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1.
Eur Rev Med Pharmacol Sci ; 26(1): 211-217, 2022 Jan.
Article in English | MEDLINE | ID: mdl-35048997

ABSTRACT

OBJECTIVE: Testicular torsion is a condition that manifests with acute pain and can lead to infertility despite urgent surgical intervention. The aim of this study is to investigate the protective and preventive effects of etomidate, an imidazole derivative, a non-barbiturate general anesthetic agent, without analgesic effect, on testicular ischemia-reperfusion injury. MATERIALS AND METHODS: Twenty-four adult male Wistar rats weighing 200-250 g were used in the study. Torsion was created in all rats by rotating left testes 720° clockwise on the day of the experiment. 30 minutes before detorsion, 4 mg/kg etomidate and 10 mg/kg propofol were administered intraperitoneally to the etomidate and propofol groups, respectively. After an hour of ischemia, the left testis was reinstated, and the tissues were repaired according to their physiology. Following 24 hours of reperfusion, the animals were euthanized after ipsilateral and contralateral testes were removed. RESULTS: Etomidate applied before testicular detorsion significantly suppressed germ cell damage and Leydig cell loss in ipsilateral tissue. It did not cause any significant changes in the percentage of necrosis, histological score, and tubule rupture in ipsilateral tissue. Propofol administered before testicular detorsion significantly suppressed the percentage of necrosis only in the ipsilateral tissue. In addition, no signs of damage were observed in the contralateral testis. CONCLUSIONS: These findings show that etomidate administered before detortion creates a protective effect by preventing testicular ischemia-reperfusion injury.


Subject(s)
Etomidate , Reperfusion Injury , Animals , Etomidate/pharmacology , Male , Malondialdehyde , Rats , Rats, Wistar , Reperfusion Injury/drug therapy , Reperfusion Injury/pathology , Reperfusion Injury/prevention & control , Testis
2.
Auton Autacoid Pharmacol ; 33(1-2): 7-16, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23461535

ABSTRACT

The nitrergic system modulates cardiovascular functions of the central nucleus of amygdala (CeA) and the posterior hypothalamus (PH) which are involved in the central regulation of the cardiovascular system. The aim of this study was to investigate the contribution of nitric oxide (NO) in the PH in eliciting cardiovascular responses produced through electrical stimulation (ES) of the CeA. Rats were implanted with a stimulation electrode and a parenchymal cannula system into the CeA and a parenchymal cannula or a microdialysis probe into the PH. The next day, the femoral artery was cannulated for haemodynamic measurement. The CeA was electrically stimulated to produce cardiovascular response. The nitric oxide synthetase inhibitor, NG-nitro-L-arginine methyl ester (L-NAME; 400 nmol/100 nl) or artificial cerebrospinal fluid were injected into the PH or the CeA before the ES of the CeA. The dialysates were collected from the PH to determine the L-citrulline and the L-glutamic acid levels. L-NAME injection into the CeA but not to the PH suppressed the increases in the mean arterial pressure produced by the ES of the CeA significantly; however, heart rate was not affected by L-NAME injection into either the PH or the CeA. L-citrulline and L-glutamic acid levels in the PH were shown to be increased by the ES of the CeA. NO is involved between the PH and the CeA which has a considerable role in the central regulation of the cardiovascular system.


Subject(s)
Amygdala/physiology , Blood Pressure/physiology , Hypothalamus, Posterior/physiology , Nitric Oxide/physiology , Amygdala/drug effects , Animals , Blood Pressure/drug effects , Citrulline/metabolism , Electric Stimulation , Enzyme Inhibitors/administration & dosage , Female , Glutamic Acid/metabolism , Heart Rate/drug effects , Heart Rate/physiology , Hypothalamus, Posterior/drug effects , Male , Microdialysis , Microinjections , NG-Nitroarginine Methyl Ester/administration & dosage , Nitric Oxide Synthase/antagonists & inhibitors , Rats , Rats, Sprague-Dawley
3.
Pharmacology ; 68(4): 190-7, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12837973

ABSTRACT

Epilepsy affects homeostasis and autonomic nervous system functions. It has been thought that the dysfunction in the autonomic neural mechanisms could be a cause of sudden unexpected death in patients with epilepsy. The kindling model of epilepsy is considered to be an animal model for complex partial seizures with secondary generalization. The objectives of this study were to investigate the extracellular gamma-aminobutyric acid (GABA), glutamate, noradrenaline and dopamine levels in the dorsomedial nucleus of the hypothalamus in non-epileptic and kindled epileptic rats and to explain some of the cardiovascular changes in the kindling model of epilepsy. Stimulation electrodes were stereotaxically implanted into the basolateral amygdala and electrical stimulation was applied 3 times a day at a constant current. The rats were then kindled to full stage 5 seizures. Microdialysis experiments were performed to demonstrate the neurotransmitter levels in the dorsomedial nucleus of the hypothalamus 3-5 days after being kindled. Decreases in noradrenaline and dopamine levels in the dorsomedial nucleus were detected in the conscious kindled animals. This finding is in agreement with prior findings that the noradrenergic system has a negative role in the process of kindling. The basal level of glutamic acid and GABA remained unchanged in the kindled group when compared to non-epileptic animals, and similarly, neither blood pressure nor heart rate responses to bicuculline or N-methyl-D-aspartate were affected by the acute kindled state. These findings suggest that the autonomic changes in kindling require further studies.


Subject(s)
Dopamine/metabolism , Dorsomedial Hypothalamic Nucleus/physiology , Glutamic Acid/metabolism , Kindling, Neurologic , Norepinephrine/metabolism , gamma-Aminobutyric Acid/metabolism , Animals , Bicuculline/pharmacology , Blood Pressure/drug effects , Chromatography, High Pressure Liquid , Epilepsy/metabolism , Epilepsy/physiopathology , Extracellular Space/metabolism , Heart Rate/drug effects , Male , Microdialysis , N-Methylaspartate/pharmacology , Rats , Rats, Sprague-Dawley , Receptors, N-Methyl-D-Aspartate/drug effects
4.
Brain Res ; 968(2): 219-26, 2003 Apr 11.
Article in English | MEDLINE | ID: mdl-12663091

ABSTRACT

Dorsomedial (DMH) and paraventricular nuclei (PVN) are two important hypothalamic structures involved in the central regulation of cardiovascular regulation. L-Glutamic acid and gamma-aminobutyric acid (GABA) were demonstrated to elicit cardiovascular responses when administered via intracerebroventricular injection or parenchymal microinjections into the hypothalamic nuclei, participating in central cardiovascular regulation. In this study the interaction between the DMH and the PVN were investigated by means of microinjection and microdialysis techniques in Sprague-Dawley rats. Stereotaxic surgery was performed for the insertion of intracerebral parenchymal microinjection cannula into the right DMH and microdialysis probe into the left PVN. After a recovery period of 3 days, the iliac artery was cannulated for monitoring pulsatile blood pressure and heart rate by means of pressure transducer connected to a polygraph. Microinjection of 50 pmol NMDA into the DMH was performed and microdialysis perfusates were collected simultaneously from the PVN in the conscious rat model. L-Glutamic acid and GABA levels were analyzed by an isocratic HPLC method with the aid of a fluorescent detector. Microinjection of 50 pmol NMDA into the DMH produced significant increases in mean arterial pressure and heart rate. NMDA microinjection into the DMH produced a significant increase in L-glutamic acid release in the PVN, but no significant change in GABA release was observed. These results may indicate that stimulation of the DMH by NMDA results in subsequent stimulation of the PVN.


Subject(s)
Blood Pressure/drug effects , Dorsomedial Hypothalamic Nucleus/physiology , Excitatory Amino Acid Agonists/pharmacology , Heart Rate/drug effects , N-Methylaspartate/pharmacology , Paraventricular Hypothalamic Nucleus/physiology , Animals , Dorsomedial Hypothalamic Nucleus/anatomy & histology , Dorsomedial Hypothalamic Nucleus/drug effects , Female , Functional Laterality , Glutamic Acid/metabolism , Male , Microdialysis/methods , Microinjections/methods , Paraventricular Hypothalamic Nucleus/anatomy & histology , Rats , Rats, Sprague-Dawley , Time Factors , gamma-Aminobutyric Acid/metabolism
5.
J Anat ; 198(Pt 4): 463-72, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11327208

ABSTRACT

The posterior hypothalamic nucleus has been implicated as an area controlling autonomic activity. The afferent input to the nucleus will provide evidence as to its role in autonomic function. In the present study, we aimed to identify the detailed anatomical projections to the posterior hypothalamic nucleus from cortical, subcortical and brainstem structures, using the horseradish peroxidase (HRP) retrograde axonal transport technique in the rat. Subsequent to the injection of HRP into the posterior hypothalamic nucleus, extensive cell labelling was observed bilaterally in various areas of the cerebral cortex including the cingulate, frontal, parietal and insular cortices. At subcortical levels, labelled cells were observed in the medial and lateral septal nuclei, the bed nucleus of stria terminalis, and various thalamic and amygdaloid nuclei. Also axons of the vertical and horizontal limbs of the diagonal band were labelled and labelled cells were localised at the CA1 and CA3 fields of the hippocampus and the dentate gyrus. The brainstem projections were from the medial, lateral and parasolitary nuclei, the intercalated nucleus of the medulla, the sensory nuclei of the trigeminal nerve, and various reticular, vestibular, raphe and central grey nuclei. The posterior hypothalamic nucleus also received projections from the lateral and medial cerebellar nuclei and from upper cervical spinal levels. The results are discussed in relation to the involvement of the posterior hypothalamic nucleus in autonomic function and allows a better understanding of how the brain controls visceral function.


Subject(s)
Autonomic Nervous System/physiology , Hypothalamus, Posterior/anatomy & histology , Neurons, Afferent/cytology , Animals , Axonal Transport , Brain Stem/cytology , Cell Count , Cerebellum/cytology , Coloring Agents , Horseradish Peroxidase , Rats , Rats, Sprague-Dawley
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