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Use of post mortem and in vitro tissue specimens for X-ray microanalysis.

Post mortem changes in the distribution of elements, as well as changes induced by dissection and incubation of tissue slices, were investigated by X-ray microanalysis of brain tissue, liver, pancreas and submandibular gland. Dissection itself causes minor changes in the intracellular ionic concentrations, but even a brief exposure of dissected tissue slices to a physiological buffer causes an increase in intracellular Na and Cl and a decrease in intracellular K concentration. The effect is most marked in brain tissue and least marked in submandibular gland slices. Incubation in fluid resembling the extracellular compartment in its ion composition results in a further increase of Na and Cl in brain tissue (cortex and hippocampus) and liver; in pancreas and submandibular gland, on the other hand, a stable situation throughout 2 h of incubation can be obtained. Incubation at lower temperature, and exchanging NaCl in the incubation medium for Na gluconate, has only relatively minor effects on the intracellular K/Na ratio. Exchanging the NaCl for K gluconate results in a high intracellular K/Na ratio throughout the incubation, but morphological evidence of tissue oedema was nevertheless observed. Physiological changes in intracellular ion content induced by cholinergic stimulation are similar in in vitro preparations as compared with stimulation in situ. The effect of dissection and brief incubation on the ionic composition of brain tissue is less pronounced 6 h after death than in a living, anaesthetized animal, but this is largely due to the post mortem changes that already have taken place.

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Post-mortem changes of neurotransmitter concentrations in the rat brain regions.

Using High Performance Liquid Chromatography coupled with electrochemical detection the post-mortem stability of noradrenaline (NA), dopamine (DA), serotonin (5-HT) and 5-hydroxy indole acetic acid (5-HIAA) were examined in the rat hypothalamus, amygdala, cerebral cortex, cerebellum and corpus striatum over an 8 hour time period. Changes in concentrations of the different neurotransmitters were less than it might be expected. The significant changes were: a. A fall in NA levels in the cerebral cortex by 4 hours and in the hypothalamus at 8 hours. b. A reduction in DA concentrations in the corpus striatum at 8 hours but a two fold rise of levels in the hypothalamus at 1 and 2 hours. c. A four-fold increase in 5-HT concentrations in the amygdala throughout the 8 hours studied. The results indicate that for comparative studies on post-mortem brain tissue correction factors should be employed to take into account differential changes in the concentrations of the various neurotransmitters.

Animals↗

Continuous monitoring of the position of the ferret mandibular canine tooth to enable comparisons with the continuously-growing rabbit incisor.

A variable capacitance displacement transducer, previously employed for continuously monitoring movements of the rabbit mandibular incisor, was modified for use with the ferret mandibular canine. Comparing this tooth of limited growth with the tooth of continuous growth, similarities were seen in the reactions to extrusive loads and the responses at death. For the tooth of limited growth, however, less creep was seen with extrusive loading and hexamethonium did not produce changes in tooth position.

Animals↗

Ultrastructural and ultrahistochemical studies of post-mortem changes and effects of hypoxia in the bony fish heart.

The ultrastructural and ultrahistochemical properties of post-mortem changed and hypoxic heart tissue of Gadus virens, Gadus morhua, and Poecilia reticulata are described. When incubated for 0.5 h at 20 degrees C the cardiac tissue is rich in vacuoles and endocardial blebs. After 1 h of incubation, the myocardial mitochondria contain some amorphous, flocculent densities (50-100 nm), which seem to increase in number and size with advancing incubation time. Furthermore, the mitochondria in heart perfused by a calcium-containing solution for 7 h at hypoxic conditions contain large numbers of highly electron dense annular-granules (35-50 nm). Numerous myocardial mitochondria exclude tannic acid in tissue incubated or perfused for up to 1.5 h, whereas all mitochondria seem permeated by this substance when incubated for 5 h or perfused at hypoxic condition for 7 h. The amount of myocardial glycogen in P. reticulata is greatly reduced in the hypoxic heart compared with the normal heart. The mitochondria and contractile material, however, seem to tolerate oxygen depletion remarkably well. The present results are compared with those reported previously for the post-mortem changes and hypoxic hearts in fishes and mammals.

Animals↗