Pharmacokinetic application for this method was performed in Sprague Dawely rats. Resperidone and fluxotine were made into suspension using 2% tweem 80. Male rats weighing 200± 20 g administered simultaneously with risperidone mg/kg and fluoxetine 0.3 mg/kg after overnight fasting. Blood was withdrawal from the retro-orbital vein under partial anesthesia at ….,….. h post dosing. Plasma separated by centrifugation of blood at 3500 rpm for 5min. The sample kept frozen at -80 °C till analysis.…
Dopaminergic innervation in sympathetic system - renal blood vessels Important steps of Neurotransmission: Synthesis, storage, release, recognition, and metabolism. Know where drugs can intervene,…
Blocks the effects of serotonin at 5-HT3 – receptor sites located in the vagal nerve terminals and the chemoreceptor trigger zone in the CNS. Therapeutic effects: decreases severity of nausea and vomiting following chemotherapy or surgery.…
Adrenergic medications affect the four receptors, a1, a2, B1 and B2. The sympathetic nervous system triggers the secretion of epinephrine and norepinephrine. Epinephrine is a hormone and norepinephrine functions as a hormone and neurotransmitter.…
The functional anatomy of anxiety involves amygdala-based neurocircuits with critical reciprocal connections to the medial prefrontal cortex (i.e. Mailizia, 1999). An understanding of the functional anatomy of anxiety allows for a new perspective on the various anxiety disorders. The neurotransmitters involved in these circuits are reviewed for their relevance to the pharmacologic choices in the treatment of anxiety (i.e. Kang, Wilson & Wilson, 2000). Much research has been conducted on gamma-aminobutyric acid (GABA) as it is the major inhibitory neurotransmitter in the mammalian Central Nervous System (CNS) (i.e. Vekovischeva, Haapalinna & Sarviharju, 1999). GABA participates in the regulation of neuronal excitability through specific membrane proteins (the GABAA receptors). The binding of GABA to these postsynaptic receptor results in an opening of chloride channel integrated in the receptor, which allows the entry of Cl-. As a consequence, this leads to the hyperpolarization of the recipient cell, which is allosterically modulated by a wide variety of chemical entities that interact with distinct binding sites at the GABAA receptor complex. One of the most thoroughly investigated modulatory sites is the benzodiazepine-binding site. The purpose of this paper is to…
Areas with altered interictal perfusion may reflect local interictal differences in neuronal metabolic activity or density. This could reflect a preexisting difference in local brain structure and/or function or be the consequence of repetitive migraine attacks or chronic adaptive mechanisms, leading to neuroplastic changes in cortical and subcortical structures. Shorter-term explanations include changes related to, for instance, the migraine cycle, the presence of some degree of interictal cerebrovascular dysregulation in migraineurs, or a (migraine disease-related) systemic condition altering vessel wall characteristics that influence regional blood flow. Most if not all currently identified areas of altered perfusion have earlier been reported…
Ronald P. Rubin, (2007). A Brief History of Great Discoveries in Pharmacology: In Celebration of the Centennial Anniversary of the Founding of the American Society of Pharmacology and Experimental Therapeutics . pharmacological review. 59 , pp.4…
Ketamine, or the chemical name Ketamine Hydrochloride, was originally created to be used as a human anaesthetic, and is still used as an anaesthetic for children, people with ppor health, and in veterinary medicine. Ketamine is also used as a recreational drug due to it's effects of causing a separation between perception and sensation. In other words, your mind drifts away from your body and you lose control of your body and the sensations that yoour body is feeling. This is why ketamine is grouped into the category named "dissociative anaesthetics" because of the way that it can separate your body and mind. Ketamine is usually sold in small pharmacy bottles but when it is used recreationally, it is often cooked into a white powder for snorted…
Daly, J.W., Butts-Lamb, P. and Padgett, W. Subclasses of adenosine receptors in the central nervous system: Interaction with caffeine and related methylxanthines. Cellular and Molecular Neurobiology. 3:69-80, 1983.…
Bennett HJ, White TD, & Semba K. 2003. Activation of Cholinergic and Adrenergic Receptors Increases the Concentration of Extracellular Adenosine in the Cerebral Cortex of Unanesthetized Rat. 117, 1, 119-127.…
Unit 7. Assignment 2. The Effects of Selected Drugs and Diseases on the Central Nervous System.…
The addiction to ketamine is a very strong mental bond. What occurs when a person uses ketamine is called disassociation. They become separate from themselves. The feeling that comes with this is an extreme feeling of euphoria followed by a near death feeling. These episodes of consciousness perforation can become extremely psychologically addicting.…
Ketamine was developed in the early 1960’s. It is dissociative anesthetic and is used in human and veterinary medicines but, it is primarily used for anesthesia. Ketamine is under the category of Hallucinogens. Hallucinogens interfere with the brain and the central nervous system by in radical distortions of a user’s perception of reality. Images, sensations, and sounds with be experienced but don’t actually exist.…
The Effect of Common Household Drugs on Circulatory Functions. N.p.: Department of Biology, n.d. Print.…
ii) On the basis of molecular targets: Biomolecules like Carbohydrates, lipids, proteins, nucleic acids etc. react with dugs. These biomolecules are called drug targets or simply target molecules. iii) On the basis of chemical structure: The drugs with some common structural features generally show similar pharmacological activity. Ex: Sulphonamides have common structural feature. So they have same chemotherapeutic action. 2. Discuss about (i) analgesics and (ii) antipyretics. Ans: Analgesics: Analgesics either reduce or totally abolish pain without causing disturbances of nervous system. These are classified as a) Narcotic analgesics: These are most potent and clinically useful agents causing depression of central nervous system and at the same time act as strong analgesics. Ex: Morphine, Codeine, Heroin etc. The term narcotic drugs now mean addictive drugs. When these are administered in medicinal doses, relieve pain and produce sleep. In high doses they produce coma, convulsions and finally death. Uses: These analgesics are chiefly used for the relief of post operative pain, cardiac pain, cancer pain, cough and induce sleep in the presence of pain.…