111/j.1439-0272.2012.01324.x-BIB0007|and1324-cit-0007) 2000; 56
Schwinn (10.1111/j.1439-0272.2012.01324.x-BIB0029|and1324-cit-0029) 2001; 88
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Sofikitis (10.1111/j.1439-0272.2012.01324.x-BIB0035|and1324-cit-0035) 1992; 15
Giuliano (10.1111/j.1439-0272.2012.01324.x-BIB0009|and1324-cit-0009) 2004; 93
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Snippet Summary Previous studies have shown that alpha1‐adrenergic receptor antagonists may alter seminal vesicle contractility and impair fertility in male rats. This...
Previous studies have shown that alpha1-adrenergic receptor antagonists may alter seminal vesicle contractility and impair fertility in male rats. This study...
Summary Previous studies have shown that alpha1-adrenergic receptor antagonists may alter seminal vesicle contractility and impair fertility in male rats. This...
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StartPage 128
SubjectTerms Adrenergic alpha-1 Receptor Antagonists - toxicity
Alpha-adrenoreceptor antagonists
Animals
catalase
Catalase - metabolism
Fertility - drug effects
lipid peroxidation
Lipid Peroxidation - drug effects
Male
Prazosin - analogs & derivatives
Prazosin - toxicity
rat prostate
Rats
Rats, Wistar
Seminal Vesicles - drug effects
Seminal Vesicles - metabolism
Seminal Vesicles - pathology
terazosin
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Title Terazosin-induced alterations in catalase expression and lipid peroxidation in the rat seminal vesicles
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