Changes in serum thyroxine and triiodothyronine concentrations during metamorphosis of the Southern Hemisphere Lamprey Geotria australis,and the effect of propylthiouracil,triiodothyronine and environmental temperature on serum thyroid hormone concentrations of ammocoetes

Serum thyroid hormone concentrations were measured during the seven stages of metamorphosis (1–7) of the southern hemisphere lamprey, Geotria australis. The respective mean concentrations ± SEM of serum thyroxine (T₄) and triiodothyronine (T₃) fell from 31.73 ± 4.09 and 5.06 ± 0.70 nM in large ammocoetes sampled in February, at the time when metamorphosis was initiated, to 4.54 ± 0.36 and 1.03 ± 0.12 nM at stage 5. Although there was a small, but significant, recovery of serum T₄ concentrations during stages 6 and 7, no such corresponding statistically significant rise occurred in serum T₃ concentrations. Serum thyroid hormone concentrations in ammocoetes sampled during the period when metamorphosis was taking place, exhibited a marked seasonal increase between February and May–June (late autumn/early winter); serum T₃ and T₄ concentrations peaked in May–June and were, respectively, > 2 fold and > 8 fold higher than those recorded for samples in late February (mid summer). By mid-July the serum T₄ and T₃ levels had declined from the peak values. Ammocoetes taken from streams at 16°C in June and acclimated to aquaria water at 25°C or 6°C had significantly lower serum T₃ and T₄ concentrations at the higher temperature, and also a lower serum T₄, but not T₃ concentration, at the lower temperature. Treatment of separate groups of ammocoetes with either propylthiouracil or T₃ for 70 days significantly depressed and raised respectively, the serum thyroid hormone and hepatic T₃ concentrations and caused significant changes in the body weight, but did not induce the onset of metamorphosis.     

Oxygen consumption and responses to hypoxia of ammocoetes of the southern hemisphere lampreyGeotria australis

The standard rate of oxygen consumption of ammocoetes (larvae) ofGeotria australis with a mean weight of c. 0.5 g was 9.6, 31.4 and 59.4l g^–1 h^–1 at 4.5, 15.5 and 25.0°C respectively, which gives an overall Q₁₀ of 2.4. The regression coefficient for the logarithmic relationship between oxygen consumption and body weight at 15.5°C was 0.704. The ammocoetes ofG. australis have a much lower rate of oxygen consumption at 15.5 and 25.0°C than those of holarctic lampreys. This presumably reflects the lower oxygen delivery pressure to their tissues and helps account for their slow growth rate. At 15.5°C, ammocoetes ofG. australis emerged from the substrate at 21–25 mm Hg and, unlike those of the Northern HemisphereIchthyomyzon greeleyi, died at 14–17 mm Hg. Thus, despite having a thinner water/blood barrier in the gills and blood with a higher oxygen affinity and capacity than holarctic ammocoetes, the larvae ofG. australis cannot survive very low dissolved oxygen tensions. This is apparently related to an inability of larvalG. australis to meet the high oxygen requirements of the respiratory pump at these oxygen tensions. During metamorphosis, oxygen consumption at 15.5°C rose from approximately 27l g^–1 h^–1 at the beginning of transformation to 33.2l g^–1 h^–1 by Stage 3 and then rapidly to 66l g^–1 h^–1 at Stage 6. It remained near this level in Stage 7 and the downstream migrant.     

Growth patterns of reed (Phragmites australis): the development of reed stands in carp ponds

Reed stands exhibit apparent differences of stem diameter, shoot length, density, and invasiveness. In carp ponds, five characteristic growth patterns can be distinguished. These growth patterns are ontogenetic states of a time-dependent stand development. Invasive reeds with short shoots are found in newly occupied habitats. With continuing establishment of the stand, the shoots in the inner regions become taller and fewer, a growth pattern described as central reed. Later, only a few shoots with thick stems remain. Two alternative pathways of stand development exist: steep shore reed and reed tussocks. By mowing, the directional development of reed stands can be turned into a circulation of growth patterns. The growth patterns have implications for the selection of reed stand areas for conservation purposes.     

Intraperitoneal injection of sulfur amino acids enhance the hepatic cysteine dioxygenase activity in rainbow trout (Oncorhynchus mykiss)

As part of the investigation into cysteine metabolism in fish, sulfur amino acids and their derivatives were injected intraperitoneally to fingerling rainbow trout (Oncorhynchus mykiss) to examine how the doses of these compounds affect the hepatic cysteine dioxygenase [EC 1.12.11.20] in this species. A dose of 0.25 mmol L-cysteine per 100 g body weight induced the enzyme activity as much as 2.5 times that of the control fish within 4h after the injection. The activity increased proportionally to the increasing dose of cysteine up to the dose of 0.15 mmol per 100 g body weight. The induction was observed to be rather specific to L-cysteine. These findings suggested that the cysteine sulfinate pathway might play an important role in the metabolism of excess cysteine in rainbow trout. The dosage of L-cysteine larger than 0.50 mmol per 100g body weight led to mortality of the fish. The pathway of cysteine catabolism was considered to function to prevent toxic accumulation of cysteine in rainbow trout, as in the case of mammals.     

Stress-induced changes in the affinity and abundance of cytosolic cortisol-binding sites in the liver of rainbow trout,Oncorhynchus mykiss (Walbaum), are not accompanied by changes in measurable nuclear binding

Plasma cortisol levels and the number (N_max) and affinity (K_d) of specific hepatic cortisol-binding sites were determined in rainbow trout subjected to chronic confinement stress for 14 days. Confinement significantly elevated plasma cortisol levels to 47.3 ± 13.5 ng ml^–1 within 24h and although levels declined to 8.0 ± 3.0 ng ml^–1 after 14 days, they were significantly higher throughout than levels in unstressed control fish (< 2.0 ng ml^–1). There was a 60% reduction in cytosolic N_max in stressed fish during the first 24h of confinement (35.8 ± 7.9 cf. 129.0 ± 15.2 fmol mg^–1 protein), a decline which was sustained at 7 days after the onset of stress but, although numbers of binding sites in the liver of stressed fish were still lower than in unstressed fish, the difference was no longer significant after 14 days of confinement. There was an accompanying significant rise in the K_d of cortisol binding in stressed fish during confinement, from 4.0 ± 0.6 nM at time 0 to 8.4 ± 0.8 nM after 24 h confinement. This increment in K_d was sustained at a level significantly higher than in control fish throughout the 14 day confinement period, despite marked reductions in cortisol levels and increases in N_max in stressed fish. Throughout the study, specific binding of cortisol could not be consistently detected in high-salt nuclear extracts from stressed or unstressed fish, suggesting either that high-affinity binding sites for cortisol were absent from these preparations, that receptors were present but unable to interact with ligand because they were occupied, or that receptors were present but not being extracted. These possibilities were investigated using a range of extraction procedures, by varying the temperature of incubation, by employing dexamethasone as ligand and by examining binding in purified, intact, nuclei. Estradiol was employed as a methodological control throughout and substantial amounts of specific estradiol binding were detected in all compartments and preparations. Specific cortisol-binding sites were detected in intact nuclei of both stressed and unstressed fish, at levels an order of magnitude lower than estradiol binding in the same preparations. These data demonstrate that activation of the pituitary-interrenal axis leads to significant changes in the nature of target-tissue binding of cortisol in rainbow trout, and reveal a clear difference in the subcellular distribution of binding-sites for estradiol and cortisol, which reflects the situation in mammalian tissues.     

Substrate concentration affects the in vitro metabolism of 17-hydroxyprogesterone by ovaries of the carp,Cyprinus carpio

Carp ovarian tissue was incubated with ³H-17-hydroxyprogesterone in the presence of 0, 0.1, 1, 10, and 100 μg ml⁻¹ unlabeled 17-hydroxyprogesterone. The pattern of metabolites formed showed a marked variation with substrate concentration. Formation of glucuronide and sulphate conjugates was important only at low substrate concentration. At high substrate concentration (10 and 100 μg ml⁻¹) 17,20α-dihydroxy-4-pregnen-3-one was the major metabolite, but at intermediate concentrations polar 7α-hydroxypregnanetetrols predominated. The results support the hypothesis that at low substrate concentrations conjugating, 5α-reducing and 7α-hydroxylating enzymes, of high activity but low capacity, act as scavengers to deactivate any steroids formed during the relatively low pituitary gonadotrophin secretions which are necessary for oocyte development, but that during the prespawning gonadotrophin surge when high levels of substrate are present these enzymes are saturated and 17,20α-dihydroxy-4-pregnen-3-one (17,20αP) becomes the major ovarian steroid. The possible role of 17,20αP during oocyte final maturation requires further examination.     

Stimulation of acetylcholinesterase activity by triiodothyronine in the brain of Singi fish,Heteropneustes fossilis (Bloch)

Three consecutive days of injections of triiodothyronine (T₃)(0.038, 0.075, 0.15 and 1.54 nmoles/g) significantly elevated the acetylcholinesterase (AchE) activity in the brain of Singi fish, Heteropneustes fossilis (Bloch). The higher doses of 0.075, 0.15 and 1.54 nmoles of T₃/g induced a greater increase in enzyme activity than 0.038 nmoles/g. A T₃ dose of 0.019 nmoles/g was found to be ineffective. The T₃ action on AchE activity was blocked by cycloheximide. Thiourea treatment for 30 days decreased the AchE activity below the control level. This reduced level of the enzyme activity was brought back even above the control level by T₃ injections. It is, therefore, suggested that thyroid hormone is involved in the sustenance of AchE activity in fish brain.