157DISCUSSION SUMMARY Dr Krueger wondered whether elevated skin temperature or blood flow contributed to the increased corticoid penetration. However, in this model it was thought the thinner horny layer and hyperkeratosis were the major determining factors.
Synopsis The unsaponifiable lipidic fractions of avocado and soya bean were administered percutaneously, on the dorsal skin of hairless rats for 15 days, in a 5% sweet almond oil solution. This treatment produced a modification of dermal connective tissue components. The biochemical analysis showed an increase of soluble proteins, especially of salt soluble collagen together with a decrease of proteins insoluble in neutral buffer. The ratio, soluble proteins:insoluble proteins, increases as well as the ratio soluble collagen: insoluble collagen. These modifications can be considered as a result of the activation of connective tissue metabolism. The above results are in agreement with those obtained when the unsaponifiables were administered per os to rats.
Synopsis The non-saponifiable lipidic fractions of avocado and soya bean applied percutaneously to hairless rats for 15 days had been shown to produce biochemical modifications of dermal connective tissue components: increases of soluble collagen and of the ratio soluble collagen/insoluble collagen. In this present study, we tried to show whether these biochemical modifications could be confirmed by biophysical analytical methods and could affect the biochemical properties of the skin. The experiments were carried out on three groups of rats treated by application to the dorsal skin, either with 0.9% NaCl (control), or sweet almond oil (vehicle), or with a mixture of 2/3 soya bean and 1/3 avocado in solution at 5% of sweet almond oil (treated group). After 15 days treatment, the rats were killed and the skin of the treated area dissected. X-ray diffraction diagrams were recorded by varying the position of previously dried samples in controlled conditions. Results indicated that the vehicle decreased the orientation degree of collagen fibres, acting on their reticulation. The addition of the non-saponifiable fraction did not significantly add to the vehicle effect. The study of thermostability of the cutaneous collagen by differential scanning calorimetry showed that non-saponifiables increased the slope of the rise of temperature of denaturation. The quantity of heat absorbed during the denaturation (enthalpy variation) reached around 0.04 J mg(-1) of collagen in the control groups and did not exceed 0.03 J mg(-1) of collagen in the treated ones. Taken in conjunction with previous work it is probable that the non-saponifiables increase the proportion of soluble collagen. The elasticity of whole skin, determined by a static method using an Instron exten-siometer was significantly modified by treatment with non-saponifiables. They produced a decrease of the elasticity module. These results correspond to a decrease of collagen reticulation degree.
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