The multicomponent phytopharmaceutical SKI306X inhibits in vitro cartilage degradation and the production of inflammatory mediators.

Clinical studies have demonstrated that SKI306X, a purified preparation of three medicinal plants, relieves joint pain and improves functionality in osteoarthritis patients. To study the biological action of SKI306X, bovine cartilage explants and human peripheral blood mononuclear cells (PBMC) were stimulated with IL-1 beta and lipopolysaccharide (LPS) respectively, in the presence or absence of SKI306X and its individual composites. All tested compounds inhibited dose-dependently IL-1 beta-induced proteoglycan release and nitric oxide production by cartilage, indicating cartilage protective activity. SKI306X and two of its compounds inhibited PGE(2), TNF-alpha and IL-1 beta production by LPS-stimulated PBMC, indicating anti-inflammatory activity. These results demonstrate that the biological effect of SKI306X is at least bipartite: (1) cartilage protective and (2) anti-inflammatory. The observed anti-inflammatory effects may provide an explanation for the outcome of the clinical studies. Long-term clinical trails are necessary to elucidate whether the in vitro cartilage protective activity results in disease-modifying effects.

Immunomodulatory and anti-inflammatory activity of Picrorhiza scrophulariiflora.

Extracts of the rhizomes of Picrorhiza scrophulariiflora Pennell (Scrophulariaceae) were investigated for their in vitro and in vivo immunomodulatory properties. Diethyl ether extracts showed potent inhibitory activity towards the classical pathway of the complement system, the respiratory burst of activated polymorphonuclear leukocytes, and mitogen-induced proliferation of T-lymphocytes. Furthermore, such extracts showed anti-inflammatory activity towards carrageenan-induced paw edema. No effects were observed in experimentally induced arthritis in mice.

Inhibition of T-lymphocyte proliferation by cucurbitacins from Picrorhiza scrophulariaeflora.

Two cucurbitacin aglycons were isolated from the dried rhizomes of Picrorhiza scrophulariaeflora and were identified as 25-acetoxy-2,3, 16,20-tetrahydroxy-9-methyl-19-norlanosta-5,23-dien-22-one (picracin, 1) and 2,3,16,20,25-pentahydroxy-9-methyl-19-norlanosta-5, 23-dien-22-one (deacetylpicracin, 2). Both compounds inhibit mitogen-induced T-lymphocyte proliferation at an IC(50) value of 1 microM.

Observations on the influence of intestinal spirochaetosis in broiler breeders on the performance of their progeny and on egg production.

Observations were made on the effect of avian intestinal spirochaetosis (AIS) in eight broiler breeder flocks on the performance of their commercial broiler progeny flocks, and also on the production of eggs and the selection of hatching eggs. The effect of treatment on egg production was analysed. The broiler breeder flocks were examined for the presence or absence of antibodies, spirochaetes and clinical signs of AIS, and correlated with the performance data from 136 commercial broiler flocks produced by them. Broiler flocks from affected breeders with clinical signs of AIS had a poorer feed conversion of approximately 90 g per kg growth, an increased number of weak chicks, slower growth and poorer feed digestion than the offspring of unaffected flocks including those previously infected with AIS but without clinical signs. Breeder flocks with clinical signs produced 7.5% less eggs than unaffected flocks. A larger number of eggs (+ 3%) was considered to have insufficient weight for successful hatching. Treatment of hens before the onset of lay prevented the negative effects on egg production but later treatment was less effective. These findings indicate that AIS in broiler breeder flocks is associated with significant production losses through decreased broiler flock performance and decreased egg production and quality.

Ayurvedic herbal drugs with possible cytostatic activity.

Ayurveda is considered to be the traditional science of health in India and is based on the principle of subjectivity. All matter is composed of five basic elements, which can be perceived by the five sense organs. All food and drugs are classified according to their pharmacological properties, which are derived from these five elements. To investigate which Ayurvedic plants might have cytostatic activity, an Ayurvedic model for the pathogenesis of cancer was made. Based on this, selection criteria were formed, that were used to select plants from a list of Ayurvedic herbal drugs. Some of the selected species could be collected in India and Nepal. The dried material of 14 species was submitted to ethanol (70% v/v) extraction and the extracts were tested for cytotoxicity on COLO 320 tumour cells, using the microculture tetrazolium (MTT) assay. The IC50-value, the concentration causing 50% growth inhibition of the tumour cells, was used as a parameter for cytotoxicity. Extracts of the flowers of Calotropis procera (Ait.) R. Br. (Asclepiadaceae) and of the nuts of Semecarpus anacardium L.f. (Anacardiaceae) displayed the strongest cytotoxic effect with IC50-values of 1.4 micrograms/ml and 1.6 micrograms/ml, respectively. The extracts of several other plants did not show a cytotoxic effect up to 100 micrograms/ml, the highest concentration tested.

Infection of broiler parent hens with avian intestinal spirochaetes: effects on egg production and chick quality.

Broiler parent hens were inoculated with avian intestinal spirochaetes several weeks before the onset of egg production. The infection persisted, wet droppings developed, and egg production, mean egg weight and carotenoid contents of the eggs were decreased. Hatching eggs were collected and incubated. In broilers which hatched from these eggs, reduced gain in body weight at 2 and 3 weeks of age, wet droppings, low plasma carotenoid concentration and elevated alkaline phosphatase activity in the blood plasma were observed. Spirochaetes were not detected in these broilers. These findings demonstrated the deleterious effects on chick quality of parental infection with avian intestinal spirochaetes. Avian intestinal spirochaetosis was diagnosed in about 2.5% of all submissions from reproductive flocks in 1991.

Infection of broiler chicks (Gallus domesticus) with human intestinal spirochaetes.

One-day-old broiler chicks were infected orally with spirochaetes isolated from cases of intestinal disorder in humans. Three different isolates were studied in an experiment of 22 days duration. No signs of clinical disease were observed; the infection did not cause changes in the concentration of carotenoids or in the activity of alkaline phosphatase in the serum. Spirochaetes were shed in the caecal faeces. At autopsy, no lesions were seen in the intestinal tracts of the birds. Large numbers of spirochaetes were present in the caecum of 30 to 100% of the infected birds; in a few birds small numbers of spirochaetes were observed in scrapings from the mucosa of the small intestine. On histological examination massive colonisation of the caecal mucosa was observed. Spirochaetes of two isolates had invaded the caecal mucosa and for one of these, they were found between enterocytes, but not below the basement membrane. The other isolate had produced gap-like lesions, subepithelial accumulations of spirochaetes and focal erosion. No signs of an inflammatory reaction were observed.

Influence of infection with avian intestinal spirochaetes on the faeces of laying hens.

Laying hens of 20 weeks of age were infected with avian intestinal spirochaetes (isolate 1380). After 20 weeks it was found that most infected birds shed 10(7) or more spirochaetes/ml caecal faeces. Faecal dry matter content was not significantly influenced by the infection, but the amount of crude fat in the faecal dry matter increased by more than 25%.

Spirochaetosis in broilers.

One-day-old broilers were inoculated with spirochaetes (isolate 1380); the inocula consisting either of spirochaetes derived from plate culture or from intestinal homogenates of previously infected birds. After 13 to 15, and 21 days after inoculation growth was depressed, serum concentrations of protein lipid, carotenoids and bilirubin were decreased and the fat content of the faeces was increased. The activity of alkaline phosphatase in the serum was increased but the activities of tau-glutamyl transferase, sorbitol dehydrogenase, aspartate aminotransferase and alanine aminotransferase of the infected groups were not affected. These findings indicate impaired resorption in the smaller intestine which cannot be explained from a direct effect of the spirochaetes on the smaller intestinal wall nor from pathological changes in the liver.

Observations on avian intestinal spirochaetosis.

Three SPF-laying hens were inoculated into the crop with avian intestinal spirochaetes which previously had been passaged in broiler chicks by oral inoculation (isolate 1380). Mild persisting gastrointestinal disorder developed; at nine months post inoculation spirochaetes were readily demonstrated in caecal faeces. Histologic examination of the caecal mucosa revealed many spirochaetes covering the mucosal surface and filling up the crypts lumina. Spirochaetes were found in intra- and subepithelial locations and in gaps running through the epithelium. These gaps often opened into subepithelial cavities crowded with spirochaetes ('gaplike lesions'). These lesions were seen mostly on the tips of the villi and in the deeper parts of the crypts. Massive erosion or desquamation of epithelium heavily infested by spirochaetes occurred. These findings indicate colonisation of the mucosal surface and of the crypts, penetration of the mucosa and colonisation of subepithelial compartments with spirochasetes in poultry suffering from intestinal spirochaetosis.

Incidence of spirochaetal infections in cases of intestinal disorder in chickens.

The incidence of intestinal spirochaetes was determined using direct fluorescent antibody microscopy on faecal and mucosal samples from chickens. Of 134 flocks with intestinal disorders 27.6% were found to be positive, but only 4.4% (of 45 flocks) were positive where signs of enteritis were absent. Flocks housed in cages or with access to litter were equally affected. No evidence was found for pigs as an aetiological factor.

Infectious typhlitis in chickens caused by spirochetes.

A weakly haemolytic spirochete was detected with an unabsorbed fluorescent antiserum to Treponema hyodysenteriae in smears and cultures of scrapings of caecal mucosa of laying hens with diarrhoea. Two groups of experimental chickens were fed a pure culture of this spirochete or homogenated intestinal contents of affected birds. Both groups showed clinical signs of disease such as increased water content of faecal material and slight retardation of growth. A non-specific typhlitis which histologically resembled milder forms of swine dysentery was seen in the birds from which spirochetes were isolated. The isolate obtained differed in cultural, biochemical, anti-genic and morphological characteristics from T. hyodysenteriae. The pathological significance of intestinal spirochetes and their possible epidemiological relation to swine dysentery are discussed.

Swine dysentery in a sow herd. I. Clinical manifestation and elimination of the disease with a combination of lincomycin and spectinomycin.

An acute outbreak of swine dysentery (Doyle) on a farrowing farm is described. Besides clinical signs of enteritis a general loss of condition was seen throughout the herd. This resulted in a decreased fertility and breeding performance among sows and an increase in piglet mortality. Several dehydrated sows aborted. The outbreak was stopped by oral treatment with lincomycin/spectinomycin 1:1. In the course of the treatment all animals and buildings were washed and disinfected. The use of pharmacotherapeutics in treating swine dysentery is discussed with emphasis on the involuntary induction of carriers.

Swine dysentery in a sow herd. II. Comparison of a direct fluorescent antibody test with selective culture in the laboratory diagnosis.

During and after an outbreak of swine dysentery (Doyle) two diagnostic techniques were compared: a direct fluorescent antibody test and a selective culture method. The latter was more sensitive, provided the animals were not medicated and the samples were processed on the day of collection. The widespread use of chemoprophylaxis makes selective culture as a diagnostic aid under Dutch conditions highly impractical.