Lipid peroxidation (LPO) of stallion spermatozoa was assessed in fresh semen and in samples of the same ejaculates after freezing and thawing. Particular attention was paid to individual differences in the susceptibility to LPO and its possible relationship with freezability.
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Innate levels of LPO were very low in fresh spermatozoa but increased after thawing, a change that was largely stallion-dependent. The level of LPO in fresh spermatozoa was not correlated with that of the thawed spermatozoa. Negative correlations existed between LPO and intact membranes post-thaw ( r=−0.789, P.
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AbstractLipid peroxidation (LPO) of stallion spermatozoa was assessed in fresh semen and in samples of the same ejaculates after freezing and thawing. Particular attention was paid to individual differences in the susceptibility to LPO and its possible relationship with freezability.
Innate levels of LPO were very low in fresh spermatozoa but increased after thawing, a change that was largely stallion-dependent. The level of LPO in fresh spermatozoa was not correlated with that of the thawed spermatozoa. Negative correlations existed between LPO and intact membranes post-thaw ( r=−0.789, P. IntroductionCryopreservation causes differential damage to the spermatozoa of all mammalian species, of either lethal or sub-lethal nature. Obviously, sperm death is the major factor explaining the lower longevity of thawed spermatozoa, but non-lethal modifications of the surviving cells also account for their reduced life-span, thus narrowing the window which spermatozoa have for successful fertilization after artificial insemination (AI;, ). In many species including horses, peroxidation of plasma membrane lipids (lipid peroxidation, LPO) has been claimed to be a major factor involved in this sub-lethal cryodamage (, ). The particular susceptibility of the sperm plasma membrane to peroxidative damage is due to a high cellular content of polyunsaturated fatty acids.
Attacks by free radicals on those fatty acids generate peroxyl (ROO.) and alkoxyl (RO.) radicals that – in order to become stable as molecules – subtract a hydrogen atom from an adjacent carbon atom in a neighboring lipid, thus generating the corresponding acid or alcohol. The subtraction of a hydrogen atom from an adjacent lipid creates a carbon-centered radical that combines with dioxygen to create another lipid peroxide, thus perpetuating the propagation of peroxidative damage throughout various cell membranes.Recently, sperm-freezing technology has become an area of increasing interest for the equine industry. One of the major problems of equine sperm cryobiology is the large inter-individual variability in sperm survival during the freezing and thawing procedures. Such variability is often ascribed to the fact that most stallions have been selected by performance and phenotype, and not for sperm quality, either directly or indirectly. However, the physiological and biochemical reasons behind this variability remain unexplained. Sperm-LPO has been studied using many methods, including the use of fluorescent probes.
Among these, the recently developed probe BODIPY-C 11 is considered most reliable and easy to assess LPO in spermatozoa (, ). BODIPY-C 11 has, therefore, been used to assess the susceptibility of stallion sperm to this insult after different oxidative challenges (, ). However, these studies did not investigate individual variation among stallions or their ejaculates in their susceptibility to cryopreservation-induced LPO. Therefore, the aim of the present study was to assess the individual responses of spermatozoa from seven stallions to freezing and thawing, including their susceptibility to LPO, as well as to study the relationship between LPO and cell damage.
Confocal laser microscopy images of stallion spermatozoa loaded with BODIPY-C 11. (A) Red fluorescence associated with the widespread incorporation of the non-oxidized probe in the spermatozoa. (B) Green fluorescence associated with the oxidized probe. (C) Transmission images.
(D) Overlaid images in which areas of lipid peroxidation appear yellow. All images were obtained with a Bio-Rad MRC confocal microscope. Magnification, 60×.Citation: REPRODUCTION 138, 1;After thawing, there was an increase in LPO, compared with the ejaculate, fresh spermatozoa ( P. Orange fluorescence represents spermatozoa depicting high mitochondrial membrane potential. Green fluorescence represents spermatozoa depicting low mitochondrial membrane potential. Orange and green fluorescence simultaneously represent spermatozoa having heterogeneous mitochondria, with high and low mitochondrial membrane potential within the same spermatozoa. Values with different superscript between rows within a column ( a–b) or between columns within a row ( A–B), differ significantly ( P.
Correlations between proportions of sperm-LPO and sperm quality variablesSignificant correlations were found between LPO and sperm quality post-thaw, expressed as sperm membrane integrity and mitochondrial membrane potential (, and ). High negative correlations were particularly seen between the proportions of spermatozoa having LPO and intact membranes post-thaw ( r=−0.789, P. DiscussionAs previously reported, cryopreservation induces LPO in stallion spermatozoa, mainly at their mid-piece. Although the effect of cryopreservation on the induction of LPO has been previously described in many species including horses (, ), this is – to the best of our knowledge – the first time that a significant stallion-to-stallion variation in susceptibility to LPO of their cryopreserved spermatozoa has been shown. The first practical implication of this finding is that differences in susceptibility to peroxidation may explain the large individual variation in the cryoresistance of the stallion ejaculate. The second fact is that innate LPO, present in the recently ejaculated spermatozoa, is not related to the peroxidation levels found after freezing and thawing, implying that the process of cryopreservation imposes peroxidative changes unrelated to the intrinsic levels of a particular stallion. Apparently, this susceptibility is not related to the antioxidant systems of the semen, since we were unable to find direct correlations among SOD or GPx activity and LPO thus, probably this susceptibility relates to the lipid composition of the sperm plasma membrane.In our work, we studied the relationship between LPO, sperm membrane integrity, mitochondrial membrane potential (Δψm), and caspase activity.
Probably for the first time, we were able to show a direct mathematical relationship between LPO, sperm membrane integrity Δψ m, and caspase activity. To explain these relationships, the factors causing cell death and sub-lethal cellular damage during freezing and thawing should be considered. Previously, the two injury-factors theory (the presence of intracellular ice crystals, acting as an agricultural plow, tearing apart membranes on one hand and dehydration of the cells causing osmotic stress) was largely accepted. However, recent research indicates that at the freezing rates currently used in animal sperm cryobiology, the formation of intracellular ice crystals is unlikely to occur, with most damage being mainly osmotic in nature, occurring both during freezing and at thawing.In addition, a large percentage of the surviving spermatozoa experience changes that reduce their lifespan within the female reproductive tract. In the past, these changes were termed as ‘cryocapacitation’.
Today, these changes, although resembling capacitation as studied using the Chlortetracycline test, appear in a different light and are called ‘capacitation-like’ (, ). Cryopreserved spermatozoa experience premature aging, involving mechanisms such as LPO and an apoptosis-like mechanism, at least in some species, including the horse (, ). The sperm mitochondria are the main source of reactive oxygen species in the spermatozoon , mainly generated at the complexes I and III of the respiratory chain.Although the sperm mitochondria have been largely ignored for years, recent research indicates a major role of these structures in many physiological and pathological processes in the spermatozoa (, ). A possible explanation for the results presented in the current study may be the following; freezing and thawing increases ROS production in the sperm mitochondria while an osmotic mechanism may increase mitochondrial membrane permeability allowing ROS to diffuse rapidly, activating cellular machinery similar to the intrinsic pathway of apoptosis. In fact, oxidative stress is a well-documented inductor of apoptosis (, ).
Data from our laboratory support this theory, since active caspases 3 and 7 (major proteins involved in the activation of apoptosis), and caspase 9 (an inductor protein involved in the activation of the mitochondrial pathway of apoptosis) have been described in fresh and frozen–thawed equine spermatozoa. In addition, and supporting the concept that apoptotic-like phenomena may occur in ejaculated stallion spermatozoa, there is a report where ejaculated spermatozoa were capable of triggering a nuclear matrix associated topoisomerase IIB that concomitantly with a nuclease can cleave the entire sperm DNA into small fragments. The theory of an apoptotic-like process being induced by LPO to explain the concept of ‘premature aging’ of cryopreserved spermatozoa, is also supported by the mathematical relationship found in our study, between LPO, membrane integrity, and Δψm.
LPO may activate an ‘apoptotic-like’ phenomenon leading to premature aging ending in a reduced lifespan of the processed spermatozoa.From our study we can infer that susceptibility to LPO explains differences in cryoresistance among stallions and ejaculates within the same stallion. However, LPO appears to be overestimated as a major factor involved in cryodamage. Innate LPO levels were low in fresh samples of ejaculated spermatozoa, and for some stallions cryopreservation only increased LPO by 2–3% after thawing. However, despite LPO not being a major factor in sperm cryodamage, it may trigger mechanisms indirectly leading to sperm damage, and as a more practical and important aspect, LPO is highly correlated to cryoresistance.The present study also confirms previous findings from our laboratory and others , indicating that the equine ejaculate is characterized by a high percentage of spermatozoa depicting caspase activity, and that the expression of caspases increases as a result of cryopreservation.
It is unlikely that the presence of active caspases in ejaculated spermatozoa represents only a pathological phenomenon. The stallions involved in the present study were of known fertility and used as donor sires for AI in our institution. Although apoptosis is a characteristic form of cell death that usually serves to remove unwanted cells, there are some examples where apoptosis-like events do not lead to death but rather are involved in the terminal differentiation of certain cell types (, ). On the other hand, since the overall survival time of the spermatozoa (both fresh and frozen–thawed) could not be prolonged by inhibitors of caspases (, ) the mere presence of active caspases does not seem to be a crucial lethal factor in ejaculated spermatozoa. We can, therefore, speculate that active caspases potentially display additional physiological roles in mature spermatozoa rather than being involved only in detrimental changes.In summary, LPO levels are low in freshly ejaculated stallion spermatozoa, but increase after cryopreservation in a stallion-dependent manner. This LPO is unlikely to represent a sign of cryopreservation-induced injury per se, but it is apparently capable of triggering apoptotic-like changes that could result in the sub-lethal cryodamage often seen among surviving spermatozoa.
Cytofluorometric assessment of activated caspasesThe caspase FITC-VAD-FMK in situ marker (Molecular Probes, Leiden, The Netherlands) was used to detect active caspases in the spermatozoa. This cell-permeable caspase inhibitor peptide is conjugated to FITC and binds covalently to active caspases serving as an in situ marker for apoptosis. A sample of 5×10 6 freshly ejaculated or post-thawed spermatozoa was suspended in 1 ml PBS, and – after adding 1 μl FITC–VAD-FMK (5 mM) – the suspension was incubated at room temperature (22–25 °C) in darkness for 20 min. After incubation, the spermatozoa were washed with PBS, followed by the addition of 1 μl ethidium homodimer (1.167 mM; Molecular Probes Europe) to detect membrane damage. Flow cytometry and fluorescence microscopy were conducted within 10 min. Evaluation of mitochondrial membrane potential (ΔΨm)The lipophilic cationic compound 5,5′,6,6′-tetrachloro-1,1′,3,3′ tetraethylbenzymidazolyl carbocianyne iodine (JC-1, Molecular Probes Europe) has the unique ability to label differentially mitochondria with low and high membrane potential. In mitochondria with high membrane potential, JC-1 forms multimeric aggregates emitting in the high orange wavelength of 590 nm, when excited at 488 nm.
However, at the same excitement wavelength (488 nm) in mitochondria with low membrane potential, the JC-1 forms monomers that emit in the green wavelength (525–530 nm). For staining, a 3 mM stock solution of JC-1 was prepared in DMSO. From each sperm suspension, 5×10 6 freshly ejaculated or post-thawed spermatozoa were placed in 1 ml PBS and stained with 0.5 μl JC-1 stock solution. The samples were incubated at 38 °C in darkness for 40 min before flow cytometric analysis. Assessment of subtle sperm membrane changes and viabilityEarly sperm membrane changes and viability were determined as described in, with modifications for adaptation to the equine species. In brief, 1 ml sperm suspension (5×10 6 spermatozoa/ml) from freshly ejaculated or post-thawed spermatozoa was loaded with 3 μl YO-PRO-1 (25 μM) and 1 μl ethidium homodimer-1 (1.167 mM; Molecular Probes Europe, Leiden, The Netherlands). After a thorough mixing the suspension was incubated at 37 °C in darkness for 16 min.
This staining distinguishes four sperm subpopulations. The first is the subpopulation of unstained spermatozoa. These spermatozoa are considered alive and without any membrane alteration. Another sperm subpopulation consists of YO-PRO-1 positive cells emitting green fluorescence. It has been demonstrated that in the early stages of apoptosis there is a modification of membrane permeability that selectively allows entry of some non-permeable DNA-binding molecules (, ). This subpopulation contains spermatozoa which may show early damage or a shift to another physiological state, since membranes become slightly permeable during the first steps of cryoinjury, enabling YO-PRO-1 but not ethidium homodimer to penetrate the plasma membrane (, ).
Neither of these probes enters intact cells. Finally, two subpopulations of cryo-induced necrotic spermatozoa were easily detected, early necrotic, spermatozoa stained both with YO-PRO-1 and ethidium homodimer (emitting both green and red fluorescence), and late necrotic spermatozoa, cells stained only with ethidium homodimer (emitting red fluorescence; ). Confocal laser microscopy images of stallion spermatozoa loaded with YO-PRO-1/ethidium staining. (A) Green fluorescence, represents spermatozoa with an initial increase in membrane permeability (YO-PRO-1 fluorescence).
(B) Green and red fluorescence represents an advanced stage of membrane damage, both YO-PRO-1 and ethidium homodimer stains the sperm nucleus. (C) Red fluorescence, ethidium homodimer, this is the advanced degree of membrane damage. All images were obtained with a Bio-Rad MRC confocal microscope. Magnification, 60×.Citation: REPRODUCTION 138, 1. Staining for detection of LPOLPO was measured using the probe BODIPY 581/591-C 11 (Molecular Probes). A suspension of 2×10 6/ml spermatozoa (freshly ejaculated or post-thawed) was loaded with the probe at a final concentration of 2 μM. Since egg yolk was found to bind the lipophilic BODIPY 581/591-C 11, the egg yolk containing freezing extender (Ghent) was first removed by centrifugation through a 35% density gradient (Pure Sperm Nidacon, Gothenburg, Sweden).
The spermatozoa were then incubated at 37 °C for 30 min, washed by centrifugation to remove the unbound probe, and analyzed using a flow cytometer and a confocal laser microscope. Positive controls were obtained after addition of 80 μM ferrous sulfate to additional sperm suspensions. Flow cytometryFlow cytometric analyses were carried out with a Coulter EPICS XL (Coulter Corporation Inc., Miami, FL, USA) flow cytometer equipped with standard optics, an argon-ion laser (Cyonics, Coherent, Santa Clara, CA, USA) performing 15 mW at 488 nm, and an EXPO 2000 software. Subpopulations were divided into quadrants, and the frequency of each subpopulation was quantified. Non-sperm events (debris) were gated out based on the forward scatter and side scatter dot-plots by drawing a region enclosing the cell population of interest. Events with scatter characteristics similar to spermatozoa but without reasonable DNA content were also gated out.
Forward and sideways light scatter were recorded for a total of 10 000 events per sample (YO-PRO-1, caspases, and BODIPY C 11), or 30 000 events for JC-1. Samples were measured at flow rate of 200–300 cells/s. Green fluorescence was detected in FL1, red fluorescence was detected in FL3, and orange fluorescence in FL2. SOD determinationSOD activity was estimated by using a SOD determination kit following the directions provided by the manufacturer (Sigma–Aldrich). Briefly, SOD activity was indirectly estimated by a colorimetric method based on the reduction of WST-1, a highly water-soluble tetrazolium salt which renders a water-soluble formazan dye upon its reduction with a superoxide anion.
Since the absorbance of WST-1 formazan at 440 nm is proportional to the amount of superoxide anion, the SOD activity was indirectly estimated by measuring the decrease in the color development at 440 nm. Frozen/thawed seminal plasma was diluted in a ratio of 1:10 in deionized water and assayed by triplicate. Each assay consisted in 20 μl diluted sample, 200 μl WST working solution, and 20 μl a solution containing active xanthine oxidase in the appropriate buffer. After the incubation for 20 min at 37 °C the color development was measured at 440 nm.
SOD activity was expressed as arbitrary units of absorbance normalized to mg of protein. GPx determinationGPx activity was determined by using a GPx assay kit following the directions provided by the manufacturer (Calbiochem, La Jolla, CA, USA). Briefly, the GPx activity was indirectly estimated by the monitorization of the oxidation of NADPH to NADP +, which is accompanied by the decrease of the absorbance at 340 nm.
Frozen/thawed seminal plasma (20 μl) was diluted with assay buffer (100 μl), mixed with 50 μl of a mixture containing NADPH, glutathione and glutathione reductase, and assayed in triplicate. In addition to samples, non-enzymatic samples (background) as well as samples containing bovine erythrocyte GPx (positive controls) were also assayed. The decrease in the absorbance at 340 nm was measured each min during 6 min at 25 °C. GPx activity was normalized to mg of protein and expressed as nmol/min per mg protein. Statistical analysisThe data were first examined using the Kolmogorov–Smirnov test to determine their distribution.
In view of the non-Gaussian distribution of some of the data gathered, multivariate ANOVA was performed, and when significant differences were found, the non-parametric Mann–Whitney U-test was used to compare pairs of values. The Spearman non-parametric test was used to study the correlation between sperm analysis pre-freezing and sperm quality post-thaw. All analyses were performed using SPSS version 15.0 for Windows (SPSS Inc., Chicago, IL, USA).
Statistical significance was set at P. Export Figures.Confocal laser microscopy images of stallion spermatozoa loaded with BODIPY-C 11. (A) Red fluorescence associated with the widespread incorporation of the non-oxidized probe in the spermatozoa.
(B) Green fluorescence associated with the oxidized probe. (C) Transmission images. (D) Overlaid images in which areas of lipid peroxidation appear yellow. All images were obtained with a Bio-Rad MRC confocal microscope.
Magnification, 60×.Correlation analysis of the relationship between LPO and intact membranes in equine spermatozoa ( r=−0.789, P. Confocal laser microscopy images of stallion spermatozoa loaded with YO-PRO-1/ethidium staining. (A) Green fluorescence, represents spermatozoa with an initial increase in membrane permeability (YO-PRO-1 fluorescence). (B) Green and red fluorescence represents an advanced stage of membrane damage, both YO-PRO-1 and ethidium homodimer stains the sperm nucleus. (C) Red fluorescence, ethidium homodimer, this is the advanced degree of membrane damage. All images were obtained with a Bio-Rad MRC confocal microscope.
Magnification, 60×.
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