Protective effect of L-carnitine on testicular ischaemia-reperfusion injury in rats

Testicular torsion is a urological emergency referred to as ‘acute scrotum’, because inappropriate treatment can lead to male subfertility and infertility. A possible cause of testicular damage is the ischaemia–reperfusion (I/R) injury attributed to oxygen free radicals. L‐carnitine, a vitamin‐like...

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Published inCell biochemistry and function Vol. 25; no. 6; pp. 611 - 618
Main Authors Dokmeci, Dikmen, Inan, Mustafa, Basaran, Umit Nusret, Yalcin, Omer, Aydogdu, Nurettin, Turan, Fatma Nesrin, Uz, Yesim Hulya
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.11.2007
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Summary:Testicular torsion is a urological emergency referred to as ‘acute scrotum’, because inappropriate treatment can lead to male subfertility and infertility. A possible cause of testicular damage is the ischaemia–reperfusion (I/R) injury attributed to oxygen free radicals. L‐carnitine, a vitamin‐like antioxidant, plays a pivotal role in the maturation of spermatozoa within the reproductive tract. The aim of the present paper was to determine the protective effect of L‐carnitine on testicular I/R‐induced injury. Thirty‐two male rats were divided into 4 groups (n = 8). Testicular torsion was created by rotating the right testis 720° in a clockwise direction. Group 1: sham‐operated control; group 2: ischaemia; group 3: I/R; group 4: ischaemia–L‐carnitine treatment–reperfusion group. L‐carnitine (500 mg kg−1, intraperitoneally) was administered before 30 min of detorsion in Group 4. After torsion (5 h) and detorsion (5 h), bilateral orchidectomy was performed. The malondialdehyde (MDA) level was evaluated in testes. Histopathologically, Johnsen's spermatogenesis criteria and mean seminiferous tubule diameter (MSTD) measurements were used. Testicular MDA levels were higher in the torsion group compared to the sham‐control group (p < 0.05). Detorsion (reperfusion) caused a further increase in MDA levels (p < 0.05). Pretreatment with L‐carnitine prevented a further increase in MDA levels (p < 0.05). Histologically, torsion caused some separation among germinal cells in the seminiferous tubules, which became much more prominent in the I/R group but was attenuated with L‐carnitine pretreatment. In conclusion, L‐carnitine pretreatment may have a protective effect in experimental testicular torsion–detorsion model in rats by its well‐known antioxidant potential. Copyright © 2006 John Wiley & Sons, Ltd.
Bibliography:istex:7D098F54BFFD428319043AED9E176611E4C919A7
This paper was presented at the 18th International Pharmacology Congress, Izmir, Turkey, October 2005.
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ArticleID:CBF1355
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0263-6484
1099-0844
DOI:10.1002/cbf.1355