Natural Agents Affecting Excitatory and Inhibitory Neurotransmission

Total Page:16

File Type:pdf, Size:1020Kb

Natural Agents Affecting Excitatory and Inhibitory Neurotransmission Natural Agents Affecting Excitatory and Inhibitory Neurotransmission Adenosine Receptor Glycine Receptor Antagonists: K Channel Antagonists: Na Channel Agents: Antagonists: • Oenanthe fistulosa (Water Dropwort) [Toxin] • Cicutoxin/Cicuta maculata (Water • Aconitine/Aconitum spp • Caffeine • Strychnine/Strychnos Nux Vomica Hemlock) AND Cicuta Virosa (Monkshood/Wolfsbane) (Cowbane or Northern Water Hemlock) • Taxine/Taxus (Yew) Ca Cl Cl Na Adenosine Adenosine Glycine DA/NE/E/S PRE-SYNAPTIC POST-SYNAPTIC K + Glutamate Other Glutamate GABA (NMDA, KA) O PLP CO O Sympathomimetics: Na +/- Ca 2 Cl + + INHIBITORY NEURON • Cathinones (Khat/Qat) H3N H3N O- O- • Cocaine/Coca Glutamic acid • Ephedra/Ephedra spp. (Ma Huang) EXCITATORY NEURON-O O decarboxylase Competitive Non-competitive • Synanceia (Stonefish) [Toxin] Glutamate Agonists: Glutamate GABA Antagonists: Antagonists: • β-N-oxalylamino-L-alanine • Bicuculline/Dicentra • Anisatin/Illicium anisatum Serotonergics: (BOAA)/Lathyrus Sativa cucullaria (Dutchman's (Japanese star anise) GAD Inhibitors: breeches) • Cicutoxin & Virol A/ Cicuta • Hypericum perforatum/ St. (Chickling Pea) • Cyanide/cyanogenic glycosides • Colchicine/Colchicum maculata (Water Hemlock) AND John's Wort • Domoic Acid/Pseudo-nitzschia australis [Amnestic Shellfish [Stonefruit] autumnale (Autumn crocus) Cicuta Virosa (Cowbane or Poisoning] • Domoic Acid/Pseudo-nitzschia • Oenanthe fistulosa (Water Northern Water Hemlock) • Ibotenic Acid/Amanita Muscaria australis [Amnestic Shellfish Dropwort) [Toxin] *Probably • Picrotoxin/Anamirta cocculus (Fly Agaric) Poisoning] competitive (Fishberries) • Kainic Acid/Digenea simplex • Gyromitrin/Gyromitra Esculenta • Thujone/Artemisia absinthium (species of seaweed) (False Morel) (Wormwood) • Kainic Acid/Digenea simplex (species of seaweed) GABA site Agonists Antagonists Barbiturate site Depressants (also ethanol?) Cl ACh Excitants? Benzodiazepine site Agonists (depressants) Antagonists Inverse agonists Steroid site Nicotinic: Unknown: Anesthetics Excitants? • Nicotine/Coniine/ conium • Camphor/Cinnamomum camphora maculatum/Nicotiana spp./etc Adapted from http://www.ncbi.nlm.nih.gov/books/ Picrotoxin site NVK28090/figure/A1185/?report=objectonly Chloride Channel Convulsants Depressants?.
Recommended publications
  • XXXV International Congress of the European Association of Poisons Centres and Clinical Toxicologists (EAPCCT) 26–29 May 2015, St Julian's, Malta
    Clinical Toxicology ISSN: 1556-3650 (Print) 1556-9519 (Online) Journal homepage: http://www.tandfonline.com/loi/ictx20 XXXV International Congress of the European Association of Poisons Centres and Clinical Toxicologists (EAPCCT) 26–29 May 2015, St Julian's, Malta To cite this article: (2015) XXXV International Congress of the European Association of Poisons Centres and Clinical Toxicologists (EAPCCT) 26–29 May 2015, St Julian's, Malta, Clinical Toxicology, 53:4, 233-403, DOI: 10.3109/15563650.2015.1024953 To link to this article: http://dx.doi.org/10.3109/15563650.2015.1024953 Published online: 26 Mar 2015. Submit your article to this journal Article views: 3422 View related articles View Crossmark data Citing articles: 2 View citing articles Full Terms & Conditions of access and use can be found at http://www.tandfonline.com/action/journalInformation?journalCode=ictx20 Download by: [UPSTATE Medical University Health Sciences Library] Date: 28 December 2016, At: 10:31 Clinical Toxicology (2015), 53, 233–403 Copyright © 2015 Informa Healthcare USA, Inc. ISSN: 1556-3650 print / 1556-9519 online DOI: 10.3109/15563650.2015.1024953 ABSTRACTS XXXV International Congress of the European Association of Poisons Centres and Clinical Toxicologists (EAPCCT) 26–29 May 2015, St Julian ’ s, Malta 1. Modelling dose-concentration-response Introduction: The American Association of Poison Control Cen- ters (AAPCC) published its fi rst annual report in 1983. Call data Ursula Gundert-Remy from sixteen US poison centers was chronicled in that report. Seven submitted data for the entire year. By July 2000, 63 centers Institute for Clinical Pharmacology and Toxicology, Charit é were part of the national poison center system, but only 59 submit- Medical School, Berlin, Germany ted data for the full year.
    [Show full text]
  • (12) Patent Application Publication (10) Pub. No.: US 2011/00284.18 A1 Parker Et Al
    US 2011 002841 8A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2011/00284.18 A1 Parker et al. (43) Pub. Date: Feb. 3, 2011 (54) USE OF GABBA RECEPTOR ANTAGONISTS Publication Classification FOR THE TREATMENT OF EXCESSIVE SLEEPINESS AND DISORDERS ASSOCATED (51) Int. Cl. WITH EXCESSIVE SLEEPINESS A63L/7028 (2006.01) A 6LX 3/557 (2006.01) (75) Inventors: Kathy P. Parker, Rochester, NY A63L/335 (2006.01) (US); David B. Rye, Dunwoody, A63L/4355 (2006.01) GA (US); Andrew Jenkins, A63L/047 (2006.01) Decatur, GA (US) A6IP 25/00 (2006.01) Correspondence Address: (52) U.S. Cl. ........... 514/29: 514/220; 514/450, 514/291; FISH & RICHARDSON P.C. (AT) 5147738 P.O BOX 1022 Minneapolis, MN 55440-1022 (US) (57) ABSTRACT (73) Assignee: Emory University, Atlanta, GA GABA receptor mediated hypersomnia can be treated by (US) administering a GABA receptor antagonist (e.g., flumazenil; clarithromycin; picrotoxin; bicuculline; cicutoxin; and (21) Appl. No.: 12/922,044 oenanthotoxin). In some embodiments, the GABA receptor antagonist is flumazenil or clarithromycin. The GABA (22) PCT Filed: Mar. 12, 2009 receptor mediated hypersomnia includes shift work sleep disorder, obstructive sleep apnea/hypopnea syndrome, narco (86). PCT No.: PCT/USO9/37034 lepsy, excessive sleepiness, hypersomnia (e.g., idiopathic hypersomnia; recurrent hyperSonmia; endozepine related S371 (c)(1), recurrent stupor; and amphetamine resistant hyperSonmia), (2), (4) Date: Sep. 10, 2010 and excessive sleepiness associated with shift work sleep disorder, obstructive sleep apnea/hypopnea syndrome, and Related U.S. Application Data hypersomnia (e.g., idiopathic hypersomnia; recurrent hyper (60) Provisional application No.
    [Show full text]
  • 1-Iodo-1-Pentyne
    MIAMI UNIVERSITY-THE GRADUATE SCHOOL CERTIFICATE FOR APPROVING THE DISSERTATION We hereby approve the Dissertation of Lizhi Zhu Candidate for the Degree: Doctor of Philosophy ________________________________ Robert E. Minto, Director ________________________________ John R. Grunwell, Reader ________________________________ John F. Sebastian, Reader ________________________________ Ann E. Hagerman, Reader ________________________________ Richard E. Lee, Graduate School Representative ABSTRACT INVESTIGATING THE BIOSYNTHESIS OF POLYACETYLENES: SYNTHESIS OF DEUTERATED LINOLEIC ACIDS & MECHANISM STUDIES OF DMDS ADDITION TO 1,4-ENYNES By Lizhi Zhu A wide range of polyacetylenic natural products possess antimicrobial, antitumor, and insecticidal properties. The biosyntheses of these natural products are widely distributed among fungi, algae, marine sponges, and higher plants. As details of the biosyntheses of these intriguing compounds remains scarce, it remains important to develop molecular probes and analytical methods to study polyacetylene secondary metabolism. An effective pathway to prepare selectively deuterium-labeled linoleic acids was developed. By this Pd-catalyzed method, deuterium can be easily introduced into the vinyl position providing deuterolinoleates with very high isotopic purity. This method also provides a general route for the construction of 1,4-diene derivatives with different chain lengths and 1,4-diene locations. Linoleic acid derivatives (12-d, 13-d and 16,16,17,17,18,18,18-d7) were synthesized according to this method. A stereoselective synthesis of methyl (14Z)- and (14E)-dehydrocrepenynate was achieved in five to six steps that employed Pd-catalyzed cross-coupling reactions to construct the double bonds between C14 and C15. Compared with earlier methods, the improved syntheses are more convenient (no spinning band distillations or GLC separation of diastereomers were necessary) and higher Z/E ratios were obtained.
    [Show full text]
  • Fall TNP Herbals.Pptx
    8/18/14 Introduc?on to Objecves Herbal Medicine ● Discuss history and role of psychedelic herbs Part II: Psychedelics, in medicine and illness. Legal Highs, and ● List herbs used as emerging legal and illicit Herbal Poisons drugs of abuse. ● Associate main plant and fungal families with Jason Schoneman RN, MS, AGCNS-BC representave poisonous compounds. The University of Texas at Aus?n ● Discuss clinical management of main toxic Schultes et al., 1992 compounds. Psychedelics Sacraments: spiritual tools or sacred medicine by non-Western cultures vs. Dangerous drugs of abuse vs. Research and clinical tools for mental and physical http://waynesword.palomar.edu/ww0703.htm disorders History History ● Shamanic divinaon ○ S;mulus for spirituality/religion http://orderofthesacredspiral.blogspot.com/2012/06/t- mckenna-on-psilocybin.html http://www.cosmicelk.net/Chukchidirections.htm 1 8/18/14 History History http://www.10zenmonkeys.com/2007/01/10/hallucinogenic- weapons-the-other-chemical-warfare/ http://rebloggy.com/post/love-music-hippie-psychedelic- woodstock http://fineartamerica.com/featured/misterio-profundo-pablo- amaringo.html History ● Psychotherapy ○ 20th century: un;l 1971 ● Recreaonal ○ S;mulus of U.S. cultural revolu;on http://qsciences.digi-info-broker.com http://www.uspharmacist.com/content/d/feature/c/38031/ http://en.wikipedia.org/nervous_system 2 8/18/14 Main Groups Main Groups Tryptamines LSD, Psilocybin, DMT, Ibogaine Other Ayahuasca, Fly agaric Phenethylamines MDMA, Mescaline, Myristicin Pseudo-hallucinogen Cannabis Dissociative
    [Show full text]
  • Is Palatability of a Root-Hemiparasitic Plant Influenced by Its Host Species?
    Oecologia (2005) 146: 227–233 DOI 10.1007/s00442-005-0192-3 PLANTANIMALINTERACTIONS Martin Scha¨dler Æ Mareike Roeder Æ Roland Brandl Diethart Matthies Is palatability of a root-hemiparasitic plant influenced by its host species? Received: 16 November 2004 / Accepted: 21 June 2005 / Published online: 19 July 2005 Ó Springer-Verlag 2005 Abstract Palatability of parasitic plants may be influ- Introduction enced by their host species, because the parasites take up nutrients and secondary compounds from the hosts. If Parasitic plants attack shoots or roots of other plants and parasitic plants acquired the full spectrum of secondary take up water, nutrients and solutes from the hosts by compounds from their host, one would expect a corre- means of specialized contact organs (haustoria, Kuijt lation between host and parasite palatability. We 1969). About 1% of all plants are parasitic and parasitic examined the palatability of leaves of the root-hemi- plants are common components of many plant commu- parasite Melampyrum arvense grown with different host nities (Molau 1995). The majority of parasitic plants are plants and the palatability of these host plants for two actually hemiparasites that have green leaves and are generalist herbivores, the caterpillar of Spodoptera lit- able to photosynthesize (Kuijt 1969). Parasitic plants can toralis and the slug Arion lusitanicus. We used 19 species drastically reduce the growth of their host plants and of host plants from 11 families that are known to con- some are important agricultural pests (Parker and Riches tain a wide spectrum of anti-herbivore compounds. 1993; Pennings and Callaway 2002). Because parasitic Growth of M.
    [Show full text]
  • Cicuta Douglasii) Tubers
    Toxicon 108 (2015) 11e14 Contents lists available at ScienceDirect Toxicon journal homepage: www.elsevier.com/locate/toxicon Short communication The non-competitive blockade of GABAA receptors by an aqueous extract of water hemlock (Cicuta douglasii) tubers * Benedict T. Green a, , Camila Goulart b, 1, Kevin D. Welch a, James A. Pfister a, Isabelle McCollum a, Dale R. Gardner a a Poisonous Plant Research Laboratory, Agricultural Research Service, United States Department of Agriculture, Logan, UT, USA b Graduate Program in Animal Science, Universidade Federal de Goias, Goiania,^ Goias, Brazil article info abstract Article history: Water hemlocks (Cicuta spp.) are acutely toxic members of the Umbellierae family; the toxicity is due to Received 22 July 2015 the presence of C17-polyacetylenes such as cicutoxin. There is only limited evidence of noncompetitive Received in revised form antagonism by C17-polyacetylenes at GABAA receptors. In this work with WSS-1 cells, we documented 9 September 2015 the noncompetitive blockade of GABA receptors by an aqueous extract of water hemlock (Cicuta dou- Accepted 14 September 2015 A glasii) and modulated the actions of the extract with a pretreatment of 10 mM midazolam. Available online 28 September 2015 Published by Elsevier Ltd. Keywords: Water hemlock Cicutoxin C17-polyacetylenes Benzodiazepines Barbiturates Midazolam Water hemlocks (Cicuta spp.) are acutely toxic members of the antagonists of the GABAA receptor by binding to the picrotoxin Umbellierae, or carrot family, that grow in wet habitats such as binding site within the chloride channel to block ion flow through streambeds or marshlands, and have been considered one of the the channel (Ratra et al., 2001; Chen et al., 2006; 2011; Olsen, most toxic plants of North America for many years (Kingsbury, 2006).
    [Show full text]
  • Dr. Duke's Phytochemical and Ethnobotanical Databases List of Chemicals for Sedative
    Dr. Duke's Phytochemical and Ethnobotanical Databases List of Chemicals for Sedative Chemical Dosage (+)-BORNYL-ISOVALERATE -- (-)-DICENTRINE LD50=187 1,8-CINEOLE -- 2-METHYLBUT-3-ENE-2-OL -- 6-GINGEROL -- 6-SHOGAOL -- ACYLSPINOSIN -- ADENOSINE -- AKUAMMIDINE -- ALPHA-PINENE -- ALPHA-TERPINEOL -- AMYL-BUTYRATE -- AMYLASE -- ANEMONIN -- ANGELIC-ACID -- ANGELICIN ED=20-80 ANISATIN 0.03 mg/kg ANNOMONTINE -- APIGENIN 30-100 mg/kg ARECOLINE 1 mg/kg ASARONE -- ASCARIDOLE -- ATHEROSPERMINE -- BAICALIN -- BALDRINAL -- BENZALDEHYDE -- BENZYL-ALCOHOL -- Chemical Dosage BERBERASTINE -- BERBERINE -- BERGENIN -- BETA-AMYRIN-PALMITATE -- BETA-EUDESMOL -- BETA-PHENYLETHANOL -- BETA-RESERCYCLIC-ACID -- BORNEOL -- BORNYL-ACETATE -- BOSWELLIC-ACID 20-55 mg/kg ipr rat BRAHMINOSIDE -- BRAHMOSIDE -- BULBOCAPNINE -- BUTYL-PHTHALIDE -- CAFFEIC-ACID 500 mg CANNABIDIOLIC-ACID -- CANNABINOL ED=200 CARPACIN -- CARVONE -- CARYOPHYLLENE -- CHELIDONINE -- CHIKUSETSUSAPONIN -- CINNAMALDEHYDE -- CITRAL ED 1-32 mg/kg CITRAL 1 mg/kg CITRONELLAL ED=1 mg/kg CITRONELLOL -- 2 Chemical Dosage CODEINE -- COLUBRIN -- COLUBRINOSIDE -- CORYDINE -- CORYNANTHEINE -- COUMARIN -- CRYOGENINE -- CRYPTOCARYALACTONE 250 mg/kg CUMINALDEHYDE -- CUSSONOSIDE-A -- CYCLOSTACHINE-A -- DAIGREMONTIANIN -- DELTA-9-THC 10 mg/orl/man/day DESERPIDINE -- DESMETHOXYANGONIN 200 mg/kg ipr DIAZEPAM 40-200 ug/lg/3-4x/day DICENTRINE LD50=187 DIDROVALTRATUM -- DIHYDROKAWAIN -- DIHYDROMETHYSTICIN 60 mg/kg ipr DIHYDROVALTRATE -- DILLAPIOL ED50=1.57 DIMETHOXYALLYLBENZENE -- DIMETHYLVINYLCARBINOL -- DIPENTENE
    [Show full text]
  • Neurochemical and Behavioral Features in Genetic Absence Epilepsy and in Acutely Induced Absence Seizures
    Hindawi Publishing Corporation ISRN Neurology Volume 2013, Article ID 875834, 48 pages http://dx.doi.org/10.1155/2013/875834 Review Article Neurochemical and Behavioral Features in Genetic Absence Epilepsy and in Acutely Induced Absence Seizures A. S. Bazyan1 and G. van Luijtelaar2 1 Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of Science, Russian Federation, 5A Butlerov Street, Moscow 117485, Russia 2 Biological Psychology, Donders Centre for Cognition, Donders Institute for Brain, Cognition and Behavior, Radboud University Nijmegen, P.O. Box 9104, 6500 HE Nijmegen, The Netherlands Correspondence should be addressed to G. van Luijtelaar; [email protected] Received 21 January 2013; Accepted 6 February 2013 Academic Editors: R. L. Macdonald, Y. Wang, and E. M. Wassermann Copyright © 2013 A. S. Bazyan and G. van Luijtelaar. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The absence epilepsy typical electroencephalographic pattern of sharp spikes and slow waves (SWDs) is considered to be dueto an interaction of an initiation site in the cortex and a resonant circuit in the thalamus. The hyperpolarization-activated cyclic nucleotide-gated cationic Ih pacemaker channels (HCN) play an important role in the enhanced cortical excitability. The role of thalamic HCN in SWD occurrence is less clear. Absence epilepsy in the WAG/Rij strain is accompanied by deficiency of the activity of dopaminergic system, which weakens the formation of an emotional positive state, causes depression-like symptoms, and counteracts learning and memory processes.
    [Show full text]
  • Studying GABAA Receptors Using AII Amacrine Cells in the Rat Retina by Tuan Van Trinh
    Studying GABAA Receptors using AII Amacrine Cells in the Rat Retina By Tuan Van Trinh MASTER THESIS IN PHARMACY Department of Biomedicine/ Centre for Pharmacy University of Bergen May 2018 The picture of AII amacrine cells in front page is adapted from Zhou et al., 2016. 2 ACKNOWLEDGEMENTS This study was carried out at the department of Biomedicine, University of Bergen, during the period August 2012 to April 2013. Due to a serious illness, the project was interrupted, and continued again in April 2018 to May 2018. I would like to thank several people for their support during this project. First I would like to express my sincere gratitude to my supervisor prof. Ph.d Margaret Lin Veruki and co-supervisor prof. dr. med. Espen Hartveit for valuable advice and much appreciated guidance during the period. Ph.d. Yifan Zhou is thanked for helping me with collecting the data, and of course thanks to Marte Nørve Årvik, Lise Skålvik Amble and all my co-workers and lab personnel that have helped me during this period. To my family and my friends thank you for supporting me during this hard period of life. Bergen, May 2018 3 TABLE OF CONTENTS ACKNOWLEDGEMENTS……………………………………………………..3 TABLE OF CONTENTS………………………………………………………..4 ABBREVIATIONS……...………………………………………………………8 AIMS……………………...…………………………………………………....11 SUMMARY……………………...…………………………………………….13 1.0 INTRODUCTION AND THEORY……………………………………………16 1.1 Nerve cell and signal communication ………………………………16 1.1.1 Cell membrane……………………………..……………………...17 1.1.2 The membrane potential………….…………………….……….……..18 1.1.3 The
    [Show full text]
  • Improved Forensic Hair Evidence for Drugs of Abuse by Mass Spectrometry
    Improved Forensic Hair Evidence for Drugs of Abuse by Mass Spectrometry Wilco F. Duvivier Thesis committee Promotor Prof. Dr M.W.F. Nielen Professor of Analytical Chemistry, with special emphasis for the detection of chemical food contaminants Wageningen University Co-promotor Dr T.A. van Beek Assistant professor, Laboratory of Organic Chemistry Wageningen University Other members Prof. Dr H.A. Schols, Wageningen University Prof. Dr R.M.A. Heeren, Maastricht University Prof. Dr A.C. van Asten, University of Amsterdam Dr F. Drijfhout, Keele University, Staffordshire, United Kingdom This research was conducted under the auspices of the Graduate School VLAG (Advanced studies in Food Technology, Agrobiotechnology, Nutrition and Health Sciences). Improved Forensic Hair Evidence for Drugs of Abuse by Mass Spectrometry Wilco F. Duvivier Thesis submitted in fulfilment of the requirements for the degree of doctor at Wageningen University by the authority of the Rector Magnificus Prof. Dr A.P.J. Mol, in the presence of the Thesis Committee appointed by the Academic Board to be defended in public on Tuesday 5 July 2016 at 4 p.m. in the Aula. Wilco F. Duvivier Improved Forensic Hair Evidence for Drugs of Abuse by Mass Spectrometry 194 pages. PhD thesis, Wageningen University, Wageningen, NL (2016) With references, with summaries in English and Dutch ISBN 978-94-6257-815-9 DOI 10.18174/381180 Table of contents List of abbreviations 7 Chapter 1: General Introduction 9 Chapter 2: Evidence Based Decontamination Protocols for the Removal of 33 External
    [Show full text]
  • (12) Patent Application Publication (10) Pub. No.: US 2012/0196835 A1 Olafield Et Al
    US 20120196835A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2012/0196835 A1 Olafield et al. (43) Pub. Date: Aug. 2, 2012 (54) ENZYME INHIBITING COMPOUNDS AND A6II 3/663 (2006.01) METHODS A6II 3/94 (2006.01) CI2N 9/99 (2006.01) (76) Inventors: Eric Olafield, Champaign, IL (US); A6II 3L/225 (2006.01) Ke Wang, Urbana, IL (US); A6II 3/662 (2006.01) Weixue Wang, Urbana, IL (US); A6II 3/665 (2006.01) Yonghui Zhang, Urbana, IL (US) A6IP3L/04 (2006.01) A6IP33/00 (2006.01) (21) Appl. No.: 13/500,845 C07F 9/113 (2006.01) A 6LX 3L/95 (2006.01) (22) PCT Filed: Oct. 8, 2010 (52) U.S. Cl. ........... 514/89; 558/152; 514/106; 558/155; 514/108: 514/574: 514/563; 514/547: 514/119; (86). PCT No.: PCT/US 10/52049 514/99: 435/184 S371 (c)(1), (2), (4) Date: Apr. 6, 2012 (57) ABSTRACT The invention provides compounds, compositions, and meth Related U.S. Application Data ods for studying the Rohmer pathway and for treating bacte (60) Provisional application No. 61/249,929, filed on Oct. rial infections or parasitic infections. The parasitic infection 8, 2009. can be a protozoan infection, such as malaria. The compounds and compositions can also be used as antibiotics, for example, O O to kill bacteria or parasites, or to inhibit bacterial or parasite Publication Classification growth. The invention further provides inhibitors of iso (51) Int. Cl. prenoid biosynthesis enzymes, and methods of inhibiting the A6 IK3I/675 (2006.01) activity ofisoprenoid biosynthesis enzymes.
    [Show full text]
  • Federal Register/Vol. 66, No. 139/Thursday, July 19, 2001/Rules
    37830 Federal Register / Vol. 66, No. 139 / Thursday, July 19, 2001 / Rules and Regulations Indian Tribal Governments (63 FR expected to affect energy supply, ENVIRONMENTAL PROTECTION 27655, May 19, 1998), do not apply to distribution, or use. AGENCY this rule. Executive Order 13175, entitled Consultation and Coordination XII. Submission to Congress and the 40 CFR Part 174 with Indian Tribal Governments (65 FR Comptroller General [OPP–300368B; FRL–6057–6] 67249, November 6, 2000), which took The Congressional Review Act, 5 effect on January 6, 2001, revokes U.S.C. 801 et seq., as added by the Small RIN 2070–AC02 Executive Order 13084 as of that date. Business Regulatory Enforcement EPA developed this rulemaking, Exemption From the Requirement of a Fairness Act of 1996, generally provides however, during the period when Tolerance Under the Federal Food, that before a rule may take effect, the Executive Order 13084 was in effect; Drug, and Cosmetic Act for Residues thus, EPA addressed tribal agency promulgating the rule must Derived Through Conventional considerations under Executive Order submit a rule report, which includes a Breeding From Sexually Compatible 13084. For the same reasons stated for copy of the rule, to each House of the Plants of Plant-Incorporated Executive Order 13084, the Congress and to the Comptroller General Protectants (Formerly Plant- requirements of Executive Order 13175 of the United States. EPA will submit a Pesticides) do not apply to this rule either. For the report containing this rule and other same reasons, this rule does not have required information to the U.S. Senate, AGENCY: Environmental Protection any substantial direct effect on States, the U.S.
    [Show full text]