Some immunological properties of female saliva and its effect on sperm motility

Overview

Background.
In this study, we investigated pH, levels of IgA, IgG, IgM, lysozyme and spermagglutinating antibodies in human saliva of healthy women, with or without hormonal contraception (HC) and their effect on sperm motility.

Methods and results.
Saliva was collected immediately after waking up from 59 healthy randomly selected women. We measured pH in sera and in saliva as well as immunoglobulin G, A and M levels in saliva by radial immunodiffusion. Sperm - saliva capillary penetration test in native saliva served for examination of sperm motility, indirect-MAR test for detection of sperm antibodies in sera, and in saliva, both observed by inverted microscope. The average pH values in native saliva according to the menstrual cycles were: from 2–5 days 6.896, from 6–17 days 7.027, and from 18 and more days 7.17. Rapid decrease of sperm motility was registered in acidic saliva in comparison with alkaline. The average concentration of IgA, IgG, IgM and lysozyme slightly differed in women with or without hormonal contraception. Moderate decreasing of sperm motility was found in saliva with higher levels of IgA. No sperm agglutinating antibodies in saliva and in serum were detected in all subjects.

Conclusions.
The pH of saliva is influenced by several causes (hormonal, immunological, microbiological factors, by meal and drinks, smoking, etc.). We demonstrated that sperm motility is lower in acidic saliva. pH is markedly changed during various days of menstrual cycles. We proved individual high levels of saliva IgA. Human saliva used as coital lubricant decreases sperm motility, but does not replace a local form of contraception..

Keywords:
human saliva – immunoglobulins – lysozyme – pH – sperm motility – sperm antibodies

INTRODUCTION

Saliva is a complex aqueous fluid composed of electrolytes (bicarbonate, potassium, sodium chloride), mucopolysaccharides and glycoproteins, some antibacterial components such as hydrogen peroxide, thiocyanate or secretory immunoglobulin A and several enzymes like alpha-amylase, lingual lipase, lysozyme, salivary lactoperoxidase, lactoferrin, beta-glucuronidase, esterases, phosphatases, kallikrein, ribonucleases (1). Immunoglobulins of all isotypes are also detected in human saliva (2, 3). Saliva is easily available through non-invasive methods and as a body fluid is constantly exposed to external factors such as smoking, food intake and internal aggressors such as microbes in dental caries that easily disturb salivary biochemical composition (3–5). Due to its properties, saliva can be involved in several important physiological mechanisms such as digestion. Properties of saliva are also influenced by disinfection and hormones (6). Currently, 15% of the couples of reproductive age suffer from infertility. Some of them use saliva as “natural lubricant”, often recommended during the initial phase of sexual intercourse. However, saliva has a negative effect on sperm motility (7, 8).

Our experimental study assesses selected immunological properties of human saliva on sperm motility in young women with and without hormonal contraception.

STUDY AND METHODS

In this study we included blood and saliva samples from 59 randomly selected healthy female students aged 14–30 years (average age 22 years); 13 of them were on HC, 46 without hormonal contraception; 50 girls were sexually active and 9 still virgin. The questionnaire given to any girl informed about basic gynaecological information. This study was approved by the Czech Institutional Ethics Committee. A written informed consent and a questionnaire were obtained from each subject participating in the study. Table 1 and 2 provide additional anamnestic data. All samples of sera and saliva were collected under fasting conditions and under abstinence of alcohol and cigarette smoking for at least 9 hours before collection. Saliva samples were collected in sterile containers and immediately after the student woke up. The saliva was then transported within half hour into laboratory.

Each sample was centrifuged (5000 rpm for 10 minutes), to remove mucin. Supernatants were stored at –80 ºC for later immunological examination. We took also 5 ml of blood and serum was obtained and stored at –20 ºC.

Fresh semen samples without spermagglutinating antibodies were collected from two healthy fertile men by masturbation for next study.

Our following experiments were performed at room temperature.

pH measurement

pH meter (Hannah Instruments, Hamilton-electrodes) was used for determination of the pH of native and supernatant of saliva, and blood serum in each sample. The pH values were distributed according to the day of the menstrual cycle, and hormonal contraception. All measurements were repeated twice and the mean value was plotted on a graph for further analysis.

Radial immunodiffusion technique

BIND A RID (The Binding Site, UK) was used for detection of IgA, IgG, IgM isotypes, and lysozyme levels in the 59 supernatants of saliva only.

Sperm motility in saliva

We used a simple sperm-saliva capillary penetration test, modification of the Kremer test for ovulatory cervical mucus (9). For our experiments, we have chosen 2 saliva samples with different pH (acidic and alkaline), and another 2 samples with different values of IgA.

A vertical tube was filled with saliva supernatants and put to a reservoir filled with 200 µl of fresh semen with a cell concentration of 60.000.000/ml from a healthy donor. Under inverted Microscope (Olympus, Japan), sperm progressive motility and vitality was measured at the intervals of start 0, 2, 5, 10 and 15–20 minutes.

Indirect mixed antiglobulin reaction test (i-MAR)

We examined sperm agglutinating antibodies in donors semen by direct MAR and in all supernatants of saliva samples by i-MAR-test).

The i-MAR test was performed to analyze the anti-sperm response in IgG and IgA class. One microliter of native sperm suspension, 1 µl of inactivated saliva, 1 µl of glutaraldehyde-fixed sheep erythrocytes pre-coated with human IgG, and IgA, were mixed together. Then, 1 µl of the corresponding antiserum anti-IgG, anti-IgA (Behringer, Hannover, Germany) was added. Finally, the mixture was covered with coverslip and incubated in humid Petri chamber for 5–10 min. The result of the sperm agglutination reaction was observed under the inverted microscope at 200× magnification. The i-MAR test was considered as positive, if more than 49% of motile spermatozoa were involved in mixed agglutinates (spermatozoa and sheep erythrocytes coated by the corresponding immunoglobulin).

RESULTS

Native saliva sample had a lower pH (average 7.10) value compared with supernatant saliva (7.4). Average pH of sera was 7.35 (Table 3).

The average pH values during menstrual cycle from 0–5 days 6.896, from 6–17 days 7.027, and in secretory phase, from 18 and more days 7.17 in all girls are shown in Figure 1.

Women using hormonal contraception have a lower (more acidic) pH value compared with no hormonal contraception Figure 2.

Two saliva samples chosen for experiment show decreased sperm motility and viability in acidic saliva (pH 5.545) compared with alkaline saliva (pH 7.1) in sperm – saliva capillary penetration test (Figure 3). The sperm motility was reduced by 50% in one minute with the more acidic saliva and after 5 min no sperm motility was observed.

The average levels of IgA, IgG, IgM isotypes and lysozyme were almost the same in women with or without HC (Fig. 4, Table 4).

In all semen samples, saliva reduced sperm progression and motility. For example Figure 5 shows the result of reduced sperm motility in a saliva sample with higher and lower IgA levels (very similar results also for IgG, IgM isotypes and lysozyme).

DISCUSSION

Previous studies (e.g. 2, 5, 10) highlight the fact that human saliva contains direct antibacterial components such as various antimicrobial peptides as thiocyanate ions, even increased amylase levels, lactoperoxidase, and lysozyme, immune cells as well as secretory IgA and other immunoglobulin isotypes, which participate in the mechanism decreasing sperm motility. Whole saliva is composed of the secretions of the parotid glands, the submandibular, the sublingual, and the minor salivary glands.

We found that the pH of saliva increases during the menstrual cycle. The fact can be explained by hormonal changes not only in physiological cycle but also by hormonal contraception. We noted a small difference in pH in supernatant and native saliva. Slightly acidic native saliva is affected by mucin (e.g. 3).

Our study demonstrates that young women with hormonal contraception have nearly the same levels of IgG, IgA, IgM isotypes and lysozyme in saliva compared with those without artificial cycles. Identification of basic immunoglobulins suggests an IgA predominance, which is powerfully secreted directly by salivary glands.

Saliva is a mirror of our body (4, 11–17) allowing detection of many hormonal and metabolic disease as diabetes, thyroid disorder, adrenal disease, cancer, viral infections etc. Our group of young women were healthy, without oral acute or chronic periodontal pathologies such as gingivitis and /or other autoimmune disease as e.g. Sjögren’s syndrome.

We have shown in this work some properties of human saliva and their differences in women with and without hormonal contraception. We modeled the situation of unprotected intercourse (using human saliva as lumbricant) as simple sperm - saliva capillary penetration test. We proved that human saliva impairs motility and progressive movement of sperm. Our data highlights to two facts:

1. The effect of saliva as lubricant for couples trying to be pregnant is not suitable because the movement of sperm into vagina and uterine cervix will be slower as we have shown in our experiments.
2. Saliva cannot be used as a local contraceptive “treatment” for fertile couples even though some spermicidal properties on the sperm are proven.

CONCLUSION

Saliva with its chemical and immunological properties used as a coital lubricant could not use as a nature form of contraception even if sperm progressive motility is impaired.

This work was supported by the project ED2.1.00/03.0076 from European Regional Development Fund  and by the grant from Charles University Grant Agency no. 969212.

ADRESA PRO KORESPONDENCI:

prof. MUDr. Zdenka Ulčová-Gallová, DrSc.

Genetika Plzeň

Parková 11A, 326 00 Plzeň

e-mail: ulcova-gallova@email.cz