Thymol, Menthol and Camphor from Indian Sources
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Technical Options for the Mitigation of Direct Methane and Nitrous Oxide Emissions from Livestock: a Review
Animal (2013), 7:s2, pp 220–234 & Food and Agriculture Organization of the United Nations 2013 animal doi:10.1017/S1751731113000876 Technical options for the mitigation of direct methane and nitrous oxide emissions from livestock: a review - P. J. Gerber1 , A. N. Hristov2, B. Henderson1, H. Makkar1,J.Oh2, C. Lee2, R. Meinen2, F. Montes3,T.Ott2, J. Firkins4, A. Rotz5, C. Dell5, A. T. Adesogan6,W.Z.Yang7, J. M. Tricarico8, E. Kebreab9, G. Waghorn10, J. Dijkstra11 and S. Oosting11 1Agriculture and Consumer protection Department, Food and Agriculture Organization of the United Nations, Vialle delle terme di Caracalla, 00153 Rome, Italy; 2Department of Animal Science, The Pennsylvania State University, University Park, PA 16802, USA; 3Plant Science Department, The Pennsylvania State University, University Park, PA 16802, USA; 4Department of Animal Sciences, The Ohio State University, Columbus OH 43210, USA; 5Department of Animal Sciences, USDA-Agricultural Research Service, Pasture Systems and Watershed Management Research Unit, University Park, PA 16802, USA; 6University of Florida, Gainesville, FL 32608, USA; 7Agriculture and Agri-Food Canada, Lethbridge AB, Canada T1J 4B1; 8Innovation Center for U.S. Dairy, Rosemont, IL 60018, USA; 9Department of Animal Sciences, University of California, Davis, CA 95616, USA; 10DairyNZ, Hamilton 3240, New Zealand; 11Department of Animal Sciences, Wageningen University, 6700 AH Wageningen, The Netherlands (Received 28 February 2013; Accepted 15 April 2013) Although livestock production accounts for a sizeable share of global greenhouse gas emissions, numerous technical options have been identified to mitigate these emissions. In this review, a subset of these options, which have proven to be effective, are discussed. -
Excluded Drug List
Excluded Drug List The following drugs are excluded from coverage as they are not approved by the FDA ACTIVE-PREP KIT I (FLURBIPROFEN-CYCLOBENZAPRINE CREAM COMPOUND KIT) ACTIVE-PREP KIT II (KETOPROFEN-BACLOFEN-GABAPENTIN CREAM COMPOUND KIT) ACTIVE-PREP KIT III (KETOPROFEN-LIDOCAINE-GABAPENTIN CREAM COMPOUND KIT) ACTIVE-PREP KIT IV (TRAMADOL-GABAPENTIN-MENTHOL-CAMPHOR CREAM COMPOUND KIT) ACTIVE-PREP KIT V (ITRACONAZOLE-PHENYTOIN SODIUM CREAM CMPD KIT) ADAZIN CREAM (BENZO-CAPSAICIN-LIDO-METHYL SALICYLATE CRE) AFLEXERYL-LC PAD (LIDOCAINE-MENTHOL PATCH) AFLEXERYL-MC PAD (CAPSAICIN-MENTHOL TOPICAL PATCH) AIF #2 DRUG PREPERATION KIT (FLURBIPROFEN-GABAPENT-CYCLOBEN-LIDO-DEXAMETH CREAM COMPOUND KIT) AGONEAZE (LIDOCAINE-PRILOCAINE KIT) ALCORTIN A (IODOQUINOL-HYDROCORTISONE-ALOE POLYSACCHARIDE GEL) ALEGENIX MIS (CAPSAICIN-MENTHOL DISK) ALIVIO PAD (CAPSAICIN-MENTHOL PATCH) ALODOX CONVENIENCE KIT (DOXYCYCLINE HYCLATE TAB 20 MG W/ EYELID CLEANSERS KIT) ANACAINE OINT (BENZOCAINE OINT) ANODYNZ MIS (CAPSAICIN-MENTHOL DISK) APPFORMIN/D (METFORMIN & DIETARY MANAGEMENT CAP PACK) AQUORAL (ARTIFICIAL SALIVA - AERO SOLN) ATENDIA PAD (LIDOCAINE-MENTHOL PATCH) ATOPICLAIR CRE (DERMATOLOGICAL PRODUCTS MISC – CREAM) Page 1 of 9 Updated JANUARY 2017 Excluded Drug List AURSTAT GEL/CRE (DERMATOLOGICAL PRODUCTS MISC) AVALIN-RX PAD (LIDOCAINE-MENTHOL PATCH) AVENOVA SPRAY (EYELID CLEANSER-LIQUID) BENSAL HP (SALICYLIC ACID & BENZOIC ACID OINT) CAMPHOMEX SPRAY (CAMPHOR-HISTAMINE-MENTHOL LIQD SPRAY) CAPSIDERM PAD (CAPSAICIN-MENTHOL -
Pre-Validation of an Acute Inhalation Toxicity Assay Using the Epiairway in Vitro Human Airway Model
Pre-Validation of an Acute Inhalation Toxicity Assay Using the EpiAirway In Vitro Human Airway Model George R. Jackson, Jr., Michelle Debatis, Anna G. Maione, Patrick J. Hayden Exposure to potentially dangerous chemicals can occur through inhalation. UNDERSTANDING HUMAN BIOLOGY IN DIMENSIONS3 2 Regulatory systems for classifying the acute inhalation toxicity of chemicals ≤ 0.05 mg/l > 0.05 ≤ 0.5 mg/l > 0.5 ≤ 2 mg/l > 2 mg/l Respirator Use Required 3 Regulatory systems for classifying the acute inhalation toxicity of chemicals 4 OECD 403/436 is the currently accepted test method for determining acute inhalation toxicity OECD Test Guidelines 403/436: In vivo rat LD50 test (dose at which 50% of the animals die) 4 hour exposure 14 Days Examination: - Death -Signs of toxicity -Necropsy should be performed (not always reported) Nose/Head only (preferred) Whole body Repeat stepwise with additional concentrations as necessary 5 Our goal is to develop & validate an in vitro test for acute inhalation toxicity UNDERSTANDING HUMAN BIOLOGY IN DIMENSIONS3 6 The EpiAirway Model EpiAirway is an in vitro 3D organotypic model of human tracheal/bronchial tissue. - Constructed from primary cells - Highly reproducible - Differentiated epithelium at the air-liquid interface - Beating cilia - Mucus secretion - Barrier function - Physiologically relevant & predictive of the human outcome Air Cilia Differentiated epithelium Microporous membrane Media 7 EpiAirwayTM acute inhalation toxicity test method Prepare 4-point dose Apply chemical to Incubate for 3 hours Examination: curve of chemical in the apical surface - Tissue viability (MTT) dH2O or corn oil Advantages of using the in vitro EpiAirway test: 1. -
Thymol Decreases Apoptosis and Carotid Inflammation Induced by Hypercholesterolemia Through a Discount in Oxidative Stress
http://www.cjmb.org Open Access Original Article Crescent Journal of Medical and Biological Sciences Vol. 4, No. 4, October 2017, 186–193 eISSN 2148-9696 Thymol decreases apoptosis and carotid inflammation induced by hypercholesterolemia through a discount in oxidative stress Roshanak Bayatmakoo1, Nadereh Rashtchizadeh2*, Parichehreh Yaghmaei1, Mehdi Farhoudi3, Pouran Karimi3 Abstract Objective: Atherosclerosis sclerosis is a chronic inflammatory disease that can lead to cardiovascular and cerebrovascular disorders that are generally along with hypercholesterolemia and oxidative stress. Various surveys have shown that thymol is a polyphenolic compound with anti-inflammatory and antioxidant properties. This study aimed to investigate the anti- inflammatory and antiapoptotic effects of thymol on carotid tissue of hypercholesterolemic rats. Materials and Methods: Forty male Wistar rats were randomly divided into 4 groups with 10 members each (n = 10): a control group with a normal diet (ND), a group with a high-cholesterol (2%) diet (HD), a group with a high-cholesterol diet combined with thymol (24 mg/kg HD + T), and a group with a thymol diet (T). After preparing serum from peripheral blood of rats, lipid measurements were obtained, including total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), and triglycerides (TG), by using a colorimetric method; the levels of oxidized LDL (OxLDL) were obtained through enzyme-linked immunosorbent assay (ELISA). The activities of superoxide dismutase (SOD) and glutathione peroxidase (GPx) antioxidant enzymes, as well as the concentrations of malondialdehyde (MDA) and serum total antioxidant capacity (TAC), were determined with the use of colorimetric methods. The protein expressions of Bcl2 and cleaved caspase 3 and the phosphorylation of p38 mitogen-activated protein kinase (MAPK) in rat carotid tissue were determined by an immunoblotting method. -
Effect of Capsaicin and Other Thermo-TRP Agonists on Thermoregulatory Processes in the American Cockroach
Article Effect of Capsaicin and Other Thermo-TRP Agonists on Thermoregulatory Processes in the American Cockroach Justyna Maliszewska 1,*, Milena Jankowska 2, Hanna Kletkiewicz 1, Maria Stankiewicz 2 and Justyna Rogalska 1 1 Department of Animal Physiology, Faculty of Biology and Environmental Protection, Nicolaus Copernicus University, 87-100 Toruń, Poland; [email protected] (H.K.); [email protected] (J.R.) 2 Department of Biophysics, Faculty of Biology and Environmental Protection, Nicolaus Copernicus University, 87-100 Toruń, Poland; [email protected] (M.J.); [email protected] (M.S.) * Correspondence: [email protected]; Tel.: +48-56611-44-63 Academic Editor: Pin Ju Chueh Received: 5 November 2018; Accepted: 17 December 2018; Published: 18 December 2018 Abstract: Capsaicin is known to activate heat receptor TRPV1 and induce changes in thermoregulatory processes of mammals. However, the mechanism by which capsaicin induces thermoregulatory responses in invertebrates is unknown. Insect thermoreceptors belong to the TRP receptors family, and are known to be activated not only by temperature, but also by other stimuli. In the following study, we evaluated the effects of different ligands that have been shown to activate (allyl isothiocyanate) or inhibit (camphor) heat receptors, as well as, activate (camphor) or inhibit (menthol and thymol) cold receptors in insects. Moreover, we decided to determine the effect of agonist (capsaicin) and antagonist (capsazepine) of mammalian heat receptor on the American cockroach’s thermoregulatory processes. We observed that capsaicin induced the decrease of the head temperature of immobilized cockroaches. Moreover, the examined ligands induced preference for colder environments, when insects were allowed to choose the ambient temperature. -
The Chemotaxonomy of Common Sage (Salvia Officinalis)
medicines Article The Chemotaxonomy of Common Sage (Salvia officinalis) Based on the Volatile Constituents Jonathan D. Craft, Prabodh Satyal and William N. Setzer * Department of Chemistry, University of Alabama in Huntsville, Huntsville, AL 35899, USA; [email protected] (J.D.C.); [email protected] (P.S.) * Correspondence: [email protected]; Tel.: +1-256-824-6519 Academic Editors: João Rocha and James D. Adams Received: 2 May 2017; Accepted: 26 June 2017; Published: 29 June 2017 Abstract: Background: Common sage (Salvia officinalis) is a popular culinary and medicinal herb. A literature survey has revealed that sage oils can vary widely in their chemical compositions. The purpose of this study was to examine sage essential oil from different sources/origins and to define the possible chemotypes of sage oil. Methods: Three different samples of sage leaf essential oil have been obtained and analyzed by GC-MS and GC-FID. A hierarchical cluster analysis was carried out on 185 sage oil compositions reported in the literature as well as the three samples in this study. Results: The major components of the three sage oils were the oxygenated monoterpenoids α-thujone (17.2–27.4%), 1,8-cineole (11.9–26.9%), and camphor (12.8–21.4%). The cluster analysis revealed five major chemotypes of sage oil, with the most common being a α-thujone > camphor > 1,8-cineole chemotype, of which the three samples in this study belong. The other chemotypes are an α-humulene-rich chemotype, a β-thujone-rich chemotype, a 1,8-cineole/camphor chemotype, and a sclareol/α-thujone chemotype. -
Estrogen Pharmacology. I. the Influence of Estradiol and Estriol on Hepatic Disposal of Sulfobromophthalein (BSP) in Man
Estrogen Pharmacology. I. The Influence of Estradiol and Estriol on Hepatic Disposal of Sulfobromophthalein (BSP) in Man Mark N. Mueller, Attallah Kappas J Clin Invest. 1964;43(10):1905-1914. https://doi.org/10.1172/JCI105064. Research Article Find the latest version: https://jci.me/105064/pdf Journal of Clinical Investigation Vol. 43, No. 10, 1964 Estrogen Pharmacology. I. The Influence of Estradiol and Estriol on Hepatic Disposal of Sulfobromophthalein (BSP) inMan* MARK N. MUELLER t AND ATTALLAH KAPPAS + WITH THE TECHNICAL ASSISTANCE OF EVELYN DAMGAARD (From the Department of Medicine and the Argonne Cancer Research Hospital,§ the University of Chicago, Chicago, Ill.) This report 1 describes the influence of natural biological action of natural estrogens in man, fur- estrogens on liver function, with special reference ther substantiate the role of the liver as a site of to sulfobromophthalein (BSP) excretion, in man. action of these hormones (5), and probably ac- Pharmacological amounts of the hormone estradiol count, in part, for the impairment of BSP dis- consistently induced alterations in BSP disposal posal that characterizes pregnancy (6) and the that were shown, through the techniques of neonatal period (7-10). Wheeler and associates (2, 3), to result from profound depression of the hepatic secretory Methods dye. Chro- transport maximum (Tm) for the Steroid solutions were prepared by dissolving crystal- matographic analysis of plasma BSP components line estradiol and estriol in a solvent vehicle containing revealed increased amounts of BSP conjugates 10% N,NDMA (N,N-dimethylacetamide) 3 in propylene during estrogen as compared with control pe- glycol. Estradiol was soluble in a concentration of 100 riods, implying a hormonal effect on cellular proc- mg per ml; estriol, in a concentration of 20 mg per ml. -
Effects of Camphor Oil Addition to Diesel on the Nanostructures and Oxidative Reactivity of Combustion-Generated Soot
Effects of camphor oil addition to diesel on the nanostructures and oxidative reactivity of combustion-generated soot Item Type Article Authors Morajkar, Pranay; Guerrero Pena, Gerardo D.J.; Raj, Abhijeet; Elkadi, Mirella; Rahman, Ramees K.; Salkar, Akshay V.; Pillay, Avinash; Anjana, Tharalekshmy; Cha, Min Suk Citation Morajkar, P., Guerrero Pena, G. D. J., Raj, A., Elkadi, M., Rahman, R. K., Salkar, A. V., … Cha, M. S. (2019). Effects of camphor oil addition to diesel on the nanostructures and oxidative reactivity of combustion-generated soot. Energy & Fuels. doi:10.1021/ acs.energyfuels.9b03390 Eprint version Post-print DOI 10.1021/acs.energyfuels.9b03390 Publisher American Chemical Society (ACS) Journal Energy & Fuels Rights This document is the Accepted Manuscript version of a Published Work that appeared in final form in Energy & Fuels, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/doi/10.1021/ acs.energyfuels.9b03390. Download date 28/09/2021 21:36:33 Link to Item http://hdl.handle.net/10754/660017 1 Effects of camphor oil addition to diesel on the nanostructures and 2 oxidative reactivity of combustion-generated soot 3 Pranay P. Morajkara,b, Gerardo D.J. Guerrero Peñac, Abhijeet Raja,*, Mirella Elkadid, Ramees 4 K. Rahmane, Akshay V. Salkarb, Avin Pillayd, Tharalekshmy Anjanaa, Min Suk Chac 5 aDepartment of Chemical Engineering, The Petroleum Institute, Khalifa University of Science 6 & Technology, Abu Dhabi, U.A.E 7 bSchool of Chemical Sciences, Goa University, Taleigao Plateau, Goa, India 8 cClean Combustion Research Centre, King Abdullah University of Science and Technology, 9 Thuwal, Saudi Arabia 10 dDepartment of Chemistry, Khalifa University of Science & Technology, Abu Dhabi, U.A.E 11 eDepartment of Chemical Engineering, University of Central Florida, Orlando, US 12 13 Abstract 14 Less viscous and low cetane (LVLC) fuels have emerged as the promising alternative fuels or 15 additives to fossil fuels. -
Thesis Has Been Carried out in the School of Pharmacy and Pharmacology and in the School of Biology and Biochemistry, Under the Supervision of Dr Michael D
University of Bath PHD Inhibitors of DNA repair processes as potentiating drugs in cancer radiotherapy and chemotherapy Watson, Corrine Yvonne Award date: 1997 Awarding institution: University of Bath Link to publication Alternative formats If you require this document in an alternative format, please contact: [email protected] General rights Copyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. • Users may download and print one copy of any publication from the public portal for the purpose of private study or research. • You may not further distribute the material or use it for any profit-making activity or commercial gain • You may freely distribute the URL identifying the publication in the public portal ? Take down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. Download date: 10. Oct. 2021 Inhibitors of DNA Repair Processes as Potentiating Drugs in Cancer Radiotherapy and Chemotherapy submitted by Corrine Yvonne Watson for the degree of PhD of the University of Bath 1997 The research work in this thesis has been carried out in the School of Pharmacy and Pharmacology and in the School of Biology and Biochemistry, under the supervision of Dr Michael D. Threadgill and Dr William J. D. Whish. COPYRIGHT Attention is drawn to the fact that copyright of this thesis rests with its author. -
Inhibitory Effects of Monoterpenes on Human TRPA1 and the Structural Basis of Their Activity
J Physiol Sci (2014) 64:47–57 DOI 10.1007/s12576-013-0289-0 ORIGINAL PAPER Inhibitory effects of monoterpenes on human TRPA1 and the structural basis of their activity Masayuki Takaishi • Kunitoshi Uchida • Fumitaka Fujita • Makoto Tominaga Received: 26 July 2013 / Accepted: 2 September 2013 / Published online: 12 October 2013 Ó The Author(s) 2013. This article is published with open access at Springerlink.com Abstract TRPA1, one of the transient receptor potential on these identified TRPA1 antagonists could lead to new channels, has been reported to be involved in nociception pain therapeutics. and inflammatory pain, suggesting that this molecule could be a promising target for the development of analgesic Keywords Monoterpene Á Pain relief Á TRPA1 Á agents. We screened several monoterpene analogs of Hydroxyl group camphor, which is known to inhibit human (h) TRPA1, to identify more effective naturally occurring TRPA1 antag- onists. Borneol, 2-methylisoborneol, and fenchyl alcohol Introduction exhibited higher inhibitory effects on hTRPA1 activity than either camphor or 1,8-cineole. Our results revealed Transient receptor potential (TRP) channels respond to a further that the S873, T874, and Y812 residues of hTRPA1 wide variety of sensory stimuli, including temperature, were involved in the inhibitory effects, suggesting that the nociceptive compounds, touch, osmolarity, and phero- hydroxyl group in the six-membered ring of the inhibitors mones [1–3]. TRPA1, one of the TRP channels, functions may be interacting with these amino acids. Further research as a receptor that responds to noxious cold temperatures and pungent compounds, including allyl isothiocyanate (AITC), a component of mustard oil [4–8]. -
Avoiding Medication Mayhem
Avoiding Medication Mayhem Penny Miller, BSc.(Pharm.), M.A. Senior Instructor, Faculty of Pharmaceutical Sciences and Department of Family Practice, UBC Pharmacotherapeutic Consultant, Lifemark Health Chronic pain Program Disclosure I have nothing to disclose concerning possible financial or personal relationships with commercial entities that may have a direct or indirect interest in the subject matter of this presentation. Goal: Provide the clinician with practical information to support the medication management of patients with chronic pain. Learning Objectives: At the end of this session, the clinician will demonstrate improved abilities to: 1. Describe the rationale, efficacy, benefits and risks associated with non-steroidal anti-inflammatory agents, opioids, antidepressants and anticonvulsants in the treatment of chronic pain. 2. Identify appropriate combinations of medications. 3. Outline the important reasons for slow upward titrations and slow tapers off medications. 4. Discuss effective monitoring for the efficacy and side effects of drugs to meet the outcomes of increased functioning, improved sleep and reduced pain. Case of Ben 45 y.o., construction worker • Low back pain x 7 months after a fall at work • Constant throbbing ache in low back • Radiates down right buttock & thigh, at times extends to right ankle (burning, shooting, electric pain) • Pain level on good day 5/10, on bad day 8/10, average 7/10 (over past week) • Sleep 3 hours nightly interrupted 3 times. • Diagnosis: Lumbar radiculopathy (neuropathy with nerve root -
Cinnamic Aldehyde
CINNAMIC ALDEHYDE Your patch test result indicates that you have a contact allergy to cinnamic aldehyde. This contact allergy may cause your skin to react when it is exposed to this substance although it may take several days for the symptoms to appear. Typical symptoms include redness, swelling, itching and fluid-filled blisters. Where is cinnamic aldehyde found? Cinnamic aldehyde is the chemical compound that gives cinnamon its flavor and odor. Cinnamic aldehyde occurs naturally in the bark of cinnamon, camphor, and cassia trees. These trees are the natural source of cinnamon, and the essential oil of cinnamon bark is about 90% cinnamic aldehyde. It is used as a flavoring in food items like chewing gum, ice cream, candy, and beverages and in some perfumes of natural, sweet, or fruity scents. Cinnamic aldehyde is also sometimes used as a fungicide and its scent is known to repel animals like cats and dogs. How can you avoid contact with cinnamic aldehyde? Avoid products that list any of the following names in the ingredients: • 2-Propenal, 3-phenyl- • Cinnamic aldehyde • 3-Phenyl-2-propenaldehyde • Cinnamylaldehyde • CAS RN: 104-55-2 • Cinnemaldehyde • Benzylideneacetaldehyde What are some products that may contain cinnamic aldehyde? Corrosion Inhibitor Fungicide: Food Flavoring: • Root Treatment • Beverages Insecticide - Cola - Vermuth Personal Care Products: • Chewing gum • Dental Floss - Ban-Smoke • Mouthwash - Big Red • Oral anaesthetics - Dentyne Fire • Toothpastes - Slim-mint Pet Care Products: • Candy • Hoffman Dog & Cat Repellent • Ice cream • Nilodor Deodorizing Cleaner Concentrate, Original Fragrances (natural, sweet, or fruity scents): • Nilodor Deodorizing Ferret Shampoo • Almond • Nilodor Nilolitter Cat Box Additive • Apricot • Butterscotch For additional information about products that might contain cinnamic aldehyde, go to the Household Product Database online (http:/ householdproducts.nlm.nih.gov) at the United States National Library of Medicine.