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Biomedical subjects

A Gibson

Publications and source records attributed to A Gibson.

At least 145 records · Page 8Linked to original sources

The oral and dental effects of q'at chewing.

A survey of 121 male volunteers who were questioned regarding their attitudes to q'at (Khat or Catha edulis) is presented. This preceded a dental examination that revealed a low caries rate, an inverse relationship between periodontal pocket depth and the chewing side, and evidence of temporomandibular joint dysfunction. Keratosis of the buccal mucosa--probably related to q'at chewing--was also seen. No evidence has been found to suggest that q'at chewing has particularly detrimental oral or dental effects.

Adolescent↗

Complex effects of Gillichthys urotensin II on rat aortic strips.

The aim of this study was to determine whether the fish neuropeptide, Gillichthys urotensin II (GUII), possesses significant biological activity on rat aortic strips. On intact strips, pre-contracted by noradrenaline (100 nM), low concentrations (0.1-0.5 nM) of GUII produced relaxations, while higher concentrations (1-10 nM) caused further contraction. On strips rubbed to remove endothelial cells, relaxations were absent but contractile responses to higher concentrations of GUII remained. GUII (0.02-10 nM) produced dose-related contractions of quiescent, intact aortic strips. These contractions consisted of two components, tonic and phasic, and were potentiated in rubbed strips and in the presence of the antioxidant drug hydroquinone (10 microM). Mepacrine (40 microM) and p-bromophenacyl bromide (50 microM) completely abolished contractions to GUII, but indomethacin (10 microM) and nordihydro-guaiaretic acid (10 microM) were without effect. The phasic, but not the tonic, component of the contractile response was inhibited by nitrendipine (200 nM), and was absent in bathing medium from which Ca2+ had been omitted. Addition of EGTA (2 mM) to Ca2+-free bathing medium abolished the residual tonic component. GUII-induced contractions were completely abolished by the calmodulin antagonists trifluoperazine (50 microM) and W-7 (30 microM). It is concluded that GUII, previously considered devoid of significant activity on mammalian tissues, produces potent endothelium-dependent relaxations and endothelium-independent contractions of rat aorta, and possible mechanisms underlying each response are discussed.

Animals↗

Hyperbaric oxygen therapy in the management of Clostridium perfringens infections.

Patients with Clostridium perfringens infections treated in Christchurch over a 14 year period to 1984 were reviewed retrospectively. Of the 46 documented cases, 21 died. Twenty-nine patients were treated with hyperbaric oxygen (HBO) therapy. Of these, nine died, whilst 12 of 17 other patients who did not receive HBO died, including five in whom the diagnosis was only made at postmortem. The clinical features and predisposing factors for clostridial infections are discussed. The importance of early vigorous treatment with a combination of surgical debridement, antibiotics and HBO to reduce the morbidity and mortality of this lethal infection is emphasised.

Adult↗

Cardiovascular effects of urotensin II in anesthetized and pithed rats.

Gillichthys urotensin II (GUII; 1.5-150 nmol kg-1) reduced blood pressure in anesthetized rats, diastolic pressure being reduced to a greater extent than systolic. The effect was slow in onset (peak at 4-5 min) and longlasting (up to 60 min), and was accompanied by a reflex tachycardia. The hypotension was not blocked by propranolol or by mepyramine. In pithed rats, GUII (150 nmol kg-1) reduced the pressor responses to sympathetic nerve stimulation, noradrenaline, and Arg-vasopressin. Somatostatin (150 nmol kg-1) had no effect on the sympathetic pressor response but reduced heart rate. It is concluded that GUII is a vasodilator in the rat, an action not shared with somatostatin.

Anesthesia↗

Effects of 6-hydroxydopamine-induced lesions of the paraventricular nucleus, and of prazosin, on the corticosterone response to restraint in rats.

In rats, with bilateral lesions of the paraventricular nuclei induced by 6-hydroxydopamine, restraint stress failed to elevate levels of corticosterone in plasma, although the resting levels in lesioned animals were similar to those of control rats. Prazosin inhibited the plasma-corticosterone response to restraint in intact rats, at doses which did not by themselves influence resting hormone levels. These results suggest a positive role for noradrenaline, acting through alpha-adrenoceptors, on the stress-induced output of corticotrophin.

Adrenergic alpha-Antagonists↗

Germination of Eucalyptus sieberi, L. Johnson seeds. I. Response to substrate and atmospheric moisture.

Consistent germination of Eucalyptus sieberi L. Johnson seeds required a low vapor pressure deficit (< 5 x 10(-6) MPa) and a high matric water potential (> -5 x 10(-3) MPa). Eucalyptus sieberi seeds, under moist but less favorable conditions, were unable to germinate but underwent changes that enabled them to germinate more rapidly when suitable conditions occurred. Such pregerminative development was interrupted but not reversed by a dry period as long as eight months. This may explain how seeds of this species germinate successfully on the surface of exposed seedbeds subject to intermittent drying.

Journal Article↗

Germination of Eucalyptus sieberi L. Johnson seeds. II. Internal water relations.

At 15-20 degrees C, seeds of Eucalyptus sieberi L. Johnson need to maintain a water content equal to 30% or more of dry weight for approximately 60 h in order to germinate. Several shorter periods of imbibition at 30% water content separated by between 6 and 120 h desiccation were as effective as an unintenupted imbibition in bringing seeds to the point of germination. Even after 8 months' desiccation an earlier imbibition shortened the time required for the completion of germination, although it did not hasten the onset of germination. The water potential of seeds sufficiently hydrated to germinate was about -0.6 MPa, whereas that of the embryo was only about -4.5 MPa. The difference was caused by the inhibition of water uptake by the inner integument of the seed coat. During germination, reserve protein in a small group of cells above the collet was hydrolyzed. Subsequent expansion of these cells caused rupture of the inner integument thereby allowing further water uptake by the embryo. The balance of water absorption and evaporative loss by the outer integument was such that most seeds on a moist substrate but exposed to dry air (6.5-8 x 10(-4) MPa) did not maintain the 30% water content necessary for germination. Thus although able to germinate on seedbeds subject to intermittent drying, E. sieberi seeds have the capacity to avoid germination except under humid conditions.

Journal Article↗

An oxytocin receptor in anococcygeus muscles isolated from male mice.

The nature of the neurohypophyseal peptide receptor in the anococcygeus muscles from male mice was investigated. The rank order of potency of naturally occurring peptides was oxytocin greater than Arg-vasotocin greater than Arg-vasopressin greater than Lys-vasopressin, which is similar to that found in the uterus and mammary gland. Selective agonists on the oxytocin (OT) receptors of the uterus and mammary gland (Thr4-OT; Gly7-OT; Thr4-Gly7-OT) were also potent agonists in the mouse anococcygeus. Competitive antagonists of uterine responses to oxytocin (dP-TyrMe-Thr4-OT; dP-TyrMe-OT; dP-Thr4-OT; dp-Orn8-OT) were also competitive antagonists of oxytocin-induced contractions of the mouse anococcygeus. It is concluded that the neurohypophyseal peptide receptor of the male mouse anococcygeus is of the oxytocin type; antagonist pA2 values suggest that this receptor resembles, but may not be identical to, the uterine oxytocin receptor. Possible physiological and pharmacological implications of these observations are discussed.

Animals↗

Magnesium ions and oxytocin sensitivity of the male mouse anococcygeus.

The sensitivity of the mouse anococcygeus to contraction by oxytocin was shown to be Mg2+-dependent. Decreasing [Mg2+]0 from the optimal concentration of 1 to 0 mM caused a 20-fold parallel rightward displacement of the oxytocin dose-response curve. Contractions to oxytocin-related peptides (Arg-vasotocin, Arg-vasopressin and Lys-vasopressin) were also Mg2+-dependent, but those to other drugs (carbachol, methoxamine and thyrotrophin releasing hormone) were not. The onset of the potentiating effect of Mg2+ was rapid, full potentiation occurring within 70 s. 1-Deaminopenicillamine 8-ornithine-vasotocin produced competitive antagonism of responses to oxytocin, but was more potent in the absence (pA2 = 8.01) than in the presence of Mg2+ (1 mM; pA2 = 7.52). Thus, physiological concentrations of [Mg2+]0 enhanced oxytocin agonist potency but decreased oxytocin antagonist potency; possible mechanisms are discussed.

Animals↗

Neuropeptide-induced contraction and relaxation of the mouse anococcygeus muscle.

Isometric tension responses to neuropeptides were recorded from anococcygeus muscles isolated from male mice. This smooth muscle tissue is innervated by inhibitory nonadrenergic, noncholinergic nerves that resemble, ultrastructurally, the peptidergic neurons of the gastrointestinal tract; the physiological function of the anococcygeus is not known. Slow sustained contractions were produced by oxytocin (0.2-20 nM), [Arg8]vasopressin (0.4-200 nM), and [Arg]-vasotocin (0.4-100 nM); the mouse anococcygeus is, therefore, one of the few examples of nonvascular smooth muscle from male mammals to respond to low concentrations of oxytocin and related peptides. Substance P (0.5-8 microM) caused distinctive, biphasic increases in muscle tone of some, but not all, preparations. Other neuropeptides producing contractions were neurotensin (2-100 microM) and thyrotropin-releasing hormone (2-100 microM); the responses were of similar time course and displayed selective cross-desensitization, suggesting that these two peptides act through a common distinct mechanism. Tetradecapeptide somatostatin (10-80 microM) and its analog urotensin II (0.1-5 microM), a dodecapeptide from the urophysis of the teleost fish Gillichthys mirabilis, produced similar slowly developing relaxations of carbachol-induced tone. Piscine urotensin II, of which there are no reported effects on nonvascular mammalian systems, was 20-50 times more potent than somatostatin, a well-established mammalian hormone. Of the peptides studied, only vasoactive intestinal polypeptide (0.05-1 microM) caused rapid powerful relaxations in low concentrations; this is consistent with its proposed involvement in nonadrenergic, noncholinergic neurotransmission in the mouse anococcygeus.

Animals↗

Incorporation of [14C]glucose into lipids of bovine oligodendroglia.

Oligodendrocytes were isolated from the white matter of ox brains. Light microscopy revealed that the cells were greater than or equal to 90% phase-bright with a mean diameter of 7.6 micron. Transmission electron microscopy was employed to identify the classic morphology associated with mature oligodendrocytes. Homogenates of the isolated cells showed negligible activity of neuronal and astrocytic cell markers. Using a suspension culture method cells were incubated with [14C]glucose. This simple precursor labelled the five complex lipids choline glycerophospholipid, ethanolamine glycerophospholipid, inositol glycerophospholipid + serine glycerophospholipid, and the two cerebroside species. The incorporation of label was shown to be dependent on glucose concentration, protein concentration, and the length of incubation. In addition the glucose uptake blocker phloretin (1 mM) reduced the degree of labelling by up to 97%, and the metabolic poisons KCN (1 mM) and iodoacetate (0.5 mM) had varying deleterious effects on the amounts of labelling of the five lipids measured.

Animals↗