Physiologic Anatomy of the Male Sexual Organs

The testis is composed of up to 900 coiled seminiferous tubules, each averaging more than one half meter long, in which the sperm are formed. The sperm then empty into the epididymis, another coiled tube about 6 meters long. The epididymis leads into the vas deferens, which enlarges into the ampulla of the vas deferens immediately before the vas enters the body of the prostate gland. Two seminal vesicles, one located on each side of the prostate, empty into the prostatic end of the ampulla, and the contents from both the ampulla and the seminal vesicles pass into an ejaculatory duct leading through the body of the prostate gland and then emptying into the internal urethra. Prostatic ducts, too, empty from the prostate gland into the ejaculatory duct and from there into the prostatic urethra. Finally, the urethra is the last connecting link from the testis to the exterior. The urethra is supplied with mucus derived from a large number of minute urethral glands located along its entire extent and even more so from bilateral bulbourethral glands (Cowper’s glands) located near the origin of the urethra.

Spermatogenesis During formation of the embryo, the primordial germ cells migrate into the testes and become immature germ cells called spermatogonia which lie in two or three layers of the inner surfaces of the seminiferous tubules (a cross section of one is shown in Figure 80–2A). The spermatogonia begin to undergo mitotic division, beginning at puberty, and continually proliferate and differentiate through definite stages of development to form sperm.

Hormonal Factors That Stimulate Spermatogenesis We shall discuss the role of hormones in reproduction later, but at this point, let us note that several hormones play essential roles in spermatogenesis. Some of these are as follows: 1. Testosterone, secreted by the Leydig cells located in the interstitium of the testis, is essential for growth and division of the testicular germinal cells, which is the first stage in forming sperm. 2. Luteinizing hormone, secreted by the anterior pituitary gland, stimulates the Leydig cells to secrete testosterone. 3. Follicle-stimulating hormone, also secreted by the anterior pituitary gland, stimulates the Sertoli cells; without this stimulation, the conversion of the spermatids to sperm (the process of spermiogenesis) will not occur. 4. Estrogens, formed from testosterone by the Sertoli cells when they are stimulated by folliclestimulating hormone, are probably also essential for spermiogenesis. 5. Growth hormone (as well as most of the other body hormones) is necessary for controlling background metabolic functions of the testes. Growth hormone specifically promotes early division of the spermatogonia themselves; in its absence, as in pituitary dwarfs, spermatogenesis is severely deficient or absent, thus causing infertility.

Testosterone and Other Male Sex Hormones Secretion, Metabolism, and Chemistry of the Male Sex Hormone Secretion of Testosterone by the Interstitial Cells of Leydig in the Testes. The testes secrete several male sex hormones, which are collectively called androgens, including testosterone, dihydrotestosterone, and androstenedione. Testosterone is so much more abundant than the others that one can consider it to be the significant testicular hormone, although as we shall see, much, if not most, of the testosterone is eventually converted into the more active hormone dihydrotestosterone in the target tissues. Testosterone is formed by the interstitial cells of Leydig, which lie in the interstices between the seminiferous tubules and constitute about 20 per cent of the mass of the adult testes, as shown in Figure 80–7. Leydig cells are almost nonexistent in the testes during childhood when the testes secrete almost no testosterone, but they are numerous in the newborn male infant for the first few months of life and in the adult male any time after puberty; at both these times the testes secrete large quantities of testosterone. Furthermore, when tumors develop from the interstitial cells of Leydig, great quantities of testosterone are secreted. Finally, when the germinal epithelium of the testes is destroyed by x-ray treatment or excessive heat, the Leydig cells, which are less easily destroyed, often continue to produce testosterone. Secretion of Androgens Elsewhere in the Body. The term “androgen” means any steroid hormone that has masculinizing effects, including testosterone itself; it also includes male sex hormones produced elsewhere in the body besides the testes. For instance, the adrenal glands secrete at least five androgens, although the total masculinizing activity of all these is normally so slight (less than 5 per cent of the total in the adult male) that even in women they do not cause significant masculine characteristics, except for causing growth of pubic and axillary hair. But when an adrenal tumor of the adrenal androgen-producing cells occurs, the quantity of androgenic hormones may then become great enough to cause all the usual male secondary sexual characteristics to occur even in the female. These effects are described in connection with the adrenogenital syndrome in Chapter 77. Rarely, embryonic rest cells in the ovary can develop into a tumor that produces excessive quantities of androgens in women; one such tumor is the arrhenoblastoma. The normal ovary also produces minute quantities of androgens, but they are not significant. Chemistry of the Androgens. All androgens are steroid compounds, as shown by the formulas in Figure 80–8 for testosterone and dihydrotestosterone. Both in the testes and in the adrenals, the androgens can be synthesized either from cholesterol or directly from acetyl coenzyme A. Metabolism of Testosterone. After secretion by the testes, about 97 per cent of the testosterone becomes either loosely bound with plasma albumin or more tightly bound with a beta globulin called sex hormone–binding globulin and circulates in the blood in these states for 30 minutes to several hours. By that time, the testosterone either is transferred to the tissues or is degraded into inactive products that are subsequently excreted. Much of the testosterone that becomes fixed to the tissues is converted within the tissue cells to dihydrotestosterone, especially in certain target organs such as the prostate gland in the adult and the external genitalia of the male fetus. Some actions of testosterone are dependent on this conversion, whereas other actions are not.

Degradation and Excretion of Testosterone. The testosterone that does not become fixed to the tissues is rapidly converted, mainly by the liver, into androsterone and dehydroepiandrosterone and simultaneously conjugated as either glucuronides or sulfates (glucuronides, particularly). These are excreted either into the gut by way of the liver bile or into the urine through the kidneys. Production of Estrogen in the Male. In addition to testosterone, small amounts of estrogens are formed in the male (about one fifth the amount in the nonpregnant female), and a reasonable quantity of estrogens can be recovered from a man’s urine.The exact source of estrogens in the male is unclear, but the following are known: (1) the concentration of estrogens in the fluid of the seminiferous tubules is quite high and probably plays an important role in spermiogenesis. This estrogen is believed to be formed by the Sertoli cells by converting testosterone to estradiol. (2) Much larger amounts of estrogens are formed from testosterone and androstanediol in other tissues of the body, especially the liver, probably accounting for as much as 80 per cent of the total male estrogen production. Functions of Testosterone In general, testosterone is responsible for the distinguishing characteristics of the masculine body. Even during fetal life, the testes are stimulated by chorionic gonadotropin from the placenta to produce moderate quantities of testosterone throughout the entire period of fetal development and for 10 or more weeks after birth; thereafter, essentially no testosterone is produced during childhood until about the ages of 10 to 13 years. Then testosterone production increases rapidly under the stimulus of anterior pituitary gonadotropic hormones at the onset of puberty and lasts throughout most of the remainder of life, as shown in Figure 80–9, dwindling rapidly beyond age 50 to become 20 to 50 per cent of the peak value by age 80.

Functions of Testosterone During Fetal Development Testosterone begins to be elaborated by the male fetal testes at about the seventh week of embryonic life. Indeed, one of the major functional differences between the female and the male sex chromosome is that the male chromosome causes the newly developing genital ridge to secrete testosterone, whereas the female chromosome causes this ridge to secrete estrogens. Injection of large quantities of male sex hormone into pregnant animals causes development of male sexual organs even though the fetus is female. Also, removal of the testes in the early male fetus causes development of female sexual organs. Thus, testosterone secreted first by the genital ridges and later by the fetal testes is responsible for the development of the male body characteristics, including the formation of a penis and a scrotum rather than formation of a clitoris and a vagina. Also, it causes formation of the prostate gland, seminal vesicles, and male genital ducts, while at the same time suppressing the formation of female genital organs. Effect of Testosterone to Cause Descent of the Testes. The testes usually descend into the scrotum during the last 2 to 3 months of gestation when the testes begin secreting reasonable quantities of testosterone. If a male child is born with undescended but otherwise normal testes, the administration of testosterone usually causes the testes to descend in the usual manner if the inguinal canals are large enough to allow the testes to pass. Administration of gonadotropic hormones, which stimulate the Leydig cells of the newborn child’s testes to produce testosterone, can also cause the testes to descend. Thus, the stimulus for descent of the testes is testosterone, indicating again that testosterone is an important hormone for male sexual development during fetal life. Effect of Testosterone on Development of Adult Primary and Secondary Sexual Characteristics After puberty, the increasing amounts of testosterone secretion cause the penis, scrotum, and testes to enlarge about eightfold before the age of 20 years. In addition, testosterone causes the secondary sexual characteristics of the male to develop, beginning at puberty and ending at maturity. These secondary sexual characteristics, in addition to the sexual organs themselves, distinguish the male from the female as follows. Effect on the Distribution of Body Hair. Testosterone causes growth of hair (1) over the pubis, (2) upward along the linea alba of the abdomen sometimes to the umbilicus and above, (3) on the face, (4) usually on the chest, and (5) less often on other regions of the body, such as the back. It also causes the hair on most other portions of the body to become more prolific. Baldness. Testosterone decreases the growth of hair on the top of the head; a man who does not have func tional testes does not become bald. However, many virile men never become bald because baldness is a result of two factors: first, a genetic background for the development of baldness and, second, superimposed on this genetic background, large quantities of androgenic hormones. A woman who has the appropriate genetic background and who develops a longsustained androgenic tumor becomes bald in the same manner as does a man. Effect on the Voice. Testosterone secreted by the testes or injected into the body causes hypertrophy of the laryngeal mucosa and enlargement of the larynx. The effects cause at first a relatively discordant, “cracking” voice, but this gradually changes into the typical adult masculine voice. Testosterone Increases Thickness of the Skin and Can Contribute to Development of Acne. Testosterone increases the thickness of the skin over the entire body and increases the ruggedness of the subcutaneous tissues. Testosterone also increases the rate of secretion by some or perhaps all the body’s sebaceous glands. Especially important is excessive secretion by the sebaceous glands of the face, because this can result in acne. Therefore, acne is one of the most common features of male adolescence when the body is first becoming introduced to increased testosterone. After several years of testosterone secretion, the skin normally adapts to the testosterone in a way that allows it to overcome the acne. Testosterone Increases Protein Formation and Muscle Development. One of the most important male characteristics is development of increasing musculature after puberty, averaging about a 50 per cent increase in muscle mass over that in the female. This is associated with increased protein in the nonmuscle parts of the body as well. Many of the changes in the skin are due  to deposition of proteins in the skin, and the changes in the voice also result partly from this protein anabolic function of testosterone. Because of the great effect that testosterone and other androgens have on the body musculature, synthetic androgens are widely used by athletes to improve their muscular performance.This practice is to be severely deprecated because of prolonged harmful effects of excess androgens, as we discuss in Chapter 84 in relation to sports physiology. Testosterone or synthetic androgens are also occasionally used in old age as a “youth hormone” to improve muscle strength and vigor, but with questionable results. Testosterone Increases Bone Matrix and Causes Calcium Retention. After the great increase in circulating testosterone that occurs at puberty (or after prolonged injection of testosterone), the bones grow considerably thicker and deposit considerable additional calcium salts. Thus, testosterone increases the total quantity of bone matrix and causes calcium retention. The increase in bone matrix is believed to result from the general protein anabolic function of testosterone plus deposition of calcium salts in response to the increased protein. Testosterone has a specific effect on the pelvis to (1) narrow the pelvic outlet, (2) lengthen it, (3) cause a funnel-like shape instead of the broad ovoid shape of the female pelvis, and (4) greatly increase the strength of the entire pelvis for load-bearing. In the absence of testosterone, the male pelvis develops into a pelvis that is similar to that of the female. Because of the ability of testosterone to increase the size and strength of bones, it is often used in older men to treat osteoporosis. When great quantities of testosterone (or any other androgen) are secreted abnormally in the still-growing child, the rate of bone growth increases markedly, causing a spurt in total body height. However, the testosterone also causes the epiphyses of the long bones to unite with the shafts of the bones at an early age. Therefore, despite the rapidity of growth, this early uniting of the epiphyses prevents the person from growing as tall as he would have grown had testosterone not been secreted at all. Even in normal men, the final adult height is slightly less than that which occurs in males castrated before puberty. Testosterone Increases Basal Metabolism. Injection of large quantities of testosterone can increase the basal metabolic rate by as much as 15 per cent. Also, even the usual quantity of testosterone secreted by the testes during adolescence and early adult life increases the rate of metabolism some 5 to 10 per cent above the value that it would be were the testes not active. This increased rate of metabolism is possibly an indirect result of the effect of testosterone on protein anabolism, the increased quantity of proteins—the enzymes especially—increasing the activities of all cells. Effect on Red Blood Cells. When normal quantities of testosterone are injected into a castrated adult, the number of red blood cells per cubic millimeter of blood increases 15 to 20 per cent. Also, the average man has about 700,000 more red blood cells per cubic millimeter than the average woman. This difference may be due partly to the increased metabolic rate that occurs after testosterone administration rather than to a direct effect of testosterone on red blood cell production. Effect on Electrolyte and Water Balance. As pointed out in Chapter 77, many steroid hormones can increase the reabsorption of sodium in the distal tubules of the kidneys. Testosterone also has such an effect, but only to a minor degree in comparison with the adrenal mineralocorticoids. Nevertheless, after puberty, the blood and extracellular fluid volumes of the male in relation to body weight increase as much as 5 to 10 per cent. Basic Intracellular Mechanism of Action of Testosterone Most of the effects of testosterone result basically from increased rate of protein formation in the target cells. This has been studied extensively in the prostate gland, one of the organs that is most affected by testosterone. In this gland, testosterone enters the prostatic cells within a few minutes after secretion. Then it is most often converted, under the influence of the intracellular enzyme 5a-reductase, to dihydrotestosterone, and this in turn binds with a cytoplasmic “receptor protein.” This combination migrates to the cell nucleus, where it binds with a nuclear protein and induces DNA-RNA transcription. Within 30 minutes, RNA polymerase has become activated and the concentration of RNA begins to increase in the prostatic cells; this is followed by progressive increase in cellular protein. After several days, the quantity of DNA in the prostate gland has also increased and there has been a simultaneous increase in the number of prostatic cells. Testosterone stimulates production of proteins virtually everywhere in the body, although more specifically affecting those proteins in “target” organs or tissues responsible for the development of both primary and secondary male sexual characteristics. Recent studies suggest that testosterone, like other steroidal hormones, may also exert some rapid, nongenomic effects that do not require synthesis of new proteins. The physiological role of these nongenomic actions of testosterone, however, has yet to be determined. Control of Male Sexual Functions by Hormones from the Hypothalamus and Anterior Pituitary Gland A major share of the control of sexual functions in both the male and the female begins with secretion of gonadotropin-releasing hormone (GnRH) by the hypothalamus (see Figure 80–10). This hormone in turn stimulates the anterior pituitary gland to secrete two other hormones called gonadotropic hormones: (1) luteinizing hormone (LH) and (2) follicle-stimulating hormone (FSH). In turn, LH is the primary stimulus for the secretion of testosterone by the testes, and FSH mainly stimulates spermatogenesis. GnRH and Its Effect in Increasing the Secretion of LH and FSH GnRH is a 10-amino acid peptide secreted by neurons whose cell bodies are located in the arcuate nuclei of the hypothalamus. The endings of these neurons terminate mainly in the median eminence of the hypothalamus, where they release GnRH into the hypothalamic-hypophysial portal vascular system. Then the GnRH is transported to the anterior pituitary gland in the hypophysial portal blood and stimulates the release of the two gonadotropins, LH and FSH. GnRH is secreted intermittently a few minutes at a time once every 1 to 3 hours. The intensity of this hormone’s stimulus is determined in two ways: (1) by the frequency of these cycles of secretion and (2) by the quantity of GnRH released with each cycle. The secretion of LH by the anterior pituitary gland is also cyclical, with LH following fairly faithfully the pulsatile release of GnRH. Conversely, FSH secretion increases and decreases only slightly with each fluctuation of GnRH secretion; instead, it changes more slowly over a period of many hours in response to longer-term changes in GnRH. Because of the much closer relation between GnRH secretion and LH secretion, GnRH is also widely known as LHreleasing hormone. Gonadotropic Hormones: LH and FSH Both of the gonadotropic hormones, LH and FSH, are secreted by the same cells, called gonadotropes, in the anterior pituitary gland. In the absence of GnRH secretion from the hypothalamus, the gonadotropes in the pituitary gland secrete almost no LH or FSH. LH and FSH are glycoproteins. They exert their effects on their target tissues in the testes mainly by activating the cyclic adenosine monophosphate second messenger system, which in turn activates specific enzyme systems in the respective target cells. Testosterone—Regulation of Its Production by LH. Testosterone is secreted by the interstitial cells of Leydig in the testes, but only when they are stimulated by LH from the anterior pituitary gland. Furthermore, the quantity of testosterone secreted increases approximately in direct proportion to the amount of LH available. Mature Leydig cells are normally found in a child’s testes for a few weeks after birth but then disappear until after the age of about 10 years. However, either injection of purified LH into a child at any age or secretion of LH at puberty causes testicular interstitial cells that look like fibroblasts to evolve into functioning Leydig cells. Inhibition of Anterior Pituitary Secretion of LH and FSH by Testosterone—Negative Feedback Control of Testosterone Secretion. The testosterone secreted by the testes in response to LH has the reciprocal effect of inhibiting anterior pituitary secretion of LH (see Figure 80–10). Most of this inhibition probably results from a direct effect of testosterone on the hypothalamus to decrease the secretion of GnRH. This in turn causes a corresponding decrease in secretion of both LH and FSH by the anterior pituitary, and the decrease in LH reduces the secretion of testosterone by the testes. Thus, whenever secretion of testosterone becomes too great, this automatic negative feedback effect, operating through the hypothalamus and anterior pituitary gland, reduces the testosterone secretion back toward the desired operating level. Conversely, too little testosterone allows the hypothalamus to secrete large amounts of GnRH, with a corresponding increase in anterior pituitary LH and FSH secretion and consequent increase in testicular testosterone secretion. Regulation of Spermatogenesis by FSH and Testosterone FSH binds with specific FSH receptors attached to the Sertoli cells in the seminiferous tubules. This causes these cells to grow and secrete various spermatogenic substances. Simultaneously, testosterone (and dihydrotestosterone) diffusing into the seminiferous tubules from the Leydig cells in the interstitial spaces also has a strong tropic effect on spermatogenesis. Thus, to initiate spermatogenesis, both FSH and testosterone are necessary. Negative Feedback Control of Seminiferous Tubule Activity— Role of the Hormone Inhibin. When the seminiferous tubules fail to produce sperm, secretion of FSH by the anterior pituitary gland increases markedly. Conversely, when spermatogenesis proceeds too rapidly, pituitary secretion of FSH diminishes.The cause of this negative feedback effect on the anterior pituitary is believed to be secretion by the Sertoli cells of still another hormone called inhibin (see Figure 80–10). This hormone has a strong direct effect on the anterior pituitary gland to inhibit the secretion of FSH and possibly a slight effect on the hypothalamus to inhibit secretion of GnRH. Inhibin is a glycoprotein, like both LH and FSH, having a molecular weight between 10,000 and 30,000. It has been isolated from cultured Sertoli cells. Its potent inhibitory feedback effect on the anterior pitu itary gland provides an important negative feedback mechanism for control of spermatogenesis, operating simultaneously with and in parallel to the negative feedback mechanism for control of testosterone secretion. Psychic Factors That Affect Gonadotropin Secretion and Sexual Activity Many psychic factors, feeding especially from the limbic system of the brain into the hypothalamus, can affect the rate of secretion of GnRH by the hypothalamus and therefore can also affect most other aspects of sexual and reproductive functions in both the male and the female. For instance, transporting a prize bull in a rough truck is said to inhibit the bull’s fertility— and the human male is hardly different. Human Chorionic Gonadotropin Secreted by the Placenta During Pregnancy Stimulates Testosterone Secretion by the Fetal Testes During pregnancy, the hormone human chorionic gonadotropin (hCG) is secreted by the placenta, and it circulates both in the mother and in the fetus. This hormone has almost the same effects on the sexual organs as LH. During pregnancy, if the fetus is a male, hCG from the placenta causes the testes of the fetus to secrete testosterone.This testosterone is critical for promoting formation of the male sexual organs, as pointed out earlier. We discuss hCG and its functions during pregnancy in greater detail in Chapter 82. Puberty and Regulation of Its Onset Initiation of the onset of puberty has long been a mystery. But it has now been determined that during childhood the hypothalamus simply does not secrete significant amounts of GnRH. One of the reasons for this is that, during childhood, the slightest secretion of any sex steroid hormones exerts a strong inhibitory effect on hypothalamic secretion of GnRH. Yet, for reasons still not understood, at the time of puberty, the secretion of hypothalamic GnRH breaks through the childhood inhibition, and adult sexual life begins. Male Adult Sexual Life and Male Climacteric. After puberty, gonadotropic hormones are produced by the male pituitary gland for the remainder of life, and at least some spermatogenesis usually continues until death. Most men, however, begin to exhibit slowly decreasing sexual functions in their late 40s or 50s, and one study showed that the average age for terminating intersexual relations was 68, although the variation was great. This decline in sexual function is related to decrease in testosterone secretion, as shown in Figure 80–9. The decrease in male sexual function is called the male climacteric. Occasionally the male climacteric is associated with symptoms of hot flashes, suffocation, and psychic disorders similar to the menopausal symptoms of the female. These symptoms can be abrogated by administration of testosterone, synthetic androgens, or even estrogens that are used for treatment of menopausal symptoms in the female. Abnormalities of Male Sexual Function Prostate Gland and Its Abnormalities The prostate gland remains relatively small throughout childhood and begins to grow at puberty under the stimulus of testosterone. This gland reaches an almost stationary size by the age of 20 years and remains at this size up to the age of about 50 years. At that time, in some men it begins to involute, along with decreased production of testosterone by the testes. A benign prostatic fibroadenoma frequently develops in the prostate in many older men and can cause urinary obstruction. This hypertrophy is caused not by testosterone but instead by abnormal overgrowth of prostate tissue itself. Cancer of the prostate gland is a different problem and is a common cause of death, accounting for about 2 to 3 per cent of all male deaths. Once cancer of the prostate gland does occur, the cancerous cells are usually stimulated to more rapid growth by testosterone and are inhibited by removal of both testes so that testosterone cannot be formed. Prostatic cancer usually can be inhibited by administration of estrogens. Even some patients who have prostatic cancer that has already metastasized to almost all the bones of the body can be successfully treated for a few months to years by removal of the testes, by estrogen therapy, or by both; after this therapy the metastases usually diminish in size and the bones partially heal. This treatment does not stop the cancer but does slow it and sometimes greatly diminishes the severe bone pain. Hypogonadism in the Male When the testes of a male fetus are nonfunctional during fetal life, none of the male sexual characteristics develop in the fetus. Instead, female organs are formed. The reason for this is that the basic genetic characteristic of the fetus, whether male or female, is to form female sexual organs if there are no sex hormones. But in the presence of testosterone, formation of female sexual organs is suppressed, and instead, male organs are induced. When a boy loses his testes before puberty, a state of eunuchism ensues in which he continues to have infantile sex organs and other infantile sexual characteristics throughout life.The height of an adult eunuch is slightly greater than that of a normal man because the bone epiphyses are slow to unite, although the bones are quite thin and the muscles are considerably weaker than those of a normal man. The voice is childlike, there is no loss of hair on the head, and the normal adult masculine hair distribution on the face and elsewhere does not occur. When a man is castrated after puberty, some of his male secondary sexual characteristics revert to those of a child and others remain of adult masculine character. The sexual organs regress slightly in size but not to a childlike state, and the voice regresses from the bass quality only slightly. Conversely, there is loss of masculine hair production, loss of the thick masculine bones, and loss of the musculature of the virile male. Also in a castrated adult male, sexual desires are decreased but not lost, provided sexual activities have been practiced previously. Erection can still occur as before, although with less ease, but it is rare that ejaculation can take place, primarily because the semenforming organs degenerate and there has been a loss of the testosterone-driven psychic desire. Some instances of hypogonadism are caused by a genetic inability of the hypothalamus to secrete normal amounts of GnRH. This often is associated with a simultaneous abnormality of the feeding center of the hypothalamus, causing the person to greatly overeat. Consequently, obesity occurs along with eunuchism. A patient with this condition is shown in Figure 80–11; the condition is called adiposogenital syndrome, Fröhlich’s syndrome, or hypothalamic eunuchism. Testicular Tumors and Hypergonadism in the Male Interstitial Leydig cell tumors develop in rare instances in the testes, but when they do develop, they sometimes produce as much as 100 times the normal quantities of testosterone. When such tumors develop in young children, they cause rapid growth of the musculature and bones but also cause early uniting of the epiphyses, so that the eventual adult height actually is considerably less than that which would have been achieved otherwise. Such interstitial cell tumors also cause excessive development of the male sexual organs, all skeletal muscles, and other male sexual characteristics. In the adult male, small interstitial cell tumors are difficult to diagnose because masculine features are already present. Much more common than the interstitial Leydig cell tumors are tumors of the germinal epithelium. Because germinal cells are capable of differentiating into almost any type of cell, many of these tumors contain multiple tissues, such as placental tissue, hair, teeth, bone, skin, and so forth, all found together in the same tumorous mass called a teratoma. These tumors often secrete few hormones, but if a significant quantity of placental tissue develops in the tumor, it may secrete large quantities of hCG with functions similar to those of LH. Also, estrogenic hormones are sometimes secreted by these tumors and cause the condition called gynecomastia (overgrowth of the breasts). Pineal Gland—Its Function in Controlling Seasonal Fertility in Some Animals For as long as the pineal gland has been known to exist, myriad functions have been ascribed to it, including its (1) being the seat of the soul, (2) enhancing sex, (3) staving off infection, (4) promoting sleep, (5) enhancing mood, and (6) increasing longevity (as much as 10 to 25 per cent). It is known from comparative anatomy that the pineal gland is a vestigial remnant of what was a third eye located high in the back of the head in some lower animals. Many physiologists have been content with the idea that this gland is a nonfunctional remnant, but others have claimed for many years that it plays important roles in the control of sexual activities and reproduction, functions that still others said were nothing more than the fanciful imaginings of physiologists preoccupied with sexual delusions. But now, after years of dispute, it looks as though the sex advocates have won and that the pineal gland does indeed play a regulatory role in sexual and reproductive function. In lower animals that bear their young at certain seasons of the year and in which the pineal gland has been removed or the nervous circuits to the pineal gland have been sectioned, the normal periods of seasonal fertility are lost. To these animals, such seasonal fertility is important because it allows birth of the offspring at the time of year, usually springtime or early summer, when survival is most likely. The mechanism of this effect is not entirely clear, but it seems to be the following. First, the pineal gland is controlled by the amount of light or “time pattern” of light seen by the eyes each day. For instance, in the hamster, greater than 13 hours of darkness each day activates the pineal gland, whereas less than that amount of darkness fails to activate it, with a critical balance between activation and nonactivation. The nervous pathway involves the passage of light signals from the eyes to the suprachiasmal nucleus of the hypothalamus and then to the pineal gland, activating pineal secretion. Second, the pineal gland secretes melatonin and several other, similar substances. Either melatonin or one of the other substances is believed to pass either by way of the blood or through the fluid of the third ventricle to the anterior pituitary gland to decrease gonadotropic hormone secretion. Thus, in the presence of pineal gland secretion, gonadotropic hormone secretion is suppressed in some species of animals, and the gonads become inhibited and even partly involuted. This is what presumably occurs during the early winter months when there is increasing darkness. But after about 4 months of dysfunction, gonadotropic hormone secretion breaks through the inhibitory effect of the pineal gland and the gonads become functional once more, ready for a full springtime of activity. But does the pineal gland have a similar function for control of reproduction in humans? The answer to this question is unknown. However, tumors often occur in the region of the pineal gland. Some of these secrete excessive quantities of pineal hormones, whereas others are tumors of surrounding tissue and press on the pineal gland to destroy it. Both types of tumors are often associated with hypogonadal or hypergonadal function. So perhaps the pineal gland does play at least some role in controlling sexual drive and reproduction in humans.