@2024 Afarand., IRAN
ISSN: 2251-8215 Sarem Journal of Reproductive Medicine 2017;1(2):59-62
ISSN: 2251-8215 Sarem Journal of Reproductive Medicine 2017;1(2):59-62
Carnitine, Fructose and Zinc Levels in Seminal Plasma of Unexplained Asthenospermic Patients Compared with Normal Individuals
ARTICLE INFO
Article Type
Original ResearchAuthors
Saremi A.T. (*)Khamesian M. (1)
Marmazi F. (1)
(*) “Sarem Fertility & Infertility Research Center (SAFIR)” and “Sarem Cell Research Center (SCRC)”, Sarem Women’s Hospital, Tehran, Iran
(1) Sarem Women’s Hospital, Tehran, Iran
Correspondence
Article History
Received: January 15, 2016Accepted: May 14, 2016
ePublished: June 15, 2017
BRIEF TEXT
Infertility has known and unknown variety of reasons. In almost 50% of infertility cases, male factors are involved alone or in combination with female factors [1].
... [2, 3]. The decrease in the number and percentage of moving sperm or reduction in the number of fast and progressive sperms is called osteospermum. Various causes such as sperm structure problems, genitourinary tract infection, anti-spasm antibodies, and relative obstruction of sperm passage can reduce sperm motility [4]. If there is no cause for low sperm motility, it is referred to as a "low motility with unknown cause". Previous research suggests that if semen plasma of semen is added to the low motility sperm, it will increase their movement. In other words, there are factors or factors in the plasma of normal semen that affect sperm motility [5-7]. Semen plasma is the result of epididymis secretions and sexually transmitted glands, mainly seminal vesicles and prostate. Carnitine, fructose and zinc are three compounds that have a very high concentration in the plasma of semen in comparison with other body fluids, the main source of which is epididymis, seminal vesicles and prostate [7, 8]. When sperm is produced in the testicle, it is motile and produces the property of fertility through epididymis. By measuring carnitine in semen plasma, the epididymis can be monitored [9, 10]. Seminal vesicles secretion has the largest contribution to the formation of semen, and one of its main components is fructose. Fructose is considered as an energy source for sperm [11]. After seminal vesicles, the prostate has the largest contribution to the formation of semen volume. Zinc is one of the compounds that are high in semen and prostate secretions. Zinc measurements have been proposed as a test to measure prostate activity [5]. There are various hypotheses regarding the role of zinc in male reproductive physiology. Zinc can inhibit oxygen consumption in the sperm [12]. ... [13-17].
Previous studies have reported contradictory results on the effects of these three factors on moving motile sperms. Therefore, this study was conducted with the aim of investigating the amounts of carnitine, fructose and zinc in seminal plasma in people with non-causative asteospermum compared to healthy subjects.
This research is an observational and case-control study.
Patients with impaired sperm motility without any cause and healthy subjects were examined from patients referring to Sarem Medical Center in a 7-month period.
In the selection of the patients group, the subjects who had spermogram tests were examined. If sperm motility was poor and the patients have no clinical disorder or complication, they were given another spermogram and hormonal tests for the next week. Hormonal tests included T3, T4, TSH, testosterone, prolactin, LH and FSH, that all of them except sperm motility were in the normal range. Data and demographic characteristics of patients were also collected through a questionnaire. 101 patients were examined. Finally, with regard to the clinical signs, hormonal findings, supplementary tests and the result of the spermogram that were performed to investigate the causes of sperm low motility, 43 cases were diagnosed as low motility sperm with no cause and entered to the study. To select the control group, those healthy individuals who had referred to the Sarem Medical Center and the reason of infertility was their wives (female infertility) were selected. They were also evaluated for clinical signs, hormonal findings and spermogram results, and if all the criteria were normal, they were selected as healthy subjects. Matching of the control group was based on age-related variables. Finally, 36 people were selected as the control group and entered the study.
Sampling and analysis of semen: Semen specimens were collected with Masturbation following 3 to 6 days of non-intercourse and were collected in sterile plastic single-use dishes. Samples were placed immediately at 37 ° C until the clot was opened. Then some samples were used for routine diagnostic tasks such as semen analysis. The samples were then poured into plastic tubes and centrifuged for 20 minutes at a speed of 200 rpm, and the plasma was transferred into four separate tubes to measure carnitine, fructose and zinc and a sample of storage. Zinc, fructose and carnitine were measured by atomic absorption spectrophotometry [18]. Sperm motility evaluation, in addition to quantity, is also important in the quality of sperm movement. In terms of motility, the sperms were divided in to four groups: Immotile groups (sperms that had no motility), low (sperms that had a slight movement in their place, had no forward movement, or they were turning around), Sluggish (those had forward movement but with slow speed and large deviation to the sides) and Full (sperms that had fast moving forward without deviations or they had slight deviations to the sides); If a sample had less than 50% of motile sperm , or lacking full motion, it was considered as the osteospermum sample.
There was no significant difference between the two groups in terms of semen volume and sperm counts in milliliters, but there was a significant difference between the total sperm count (× 106/ ejac), the percentage of moving sperm and percentage of progressive movement, that all three variables were less in the group of patients with osteospermum without a specific cause (Table 1). Mean concentration of zinc (mg/dl) and fructose (mg/dl) were not significantly different between the two groups, but the mean of carnitine concentration (nmol/ml) was significantly lower in the patients that in those of healthy subjects (p=0.015; Table 2). No significant correlation was found between total zinc and fructose in seminal plasma with the percentage of moving sperm and percentage of progressive movement, while there was a direct and significant correlation between total carnitine content and total percentage of sperm motility (p = 0.001). Also, there was a direct and significant correlation between total carnitine content and percentage of progressive movement (p = 0.001).
Studies have shown that if seminal plasma of healthy people is added to the low motile sperm, the sperm movement increases. This suggests that the combination of seminal plasma of normal people with this group of patients is different or have some differences [5, 7]. In this study, there was a positive and significant correlation between plasma carnitine concentration and sperm motility (p <0.01) and progressive movement (p <0.01). Previous studies have confirmed this relationship [14, 19]. Also, in assessing the amount of total carnitine, a positive and significant relationship was found between total carnitine content and sperm motility (p <0.01), as well as between total carnitine content with progressive movement percentage (p <0.01). Previous studies by Carpino, Pruneda, and Fabris have also emphasized this correlation [5, 6, 8]. According to the results obtained in this study, it can be concluded that the low motility of sperms in patients undergoing research is due to reduction of carnitine in seminal plasma or reduction of epididymal function. In this study, the mean zinc concentration in seminal plasma of healthy individuals was 13.7 mg / dl and in subjects with sperm low motility, it was 12.7 mg / dl, which was not significantly different. Considering that there was no significant difference in the amount of zinc present in the seminal plasma of normal individuals and people with osteospermum without a specific cause, and considering that zinc value in semen is known as a sign of prostate activity, it can be concluded that the patients studied in The study did not have a specific disorder for prostate function. Also, considering that the patients in the study did not differ from normal subjects in terms of the amount of fructose present in the seminal plasma, it can be said that they have no problems in terms of seminal vesicles.
Reducing carnitine with a potential mechanism for epididymal function decreases sperm motility. Since several interfering factors are effective in sperm movement, comparing different parameters of the seminal fluid simultaneously can be very useful and enlightening for sperm motility against different concentrations of these compounds in vitro. In addition, other seminal fluid factors can be compared simultaneously.
TABLES and CHARTS
Show attach fileCITIATION LINKS
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[6]Check DJ, Check JH, Bollendorf A. Fresh versus frozen seminal plasma for enhancing sperm motility in asthenozoospermic males. Arch Androl. 1991;26(2):79-81.
[7]Karacagil M, Sade M, TÜRkyilmaz RK. The effect of zinc, arginine, fructose and seminal supernatant of normal semen on the triple adenosine triphosphatase activities of the spermatozoa from males with oligoasthenozoospermia. Andrologia. 1985;17(4):383-8.
[8]Pruneda A, Yeung CH, Bonet S, Pinart E, Cooper TG. Concentrations of carnitine, glutamate and myo-inositol in epididymal fluid and spermatozoa from boars. Anim Reprod Sci. 2007;97(3-4):344-55.
[9]Jeulin C, Lewin LM. Role of free L-carnitine and acetyl-L-carnitine in post-gonadal maturation of mammalian spermatozoa. Hum Reprod Update. 1996;2(2):87-102.
[10]Kobayashi D, Tamai I, Sai Y, Yoshida K, Wakayama T, Kido Y, et al. Transport of carnitine and acetylcarnitine by carnitine/organic cation transporter (OCTN) 2 and OCTN3 into epididymal spermatozoa. Reproduction. 2007;134(5):651-8.
[11]Andrade-Rocha FT. Seminal fructose levels in male infertility: Relationship with sperm characteristics. Int Urol Nephrol. 1999;31(1):107-11.
[12]Henkel R, Bittner J, Weber R, Huther F, Miska W. Relevance of zinc in human sperm flagella and its relation to motility. Fertil Steril. 1999;71(6):1138-43.
[13]Andrews JC, Nolan JP, Hammerstedt RH, Bavister BD. Role of zinc during hamster sperm capacitation. Biol Reprod. 1994;51(6):1238-47.
[14]Colagar AH, Marzony ET, Chaichi MJ. Zinc levels in seminal plasma are associated with sperm quality in fertile and infertile men. Nutr Res. 2009;29(2):82-8.
[15]Bjorndahl L, Kjellberg S, Kvist U. Ejaculatory sequence in men with low sperm chromatin-zinc. Int J Androl. 1991;14(3):174-8.
[16]Srivastava A, Chopra SK, Dasgupta PR. Biochemical analysis of human seminal plasma. I. Fructose, ascorbate, cholesterol, adenosine triphosphatase and lactic dehydrogenase. Andrologia. 1983;15(5):431-5.
[17]Matalliotakis I, Koumantaki Y, Evageliou A, Matalliotakis G, Goumenou A, Koumantakis E. L-carnitine levels in the seminal plasma of fertile and infertile men: Correlation with sperm quality. Int J Fertil Womens Med. 2000;45(3):236-40.
[18]Burtis CA, Ashwood ER, Bruns DE. Tietz Fundamentals of Clinical Chemistry. 6th ed. Amsterdam: Saunders Elsevier. 2008. P.976.
[19]Li K, Li W, Huang YF, Shang XJ. Level of free L-carnitine in human seminal plasma and its correlation with semen quality. Zhonghua Nan Ke Xue. 2007;13(2):143-6.
[2]Zavos PM, Abou-Abdallah M, Aslanis P, Correa JR, Zarmakoupis-Zavos PN. Use of the Multi-ZSC one-step standardized swim-up method: Recovery of high-quality spermatozoa for intrauterine insemination or other forms of assisted reproductive technologies. Fertil Steril. 2000;74(4):834-5.
[3]Chen ZJ. Clinical progress in gynecologic reproductive endocrinology. Zhonghua fu chan ke za zhi. 2009;44(9):655-7. [Chinese]
[4]Hanash KA. Book review: Campbell's urology, 7th ed. Ann Saudi med. 1998;18(6):570-1.
[5]Carpino A, Sisci D, Aquila S, Salerno M, Siciliano L, Sessa M, et al. Adnexal gland secretion markers in unexplained asthenozoospermia. Arch Androl. 1994;32(1):37-43.
[6]Check DJ, Check JH, Bollendorf A. Fresh versus frozen seminal plasma for enhancing sperm motility in asthenozoospermic males. Arch Androl. 1991;26(2):79-81.
[7]Karacagil M, Sade M, TÜRkyilmaz RK. The effect of zinc, arginine, fructose and seminal supernatant of normal semen on the triple adenosine triphosphatase activities of the spermatozoa from males with oligoasthenozoospermia. Andrologia. 1985;17(4):383-8.
[8]Pruneda A, Yeung CH, Bonet S, Pinart E, Cooper TG. Concentrations of carnitine, glutamate and myo-inositol in epididymal fluid and spermatozoa from boars. Anim Reprod Sci. 2007;97(3-4):344-55.
[9]Jeulin C, Lewin LM. Role of free L-carnitine and acetyl-L-carnitine in post-gonadal maturation of mammalian spermatozoa. Hum Reprod Update. 1996;2(2):87-102.
[10]Kobayashi D, Tamai I, Sai Y, Yoshida K, Wakayama T, Kido Y, et al. Transport of carnitine and acetylcarnitine by carnitine/organic cation transporter (OCTN) 2 and OCTN3 into epididymal spermatozoa. Reproduction. 2007;134(5):651-8.
[11]Andrade-Rocha FT. Seminal fructose levels in male infertility: Relationship with sperm characteristics. Int Urol Nephrol. 1999;31(1):107-11.
[12]Henkel R, Bittner J, Weber R, Huther F, Miska W. Relevance of zinc in human sperm flagella and its relation to motility. Fertil Steril. 1999;71(6):1138-43.
[13]Andrews JC, Nolan JP, Hammerstedt RH, Bavister BD. Role of zinc during hamster sperm capacitation. Biol Reprod. 1994;51(6):1238-47.
[14]Colagar AH, Marzony ET, Chaichi MJ. Zinc levels in seminal plasma are associated with sperm quality in fertile and infertile men. Nutr Res. 2009;29(2):82-8.
[15]Bjorndahl L, Kjellberg S, Kvist U. Ejaculatory sequence in men with low sperm chromatin-zinc. Int J Androl. 1991;14(3):174-8.
[16]Srivastava A, Chopra SK, Dasgupta PR. Biochemical analysis of human seminal plasma. I. Fructose, ascorbate, cholesterol, adenosine triphosphatase and lactic dehydrogenase. Andrologia. 1983;15(5):431-5.
[17]Matalliotakis I, Koumantaki Y, Evageliou A, Matalliotakis G, Goumenou A, Koumantakis E. L-carnitine levels in the seminal plasma of fertile and infertile men: Correlation with sperm quality. Int J Fertil Womens Med. 2000;45(3):236-40.
[18]Burtis CA, Ashwood ER, Bruns DE. Tietz Fundamentals of Clinical Chemistry. 6th ed. Amsterdam: Saunders Elsevier. 2008. P.976.
[19]Li K, Li W, Huang YF, Shang XJ. Level of free L-carnitine in human seminal plasma and its correlation with semen quality. Zhonghua Nan Ke Xue. 2007;13(2):143-6.