An Overview on “Stages of Anesthesia and Some Novel General Anesthetics Drug”
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Callistephin Enhances the Protective Effects of Isoflurane on Microglial Injury Through Downregulation of Inflammation and Apoptosis
802 MOLECULAR MEDICINE REPORTS 20: 802-812, 2019 Callistephin enhances the protective effects of isoflurane on microglial injury through downregulation of inflammation and apoptosis LILI ZHAO, SHIBIAO CHEN, TIANYIN LIU, XIUHONG WANG, HAIJIN HUANG and WEICHENG LIU Department of Anesthesiology, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi 330006, P.R. China Received June 18, 2018; Accepted March 15, 2019 DOI: 10.3892/mmr.2019.10282 Abstract. Microglia are the major immune cells in the central enhanced the effects of isoflurane. Callistephin may therefore nervous system. Microglial activation can be beneficial or constitute a candidate drug agent that may target inflammatory detrimental depending on the stimuli and the physiopathological and growth regulatory signaling pathways, thus ameliorating environment. Microglial activation is involved in a variety certain aspects of neurodegenerative diseases. of neurodegenerative disorders. Different anesthetic agents have exhibited diverse effects on microglial activation and Introduction the engulfment process. The anthocyanin callistephin has been demonstrated to have antioxidant and anti‑inflammatory Microglial cells are the major immune cell in the central properties, and these were assessed in the present study, with a nervous system (CNS), responding against types of endog- focus on its effect on microglial activation. Mouse microglial enous and exogenous stimuli, including infection by bacteria, cells C8-4B were treated with 100 ng/µl lipopolysaccharide viruses, prions and β-amyloid plaques (1). Microglia are (LPS) and 1 ng/µl interferon-γ. Cells were subsequently treated activated upon exposure to different stimuli and, depending with 2% isoflurane, 100 µM callistephin or both. LPS promoted on the environmental context, this may be beneficial or detri- apoptosis in C8-B4 cells, and this was reduced following mental to the functionality and physiology of the CNS (2). -
Effect of Rutin on Gentamicin-Induced Ototoxicity in Rats: a Biochemical and Histopathological Examination
ORIGINAL ARTICLE ENT UPDATES 11(1):8-13 DOI: 10.5152/entupdates.2021.887158 Effect of Rutin on Gentamicin-Induced Ototoxicity in Rats: A Biochemical and Histopathological Examination Abstract Objective: Gentamicin is a broad-spectrum aminoglycoside antibiotic administered parenterally for moderate to severe gram-negative infections. Ototoxicity is an im- portant side effect that limits gentamicin use. The aim of this study is to investigate the effect of rutin on gentamicin-induced ototoxicity in rats biochemically and histo- pathologically. Methods: Distilled water was administered by oral gavage to healthy controls (HG) and cobalt administered group (GC). 50 mg/kg rutin was administered by oral gavage to rutin + gentamicin (RGG) group. After one hour, 100 mg/kg gentamicin was injected intraperitoneally (i.p) to the RGG and GC animal groups. This procedure was repeated once a day for 14 days. Results: Malondialdehyde (MDA), nuclear factor-κB(NF-κB), tumor necrosis factor alpha (TNF-α) and interleukin-1 beta(IL-1β) levels in the cochlear nerve tissue of gen- tamicin-treated animals were significantly higher compared to healthy controls and rutin + gentamicin treated rats. On the other hand, the amount of total Glutathione (tGSH) was significantly lower compared to the control and rutin group. Histopatho- logical examination revealed degenerated myelinated nerve fibers in the gentamicin group and Schwann cell nuclei were generally not seen. There was a high accumula- tion of collagen fiber in the tissue and dilated blood capillaries. In the rutin group, my- elinated nerve fibers mostly exhibited normal morphology, Schwann cell nuclei were İsmail Salcan1 evident and the vessels were normal. -
Aldrich Raman
Aldrich Raman Library Listing – 14,033 spectra This library represents the most comprehensive collection of FT-Raman spectral references available. It contains many common chemicals found in the Aldrich Handbook of Fine Chemicals. To create the Aldrich Raman Condensed Phase Library, 14,033 compounds found in the Aldrich Collection of FT-IR Spectra Edition II Library were excited with an Nd:YVO4 laser (1064 nm) using laser powers between 400 - 600 mW, measured at the sample. A Thermo FT-Raman spectrometer (with a Ge detector) was used to collect the Raman spectra. The spectra were saved in Raman Shift format. Aldrich Raman Index Compound Name Index Compound Name 4803 ((1R)-(ENDO,ANTI))-(+)-3- 4246 (+)-3-ISOPROPYL-7A- BROMOCAMPHOR-8- SULFONIC METHYLTETRAHYDRO- ACID, AMMONIUM SALT PYRROLO(2,1-B)OXAZOL-5(6H)- 2207 ((1R)-ENDO)-(+)-3- ONE, BROMOCAMPHOR, 98% 12568 (+)-4-CHOLESTEN-3-ONE, 98% 4804 ((1S)-(ENDO,ANTI))-(-)-3- 3774 (+)-5,6-O-CYCLOHEXYLIDENE-L- BROMOCAMPHOR-8- SULFONIC ASCORBIC ACID, 98% ACID, AMMONIUM SALT 11632 (+)-5-BROMO-2'-DEOXYURIDINE, 2208 ((1S)-ENDO)-(-)-3- 97% BROMOCAMPHOR, 98% 11634 (+)-5-FLUORODEOXYURIDINE, 769 ((1S)-ENDO)-(-)-BORNEOL, 99% 98+% 13454 ((2S,3S)-(+)- 11633 (+)-5-IODO-2'-DEOXYURIDINE, 98% BIS(DIPHENYLPHOSPHINO)- 4228 (+)-6-AMINOPENICILLANIC ACID, BUTANE)(N3-ALLYL)PD(II) CL04, 96% 97 8167 (+)-6-METHOXY-ALPHA-METHYL- 10297 ((3- 2- NAPHTHALENEACETIC ACID, DIMETHYLAMINO)PROPYL)TRIPH 98% ENYL- PHOSPHONIUM BROMIDE, 12586 (+)-ANDROSTA-1,4-DIENE-3,17- 99% DIONE, 98% 13458 ((R)-(+)-2,2'- 963 (+)-ARABINOGALACTAN BIS(DIPHENYLPHOSPHINO)-1,1'- -
Pharmacology – Inhalant Anesthetics
Pharmacology- Inhalant Anesthetics Lyon Lee DVM PhD DACVA Introduction • Maintenance of general anesthesia is primarily carried out using inhalation anesthetics, although intravenous anesthetics may be used for short procedures. • Inhalation anesthetics provide quicker changes of anesthetic depth than injectable anesthetics, and reversal of central nervous depression is more readily achieved, explaining for its popularity in prolonged anesthesia (less risk of overdosing, less accumulation and quicker recovery) (see table 1) Table 1. Comparison of inhalant and injectable anesthetics Inhalant Technique Injectable Technique Expensive Equipment Cheap (needles, syringes) Patent Airway and high O2 Not necessarily Better control of anesthetic depth Once given, suffer the consequences Ease of elimination (ventilation) Only through metabolism & Excretion Pollution No • Commonly administered inhalant anesthetics include volatile liquids such as isoflurane, halothane, sevoflurane and desflurane, and inorganic gas, nitrous oxide (N2O). Except N2O, these volatile anesthetics are chemically ‘halogenated hydrocarbons’ and all are closely related. • Physical characteristics of volatile anesthetics govern their clinical effects and practicality associated with their use. Table 2. Physical characteristics of some volatile anesthetic agents. (MAC is for man) Name partition coefficient. boiling point MAC % blood /gas oil/gas (deg=C) Nitrous oxide 0.47 1.4 -89 105 Cyclopropane 0.55 11.5 -34 9.2 Halothane 2.4 220 50.2 0.75 Methoxyflurane 11.0 950 104.7 0.2 Enflurane 1.9 98 56.5 1.68 Isoflurane 1.4 97 48.5 1.15 Sevoflurane 0.6 53 58.5 2.5 Desflurane 0.42 18.7 25 5.72 Diethyl ether 12 65 34.6 1.92 Chloroform 8 400 61.2 0.77 Trichloroethylene 9 714 86.7 0.23 • The volatile anesthetics are administered as vapors after their evaporization in devices known as vaporizers. -
Reactions of Some 1-Arylpiperazines and 1-Aryl-4-(2-Hydroxy-3
Reactions of Some l-Arylpiperazines and -Aryl-4- (2-Hydroxy-3-Methoxypropyl) Piperazines By HILDA HOWELL A DISSERTATION PRESENTED TO THE GRADUATE COUNQL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY UNIVERSITY OF FLORIDA August, 1961 5 ACKNOWLEDGMENTS The author would like to thank Parke, Davis and Company who provided a graduate fellowship during part of this work. The able assistance of the faculty, staff, and fellow graduate students of the Chemistry Department has made this research quite pleasant. Thanks are also due to Miss Joan Merritt, Mrs. Marie Eckart, Mr. T. W. Brooks, and Mr. Ralph Damico for their help with the typing, drawings, and proofreading of this report. The special consideration of Mr. P. L. Bhatia who shared this laboratory is appreciated. Special recognition is offered to D». C. B. Smith, Commdr. N. L. Smith, Dr. W. M. Jones, and Dr. G. B. Butler, each of whom from his own ability and opportunity has been of inestimable help. The moral support of her parents, family, and friends has significantly contributed to the success of this graduate program. She is deeply indebted to Dr* C. B. Pollard for his inspiration and direction !n the early part of this work and to her graduate ccKnmittee for their friendship demonstrated particularly since his death. She is especially indebted to Dr. Harry H. Slsler for the under- standing way in which he has directed the completion of this research. His friexidship and encouragement have made graduate work an enjoyable experience. ^ TABLE OF CONTENTS Page ACKNOWLEDGMENTS. -
Air Pollution Control General Definitions Regulation, State Of
STATE RHODE ISLAND AND PROVIDENCE PLANTATIONS DEPARTMENT OF ENVIRONMENTAL MANAGEMENT OFFICE OF AIR RESOURCES AIR POLLUTION CONTROL GENERAL DEFINITIONS REGULATION Applicability Unless otherwise expressly defined by an individual Air Pollution Control Regulation, the terms, definitions and unit of measure abbreviations contained herein shall be generally applicable to all Rhode Island Air Pollution Control Regulations adopted or amended at the same time as or after the adoption of these definitions. Definitions “Act” or “Clean Air Act” or “CAA” means the Federal Clean Air Act, as amended 42 U.S.C. 7401, et seq. “Actual heat input” means the gross heat release potential based upon the actual BTU content of the fossil fuel being burned and the rate at which it is burned. “Administrator” means the Administrator of the United States Environmental Protection Agency or the Administrator's duly authorized representative. “Aerodynamic downwash” means the rapid descent of a plume to ground level with little dilution and dispersion due to alteration of background air flow characteristics caused by the presence of buildings or other obstacles in the vicinity of the emission point. “Air contaminant” means soot, cinders, ashes, any dust, fumes, gas, mist, smoke, vapor, odor, toxic or radioactive material, particulate matter, or any combination of these. “Air pollution” means the presence in the outdoor atmosphere of one or more air contaminants in sufficient quantities which, either alone or in connection with other emissions, by reason of their concentration and duration, may be injurious to human, plant or animal life, or cause damage to property or which unreasonably interferes with the enjoyment of life and property. -
Visualizing Anesthesia-Induced Vasodilation of Cerebral Vasculature Using Multi-Exposure Speckle Imaging
bioRxiv preprint doi: https://doi.org/10.1101/2020.06.26.174227; this version posted June 29, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Visualizing anesthesia-induced vasodilation of cerebral vasculature using multi-exposure speckle imaging Colin T. Sullendera, Lisa M. Richardsa, Fei Heb, Lan Luanb,c, Andrew K. Dunna,* aDepartment of Biomedical Engineering, University of Texas at Austin, 107 W. Dean Keeton Street Stop C0800, Austin, Texas, 78712, United States bDepartment of Electrical and Computer Engineering, Rice University, 6100 Main Street, Houston, TX, 77005, United States cDepartment of Bioengineering, Rice University, 6100 Main Street, Houston, TX, 77005, United States Abstract. Anesthetized animal models are used extensively during neurophysiological and behavioral studies despite systemic effects from anesthesia that undermine both accurate interpretation and translation to awake human physi- ology. In this paper, we characterize the impact of isoflurane on cerebral blood flow (CBF) during the induction of general anesthesia in awake mice using multi-exposure speckle imaging (MESI). We highlight the large anatomical changes caused by the vasodilatory inhalant with wide-field imagery and quantify the cortical hemodynamics with MESI across multiple subjects and imaging sessions. Compared to the awake state, we measured, on average, an 18% increase in surface vessel diameter accompanied by a 135% increase in vascular flux and 92% increase in parenchyma perfusion. These large alterations to the cortical vasculature and CBF are unrepresentative of normal physiology and provide further evidence that neuroscience experiments would benefit from transitioning to un-anesthetized awake animal models. -
Pharmacological Classification of the Abuse-Related Discriminative
Ashdin Publishing Journal of Drug and Alcohol Research ASHDIN Vol. 3 (2014), Article ID 235839, 10 pages publishing doi:10.4303/jdar/235839 Research Article Pharmacological Classification of the Abuse-Related Discriminative Stimulus Effects of Trichloroethylene Vapor Keith L. Shelton and Katherine L. Nicholson Department of Pharmacology and Toxicology, School of Medicine, Virginia Commonwealth University, P.O. Box 980613, Richmond, VA 23298, USA Address correspondence to Keith L. Shelton, [email protected] Received 10 December 2013; Revised 2 January 2014; Accepted 27 January 2014 Copyright © 2014 Keith L. Shelton and Katherine L. Nicholson. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Inhalants are distinguished as a class primarily based upon common means of administration suggests a homogeneity of a shared route of administration. Grouping inhalants according to mechanism and behavioral effects that may be scientifically their abuse-related in vivo pharmacological effects using the drug unwarranted. As an illustration of the inadequacy of this discrimination procedure has the potential to provide a more relevant classification scheme to the research and treatment community. simplistic taxonomic approach, consider the fact that if a Mice were trained to differentiate the introceptive effects of the similar system was applied to other common drugs of abuse, trichloroethylene vapor from air using an operant procedure. then tobacco, crack cocaine, and marijuana would be treated Trichloroethylene is a chlorinated hydrocarbon solvent once used as a single category. Instead, other classes of abused drugs as an anesthetic as well as in glues and other consumer products. -
The Cardiovascular and Respiratory Effects of Isoflurane-Nitrous Oxide Anaesthesia
THE CARDIOVASCULAR AND RESPIRATORY EFFECTS OF ISOFLURANE-NITROUS OXIDE ANAESTHESIA WILLIAM M. DOLAN, M.D.S, WENDELL C. STEVENS, M.D.,O EDMOND I. EGER, II, M.D.,* TnOlX~AS H. CROMWELL, M.D,, c* MICHAEL J. HALSEY, PH.D.,C* THOMAS F. SHAKESPEAlqE, Ik~.D.,c* AND RONALD D. MILLER, M.D. c* INTRODUCTION ISOFLURAnE (Forane| 1 chloro-2-2-2 trifluoroethyl, difluoromethyl ether), is a halogenated ether currently being evaluated for use as an inhalational anaesthetic. Its favourable properties include non-flammability, 1 relatively low blood and fat solubilities (blood-gas and oil-gas partitions of 1.4 and 99, respectively), 1,2 mole- cular stability resulting in resistance to dehydrohalogenation and hepatic meta- bolism, 1,~ lack of sensitization of the heart to catecholamines, 4 and favourable depression of neuromuscular function and potentiation of muscle relaxants. ~ However, isoflurane can produce profound depression of ventilation and blood pressure. ~ Since the concurrent use of nitrous oxide with halothane attenuates the hypotension and ventilatory depression caused by halothane, s,'~,l~ we asked whether nitrous oxide would produce similar changes towards awake values dur- ing isoflurane anaesthesia. METHODS We studied the cardiovascular and respiratory effects of anaesthesia with iso- flurane and 70 per cent nitrous oxide in eight healthy, unpremedicated volun- teers. The volunteers were 25 --4- 1 (SD) years of age and were informed of the purposes, procedures, and hazards of the study. The protocol was approved by the Committee on Human Experimentation of the University of California, San Francisco. A normal medical history, physical examination, chest roentgenogram, complete blood count, serum glutamic oxaloacetic transanainase and lactic de- hydrogenase were required before a volunteer was accepted for anaesthesia. -
Synthetic Method for Fluoromethylation Of
Europäisches Patentamt *EP001286941B1* (19) European Patent Office Office européen des brevets (11) EP 1 286 941 B1 (12) EUROPEAN PATENT SPECIFICATION (45) Date of publication and mention (51) Int Cl.7: C07C 43/12, C07C 41/16, of the grant of the patent: C07C 41/22, C07C 41/28, 20.07.2005 Bulletin 2005/29 C07C 41/52, C07C 43/313 (21) Application number: 01939633.2 (86) International application number: PCT/US2001/017348 (22) Date of filing: 30.05.2001 (87) International publication number: WO 2001/092193 (06.12.2001 Gazette 2001/49) (54) SYNTHETIC METHOD FOR FLUOROMETHYLATION OF HALOGENATED ALCOHOLS VERFAHREN ZUR FLUORMETHYLIERUNG VON HALOGENIERTEN ALKOHOLEN PROCEDE DE SYNTHESE DE FLUOROMETHYLATION D’ALCOOLS HALOGENES (84) Designated Contracting States: (72) Inventors: AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU • BIENIARZ, Christopher MC NL PT SE TR Highland Park, IL 60035 (US) Designated Extension States: • RAMAKRISHNA, Kornepati, V. RO SI Libertyville, IL 60048 (US) (30) Priority: 01.06.2000 US 587421 (74) Representative: Modiano, Guido, Dr.-Ing. et al Modiano, Josif, Pisanty & Staub, (43) Date of publication of application: Baaderstrasse 3 05.03.2003 Bulletin 2003/10 80469 München (DE) (73) Proprietor: Abbott Laboratories (56) References cited: Abbott Park, IL 60064-6050 (US) EP-A- 0 822 172 GB-A- 1 250 928 Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. -
Chapter 14 Ethers
Chapter 14 Ethers, Epoxides, and Sulfides Chem 233 Dr. Hoeger Introduction • Formula R-O-R′ where R and R′ are alkyl or aryl. • Symmetrical or unsymmetrical • Examples: CH3 O CH3 O O CH3 Ethers Ethers 2 1 Structure and Polarity • Bent molecular geometry • Oxygen is sp3 hybridized • Tetrahedral angle => Ethers Ethers 3 Boiling Points Similar to alkanes of comparable molecular weight. => Ethers Ethers 4 2 Hydrogen Bond Acceptor • Ethers cannot H-bond to each other. • In the presence of -OH or -NH (donor), the lone pair of electrons from ether forms a hydrogen bond with the -OH or -NH. => Ethers Ethers 5 Solvent Properties • Nonpolar solutes dissolve better in ether than in alcohol. • Ether has large dipole moment, so polar solutes also dissolve. • Ethers solvate cations. • Ethers do not react with strong bases. => Ethers Ethers 6 3 Ether Complexes • Grignard reagents H + _ • Electrophiles O B H H BH3 THF • Crown ethers => Ethers Ethers 7 Common Names of Ethers • Alkyl alkyl ether • Current rule: alphabetical order • Old rule: order of increasing complexity • Symmetrical: use dialkyl, or just alkyl. • Examples: CH3 CH3 O C CH3 CH3CH2 O CH2CH3 CH3 diethyl ether or t-butyl methyl ether or ethyl ether methyl t-butyl ether => Ethers Ethers 8 4 IUPAC Names • Alkoxy alkane • Examples: CH 3 O CH3 CH3 O C CH3 CH3 2-methyl-2-methoxypropane Methoxycyclohexane => Ethers Ethers 9 Cyclic Ethers • Heterocyclic: oxygen is in ring. O Epoxides (oxiranes) • H2C CH2 O • Oxetanes • Furans (Oxolanes ) O O • Pyrans (Oxanes ) O O O •Dioxanes => O Ethers Ethers 10 5 Naming Epoxides • Alkene oxide, from usual synthesis method H peroxybenzoic acid O cyclohexene oxide H • Epoxy attachment to parent compound, 1,2-epoxy-cyclohexane • Oxirane as parent, oxygen number 1 O H CH3 trans-2-ethyl-3-methyloxirane => CH3CH2 H Ethers Ethers 11 Spectroscopy of Ethers • IR: Compound contains oxygen, but O-H and C=O stretches are absent. -
Delivery of Carbon Monoxide Via Halogenated Ether Anesthetics
Nitric Oxide 89 (2019) 93–95 Contents lists available at ScienceDirect Nitric Oxide journal homepage: www.elsevier.com/locate/yniox T Delivery of carbon monoxide via halogenated ether anesthetics ARTICLE INFO Keywords: Anesthetics CORM Carbon monoxide Heme oxygenase Desflurane Sevoflurane Organ transplantation Letter to the Editor across preclinical models. Whereas preclinical models have experi- mental flexibility, stringent safety constraints have prevented physi- The therapeutic potential of carbon monoxide (CO) has been well- cians from attaining high COHb levels in humans. Interestingly, a characterized over the past decades [1]. Organ transplantation is an widely used general anesthetic, desflurane, has been associated with exemplary unmet medical need where CO has emerged as a protective significantly increased intraoperative COHb levels ranging between 7% agent [2]. Translational efforts have focused on CO inhalation proto- and 36% when administered through dried carbon dioxide absorbents cols, carboxyhemoglobin infusion, heme oxygenase (HO) induction, [18]. Though 36% COHb is an extraordinary case, it seems possible that and local delivery of CO-releasing molecules (CORMs); however, a anesthesia protocols utilizing HEAs can be optimized to deliver a CO clinical breakthrough has yet to emerge [3]. Interestingly, halogenated payload to achieve high COHb levels in a clinical setting. ether anesthetics (HEAs) (Fig. 1) have been linked to elevated in- The phenomenon of CO being liberated from HEAs within an an- traoperative carboxyhemoglobin (COHb) levels [4,5]. A recent rando- esthesia machine apparatus has been well-documented [4]. The pro- mized clinical trial indicated patients receiving HEAs have demon- posed mechanism for desflurane is specifically dependent upon are- strated improved graft survival prognosis relative to patients receiving action with partially dried carbon dioxide absorbents (< 4.8% water a different anesthetic.