After I get home from the gym, shower and eat...I get on the computer to unwind and I am ready to go and can't shake the freaking thought!!

A few months ago I had decided to just stop and I would go 5-7 days without jerking off. I met a ton of girls during this time. I got "one-itis" with this one chick and totally gave up on what I was doing.

Now I'm going for it every night. This wouldn't be a problem except it makes me less motivated to go after girls. (edit) A LOT LESS motivated. My nerves kick in wayyyy more if I don't got the testosterone stored up.

Anyone else gone through something similar? Psh I hope I have this problem when I have a steady girl!!

Exercise, particularly heavy cardio, helps out a lot. It'll relax your mind and body without sacrificing testosterone.

You don't have a problem buddy, you're very healthy.

If you don't have a high sex drive you are NOT healthy. So enjoy it, eat well, lift weights (in good form) and study/practice game.

_________________
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On that note, anyone know of any good ways to boost your sex drive?

I notice a trend when your getting pussy you dont jack it when your not you do....aquire pussy

The common theme is always have something choking your dick and everything will be A ok

Actually there's evidence that ACUTE masterbation leads to decreased levels of testosterone in males. Keep in the sample size is too small to be clinical significant at n=10 (10 subjects). Take it with a grain of salt, or jizz.



World J Urol. 2001 Nov;19(5):377-82.
Endocrine response to masturbation-induced orgasm in healthy men following a 3-week sexual abstinence.
Exton MS, Krüger TH, Bursch N, Haake P, Knapp W, Schedlowski M, Hartmann U.
Source

Institut für Medizinische Psychologie, Universitätsklinikum Essen, Germany. michael.exton@uni-essen.de
Abstract

This current study examined the effect of a 3-week period of sexual abstinence on the neuroendocrine response to masturbation-induced orgasm. Hormonal and cardiovascular parameters were examined in ten healthy adult men during sexual arousal and masturbation-induced orgasm. Blood was drawn continuously and cardiovascular parameters were constantly monitored. This procedure was conducted for each participant twice, both before and after a 3-week period of sexual abstinence. Plasma was subsequently analysed for concentrations of adrenaline, noradrenaline, cortisol, prolactin, luteinizing hormone and testosterone concentrations. Orgasm increased blood pressure, heart rate, plasma catecholamines and prolactin. These effects were observed both before and after sexual abstinence. In contrast, although plasma testosterone was unaltered by orgasm, higher testosterone concentrations were observed following the period of abstinence. These data demonstrate that acute abstinence does not change the neuroendocrine response to orgasm but does produce elevated levels of testosterone in males.

Pharmacological and physiological aspects of sexual exhaustion in male rats

Alonso Fernández-Guasti*,
Gabriela Rodríguez-Manzo

Article first published online: 27 JUN 2003

DOI: 10.1111/1467-9450.00343

Issue
Scandinavian Journal of Psychology
Scandinavian Journal of Psychology

Volume 44, Issue 3, pages 257–263, July 2003


The present article reviews the current findings on the interesting phenomenon of sexual satiety. Knut Larsson in 1956 reported on the development of sexual exhaustion in the male rat after repeated copulation. We have studied the process and found the following results. (1) One day after 4 hours of ad libitum copulation, two-thirds of the population showed complete inhibition of sexual behavior, while the other third displayed a single ejaculatory series from which they did not recover. (2) Several pharmacological SPAM, including 8-OH-DPAT, yohimbine, naloxone and naltrexone, reverse this sexual satiety, indicating that the noradrenergic, serotonergic and opiate systems are involved in this process. Indeed, direct neurochemical determinations showed changes in various neurotransmitters during sexual exhaustion. (3) Given enough stimulation, by changing the stimulus female, sexual satiety was prevented, suggesting that there are motivational components of the sexual inhibition that characterizes sexual exhaustion. (4) The GABA antagonist bicuculline, or the electrical stimulation of the medial preoptic area, did not reverse sexual exhaustion. These data suggest, on the one hand, that sexual exhaustion and the postejaculatory interval (which is shortened by bicuculline administration) are not mediated by similar mechanisms and, on the other, that the medial preoptic area does not regulate sexual satiety. (5) The androgen receptor density in brain areas closely related to the expression of masculine sexual behavior, such as the medial preoptic nucleus, was drastically reduced in sexually exhausted animals. Such reduction was specific to certain brain areas and was not related to changes in the levels of androgens. These results suggest that changes in brain androgen receptors account for the inhibition of sexual behavior present during sexual exhaustion. (6) The recovery process of sexual satiety after 4 hours of ad libitum copulation reveals that, after 4 days, only 63% of the males are able to show sexual behavior while after 7 days all animals display copulatory activity.