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Biomedical subjects

D F Opdyke

Publications and source records attributed to D F Opdyke.

At least 19 recordsLinked to original sources
PubMed1984

Vascular recovery following hemorrhage in the dogfish shark Squalus acanthias.

Cardiovascular regulatory systems were examined in the dogfish shark after hemorrhage of 1% of body weight. An immediate 45% decrease in mean dorsal aortic pressure and delayed increases in plasma epinephrine concentration and plasma norepinephrine concentration were noted. During the recovery period following hemorrhage, the catecholamine levels peaked (epinephrine 203% of control, norepinephrine 148% of control) and then returned toward control values. Hematocrit, however, continued to decline as blood pressure recovered. Phentolamine pretreatment, which in itself caused a 55% decrease in dorsal aortic pressure, did not prevent the recovery of blood pressure after hemorrhage. This study indicates that 1) hemorrhage causes an increase in circulatory catecholamine concentration, possibly by a baroreceptor reflex; 2) volume recruitment, as indicated by the drop in hematocrit, is a major mechanism contributing to the recovery of dorsal aortic pressure after hypotension; and 3) alpha-adrenergic receptors are not necessary for the recovery of dorsal aortic pressure after hemorrhage.

Animals↗
PubMed1983

Dual mechanism for catecholamine secretion in the dogfish shark Squalus acanthias.

Both 1,1-dimethyl-4-phenylpiperazinium iodide, a ganglionic stimulating drug (DMPP), and potassium ion (K+) cause a pressor response when injected into Squalus acanthias, an elasmobranch. The pressor responses are due to increased secretion of epinephrine and norepinephrine. The pressor response to DMPP can be blocked by prior infusion of hexamethonium, a ganglionic blocking drug. However, ganglionic blockade does not inhibit the pressor response to K+. Plasma catecholamine concentrations do not increase significantly in response to challenge with DMPP after hexamethonium infusion, but exceedingly high levels of plasma catecholamines quickly appear after K+ injection following hexamethonium infusion. It is concluded that there are at least two mechanisms controlling catecholamine secretion in the dogfish, one of which involves the ganglion cells that are intimately associated with chromaffin cells in the chromophil bodies that are so characteristic of this species and elasmobranchs in general.

Animals↗
PubMed1983

Effect of ganglionic blockade on catecholamine secretion in exercised dogfish.

A brief bout of vigorous exercise results in significant increases in plasma epinephrine (E) and norepinephrine (NE) in the dogfish, Squalus acanthias. Since the presence of a functioning sympathetic nervous system in dogfish is in doubt, experiments were undertaken to show whether or not exercise-induced catecholamine (CA) secretion is under autonomic neurogenic control. Changes in plasma E and NE in a control group of exercised fish were compared with changes in fish exercised while under the influence of ganglionic blockade. Ganglionic blockade was induced in dogfish by hexamethonium infusion before exercise. CA secretion in response to a subsequent bout of exercise was significantly reduced without impairment of the ability of the fish to exercise. The pattern of systemic arterial pressure response to exercise and recovery (initial decrease during exercise followed by a prompt recovery to control level) was not significantly altered by ganglionic blockade. It is concluded that in dogfish some fraction of CA secretion capacity is possibly or potentially under neurogenically related control. Apparently the fraction of CA secretion under such control is not essential for performing exercise. The pattern of CA secretion accompanying the events of exercise and recovery in dogfish suggests that CA may play a more important role in recovery from exercise than in its performance.

Animals↗
PubMed1982

Effect of angiotensin II on vascular resistance in whole-body perfused dogfish.

1. The effect of angiotensin II (AII), norepinephrine (NE), epinephrine (E) and isoproterenol (ISO) was observed on the branchial and systemic circulations in a whole-body-pump perfused dogfish preparation. 2. NE and E increased systemic blood flow resistance, but decreased branchial resistance. 3. ISO decreased both systematic and branchial blood flow resistance. 4. AII had no significant effect on either branchial or systemic resistance.

Angiotensin II↗
PubMed1982

Dogfish pressor response to potassium blocked by magnesium and phentolamine.

In vivo infusion of MgCl2 blocks the dogfish pressor response to K+. This action of Mg2+ was contrasted to phentolamine in in vivo and in vitro experiments. Mg2+ blocks the spontaneous release of catecholamines from dogfish chromaffin tissue but does not alter the norepinephrine-induced contraction of the isolated dogfish artery. In vivo infusion of Mg2+ causes a significant decrease in resting catecholamine levels and diminishes the catecholamine release caused by K+ challenge. Both Mg2+ and phentolamine block the pressor action of K+, Mg2+ by preventing the K+-induced release of catecholamines and phentolamine by preventing the circulating catecholamines from interacting with alpha-adrenergic receptor sites.

Animals↗
PubMed1982

Catecholamine release and blood pressure changes induced by exercise in dogfish.

Plasma norepinephrine (NE), epinephrine (E), and potassium (K+) were measured before, during a 3-min bout of exercise, and at intervals after exercise in Squalus acanthias. The dorsal aortic pressure response following 1 min of exercise was observed in another series of experiments. Plasma E, NE, and K+ increased significantly and progressively during the exercise period and for 2 min after exercise. Plasma E increased significantly during the 1st min; NE during the 2nd min; but K+ did not increase significantly until the 3rd min of exercise. Blood pressure decreased significantly during 1 min of exercise but increased over control level within 4 min after the end of exercise coincident with the peak of plasma E and NE concentrations. Plasma NE, E, and blood pressure decreased slowly in parallel fashion during the 37-min postexercise period of observation. Increased plasma K+ from skeletal muscle is probably not the primary stimulus for early catecholamine release in exercising dogfish, but increased plasma K+ does contribute to releasing and maintaining plasma NE and E levels in the postexercise period. This results in a sustained pressor effect that promotes blood flow and aids in metabolic recovery.

Animals↗
PubMed1982

Evolution of angiotensin II-induced catecholamine release.

The interaction between angiotensin II (ANG II) and catecholamines was examined in nonmammalian vertebrates. ANG II challenge caused a significant pressor response in representatives of the seven vertebrate classes. Additionally, plasma levels of both epinephrine and norepinephrine increased following intravascular ANG II injection in the conscious lumpfish, bullfrog, and turtle, and the anesthetized chicken. Phentolamine pretreatment totally abolished ANG II pressor action in the hagfish and chicken and diminished the ANG II pressor response in other classes of vertebrates. The ability of ANG II to release catecholamines appears to be a phylogenetically ancient interaction and indicates that catecholamines may play an important role in the physiological expression of ANG II action in lower vertebrates.

Angiotensin II↗
PubMed1976

Response to angiotensins I and II and to AI-converting-enzyme inhibitor in a shark.

The spiny dogfish shark, which does not have renal juxtaglomerular cells, exhibits a strong pressor response to both angiotensin I and II. A nonapeptide, angiotensin I-converting-enzyme inhibitor, blocks the pressor response to angiotensin I in this fish. The pressor response to both angiotensin II and norepinephrine is completely blocked by the adrenergic blocking drug phentolamine.

Adrenergic alpha-Antagonists↗
PubMed1975

Vascular volume-distensibility characteristics of the isolated dogfish gut.

The vascular capacitance and volume distensibility of the isolated dogfish gut and segments of dogfish arteries and veins were investigated. The volume-distensibility curves for dogfish arteries and veins are very similar to comparable curves derived from arteries and veins of dogs or man. The vascular volume-distensibility curve of the gut, however, shows a greater distensibility at higher systemic pressure than at lower pressure. Evidence is presented that significant amounts of fluid leave the vascular compartment at a lower systemic pressure than in an isolated dog hindlimb preparation. However, this alone does not explain the atypical vascular volume-distensibility curve obtained from the dogfish gut. It is suggested that in the dogfish capillary filtration pore enlargement takes place at a very low capillary pressure or volume (compared to mammals) and this complicates the construction of a volume-distensibility curve because initial vascular volume is not constant.

Animals↗