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Different rations were used in successive experimental periods (Dried green feeds (I), fresh green feed from sugar beet tops (II), concentrates (III, IV), and maize silage (V), to test the effect they have on the structure and oxidative functions of the ruminal mucosa in cattle. Rations I, II, IV, and V were both energy and protein equivalent. Biopsy specimens from ruminal papillae were taken on the day when rations were suddenly changed and on the 21st and 22nd day of the feeding period; they were then investigated histologically and manometrically. It was found that some characteristics, (viz. the type and thickness of the stratum corneum, the thickness of epithelia, the size of cell nuclei in the stratum basale of the epitheliumas well as the state of the lamina propria and the oxygen uptake were subject to alterations depending on nutrition. Nutrition with energy-equivalent, but otherwise extremely different diets representing particular types of rations led to the development of different and quite specific functional states of the ruminal mucosa. All these functional states of the mucosa were found to be within the limits of normality but seemed to have a definitely more favourable functional effect in the case of rations I and IV than in the case of rations II and V. The feeding of concentrates (III, V) increased the energy intake to an amount of 6.6 kEFr, i.e. double that of the other rations, and brought about changes in quantitative parameters. These, in turn, indicated that proliferative and oxidative processes had been stimulated. Changes of this kind were accompanied by increases in the concentration of volatile fatty acids in the ruminal fluid which rose from a maximum of 9 mMol per 100 ml (ration IV) to 12.5 mMol per 100 ml (ration III). Immediately after any change in nutrition brought about by a change of rations, processes of adaptation occurred in the ruminal mucosa. A balanced state of the mucosa was again achieved after a period of not more than 3 weeks.

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Three non-lactating cows (Deutsches Schwarzbuntes Rind) with large ruminal fistulas were fed coarsely structured food. Within a trial period of 21 weeks infusion periods lasting 3 weeks alternated with equally long control periods (K). During the 3 infusion periods, 8.4 mMol of propionic acid (P), 14.8 mMol of acetic acid (E) and 4,5 mMol of butyric acid (B) per kg liveweight per day were administered through the fistula, the total quantity being 19 litres of solution. In the periods K1...4 the ruminal fluid contained an average of 68 Mol% E, 19 Mol% P, 13 Mol% B (maximum of 10.25 mMol free fatty acids (FFS) per 100 ml, minimum pH 6.4). In the course of the 10 hrs of infusion the Mol percentages of the particular acids infused increased to 27% P (maximum of 11.14 mMol FFS per 100 ml, minimum pH 6.4) or 79% E (maximum of 12,99 mMol FFS per 100 ml, minimum pH 6.0 (5.5)) or 25% B (maximum of 10.34 mMol FFS per 100 ml, minimum pH 6.0 (5.5)). Infusions of E and B had the most pronounced effect on the ruminal mucosa compared with the K periods. All fatty acids increased the process of keratinization and decreased the size of cell nuclei in the stratum basale. As specific effect, P infusions produced a thickening of the lamina propria; B infusions caused a thickening of the stratum germinativum (proliferative effect) while e infusions led to a drastically reduced thickness of villi (antiproliferative effect) due to reductions in the stratum germinativum and the lamina propria. According to the morphological situation high specific mucosal function is suggested during the B-period. The mucosa appeared quite normal during all periods investigated, with the exception of the E period, where hyperkeratosis, atrophy and necrosis were observed in 34% of the sample. Changes in the state of the mucosa appeared as early as 1 week after the beginning of the respective trial periods. Keratin consolidation was the primary cause for chemically induced keratosis. The development of hyperkeratosis seemed to be favoured if low pH values occurred in the rumen in combination with small amounts of metabolites inducing proliferation, both representing synergistic factors.

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