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Mental roots of sexual orientation

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A theory about the development of sexual orientation and sexual arousal suggests that these behavior patterns are learned unconsciously from asexual experiences during childhood. The learning begins when the child distinguishes between men and women by the pitch of their voice. Using conditioning, the brain develops mental images of ‘man’ and ‘woman’ that consist of features typical to men and women in the child’s surroundings. Throughout childhood, relying on asexual experiences, the brain continues to develop the patterns of sexual behavior around those mental images. After puberty, behavior patterns that were learned from sexual experiences are added to those learned from asexual experiences during childhood.[1][2]

Underlying causes of sexual diversity[edit]

While body differences between men and women are due to differences in their chromosomes, no one-to-one correlation between genes and sexual orientation was found. Pre- and post-natal concentrations of sex hormones affect the development of the sex organs, but no correlation was found between the concentration levels of hormones and sexual orientation.[3][4] Concentration of sex hormones may affect the libido and other emotional traits such as aggressiveness, but they do not alter sexual orientation.[5][6] There is no correlation between the family-structure of the child (mother and father, a single parent, two parents of the same sex) and the sexual orientation of the grown-up child.[7][8]

Differentiation of some brain structures has been correlated with sexual orientation. For instance, the size of the INAH-3, which is a part of the hypothalamus, a brain area that among other things controls physical aspects of sexual activity, is larger in gay men than in heterosexual men and women.[9] The hypothalamus also reacts to certain chemical compounds in accordance with the sexual orientation of the individual.[10][11][12][13] The amygdala, a brain area involved in emotional activities such as fear, was found to be involved in sexual activities.[14][15][16][17][18] The inner ear shows sex and sexual orientation differentiations. The cochleae of human females are 8-13% shorter than those of males.[19] Otoacoustic emission (OAE), which is sound generated by the cochlea in response to external sound, was found to have sex differences even in newborns, and in adult women such differences correlate with sexual orientation. Auditory evoked potentials, which are presumed to correspond to populations of neurons from the auditory nerve through auditory cortex, showed differences in mean latency or amplitude that correlate with sex and with sexual orientation of women.[20]

The role of conditioning[edit]

Conditioning is an innate learning mechanism that enables animals to develop beneficial behaviors in the environment in which they happen to live. In Pavlov's experiments, the taste of food is the innate cue that triggers the conditioning process. Events associated with that cue (e.g. a whistle) become new triggers of salivation and the feeling of gratification, which are the innate root responses. A learned (conditioned) cue may serve in subsequent events as a trigger of additional conditioning processes. For example, additional stimuli or activities that are associated with the whistle are perceived by the dog as gratifying, and are internalized as such. That is one way in which simple root mechanisms direct the development of elaborate behaviors, which consists of a variety of cues and activities. It has been demonstrated that humans can acquire new sexual cues by conditioning.[21]

In Pavlov's experiment, the sensation of food triggers the reactions of salivation and gratification. Food also triggers the process of learning new behaviors. The pitch of human voice is the analog of food when humans learn sexual behavior during childhood. The same way that the taste of food creates in the brain of the animal representations of targeted foods, the voice of a speaker creates in the brain of a child representation of sexual attraction targets. The pitch of the voice serves as a detector of the sex of the speaker. Based on this detection, the brain of the child builds representations of ‘man’ and ‘woman’. Through conditioning, the brain then uses these representations and builds mental models of who is sexually attractive, and what activities cause sexual arousal. Three main groups of brain centers are involved in the development of the mental records: the auditory system provides the root sensory cues; emotion centers, such as the amygdala, provide root emotional cues, and controllers of the physical aspects of the behavior, such as the hypothalamus, provide the connections to the sex organs. Based on the hardware of the auditory system and its connections to brain centers, such as the hypothalamus, some children develop sexual attraction to men, and others to women.[1][2]

Sexual orientation emerges at puberty. At puberty, boys and girls whose physical-sex-controllers have been innately tuned to women’s voice will be sexually attracted to women. At puberty, boys and girls whose physical-sex-controllers have been innately tuned to men’s voice will be sexually attracted to men. Boys and girls whose physical-sex-controllers have been initially tuned to men’s and women’s voice in the same amount will be sexually attracted, at puberty, to both men and women.[1][2]

The mental roots[edit]

Voice is generated and detected by genetically controlled organs, which are sex differentiated. It is robust and universal – it is one of the most reliable and commonly used cues for detecting the sex of a person. The distinction between men’s and women’s voices is based on differences in sound frequencies. Those are detected and processed by the inner ear and by the auditory neural networks, which project that information to various brain areas.[19][20] It was found that concentration of sex hormones affects the development and connectivity of neural networks,[22][23] and thus the outcomes of information that they process.

The root cues of human voice are sufficient, but not necessary, for the development of sexual orientation. Other cues may also play a role. For instance, after puberty, other root cues that depend on experiencing sexual pleasures come into play. Also, in deaf children, other mechanisms, which are still unexplored, replace the reliance on sound.[1][2]

In addition to sensory cues, also arousal cues contribute to the identification of targets of sexual attraction. It was suggested[1][2] that a combination of two innate emotions, fear and the feeling of safety, is a root cue of sexual arousal. These emotions are genetic, universal and robust. In general, their combination creates excitement. For example, the excitement of riding a roller coaster or driving a fast car is attributed to a combination of the feelings of fear and safety. Analysis has shown [1][2] that a common thread of many sexual fantasies and behaviors is a combination of those emotions.

References[edit]

  1. 1.0 1.1 1.2 1.3 1.4 1.5 Salu, Y. The roots of sexual arousal and sexual orientation. Medical Hypotheses 76 (2011) 384-387. doi:10.1016/j.mehy.2010.10.048, PMID 21095066, Preprint: http:/ / www.micropsychology. org/ The_Roots_of_Sexual_Arousal_and_Sexual_Orientation. htm.
  2. 2.0 2.1 2.2 2.3 2.4 2.5 Salu Y. Micropsychology, ISBN 1-4348-4781-0, Create Space, 2008; pp 31-78 Cite error: Invalid <ref> tag; name "S2" defined multiple times with different content
  3. Meyer-Bahlburg HF. Sex hormones and female homosexuality: A critical examination. Arch. Sex. Behav. 1979, vol 8, 2101-119.
  4. Banks A, Gartrell NK. Hormones and sexual orientation: a questionable link, J. Homosex 1995; 30, 247-268.
  5. Meyer-Bahlburg HF, Dolezal C, Baker SW, Carlson AD, Obeid JS, New MI. Prenatal androgenization affects gender-related behavior but not gender identity in 5-12-year-old girls with congenital adrenal hyperplasia. Arch Sex Behav. 2004; 33, 97-104.
  6. Gooren L. The biology of human psychosexual differentiation. Horm. Behav 2006; 50, 589-601.
  7. Golombok S., Tasker F. Children in lesbian and gay families: theories and evidence. Ann. Rev. of Sex Res., 1994; 5, 73–100.
  8. Tasker F. Children in Lesbian-Led Families: A Review. Clinical Child Psychology and Psychiatry 1999; 4, 153-166.
  9. LeVay S. A difference in hypothalamic structure between heterosexual and homosexual men. Science. 1991;253:1034–1037.
  10. Kinnunen LH, Moltz H, Metz J, Cooper M. Differential brain activation in exclusively homosexual and heterosexual men produced by the selective serotonin reuptake inhibitor, fluoxetine. Brain Res. 2004;1024:251–254.
  11. Savic I, Berglund H, Lindström P. Brain response to putative pheromones in homosexual men. Proc Natl Acad Sci USA. 2005;102:7356–7361.
  12. Berglund H, Lindström P, Savic I. Brain response to putative pheromones in lesbian women. Proc Natl Acad Sci USA. 2006;103:8269–8274.
  13. Swaab DF, Chung WC, Kruijver FP, Hofman MA, Ishunina TA. Sexual differentiation of the human hypothalamus. Adv Exp Med Biol. 2002;511:75-100; discussion 100-5.
  14. Rupp H, Wallen, K. Sex Differences in Response to Visual Sexual Stimuli: A Review. Arch Sex Behav. 2008; 37(2): 206–218.
  15. Giuliano F, Rampin O. Neural control of erection. Physiol Behav. 2004; 83(2):189-201.
  16. Berman JR. Physiology of female sexual function and dysfunction. International Journal of Impotence Research 2005; 17, S44–S51.
  17. Giedd JN, Castellanos FX, Rajapakse JC, Vaituzis AC, Rapoport JL. Sexual dimorphism of the developing human brain. J Am Acad Child Adolesc Psychiatry. 2001;40(9):1012-20.
  18. Durston S, Hulshoff Pol HE, Casey BJ, Giedd JN, Buitelaar JK, van Engeland H. Anatomical MRI of the developing human brain: what have we learned? J. Am. Acad.Child Adolesc. Psychiatry, 2001; 40(9):1012–1020.
  19. 19.0 19.1 McFadden D. Masculinization of the Mammalian Cochlea. Hear Res. 2009; 252(1-2): 37–48.
  20. 20.0 20.1 McFadden D, Champlin CA. Comparison of auditory evoked potentials in heterosexual, homosexual, and bisexual males and females. J Assoc Res Otolaryngol. 2000;1(1):89-99.
  21. Klucken T, Schweckendiek J, Merz CJ, Tabbert K, Walter B, Kagerer S, Vaitl D, Stark R. Neural activations of the acquisition of conditioned sexual arousal: effects of contingency awareness and sex. J Sex Med. 2009; 6(11):3071-85.
  22. Tobet S, Knoll G, Hartshor C, et al. Brain sex differences and hormone influences; A moving experience? J Neuroendocrinol. 2009; 21(4): 387–392.
  23. Tobet SA, Hanna IK. Ontogeny of sex differences in the mammalian hypothalamus and preoptic area. Adv Exp Med Biol. 2002;511:75-100; discussion 100-5.


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