Androstenol, also known as 5α-androst-16-en-3α-ol, is a steroidal pheromone and neurosteroid in humans and other mammals, notably pigs. It possesses a characteristic musk-like odor. Androstenol, or a derivative, is found in truffles. This was offered as an explanation for how pigs locate them deep in the ground: Androstenol is produced in the saliva of male pigs. However, experiments in France using pigs to scent truffles, truffle extract and purified androstenol showed that pigs responded to the first two, but ignored the androstenol. A positional isomer of androstenol, 3β-androstenol, is also endogenous to humans, behaving as a pheromone and contributing to axillary odor.
Considerable amounts of androstenol are present in human urine, and it is also present in the blood plasma and saliva of humans and pigs as well as in the axillary sweat of humans. Due to its ability to cross the blood-brain-barrier, androstenol is likely present in the central nervous system as well.
Biological activity
Androstenol, similarly to the related endogenous steroids 3α-androstanediol and androsterone, has been found to act as a potent positive allosteric modulator of the GABAA. It has been proposed that this action may mediate the pheromone effects of androstenol. Moreover, as androstadienol, androstadienone, and androstenone are all converted into androstenol, it could mediate their pheromone effects as well. In animals, androstenol has been found to produce anxiolytic-like, antidepressant-like, and anticonvulsant effects. Androstenol has also been found to modify the behavioral and social responses of humans. In addition, androstenol has been found to decreaseluteinizing hormone pulse frequency during the follicular phase of the human menstrual cycle. In accordance, it has been proposed that androstenol may be involved in the menstrual synchrony of women. In contrast to androstenol, its 3β-epimer, 3β-androstenol, does not potentiate the GABAA receptor, even at high concentrations. This is in accordance with other 3β-hydroxy steroids, including isopregnanolone, epipregnanolone, 3β-dihydroprogesterone, and 3β-androstanediol, which similarly do not act as such, in contrast to their 3α-hydroxy variants. Androstenol, along with several isomers of androstanol, is an antagonist of the constitutive androstane receptor. Androstenol has minimal or no androgenic activity.