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T E Hopkins

Publications and source records attributed to T E Hopkins.

5 recordsLinked to original sources
PubMed1998

Structure and function of the axillary organ of the gulf toadfish, Opsanus beta (Goode and Bean).

The structure of the axillary organ of a batrachoidid species, the gulf toadfish (Opsanus beta Goode and Bean 1879), has been examined and several simple experiments designed to elucidate its function performed. Electron microscopy (EM) studies revealed cells and structures suggesting secretory and iono regulatory roles (e.g., abundant intracytoplasmic secretory particles, rough endoplasmic reticulum, sparse Golgi bodies, indented epithelial cells with microvilli, numerous endocytotic vesicles, etc.). Our physiological experiments allowed us to reach several conclusions: the organs do not excrete significant quantities of urea relative to other areas of the fish (head and gills), the organs do not secrete a substance that is toxic to a teleost test fish (Gambusia affinis), the secretions do not induce short-term modifications in locomotory activity of other gulf toadfish (e.g., by pheromonal means) and the secretions do not inhibit the growth of several species of microorganisms in culture. The function of the organ and its secretions remains unknown, representing a fertile area for research on structure and function in comparative physiology.

Animals↗
PubMed1996

Poor glycemic control induces hypertension in diabetes mellitus.

We conducted this study to test the hypothesis that hypertension is a primary consequence of poor glycemic control per se very early in insulin-dependent diabetes mellitus. Sprague-Dawley rats (n=15) were instrumented with artery and vein catheters, placed in metabolic cages, and sodium intake was clamped throughout the study. Mean arterial pressure was measured 24 h/d. After a precontrol period, streptozotocin (70 mg/kg IV) was administered, and 15 hours later a continuous intravenous infusion was begun at 4 U/rat per day. The insulin infusion was titrated on an individual rat basis to maintain good glycemic control, and after this 7-day control period, blood glucose, urinary sodium excretion, and mean arterial pressure were not different from precontrol values, averaging 8.8 +/- 0.6 mmol/L, 2.8 +/- 0.2 mmol/d, and 103 +/- 2 mm/Hg, respectively, for control days 5 through 7. Subsequently, a 4-day period of poor glycemic control was initiated by reducing the insulin infusion rate. Blood glucose, urinary sodium excretion, and mean arterial pressure began to increase on day 1; for diabetes days 3 and 4, they averaged 23.4 +/- 1.0 mmol/L, 3.6 +/- 0.1 mmol/d, and 110 +/- 2 mm Hg, respectively. All were significantly elevated. When insulin treatment was restored, all variables returned to control levels during the next 4 days. A second 4-day diabetic period yielded similar results. These results indicate that elevated blood pressure is a primary consequence of poor glycemic control in insulin-dependent diabetes, occurring before renal injury has had time to develop, and therefore, may be a factor contributing to the initiation of end-organ injury.

Animals↗
PubMed1995

Interactions of cortisol and nitrogen metabolism in the ureogenic gulf toadfish Opsanus beta.

We examined the relationship between plasma cortisol levels, hepatic glutamine synthetase (GNS) activity and the form of nitrogen excreted (e.g. urea, ammonia) in undisturbed versus confined/crowded (acutely stressed) gulf toadfish. Specifically, we tested the hypothesis that acute increases in plasma cortisol levels are required to trigger the increase in GNS activity induced by the confinement/crowding stress. Toadfish responded to the stress of confinement/crowding with an initial cortisol surge (approximately 37 ng ml-1 at 2 h), which was rapidly cleared and was indistinguishable from resting levels (approximately 10 ng ml-1 by 24 h). Treatment of fish with metyrapone (which inhibits cortisol synthesis) successfully blocked the acute 2 h confinement/crowding-induced surge in plasma cortisol levels. Additionally, GNS activity in confined fish 24 h after metyrapone injection also did not differ from that of control fish, indicating that acute GNS activation probably requires the earlier (2 h) cortisol peak. In post-absorptive fish, a strong relationship between total nitrogen excretion rate and plasma cortisol levels was evident. The percentage of nitrogen excreted as ammonia was inversely related to liver GNS activity. However, GNS activity explained only part (at most 57%) of the variability in the percentage of nitrogen excreted as ammonia/urea, suggesting that this is not the sole factor setting the degree of ureogenesis. When toadfish are fed, the relationships between total nitrogen excretion rate and cortisol levels, and between percentage nitrogen excreted as ammonia and GNS activity, are virtually absent. Taken together, our results indicate that a stress response may be only one of several mechanisms by which ureogenesis is activated in gulf toadfish.

Animals↗