# Estrenes for inducing hypothalamic effects

**URL:** <https://pheromonetalk.com/t/estrenes-for-inducing-hypothalamic-effects/496>\
**Category:** Studies & Abstracts\
**Created:** [July 13, 2006, 11:11am UTC](https://pheromonetalk.com/t/estrenes-for-inducing-hypothalamic-effects/496 "2006-07-13T11:11:48Z")\
**Posts on this page:** 1\
**Page:** 1

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**Author:** ![itwow](https://sea2.discourse-cdn.com/flex016/user_avatar/pheromonetalk.com/itwow/32/1493_2.png) [@itwow](https://pheromonetalk.com/u/itwow)\
**Post date:** [July 13, 2006, 11:11am UTC](https://pheromonetalk.com/t/estrenes-for-inducing-hypothalamic-effects/496/1 "2006-07-13T11:11:48Z")

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> **[Estrenes for inducing hypothalamic effects - Pherin Corporation](https://www.freepatentsonline.com/5633392.html?s_id=25a1612519fd658844968b63e6f1d01c)**
>
> The invention relates to estrene steroids, which bind to neuroepithelial receptors. The steroid is preferably administered in the form of a pharmaceutical composition containing one or more pharmaceut

A = 1, 3, 5(10),16-Estratetraen-3-yl acetate  
B = Androsta-4,16-dien-3-one (i.e. **A1** )  
C = 1,3,5(10),16-Estratetraen-3-ol (i.e. **EST** )  
D = 3-Methoxy-Estra-1,3,5(10),16-tetraene  
E = Androsta-4,16-dien-3.alpha.-ol  
F = Androsta-4,16-dien-3.beta.-ol  
G = Androst-4-en-3-one  
H = Androsta-4,16-diene-3,6-dione  
J = 10,17-Dimethylgona-4,13(17)-dien-3-one  
K = 1,3,5(10),16-Estratetraen-3-ol-methyl ether [E0723-080 Steraloids]  
L = 1,3,5(10),16-Estratetraen-3-yl-propionate  
M = 1,3,5(10)-Estratrien-3-ol [R187798 (Aldrich)]

E12/N1 = Estra-1,3,5(10),16-tetraen-3,6.beta.-diol  
E8/N1 = 3-MethoxyEstra-2,5(10),16-triene  
E7/N1 = 10-HydroxyEstra-4,16-dien-3-one

OE = olfactory epithelium  
CNS = central nervous system  
EVG = Electro-vomeronasogram  
EOG = Electro-olfactgram

**EFFECTS ON THE EVG**

- A, C and D produced significant effects, that were consistent in all individual cases (males).

- Vomeropherins active in male subjects produced larger responses than the diluent. B, F and similar concentrations of olfactants induced significantly reduced responses in the male VNO.

- Among the vomeropherins, F produced the most significant differences within the group (females). Here, A induced a small effect that was significantly different from F.

- In both populations of subjects, active vomeropherins induced receptor responses having large standard deviations. When the frequency distribution of the effects of A and F was studied in males and females respectively, we found a bimodal distribution. The significance of this observation is being studied at this point.

E, a stereoisomer of F, does not stimulate the VNO in female subjects while F does. This is a demonstration of the specificity of VNO recognition of vomeropherins. In this regard it is interesting to note that while F is a superior vomeropherin, E generates a stronger olfactory effect than does F.

**EFFECTS ON THE EOG**

- In contrast to the sensitivity of the VNO to vomeropherins, the OE is less sensitive to these substances. This is true for both males and females.

- In this study, B was the only vomeropherin having significant effect in the OE.

- This finding reveals that at the concentrations used in our study, most vomeropherins are not effective stimulants of the olfactory receptors, but do have a clear effect on vomeronasal receptors.

**REFLEX EFFECTS**

- A and C induced a significant increase in skin temperature in 30 male subjects; however D induced significant temperature decrease.

- In 30 female subjects, B and F evoked a significant increase in skin temperature compared to A and C.

- In males, A, C and D significantly increased alpha cortical activity (D and A evoked the strongest effect).

- In females, B or F applied to the VNO increased alpha cortical independent of the response of olfactory receptors.

- The steroid E12/N1 exhibited the best EEG-alpha activity in men. The steroid E8/N1 exhibited the best EEG-beta activity in men.

- The steroid E7/N1 exhibited the best EEG-alpha activity in women. Additionally, it is noted that E7/N1 exhibited excellent organ response, as shown by the EVG data, in both men and women, but there were gender differences in the CNS (high EEG-alpha in women, high EEG-beta in men).

Sexual differences were noted in the specificities and effects of two groups of vomeropherins, A, C and D; and B and F.
