In vivo kinetic study on uptake and distribution of intramuscular tritium-labeled polysulfated glycosaminoglycan in equine body fluid compartments and articular cartilage in an osteochondrial defect model

The uptake and distribution of intramuscularly (IM) administered tritium-labeled polysulfated glycosaminoglycan (³H-PSGAG) in serum, synovial fluid, and articular cartilage of eight horses was quantitated, and hyaluronic acid (HA) concentration of the middle carpal joint was evaluated in a pharmacokinetic study. A full-thickness articular cartilage defect, created on the distal articular surface of the left radial carpal bone of each horse served as an osteochondral defect model. ³H-PSGAG (500 mg) was injected IM, between 14 and 35 days after creation of the defects. Scintillation analysis of serum and synovial fluid, collected from both middle carpal joints at specific predetermined times up to 96 hours post-injection, revealed mean ³H-PSGAG concentrations peaked at 2 hours post-injection. ³H-PSGAG was detected in cartilage and subchondral bone 96 hours post-injection in samples from all eight horses. There were no statistically significant differences in ³H-PSGAG concentration of synovial fluid or cartilage between cartilage defect and control (right middle carpal) joints.

HA assay of synovial fluid revealed concentrations significantly increased at 24, 48, and 96 hours post-injection in both joints. The concentration nearly doubled 48 hours post-injection. However, no statistically significant differences were found between synovial concentrations of HA in cartilage defect and control joints.

³H-PSGAG administered IM to horses, was distributed in the blood, synovial fluid, and articular cartilage. HA concentrations in synovial fluid increased after IM administration of polysulfated glycosaminoglycan.     

Fever and acute phase response induced in dwarf goats by endotoxin and bovine and human recombinant tumour necrosis factor alpha

Tumour necrosis factor (TNF), a polypeptide produced by mononuclear phagocytes, has been implicated as an important mediator of inflammatory processes and of clinical manifestations in acute infectious diseases. To study further the potential role of TNF in infectious diseases, recombinant Escherichia coli (E. coli) derived human (r.HuTNF-alpha) and bovine TNF (r.BoTNF-alpha) were intravenously (i.v.) administered in dwarf goats. Rectal temperature, heart rate, rumen motility, plasma zinc and iron concentrations, and certain other blood biochemical and haematological values were studied and compared with the changes seen after E. coli endotoxin (LPS) was administered (dose: 0.1 microgram/kg i.v.). Following a single injection of 4 micrograms/kg of r.BoTNF-alpha, shivering and biphasic febrile response were observed, accompanied by tachycardia, inhibition of rumen contractions, drop in plasma zinc and iron concentrations, lymphopenia, and neutropenia followed by neutrophilia. The i.v. administration of a single injection of 4 micrograms/kg r.HuTNF-alpha induced shivering and biphasic febrile responses, accompanied by anorexia and a similar drop in plasma trace metal concentrations when compared with r.BoTNF-alpha-treated goats. The TNF-alpha-induced symptoms were essentially the same as those that occurred after LPS administration. However, the time of onset of these changes after the injection of TNF-alpha was significantly shorter than after LPS. Moreover, the r.BoTNF-alpha induced a longer lasting neutrophilic leucopenia, less neutrophilia, and a more persistent lymphopenia than after LPS injection. Neither r.BoTNF-alpha nor LPS caused severe haemo-concentration. Furthermore, no cross-tolerance between r.BoTNF-alpha and LPS could be demonstrated. We conclude that both r.BoTNF-alpha and r.HuTNF-alpha induce many of the physiologic, haematologic and metabolic changes that characterize the acute phase response to LPS. The overlapping biological activities of r.BoTNF-alpha, r.HuTNF-alpha and LPS in dwarf goats may indicate that both recombinant tumour necrosis factors have some homology with caprine TNF-alpha.     

Single species island biogeography and Montana mule deer

The theory of island biogeography supplemented with dynamic concepts from other areas of biology can be applied to a single species. Data series from mule deer Odocoileus hemonius hemonius populations inhabiting diverse mountain as well as prairie habitats were compared. The fawn-doe ratios obtained at 6 months of age were inversely correlated (r = ?0·97; p < 0·01) with ‘island’ size as indicated by the percentage of cover. Populations inhabiting small islands of cover in the prairie consistently had higher winter fawn-doe ratios than those of the relatively secure mountain habitats. Cover fragmentation and low security level of the prairi populations relates to a high annual turnover rate compared with that of the mountain populations. The impact of cover fragmentation is consistent with this interpretation of theory which pictures reproduction as annual recolonisation. This approach may be useful in predicting hunting and ecological impact effects.     

Peridermium pini (Pers.) Lev. and the Resin-top Disease of Scots Pine: II. Lesion Anatomy

The stages in the formation of Peridermium pini lesions aredescribed. The hyphae of the parasite were septate, uninucleate,and intercellular, with unbranched haustoria penetrating allphloem cells and xylem parenchyma cells. Lesion extension occurredby apical growth of the hyphae along the outer edge of the functionalphloem. The hyphae stretched unbroken across the active cambium.Active centripetal and longitudinal growth of the mycelium occurredin the resin ducts of the xylem, the hyphae commonly reachingthe pith. Spermogonia were produced in late summer and fall,aecia appeared in spring. In lesion xylem, tracheids were shorter,rays taller, more numerous and wider, but ray cell height remainedunchanged. Fusiform rays increased in number and size and verticalresin ducts increased in number. Changes in xylem tissues didnot become evident until two to four years after invasion ofthe cambium by the mycelium. Invasion of the secondary phloemresulted in an increase in number and size of the longitudinalphloem parenchmya cells, while changes in phloem rays were similarto those in xylem rays.