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1.
Int. j. morphol ; 41(1): 85-89, feb. 2023. ilus
Article in Spanish | LILACS | ID: biblio-1430538

ABSTRACT

Este estudio tuvo como objetivo demostrar la existencia de variaciones morfológicas en el tejido conectivo de la glándula submandibular de ratas obesas expuestas a glutamato monosódico (GMS). Se utilizaron 12 ratas Sprague Dawley machos recién nacidas (6 ratas para el grupo 1, control; 6 ratas para el grupo 2 (GMS), 4 mg/g de glutamato monosódico de peso (5 dosis) mantenidas por 16 semanas respectivamente con una dieta y agua ad libitum. En el estudio se realizó un análisis estereológico e histológico, demostrándose una variación en el tejido conectivo presentando una disminución del volúmen glandular, mayor fibrosis, y disminución de adipocitos a nivel periférico siendo reemplazado por tejido rico en colágeno. Los vasos sanguíneos observados a nivel estereológico no presentan mayores cambios en cuanto a volumen, superficie y área.


SUMMARY: This study aims to demonstrate the existence of morphological variations in the connective tissue of the submandibular gland of obese rats exposed to MSG. Twelve male newborn Sprague Dawley rats were used (6 rats for group 1, control; 6 rats for group 2 (MSG), 4 mg/g of monosodium glutamate of weight (5 doses) maintained for 16 weeks respectively with a diet and water ad libitum. In the study, a stereological and histological analysis was carried out, demonstrating a variation in the connective tissue, presenting a decrease in the glandular volume, greater fibrosis, and a decrease in adipocytes at the peripheral level, being replaced by tissue rich in collagen. Blood cells observed at the stereological level do not present major changes in terms of volume, surface and area, but in the histological study greater vascularization is observed.


Subject(s)
Animals , Male , Rats , Sodium Glutamate/administration & dosage , Submandibular Gland/drug effects , Obesity , Sodium Glutamate/pharmacology , Blood Vessels/drug effects , Body Weight , Fibrosis , Rats, Sprague-Dawley , Connective Tissue/drug effects , Animals, Newborn
2.
Braz. J. Pharm. Sci. (Online) ; 55: e17754, 2019. tab, graf
Article in English | LILACS | ID: biblio-1039063

ABSTRACT

The study evaluated the vasorelaxant effect induced by the ethanolic extract of the leaves of Zanthoxylum rhoifolium Lam (EEtOH-Zr/leaves). Wistar rats were treated with the leaf extract containing a single dose of 2,000 mg / kg, v.o. After 14 days, the animals were anesthetized for blood collection and subsequent analysis of the biochemical parameters; they were then euthanized (sodium pentobarbital-100 mg/kg, i.p.) for the removal and morphological analysis of the heart, lung, liver and kidney. The vasorelaxation activity the and vascular reactivity of EEtOH-Zr/leaves were evaluated on artery mesenteric rings isolated from rats. The extract showed no signs of toxicity and no significant difference in the values of the biochemical parameters between the control group and the group of treated animals. In the evaluation of pharmacological activity in the smooth muscle, the EEtOH-Zr/leaves caused vasorelaxant effect on the tonic contraction induced by phenylephrine in mesenteric artery preparations in the presence (pD2=2.17±0.05 µg/mL; Emax=99.8±5.2%) and absence (pD2=2.14±0.05 µg/mL; Emax=95.3±6.4%) of the vascular endothelium. Oral administration of EEtOH-Zr/leaves reduced the contraction induced by the cumulative addition of PHE. It is concluded that the EEtOH-Zr/leaves promote vasorelaxation and reduce vascular reactivity of adrenergic alpha-1 agonist in the mesenteric artery. The results did not show toxic effects of the extract.


Subject(s)
Animals , Male , Rats , Plant Extracts/adverse effects , /analysis , Zanthoxylum/toxicity , Mesenteric Arteries/drug effects , Blood Vessels/drug effects
3.
J. appl. oral sci ; 24(5): 509-517, Sept.-Oct. 2016. tab, graf
Article in English | LILACS, BBO | ID: lil-797983

ABSTRACT

ABSTRACT Tooth bleaching is a technique of choice to obtain a harmonious smile, but bleaching agents may damage the dental pulp. Objective: This study evaluated the inflammatory responses of human dental pulp after the use of two bleaching techniques. Material and Methods: Pulp samples were collected from human third molars extracted for orthodontic reasons and divided into three groups: control - no tooth bleaching (CG) (n=7); at-home bleaching with 15% carbamide peroxide (AH) (n = 10), and in-office bleaching with 38% hydrogen peroxide (IO) (n=12). Pulps were removed and stained with hematoxylin-eosin for microscopic analysis of inflammation intensity, collagen degradation, and pulp tissue organization. Immunohistochemistry was used to detect mast cells (tryptase+), blood vessels (CD31+), and macrophages (CD68+). Chi-square, Kruskal-Wallis, and Mann Whitney tests were used for statistical analysis. The level of significance was set at p<.05. Results: The inflammation intensity and the number of macrophages were significantly greater in IO than in AH and CG (p<0.05). The results of CD31+ (blood vessels per mm2) were similar in CG (61.39±20.03), AH (52.29±27.62), and IO (57.43±8.69) groups (p>0.05). No mast cells were found in the pulp samples analyzed. Conclusion: In-office bleaching with 38% hydrogen peroxide resulted in more intense inflammation, higher macrophages migration, and greater pulp damage then at-home bleaching with 15% carbamide peroxide, however, these bleaching techniques did not induce migration of mast cells and increased the number of blood vessels.


Subject(s)
Humans , Pulpitis/chemically induced , Tooth Bleaching/adverse effects , Dental Pulp/drug effects , Tooth Bleaching Agents/toxicity , Peroxides/toxicity , Pulpitis/pathology , Time Factors , Tooth Bleaching/methods , Urea/analogs & derivatives , Urea/toxicity , Blood Vessels/drug effects , Blood Vessels/pathology , Immunohistochemistry , Antigens, Differentiation, Myelomonocytic , Random Allocation , Antigens, CD , Cell Count , Collagen/drug effects , Statistics, Nonparametric , Platelet Endothelial Cell Adhesion Molecule-1 , Dental Pulp/pathology , Hydrogen Peroxide/toxicity
4.
J. appl. oral sci ; 23(1): 42-48, Jan-Feb/2015. tab, graf
Article in English | LILACS, BBO | ID: lil-741586

ABSTRACT

Objective: To evaluate the response of rat subcutaneous tissue in implanted polyethylene tubes that were filled with GMTA Angelus and Portland cements containing different arsenic concentrations. Material and Methods: Atomic absorption spectrophotometry was utilized to obtain the values of the arsenic concentration in the materials. Thirty-six rats were divided into 3 groups of 12 animals for each experimental period. Each animal received two implants of polyethylene tubes filled with different test cements and the lateral of the tubes was used as a control group. After 15, 30 and 60 days of implantation, the animals were killed and the specimens were prepared for descriptive and morphometric analysis considering: inflammatory cells, collagen fibers, fibroblasts, blood vessels and other components. The results were analyzed utilizing the Kuskal-Wallis test and the Dunn's Multiple test for comparison (p<0.05). Results: The materials showed, according to atomic absorption spectrophotometry, the following doses of arsenic: GMTA Angelus: 5.01 mg/kg, WPC Irajazinho: 0.69 mg/kg, GPC Minetti: 18.46 mg/kg and GPC Votoran: 10.76 mg/kg. In a 60-day periods, all specimens displayed a neoformation of connective tissue with a structure of fibrocellular aspect (capsule). Control groups and MTA Angelus produced the lower amount of inflammatory reaction and GPC Minetti, the highest reaction. Conclusions: There was no direct relationship between the concentration of arsenic present in the composition of the materials and the intensity of the inflammatory reactions. Higher values, as 18.46 mg/kg of arsenic in the cement, produce characteristics of severe inflammation reaction at the 60-day period. The best results were found in MTA angelus. .


Subject(s)
Animals , Male , Arsenic/toxicity , Bismuth/toxicity , Calcium Compounds/toxicity , Dental Cements/toxicity , Oxides/toxicity , Silicates/toxicity , Subcutaneous Tissue/drug effects , Arsenic/administration & dosage , Bismuth/chemistry , Blood Vessels/drug effects , Collagen/drug effects , Dental Cements/chemistry , Fibroblasts/drug effects , Materials Testing , Oxides/chemistry , Polyethylene/chemistry , Rats, Wistar , Reference Values , Spectrophotometry, Atomic , Time Factors
5.
Acta cir. bras ; 28(12): 863-869, Dec. 2013. ilus, tab
Article in English | LILACS | ID: lil-695971

ABSTRACT

PURPOSE: To evaluate the effects of copaiba oil ointment (Copaifera langsdorffii) on dorsal skin flaps in rats. METHODS: Adult male rats (n=30) were distributed into three groups of ten animals each, as follows: GC - control; GCA - absolute control and GT - treated with copaiba ointment. The rats were subjected to dorsal cutaneous skin flap surgery and the animals from the GC and GT received post-operative treatment for eight consecutive days. The animals from the GCA group did not receive treatment while the animals from the GC group received daily topical treatment of ointment without the active ingredient and the animals from the GT group were daily treated with 10% copaiba oil ointment. At the end of each experimental period the lesions were evaluated according to the percentage of necrotic area. Then, fragments from cranial, median and caudal parts were fixed in Boüin's solution and processed for paraffin embedding. The morphology of histological sections (5µm) was evaluated and the number of leucocytes, fibroblasts and blood vessels was also analyzed. The data obtained were submitted to ANOVA test complemented by Tukey-Kramer test (p<0.05). RESULTS: The necrotic area was lower in the group treated with copaiba ointment when compared to the control groups (GCA>GC and GT), while the morphology showed larger granulation tissue with bulky fibroblasts and collagen fibers more arranged in the GT group. The morphometry showed a significant higher number of blood vessels in the median and caudal parts (GT>GCA and GC), leucocytes in the cranial part (GT>GC>GCA), and also fibroblasts in the median (GT and GC> GCA) and caudal parts (GT>GC and GCA) (p<0.05). CONCLUSION: The copaiba oil ointment favors angiogenesis and accelerates the viability of random skin flaps in rats.


Subject(s)
Animals , Male , Rats , Fabaceae/chemistry , Ointments/pharmacology , Plant Oils/pharmacology , Surgical Flaps , Tissue Survival/drug effects , Administration, Topical , Blood Vessels/drug effects , Fibroblasts/drug effects , Leukocyte Count , Random Allocation , Reproducibility of Results , Skin/drug effects
6.
Acta odontol. latinoam ; 23(3): 249-256, Dec. 2010. tab
Article in English | LILACS | ID: biblio-949672

ABSTRACT

Vascular endothelial growth factor (VEGF) is a protein that increases vascular permeability and induces the proliferation, migration and survival of endothelial cells. Bisphosphonates (BPs) are antiresorptive drugs that are widely used in the treatment of bone metabolism diseases and bone metastases. Since 2003, cases of bisphosphonate-related osteonecrosis of the jaw (BRONJ) have been reported. Few papers explain the mechanisms that induce BRONJ; some authors mention alterations in bone remodelling and a certain antiangiogenic effect of BPs. The aim of this study is to evaluate the expression of VEGF in bone marrow cells and the number of blood vessels and area occupied by them in animals treated with the BP sodium olpadronate (OPD). We used 16 Wistar rats, 60 days old, divided into two groups, experimental (OPD) and control. The OPD group received 0.3 mg/kg/week intraperitoneal OPD for 5 weeks. The control group received an equivalent intraperitoneal volume of physiological saline solution. After euthanasia, hemimandibles were processed and mesio-distal histological sections of the first molar were prepared. Sections were stained with hematoxylin-eosin (HE), immunohistochemical detection of VEGF was performed (sc- 7269) and the following histomorphometric parameters were evaluated: In HE-stained sections - number of blood vessels per sq. mm. and percentage (%) of area occupied by blood vessels in relation to total area evaluated; in sections with immunohistochemical detection of VEGF – number of VEGF+ bone marrow cells per sq. mm. Data underwent statistical analysis. Number of blood vessels/mm2 was significantly lower in the OPD group (OPD: 92 ± 16; Control: 140 ± 31; p<0.05) and % vascular area/ total area evaluated showed no significant difference (OPD: 15.6 ± 6.1; Control: 10.2 ± 4.2). Number of VEGF+ cells/mm2 was lower in the OPD group than in the control group, with statistically significant differences (OPD: 7804.8 ± 597; Control: 13187.6 ± 894; p<0.001). The results of this study suggest that monosodium olpadronate has an antiangiogenic effect. Further studies are needed to reveal its potential as an antitumor agent and its connection with the onset of BRONJ.


El factor de crecimiento vascular (VEGF) es una proteina que incrementa la permeabilidad vascular, induce la proliferacion, migracion y supervivencia de las celulas endoteliales. Los bifosfonatos (BFs) son drogas antirresortivas ampliamente utilizadas en el tratamiento de enfermedades que alteran el metabolismo oseo y de metastasis oseas. Desde el 2003 se han reportado casos de osteonecrosis de maxilar asociada al uso de BFs (ONAB). Escasas publicaciones explican los mecanismos que inducen la ONAB, algunos autores mencionan las alteraciones en la remodelacion osea y un cierto efecto antiangiogenico de los BFs. El objetivo del presente trabajo es evaluar la expresion de VEGF en celulas de la medula osea y el numero y el area ocupada por vasos sanguineos en animales tratados con el BF olpadronato monosodico (OPD). Se utilizaron 16 ratas Wistar de 60 dias divididas en dos grupos, experimental (OPD) y control. El grupo OPD, recibio 0,3 mg/kg/sem de OPD via IP, durante 5 semanas. El grupo control, recibio un volumen equivalente via IP de solucion fisiologica. Luego de practicada la eutanasia se obtuvieron las hemimandibulas y se procesaron para obtener cortes histologicos mesio-distales del primer molar. Se realizo la coloracion hematoxilina-eosina (HE) y la deteccion inmunohistoquimica de VEGF (sc-7269) y se evaluaron los siguientes parametros histomorfometricos: En cortes con H&E: Numero de vasos sanguineos por mm2 y porcentaje (%) de area ocupada por los vasos sanguineos en relacion al area total evaluada; en cortes con la deteccion inmunohistoquimica de VEGF: Numero de celulas medulares VEGF+ por mm2. Los datos fueron estadisticamente analizados. El N° vasos sanguineos/mm2 fue significativamente menor en el grupo OPD (OPD: 92 ± 16; control: 140 ± 31; p<0,05) y el % area vascular/area total evaluada no mostro diferencias significativas (OPD: 15,6 ± 6.1; Control: 10.2 ± 4.2). El N° de celulas VEGF+/mm2 en el grupo OPD fue menor que en el grupo control con diferencias estadisticamente significativas (OPD: 7804,8 ± 597; Control: 13187,6 ± 894; p<0,001). Los resultados de este estudio sugieren que el olpadronato monosodico tiene un efecto antiangiogenico. Futuros estudios revelaran su potencial como agente antitumoral asi como tambien su relacion con la aparicion de ONAB.


Subject(s)
Animals , Rats , Bone Marrow/pathology , Vascular Endothelial Growth Factor A/analysis , Diphosphonates/pharmacology , Bone Density Conservation Agents/pharmacology , Mandible/pathology , Blood Vessels/drug effects , Blood Vessels/pathology , Bone Marrow/drug effects , Bone Marrow/blood supply , Bone Marrow Cells/drug effects , Bone Marrow Cells/pathology , Immunohistochemistry , Rats, Wistar , Angiogenesis Inhibitors/pharmacology , Densitometry , Dental Arch/drug effects , Dental Arch/blood supply , Dental Arch/pathology , Diphosphonates/administration & dosage , Bone Density Conservation Agents/administration & dosage , Injections, Intraperitoneal , Mandible/drug effects , Mandible/blood supply , Molar/pathology
7.
Indian J Biochem Biophys ; 2009 Feb; 46(1): 25-30
Article in English | IMSEAR | ID: sea-28707

ABSTRACT

The development of immunosuppressant compounds, such as cyclosporine and tacrolimus was crucial to the success of transplant surgery and for treatment of autoimmune diseases. However, immunosuppressant therapy may increase the concentrations of reactive oxygen species (ROS), inducing oxidative damage such as an increased vascular damage. The major source of ROS in the vascular endothelial cells is NADPH oxidase. The subunit structure and function of this enzyme complex in vascular cells differs from that in phagocytic leucocytes. The enzyme subunits Nox1, Nox2 and Nox4 are only found in vascular cells. The GTP-dependent protein subunit Rac 1 needs to be activated for this enzyme to function. Inhibiting this protein subunit should reduce NADPH oxidase-induced oxidative stress. In the cardiovascular system, oxidative stress is observed as hypertension, hypertrophy, fibrosis, conduction abnormalities and endothelial dysfunction, as well as cardiac allograft vasculopathy in transplant patients. In contrast to cyclosporine and tacrolimus, the immunosuppressant mycophenolate inhibits the Rac 1 subunit thus inhibiting NADPH oxidase in the vasculature. This may reduce oxidative stress, prevent the development of cardiac allograft vasculopathy, decrease the deterioration of vascular function and improve cardiovascular function chronically in transplant patients. This overview discusses whether this antioxidant immunosuppressive property could translate into a more general protective role for mycophenolate in the prevention of cardiovascular disease.


Subject(s)
Animals , Antioxidants/pharmacology , Antioxidants/therapeutic use , Blood Vessels/drug effects , Blood Vessels/physiology , Blood Vessels/transplantation , Calcineurin/antagonists & inhibitors , Cardiovascular Diseases/drug therapy , Cardiovascular Diseases/physiopathology , Cardiovascular Diseases/prevention & control , Cardiovascular System/drug effects , Cardiovascular System/physiopathology , Cyclosporine/metabolism , Cyclosporine/pharmacology , Endothelial Cells/drug effects , Endothelial Cells/metabolism , Heart Transplantation , Humans , Immunosuppressive Agents/pharmacology , Immunosuppressive Agents/therapeutic use , Mycophenolic Acid/pharmacology , Mycophenolic Acid/therapeutic use , NADPH Oxidases/antagonists & inhibitors , NADPH Oxidases/metabolism , Oxidative Stress/drug effects , Reactive Oxygen Species/metabolism , Tacrolimus/pharmacology , rac1 GTP-Binding Protein/antagonists & inhibitors , rac1 GTP-Binding Protein/metabolism
8.
Indian J Exp Biol ; 2006 Nov; 44(11): 875-9
Article in English | IMSEAR | ID: sea-57239

ABSTRACT

The present study aimed at investigating the influence of increased dietary calcium on Na(+)-K(+)-ATPase activity in heart and aorta of female Sprague-Dawley rats treated with oral contraceptive (OC) steroids. Rats were grouped as control (CR), OC-treated and OC+calcium-treated. OC-treated and OC+calcium-treated received a combination of OC steriods (ethinyloestradiol and norgestrel; ig). OC+calcium-treated rats were fed with 2.5% calcium diet, while OC-treated and CR groups were fed on 0.9% calcium diet. The activity of Na(+)-K(+)-ATPase in heart and aorta was significantly lower in OC-treated rats than those in the other groups. OC treatment caused significant increase in plasma glucose and significant decrease in plasma K+ as compared to control group. Decrease in Na(+)-K(+)-ATPase activity and plasma K+ was abrogated by increased calcium intake, while increase in plasma glucose was not normalized by calcium supplementation. Plasma levels of Na+, lipid peroxidation index and ascorbic acid were comparable among the three groups. These results showed that OC treatment could lead to impaired activity of cardiac and vascular Na(+)-K(+)-ATPase, possibly due to reduced plasma K+ level and these effects could be abolished by high calcium diet.


Subject(s)
Animals , Aorta, Thoracic/drug effects , Blood Glucose/analysis , Blood Vessels/drug effects , Calcium, Dietary/pharmacology , Contraceptives, Oral/pharmacology , Female , Heart/drug effects , Malondialdehyde/blood , Myocardium/enzymology , Oxidative Stress/drug effects , Potassium/blood , Rats , Rats, Sprague-Dawley , Sodium/blood , Sodium-Potassium-Exchanging ATPase/metabolism
9.
Egyptian Journal of Medical Laboratory Sciences. 1998; 7 (1): 37-45
in English | IMEMR | ID: emr-47921
10.
Egyptian Journal of Medical Laboratory Sciences. 1998; 7 (1): 87-95
in English | IMEMR | ID: emr-47926
11.
Medical Journal of the Islamic Republic of Iran. 1998; 12 (2): 153-157
in English | IMEMR | ID: emr-48743

ABSTRACT

Previous in vitro work on rabbit knee joint vessels showed that vasoconstrictor effects of nerve stimulation and administration of a-adrenoceptor agonists were mediated predominantly by alpha1-adrenoceptors. The present experiments were performed to assess the nature of alpha -adrenoceptor subtypes within these blood vessels in vivo. Dose/response relationships for adrenaline and noradrenaline produced a similar pattern of increasing constriction of articular vessels with increasing doses of drug. The alpha 1 agonist phenylephrine also produced dose-dependent constrictor responses which were diminished by prazosin. Using the alpha 2 agonists clonidine and UK -14304, responses in vivo differed from those previously observed in vitro. There was virtually no response to clonidine in vitro while responses were obvious in vivo. Although UK-14304 was found to have small effects in vitro, but only at high doses, this agent exerted more potent effects in vivo, significantly greater than those obtained with phenylephrine. Responses to the alpha 2 agonists were not altered significantly by prazosin but were reduced by rauwolscine. Following injection of UK-14304, the constrictor response to nerve stimulation was reduced. The results suggest that both alpha 1 and alpha 2 adrenoceptors are present postjunctionally within articular blood vessels, and also that prejunctional alpha 2 receptors are present which presumably regulate neurotransmitter release from sympathetic nerve endings in the joint capsule


Subject(s)
Animals, Laboratory , Adrenergic alpha-Antagonists/pharmacology , Rabbits , Blood Vessels/drug effects , Blood Vessels/physiology , Receptors, Adrenergic , Joints/physiology
12.
New Egyptian Journal of Medicine [The]. 1995; 12 (2): 168-175
in English | IMEMR | ID: emr-38796

ABSTRACT

In the present study, the administration of calcium dobesilate led to various histological and histochemical changes in the femoral artery in the form of dose related increase in mitotic figures in the tunica media in addition to mononuclear cellular infiltration in the tunica adventitia. Endothelial cell enlargement and foreign body multinucleated giant cells were noticed in all treated groups of animals except those which received therapeutic doses of the drug for 2 weeks. Meanwhile, in the femoral vein enlargement of the endothelial cells and an apparent decrease in the thickness of wall ranging from moderate to marked were also seen. Moreover, calcium dobesilate treatment causes a dose-related increase in the amount of collagenous fibers and in the PAS positive material. An increase in the alkaline phosphatase enzyme activity was observed in all treated groups of animals which received the drug for 2 and 4 weeks. On the contrary, a progressive decrease in the density of internal and external elastic lamina is shown in the femoral artery and vein


Subject(s)
Blood Vessels/drug effects
13.
Indian J Physiol Pharmacol ; 1992 Jan; 36(1): 65-9
Article in English | IMSEAR | ID: sea-106965

ABSTRACT

Vascular autonomic receptors in amphibians exhibit difference from more evolved mammalian species. Vascular perfusion studies in frog indicate constrictions by prominent muscarinic but rudimentary nicotinic constrictive regulation by cholinergic systems. Difference from classical effect-patterns of pharmacological interventions, observed in the study, make room to visualise complexity of additional regulatory mechanisms.


Subject(s)
Adrenergic alpha-Antagonists/pharmacology , Animals , Autonomic Nerve Block , Autonomic Nervous System/drug effects , Blood Vessels/drug effects , Choline/analogs & derivatives , Cholinergic Fibers/drug effects , Dose-Response Relationship, Drug , Drug Interactions , Esters/pharmacology , Female , Ganglia, Autonomic/drug effects , Male , Models, Biological , Muscarinic Antagonists , Ranidae/physiology , Vasoconstrictor Agents/pharmacology
17.
Southeast Asian J Trop Med Public Health ; 1979 Jun; 10(2): 276-9
Article in English | IMSEAR | ID: sea-31014
20.
Indian J Physiol Pharmacol ; 1977 Apr-Jun; 21(2): 133-6
Article in English | IMSEAR | ID: sea-108484

ABSTRACT

Actions of glucagon on the perfused vessels of the isolated rabbit ear were investigated. The two main actions of glucagon on the perfused ear vessels of the rabbit are: (i) release of noradrenaline which accounts for the constrictor response in low tone preparations. The response depends on the level of 3, 5 AMP. If the level rises as a result of noradrenaline action, contriction sets in. (ii) Glucagon may stimulate the adenylcyclase. In the high tone preparation 3,5 AMP levels are probably high. Release of noradrenaline by glucagon would have little additonal effect.


Subject(s)
Animals , Blood Vessels/drug effects , Ear/blood supply , Female , Glucagon/pharmacology , Male , Perfusion , Rabbits , Time Factors , Vasomotor System/drug effects
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