Amitriptyline potentiates morphine analgesia by a direct action on the central nervous system

1983 ◽  
Vol 13 (2) ◽  
pp. 160-164 ◽  
Author(s):  
Mitchell Botney ◽  
Howard L. Fields
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Direct Action ◽  
Morphine Analgesia ◽  
The Central Nervous System

Brain Respiration and Glycolysis in Cardiazol Convulsions

1940 ◽  
Vol 86 (361) ◽  
pp. 276-280 ◽  
Author(s):  
Leslie Dundonald MacLeod ◽  
Max Reiss
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Direct Action ◽  
Reducing Power ◽  
Liver Glycogen ◽  
Potassium Ions ◽  
Blood Picture ◽  
The Central Nervous System ◽  
Respiratory Centre ◽  
Convulsant Effect

Since Hildebrandt (1926) described the convulsant effect of cardiazol injection, several studies have been carried out on the mechanism of such convulsions. Zung and Tremonti (1931) suggested a direct action on the respiratory centre when cardiazol is used as a stimulant; Kerr and Antaki (1937) found no effect on brain glycogen or phosphocreatine in cardiazol-induced convulsions; Hashimoto (1937) found differences in distribution of calcium and potassium ions in the central nervous system after cardiazol. Goodwin and Lloyd (1938) recorded a direct effect on brain potential changes as shown on oscillographic records. Leibel and Hall (1938) found a large (75 per cent.) diminution of cerebral blood-flow at the onset of cardiazol convulsions. Weigand (1938) found no effect on liver glycogen or vitamin A content, reducing power of suprarenal cortex or blood picture. Denyssen and Watterson (1938) and Watterson and Macdonald (1939) attribute the convulsions to action on the vasomotor centre and note the action of vasodilator drugs in inhibiting convulsions. Wortis (1938) quoted by Quastel (1939) found no effect on brain respiration.

Interleukin-8 modulates feeding by direct action in the central nervous system

1993 ◽  
Vol 265 (4) ◽  
pp. R877-R882 ◽  
Author(s):  
C. R. Plata-Salaman ◽  
J. P. Borkoski
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Food Intake ◽  
Direct Action ◽  
Intraperitoneal Administration ◽  
Interleukin 8 ◽  
Short Term ◽  
Lipopolysaccharide Endotoxin ◽  
The Central Nervous System ◽  
Necrosis Factor

Interleukin-8 (IL-8) is released in response to infection, inflammation, and trauma. The most important stimuli for IL-8 release during these pathological processes are IL-1, tumor necrosis factor, and bacterial lipopolysaccharide (endotoxin), factors that have been shown to suppress feeding. In the present study, the participation of IL-8 on the central regulation of feeding was investigated. Intracerebroventricular (icv) microinfusion of recombinant human IL-8 (rhIL-8, 1.0-100 ng/rat) suppressed the short-term (2-h) food intake. The most effective dose of rhIL-8, 20 ng, decreased 2-h food intake by 25% and nighttime food intake by 23%. Intracerebroventricular microinfusion of anti-rhIL-8 antibody (200 and 500 ng) blocked the effect of 20 ng rhIL-8 on 2-h and nighttime food intakes. Computerized analysis of behavioral patterns for the 2-h period demonstrated a specific reduction of meal size (by 33%), whereas meal frequency and meal duration were not affected after the icv microinfusion of 20 ng rhIL-8. This short-term food intake suppression by icv rhIL-8 was accompanied by a small, but significant, increase in cerebrospinal fluid-brain and rectal temperatures. Intraperitoneal administration of rhIL-8 in doses equivalent to those administered centrally had no effect on food intake. The results suggest that IL-8 acts directly in the central nervous system to decrease feeding. This effect of IL-8 may contribute to the food intake suppression frequently accompanying pathological processes.

Pharmacological Induction of Plasticization in the Abdominal Cuticle of Rhodnius

1974 ◽  
Vol 61 (3) ◽  
pp. 705-718
Author(s):  
STUART E. REYNOLDS
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Hormone Receptor ◽  
Body Wall ◽  
Direct Action ◽  
The Body ◽  
Malpighian Tubules ◽  
Diuretic Hormone ◽  
The Central Nervous System ◽  
The Relationship

Injections of 5-hydroxytryptamine (5-HT, serotonin) are found to cause plasticization of the abdominal cuticle of Rhodnius larvae. This plasticization is a direct action of 5-HT on some element in the body wall; the central nervous system is not required. It is probable that 5-HT acts directly at a receptor on the epidermal cells. The relationship between structure and plasticizing activity for a number of 5-HT analogues has been investigated. The receptor resembles other ‘classical’ 5-HT receptors in its requirements, but is unlike the 5-HT/diuretic hormone receptor of Rhodnius Malpighian tubules.

scholarly journals Evidence of Direct Toxicological Effects of Scorpion Venom on Central Nervous System in Tunisian Children

2018 ◽  
Vol 2018 ◽  
pp. 1-3 ◽  
Author(s):  
Mabrouk Bahloul ◽  
Basma Souissi ◽  
Olfa Turki ◽  
Mariem Dlela ◽  
Khaireddine Ben Mahfoudh ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Direct Action ◽  
Scorpion Venom ◽  
Neurological Manifestations ◽  
Scorpion Sting ◽  
Scorpion Envenomation ◽  
Toxicological Effects ◽  
Cerebral Mri ◽  
The Central Nervous System

Background. Severe scorpion envenomation can lead to severe neurological manifestations, which are an indicator of the severity of the scorpion sting. The direct action of scorpion venom on the central nervous system can explain partly these neurological disorders. Methods and Findings. We report a case of severe scorpion envenomation in 16-month-old boy with no pathological history admitted in ICU for severe scorpion envenomation. The result of cerebral MRI agrees with the hypothesis of direct action of scorpion venom on the central nervous system. Patient had improved; however, he has kept as neurological sequelae language disorders and blindness. The boy was discharged 21 days after ICU admission. Conclusion. Our observation confirms that severe scorpion envenomation can be complicated by severe neurological manifestations. Although one case report is not enough to conclude such important hypothesis regarding the direct effect of scorpion venom on central nervous system (especially that the age of patient is more than one year), our case agrees with this hypothesis.

Adrenal sympathetic efferent nerve and catecholamine secretion excitation caused by capsaicin in rats

1988 ◽  
Vol 255 (1) ◽  
pp. E23-E27 ◽  
Author(s):  
T. Watanabe ◽  
T. Kawada ◽  
M. Kurosawa ◽  
A. Sato ◽  
K. Iwai
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Adrenal Gland ◽  
Direct Action ◽  
Atropine Sulfate ◽  
Catecholamine Secretion ◽  
Nerve Activity ◽  
Efferent Nerve ◽  
The Central Nervous System ◽  
Alpha Chloralose

Capsaicin enhances adrenal medullary catecholamine secretion. The participation of the central nervous system on this enhancement by capsaicin was investigated in alpha-chloralose-urethan- or halothane-anesthetized rats. Intravenous administration of capsaicin caused a rapid and marked increase in adrenal sympathetic nerve activity. The nerve activity began to show an increase with the administration of capsaicin at a dosage of 20 micrograms/kg and significantly increased with a dosage of 200 micrograms/kg, i.e., capsaicin was found to cause a dose-dependent increase in adrenal nerve activity. Cholinergic blocking with hexamethonium bromide and atropine sulfate (1 and 5 mg/kg iv, respectively) attenuated the adrenal epinephrine secretion caused by capsaicin. The direct action of capsaicin on adrenal catecholamine secretion was examined using a retrograde perfusion system of left adrenal gland. Up to 8.2 X 10(-5) M capsaicin did not enhance catecholamine secretion from the adrenal gland. These results suggest that the enhancement of physiological catecholamine secretion by capsaicin is mainly through activation of the central nervous system.

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