A unique urinary constituent, 6-hydroxy-6-methyl-3-heptanone, is a pheromone that accelerates puberty in female mice.

BACKGROUND: Olfactorily mediated puberty acceleration in female mice (measured by an increase in uterine weight) has been observed since the 1960s without the active chemosignal being structurally identified. There are many controversies in the literature as to whether this male-originated pheromone is a volatile substance. We investigated the chemical nature of the urinary fractions that are responsible for the characteristic uterine weight increases. RESULTS: The active pheromone was identified as 5,5-dimethyl-2-ethyltetrahydrofuran-2-ol and/or its open-chain tautomer (6-hydroxy-6-methyl-3-heptanone). A series of cyclic vinyl ethers were isolated from chromatographically active fractions of the urine. Because these compounds did not accelerate puberty, we postulated that these ethers were degradation products of a lactol (5,5-dimethyl-2-ethyltetrahydrofuran-2-ol). The lactol was then detected directly in the mouse urine extract using a silylation agent. Synthetic 6-hydroxy-6-methyl-3-heptanone had strong biological activity, whereas its close structural analogs did not. CONCLUSIONS: The male house mouse excretes into its urine a large quantity of a volatile substance that has a unique lactol/hydroxyketone structure. This substance is capable of binding to the less volatile urinary constituents, such as proteins or peptides, and is active in puberty-acceleration bioassays. The controversies regarding the volatility of the puberty-accelerating pheromones can now be explained by considering a complex of volatile lactol/hydroxyketone and urinary proteins.

Socio-sexual olfactory preference in female mice: attractiveness of synthetic chemosignals.

Two sesquiterpenic compounds, E,E,-alpha-farnesene and E-beta-farnesene, which were previously found as major constituents of the male mouse preputial glands, were tested for their attractiveness to female mice. Sexually naive and sexually experienced females were given the opportunity to choose between natural stimuli and synthetic analogs of preputial chemosignals. Naive females preferred investigating the odors of intact males' urine and synthetic farnesenes when spiked in high concentration in bladder urine or water over control stimulus (water or bladder urine alone). Investigatory preference was not observed when synthetic farnesenes were presented to naive females in low concentration, i.e., only twice the natural content in the dominant male urine. However, sexually experienced females were clearly able to recognize and prefer samples with synthetic farnesenes, even in low concentration. We suggest that those sesquiterpenic compounds may play a wide-ranging role in the female recognition of sexually mature and socially dominant males.

Urine marking in male mice: responses to natural and synthetic chemosignals.

The effects of natural chemosignals and their synthetic terpenic analogs on urinary marking in mice were investigated. The number and size of marking spots, and percentage of response and avoidance/counter-marking behavior, were measured for dominant and subordinate males. The males' marking behavior was found to differ significantly based on the type of stimulus sample used. Marking behavior in response to female urine was significantly altered by addition of synthetic analogs (farnesene isomers) to it. Both dominant and subordinate males avoided marking the section of the test area soiled with stimulus samples containing either natural or synthetic farnesenes. Differential responses of the dominant and subordinate male mice were observed.

Puberty-affecting synthetic analogs of urinary chemosignals in the house mouse, Mus domesticus.

Endocrinologically- and socially-dependent volatile constituents of female mouse urine, identified in a previous study, were tested for their capability to accelerate puberty and extend the estrous period in young females. Several volatile ketones advanced puberty by approximately three days and extended the period of vaginal cornification in 55-75% of exposed females. High High concentrations of these substances were capable of overriding the known puberty-delaying chemosignals. Volatile cyclic enol ethers were also effective in extending estrus, but not puberty acceleration.

A molecular and carbon isotopic study towards the origin and diagenetic fate of diaromatic carotenoids.

Pyrolysates of high-molecular-weight sedimentary fractions of the Duvernay Formation (Western Canada Basin) are dominated by 1,2,3,4- and 1,2,3,5-tetramethylbenzene, which, generated via beta-cleavage, indicate the presence of diaromatic carotenoids in the macromolecular aggregates. This was substantiated by desulphurization of sulphur-rich aggregates of the polar fraction, which released (partly) hydrogenated carotenoids. Furthermore, these components were important constituents of the aromatic hydrocarbon fractions and related oils. Apart from renieratane and isorenieratane, 1H NMR analysis established the aromatic substitution pattern of the most abundant component present, which was identified as a diaromatic compound with an unprecedented 2,3,6-/3,4,5-trimethyl aromatic substitution pattern. Molecular and isotopic analyses of both soluble and insoluble fractions of organic matter revealed relationships between diagenetically-derived carotenoids found in bitumen and related oils and their precursors incorporated into high-molecular-weight fractions. Aryl isoprenoids, important components in extracts and oils, were apparently derived from thermal cracking of bound diaromatic carotenoids rather than cleavage of free carotenoids as previously suggested. Furthermore, products derived from diaromatic carotenoids were substantially enriched in 13C relative to n-alkanes of algal origin. Together with the characteristic carotenoids, this isotopic enrichment provides evidence of significant contributions from photosynthetic green sulphur bacteria (Chlorobiaceae), which fix carbon via the reversed tricarboxylic acid (TCA) cycle. In spite of the prominence of these molecular signals, the overall isotopic composition of the organic matter indicated that only a very small portion of the preserved organic carbon was derived from the biomass of photosynthetic green sulphur bacteria.

Direct determination of trace amounts of chlorophenols in fresh water, waste water and sea water.

Chlorophenols were acetylated and the derivatives extracted by the simultaneous addition of acetic anhydride and hexane directly to the water sample. The extracts were then analysed by glass capillary column gas chromatography with electron-capture detection. Determination of chlorinated phenols at micrograms/l concentration levels requires only 5 ml of sample. At ng/l levels a 100-ml sample is sufficient. The total time of analysis is 18 min per sample. A comparison between pentafluorobenzoylation and acetylation showed that the acetylated derivatives of chlorophenol isomers separated better on the column. The method has been applied to drinking water, sea water and waste water from a sulphate pulp mill.

Thet complex of the mouse: Chemical characterization by urinary volatile profiles.

Urine samples from C3H congenic house mice (Mus domesticus) differing only at thet complex were examined by capillary gas chromatography to assess variations in the volatile components that may cause olfactory discrimination between animals bearingt lethal and+(wild-type) haplotypes. Urine was collected from 192 males and females varying in age from 1 to 9 months. C3H congenic mice that have the same genetic background at all loci but differed in theirt complex genotypes: +/ +, +/tw1,T/t w1, T/+ were used. No urinary volatiles were unique to thet complex. However, significant differences amongt complex genotypes and among ages occurred for concentrations of 12 male volatiles and four female volatiles. Usually young males (1-2 months of age) had significantly higher concentrations of cyclic enol ethers and ketones than older males (4-9 months of age). Moreover, some urinary volatiles (cyclic enol ethers, one ketone, dehydrobrevicomin, and thiazoline) were excreted in the urine of T/+and/orT/t males in significantly higher concentration than in the urine of +/+ males. Age andt complex genotype influences on the urinary volatiles in females were observed for four ketones. Gas chromatography of urinary components has the potential to be used in field studies of thet complex because the two t complex genotypes found in wild populations, +/+ and +/t, had significant differences in concentration for two males volatiles and three female volatiles.

Stereoselectivity in mammalian chemical communication: male mouse pheromones.

Two male mouse pheromones, 3,4-dehydro-exo-brevicomin (DHB) and 2-sec-butyldihydrothiazole (SBT), are chiral molecules which were previously tested in their respective bioassays as racemic mixtures. The focus of this study has been to determine the absolute configuration of their natural forms and its relation to stereospecific biological action. DHB was established as the R,R-enantiomer possessing biological activity. Due to an extremely easy racemization of SBT under very mild conditions, enantioselectivity of its transmission and its action at the receptor site appear to be of secondary importance.