It has been demonstrated for decades of years that the hypothalamic nuclei manifest heterogeneity in degeneration during aging in mammals [10] [16] [17] [18] [19] . The paraventricular nucleus (PVN) is responsible for stress response and is functional throughout the lifespan, maintaining its neuron number in senescence in humans [10] [16] . In contrast, the suprachiasmatic nucleus (SCN), the main controller of circadian rhythm, is decreased in its number of neurons during the aging process in humans and marmosets [10] [16] [18] . Moreover, the sexually dimorphic nucleus in preoptic area (SDN-POA) declines sharply in cell number after aging in male humans and rats [10] [16] [17] [19] . In these respects, the hypothalamic nuclei manifest heterogeneity in degeneration during the complex processes of senescence.

The brain aging is characterized as the accumulation of amyloid-beta [4] [14] . Brain aging is a plausible cause of senescence of hypothalamus. Recently, it was demonstrated that sleep helped biophysical clearance of amyloid-beta from the adult brain [15] [20] , implicating that the neurons of brain were homogeneously subjected to the aging toxicity of amyloid-beta. In this regard, the various hypothalamic nuclei would in turn be subjected to the homogeneous toxicity of amyloid-beta from the forebrain, and would be homogeneously affected by amyloid-beta during aging.

However, as has just been mentioned, each cell group of the hypothalamic nuclei has its own specific pattern of aging, some decreasing while others maintaining in volume during aging [10] [16] [17] [18] [19] . Since the homogeneity of biophysical clearance of forebrain amyloid-beta [15] [20] would cause the homogeneous degeneration of the hypothalamic nuclei, the heterogeneity in degeneration of hypothalamic nuclei [10] [16] [17] [18] [19] indicates that the hypothalamic aging would result from the aging mechanisms other than the toxicity of amyloid-beta from forebrain.

Cai suggested early that, due to the neuronal plasticity of learning and memory, the gradual accumulation of various randomly learned memories in the limbic structures would inevitably imbalance and disorganize the emotional behaviors so that sleep should be developed in evolution to adjust and reorganize the emotions [21] [22] [23] [24] . Consequently, the influences from forebrain to the hypothalamus are random and various, changing from time to time. In this regard, if the hypothalamic aging resulted from the random and irregular plastic changes in the neural activities in forebrain, it would be difficult for the hypothalamus to specifically maintain the paraventricular nucleus (PVN) intact [10] [16] while only reduce the neurons in the suprachiasmatic nucleus (SCN) [10] [16] [18] and male preoptic sexually dimorphic nucleus (SDN-POA) [10] [16] [17] [19] . Therefore, it is as well deduced that the hypothalamic aging might result from the mechanisms other than those from the forebrain.

Because of the above mentioned dissociation of the hypothalamic aging from the forebrain changes, Cai recently suggested a new peripheral hypothesis to explain the hypothalamic aging on suprachiasmatic nucleus (SCN) [25] . On the one hand, the continuous decrement in duration of slow-wave sleep (SWS) demonstrated in many senescent observations [25] [26] [27] [28] would cause the continuous functional degeneration of suprachiasmatic nucleus (SCN) in hypothalamus during aging [10] [16] [18] [25] . On the other hand, the skin underwent aging from exposure to the environmental sunshine and oxygen as well as from genetic shortening of the telomere [25] . The skin senescence was reported repeatedly to result in reduction in the electrodermal activities [25] , which would reduce the emotional responses and memories in brain, and would in turn reduce the requirement for slow wave sleep (SWS) [21] [22] [23] [25] . In these two respects, from skin senescence to slow wave sleep (SWS), it was formulated a new degenerative aging pathway to explain the chronological change of hypothalamic suprachiasmatic nucleus (SCN) during aging [25] .

It is noted herein that the key to cause the aging of hypothalamic suprachiasmatic nucleus (SCN) [10] [16] [18] in this hypothesis was the decrement in duration of slow wave sleep (SWS) as demonstrated in many senescent observations [25] [26] [27] [28] . Besides the skin aging as the good cause to reduce the duration of slow wave sleep (SWS) in this hypothesis [25] , there are still many other causes which may also reduce the duration of slow wave sleep (SWS), such as the cholesterol, hypertension, and so on. It is necessary to point out that the peripheral aging from the intracellular changes is homogenous within an organ, while that from cholesterol or angiemphraxis is relatively more heterogeneous, which requires more investigations.

The aging-related disorganization in expression of core clock genes in various brain regions supports this hypothetic pathway. It is common knowledge that the hippocampus is responsible for learning and memory [24] . It was demonstrated that the expression of Clock, Bmal1 and Per 2 genes in hippocampus lost circadian rhythm earlier than those in hypothalamic suprachiasmatic nucleus (SCN) [29] [30] , implicating that the hippocampal circadian rhythm relevant to sleep and memories actually decreased earlier in response to the reduction of emotional responses, while such dysfunctions later began to affect the hypothalamic suprachiasmatic nucleus (SCN) [25] . If the degeneration of hypothalamic suprachiasmatic nucleus (SCN) during aging results from the changes in the secretion of growth hormone, there would not have shown this pattern of disorganization in expression of core clock genes earlier in the hippocampus and then in the hypothalamic suprachiasmatic nucleus (SCN) [29] [30] .

Therefore, the decrement in duration of slow wave sleep (SWS) as demonstrated in many senescent observations [25] [26] [27] [28] is the most plausible cause for the degeneration of hypothalamic suprachiasmatic nucleus (SCN) during aging [10] [16] [18] [25] . In further, the senescent decrement in duration of slow wave sleep (SWS) [25] [26] [27] [28] may in turn result from the skin senescence as postulated by Cai [25] , while may result also from other populationally more heterogeneously distributed causes such as the cholesterol, hypertension, and so on.

The hypothetic peripheral causes of senescence of hypothalamic suprachiasmatic nucleus (SCN) are shown in Figure 1.

In similarity to the aging pathway from skin to hypothalamic suprachiasmatic nucleus(SCN) via slow wave sleep (SWS), on July 4, 2016, the European people in television commented that there was an additional senescent pathway for male reproduction from the common knowledge of adipose accumulation and reduction of spermatogenesis in middle age/early old age to analogously elicit the degeneration of hypothalamic preoptic area (POA) [25] [31] , while the senescence of female reproduction likewise resulting also from ovary menopause.

Because the senescent degeneration of hypothalamic suprachiasmatic nucleus (SCN) from skin senescence via slow wave sleep (SWS) would as well affect the reproductive system of animals, this pathway from adipose accumulation would provide an additional cause for the degeneration of male hypothalamic preoptic area (POA) [25] [31] , making it degenerate sharply in the course of senescence as observed [10] [16] [17] [19] .

As mentioned above, it was indeed observed that the male sexually dimorphic nucleus in preoptic area (SDN-POA) declined in cell number after aging [10] [16] [17] [19] . Besides, it was even shown that the higher estradiol resulted in the neuronal loss in the preoptic sexually dimorphic nucleus (SDN-POA) in male rats [17] , while the testosterone reversed the neuronal degeneration within the preoptic sexually dimorphic nucleus (SDN-POA) in male rats [19] , demonstrating that the hormonal levels directly able to result in the neuronal degeneration within the male preoptic sexually dimorphic nucleus (SDN-POA).

In this regard, via looking at those affecting the hormonal levels of testosterone and estradiol [17] [19] , it would be possible to find out the peripheral causes resulting in the neuronal degeneration within the preoptic sexually dimorphic nucleus (SDN-POA) during male aging.

The European view on hypothalamic aging of preoptic area (POA) from adipose accumulation [25] [31] implicated the premise that it resulted from the intrinsic aging process genetically set in development and growth. The morphogenetic development in animals is controlled by both induction and termination [32] . Induction initiates the morphogenetic development while termination controls the final shape of the generated organ during morphogenesis [32] . Many animal models can demonstrate the induction and termination as the key developmental control for the morphological changes, such as the sexual dimorphism in mammary glands, the epidermal scale in reptiles, the tail metamorphosis in amphibians, the variation in limb digits in vertebrates, and so on [32] .

In vertebrates, the fat depot sizes reach a peak by middle age or early old age, followed by a substantial decline in advanced old age [33] . Fat tissue growth occurs by increase in size and number of fat cells. Beginning at middle age, the subcutaneous fat loses earlier and consequently the intra-abdominal fat increases relatively in the course toward aging [33] , resulting in insulin resistance and increased risk of atherosclerosis and diabetes, even in lean subjects [33] . Nutrients, hormonal effectors such as insulin, leptin, IGF-1, glucocorticoids, and so on are responsible for the regulation of adipose size and redistribution in development and aging [33] [34] .

The enzyme aromatase in vertebrates converts the testosterone to estradiol and decreases the testosterone levels [35] [36] . The aromatase is expressed in the differentiated adipose cells [35] . Accordingly, Cohen suggested earlier that the increase in adipose tissue in middle age be associated with an increase in the enzyme aromatase and lead to diminished testosterone levels during male aging [36] .

It seems not convincing to overemphasize the special role of only one enzyme as aromatase in disturbing the male reproductive functions in aging. However, aromatase is really a remarkable enzyme and even plays more dramatic roles in sex determination. Aromatase is an evolutionary conserved enzyme present in amphioxus [37] , fishes [38] [39] , amphibians [40] , reptiles [41] , and mammals including humans [35] [36] . It is suggested as the key enzyme in the epigenetic determination of sex as male or female during ontogeny in many species of vertebrates [42] , as demonstrated in African cichlid fishes [39] , Japanese frog Ranarugosa [40] and some reptiles [41] .

In this regard, due to the significant effects of aromatase demonstrated in sex determination in many vertebrates [39] [40] [41] [42] , it is obvious that the increase in aromatase from increment of fat size in middle age is sufficient to significantly disturb the male reproductive system via converting the testosterone to estradiol.

The disturbance on male reproductive system from adipose and aromatase in aging can even be assayed in vivo. In one report, it was demonstrated that the free and bioavailable estradiol levels decreased modestly with age as did the ratio of free testosterone to free estradiol, the latter testifying to the age-related increase in aromatization of testosterone [43] . The estradiol levels were highly, significantly and positively related to the body fat mass [43] . In another paper comparing BMI in relation to sperm count, it was shown that the overweight and obesity were associated with an increased prevalence of azoospermia or oligozoospermia [44] .

In this regard, due to the regulation of neuronal numbers within the preoptic sexually dimorphic nucleus (SDN-POA) by the testosterone and estradiol [17] [19] , the increment of adipose and aromatase converting the testosterone to estradiol in aging [43] would cause the neuronal degeneration within the male sexually dimorphic nucleus in preoptic area (SDN-POA).

Because the degeneration of suprachiasmatic nucleus (SCN) from skin aging via slow wave sleep (SWS) would also affect the function of reproduction, the cause from adipose accumulation for the degeneration of male preoptic sexually dimorphic nucleus (SDN-POA) would make an additional contribution to its senescent degeneration, so that make its cells decline sharply after aging as observed [10] [16] [17] [19] .

It is noted that the regulation of the testosterone by lipid may not solely via the rise in aromatase during male aging, even though the rise in aromatase is sufficient to remarkably disturb the male reproductive system in senescence. In parallel, it has also been demonstrated that the level of testosterone is associated with the risk of hypertension [45] [46] [47] . Due to the limited data available, it is uncertain about the regulation of testosterone by hypertension during aging. It is necessary to carry out more investigations on this issue.

In this section, it is demonstrated the European view on the aging of male hypothalamic preoptic area (POA) from adipose accumulation and the relevant supporting facts, as the followings: 1) The genetic increase and redistribution of fat tissue in male middle age. 2) The aromatase, able to determine the sex differentiation in vertebrates, being expressed in adipose tissue to convert the testosterone to estradiol during male aging. 3) The observed disturbance on male reproductive hormones from increment of adipose and aromatase in aging. 4) In response to the hormonal outcomes from the rise in aromatase, the neuronal degeneration within the sexually dimorphic nucleus in preoptic area (SDN-POA) after male aging. 5) The necessity to carry out more investigations about the regulation of testosterone by hypertension during aging.

It is necessary to point out that, for the adipose cause of neuronal degeneration within the sexually dimorphic nucleus in preoptic area (SDN-POA) after male aging, the European view in television adopted the reduction of spermatogenesis as the key mediator, while in literature there were evidences that the ratio of testosterone to estradiol played the key role.

The hypothetic peripheral causes of senescence of male hypothalamic sexually dimorphic nucleus in preoptic area (SDN-POA) are shown in Figure 2.