Vegetable Food Toxicants and Their Harmful Effects on Health

Total Page:16

File Type:pdf, Size:1020Kb

Vegetable Food Toxicants and Their Harmful Effects on Health Int.J.Curr.Microbiol.App.Sci (2020) Special Issue-11: 1923-1936 International Journal of Current Microbiology and Applied Sciences ISSN: 2319-7706 Special Issue-11 pp. 1923-1936 Journal homepage: http://www.ijcmas.com Original Research Article Vegetable Food Toxicants and their Harmful Effects on Health Amreena Sultan1*, Baseerat Afroza1, Shahnaz Mufti1, Ajaz A. Malik1, Najmu Sakib2, Afroza Akhter1, Sayed Azrah Indrabi1 and Insha Javeed1 1Department of Vegetable Science, 2Department of Plant Pathology, Sher-e-Kashmir University of Agricultural Sciences and Technology of Kashmir, Shalimar Campus-190025, Srinagar, J&K, India *Corresponding author ABSTRACT Plant toxins are substances produced as secondary metabolites that are identical to extra cellular bacterial toxins in their properties. They show both useful and harmful effects to human beings. They show a wide range of side effects from minor itching, nausea, vomiting to adverse effects like psychosis, teratogenicity, arrhythmias. Natural toxins are present in numerous types of plants. These types of compounds whenever consumed in large quantity or when they are not cooked properly may lead to food K e yw or ds poisoning. Plant toxins are found naturally in vegetables and fruits which have been the common food sources. Natural toxins can also be found in Plant toxin, Secondary plants because of natural choice as well as new reproduction methods which metabolites, Alkaloids, enhance these defensive mechanisms. Different kinds of natural toxins can Flavonoids be present in various parts of a plant like roots, tubers, stems, fruits, buds and foliage. There are many classes of toxic compounds like phenols, alkaloids, terpenoids, flavonoids, tannins, anti-vitamins, proteins, etc. plant toxins are descri bed according to the organ system in the human body which they affect, e.g., cardiotoxins, neurotoxins, etc. The degree of toxicity also depends on the location, climatic factors, growing season, variety and age. The people are advised to be cautious in the amount of intake and are recommended to observe the effects after ingestion. Introduction minor itching, nausea, vomiting to adverse effects like psychosis, paralysis, Plant toxins are substances produced as teratogenicity, arrhythmias. They are useful secondary metabolites that are identical to in production of cosmetics, ulcers, menstrual extra cellular bacterial toxins in their cramping, cancer and in treatment of man properties. They show both useful and ailments and diseases. Toxins may enter into harmful effects in human beings and animals. the by body either by inhalation, swallowing They show a wide range of side effects from or by contact. The action is based on their 1923 Int.J.Curr.Microbiol.App.Sci (2020) Special Issue-11: 1923-1936 chemical constituents which are classified several plants produces nonspecific clinical into alkaloids, phenols, peptides, amino acids, signs that could not be distinguished from glycosides, proteins, oxalates, anti-vitamins, other disease conditions. Additionally, death tannins, volatile ether layers etc. They act by caused by toxic plant ingestion frequently altering specific mechanisms involving does not result in characteristic post-mortem enzymes, receptors and even genetic material lesions, due to relatively limited numbers of at particular cells and tissues. They can be tests are available to identify the plant toxic modified to exemplify improved affinity and compounds in post mortem or ante-mortem efficacy for health endorsement. Poisonous samples. In many instances, the simplest way plants have a seed, root, leaf, stalk, fruit or to help the diagnosis of the plant poisoning is juice where even a relatively small amount, to confirm the existence of the poisonous taken either internally or eternally, can lead plant in the environment, ensure that the plant to injury to the human body. In some species was ingested and correlate clinical findings, if the poisonous constituents occur throughout it is possible, with those known to be the whole plant. In others they are associated with the suspect plant (Deependra concentrated in one or more parts. Plants singh et al., 2013). evolve to generate natural products as a means of defence against animals (Saravanan The degree of toxicity also depends on the et al., 2016) location (including height above sea level), climatic factors including the local micro Plants have a wide range of climate (light, warmth, humidity), the pharmacologically effective phytochemicals. growing season, type of soil, fertilization, Many of these have been discovered to be plant variety and age. The condition of the really helpful for the treatment of a variety of poisonous plant material is equally important human as well as animal diseases (e.g. (dried, chewed, cooked, as tea). The dose of colchicines, atropine and digitoxin); although course is the most important factor (Table 1– few plant phytochemicals produce harmful 4). effects after exposure. The onset of harmful effects could be really immediate or taken a Classification of plant toxins little time to develop. Fortunately, among thousands of plants present in the Alkaloids include indole alkaloids, environment, relatively few of the plants only pyrrolizidine alkaloids, tropane alkaloids, cause acute and life-threatening diseases opium alkaloids, vicine and covicine when ingested. The variety of chemical alkaloids. components in the plants is really amazing and in most of the cases, still the function a Glycosidal toxins include cardiac glycosides, specific phytochemical substance, i.e. the goitrogenic glycosides, anthraquinonr normal ecology of the plant remains glycosides, mustard oil glycosides, saponin unknown. The inclusion of toxic glycosides, cyanogenetic glycosides. phytochemical substances in the plants is considered to confer some extent of defense Tannins like pyrogallol. against plant potential predators like ruminants and insects. Proteins like lectin, abrin, ricin, cicutoxin, anisatin, gelonin, falcarinol, oenotheatoxin, The medical diagnosis of plant poisonings is etc. very challenging since the ingestion of 1924 Int.J.Curr.Microbiol.App.Sci (2020) Special Issue-11: 1923-1936 Antivitamins like thiaminases. poisonous cyanogenic glycosides, called Phytoestrogens like coumestrol. amygdalin. Amygdalin derived from aromatic amino acid phenylalanine. It is hydrolysed by Volatile etheric layers such as ushuriol, photo ᵝ-glucosidase and amygdalase to afford L- sensitizing substances including hypericin. mandelonitrile and gentiobiose. Mandelonitrile is further hydrolysed to Enzyme inhibitors like cholinesterase hydrogen cyanide and benzaldehyde. inhibitors, protease inhibitors, amylase Hydrogen cyanide causes cyanide poisoning. inhibitors. The quantities of amygdalin present in the seeds not enough to be dangerous to human Others include lathyrogens, Anti-thiamin health, but consumption of more quantity of compounds, Avidin. seeds may lead to a fatal dose (Saravanan, 2016). Various types of toxins produced by different vegetable crops (Fig. 1–18) Lotaustralin Glycoalkaloids Is a cyanogenic glycoside found in austral trefoil, cassava and lima bean. It is the Cyanogenic glycosides glycoside of methyl ethyl ketone cyanohydrins. Lotaustralin hydrolysed by the Glucosinolates enzyme linamerase to form glucose and toxic compound hydrogen cyanide. Hydrogen Tomatine cyanide causes a drop in blood pressure rapid respiration, rapid pulse, headache, dizziness, Pyrrolizidine alkaloids mental confusion, vomiting, stomach pains and diarrohea. Zucchini and Cucurbitacins Linamarin Amylase inhibitors Is another cyanogenic glycoside present in Lectins the leaves and roots of lima beans, cassava and flax. It is decomposed by gut flora in the Coumarins human intestine to form hydrogen cyanide. Consumption of food prepared from Furocoumarins insufficiently processed plant material containing linamarin to produce dietry Safrozole toxicity, called Konzo disease. Dietary exposure to linamarin was also been reported Myristicins as a risk factor in developing diabetes and glucose intolerance. Toxins in food plants Oxalyl-di-amino propionic acid (ODAP) Amygdalin This is a structural analogue for the The seeds of apple, apricot, plum, bitter neurotransmitter glutamate found in the grass almond and peach contain small amount of a pea and Indian pea. It is the neurotoxic amino 1925 Int.J.Curr.Microbiol.App.Sci (2020) Special Issue-11: 1923-1936 acid responsible for motor neuron Oxalic acid degeneration syndrome, neurolathyrism, characterized by pyramidal tract neurons in Present in spinach, rhubarb (0.2-1.3%),tea the area of cortex controlling legs and in the (0.3-2.0%), spinach (1.7%), purslane and in spinal cord. As a result, lower body paralysis. parsley (1.7%). It can bind with calcium and minerals, making them insoluble and thus Phytohaemagglutinin reducing the bioavailability. Consumption of foods containing oxalates could cause kidney It is a lectin found in high concentration in stones, decreased bone growth, renal toxicity, uncooked red and white kidney beans and in diarrhea, convulsions and coma. low concentration in green, broad and Approximately 65% of kidney stones consists common beans. of Calcium oxalates. Phytohaemagglutinin has complex Ipomeamarone oligosaccharide conyaining mannose, galactose and N-acetylglucosamine. It is Is found in kumara, which is a member of the causing severe stomach ache, diarrhea, and sweet potato family. It can produce harmful vomiting in humans when consumed as raw toxins due
Recommended publications
  • 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]
  • 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]
  • 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
    [Show full text]
  • Dr. Duke's Phytochemical and Ethnobotanical Databases List of Chemicals for Tinnitus
    Dr. Duke's Phytochemical and Ethnobotanical Databases List of Chemicals for Tinnitus Chemical Activity Count (+)-ALPHA-VINIFERIN 1 (+)-AROMOLINE 1 (+)-BORNYL-ISOVALERATE 1 (+)-CATECHIN 1 (+)-EUDESMA-4(14),7(11)-DIENE-3-ONE 1 (+)-HERNANDEZINE 2 (+)-ISOLARICIRESINOL 1 (+)-NORTRACHELOGENIN 1 (+)-PSEUDOEPHEDRINE 1 (+)-SYRINGARESINOL-DI-O-BETA-D-GLUCOSIDE 1 (+)-T-CADINOL 1 (-)-16,17-DIHYDROXY-16BETA-KAURAN-19-OIC 1 (-)-ALPHA-BISABOLOL 1 (-)-ANABASINE 1 (-)-APOGLAZIOVINE 1 (-)-BETONICINE 1 (-)-BORNYL-CAFFEATE 1 (-)-BORNYL-FERULATE 1 (-)-BORNYL-P-COUMARATE 1 (-)-CANADINE 1 (-)-DICENTRINE 1 (-)-EPICATECHIN 2 (-)-EPIGALLOCATECHIN-GALLATE 1 (1'S)-1'-ACETOXYCHAVICOL-ACETATE 1 (E)-4-(3',4'-DIMETHOXYPHENYL)-BUT-3-EN-OL 1 1,7-BIS-(4-HYDROXYPHENYL)-1,4,6-HEPTATRIEN-3-ONE 1 1,8-CINEOLE 4 Chemical Activity Count 1-ETHYL-BETA-CARBOLINE 2 10-ACETOXY-8-HYDROXY-9-ISOBUTYLOXY-6-METHOXYTHYMOL 1 10-DEHYDROGINGERDIONE 1 10-GINGERDIONE 1 12-(4'-METHOXYPHENYL)-DAURICINE 1 12-METHOXYDIHYDROCOSTULONIDE 1 13',II8-BIAPIGENIN 1 13-HYDROXYLUPANINE 1 13-OXYINGENOL-ESTER 1 16,17-DIHYDROXY-16BETA-KAURAN-19-OIC 1 16-HYDROXY-4,4,10,13-TETRAMETHYL-17-(4-METHYL-PENTYL)-HEXADECAHYDRO- 1 CYCLOPENTA[A]PHENANTHREN-3-ONE 16-HYDROXYINGENOL-ESTER 1 2'-O-GLYCOSYLVITEXIN 1 2-BETA,3BETA-27-TRIHYDROXYOLEAN-12-ENE-23,28-DICARBOXYLIC-ACID 1 2-METHYLBUT-3-ENE-2-OL 2 2-VINYL-4H-1,3-DITHIIN 1 20-DEOXYINGENOL-ESTER 1 22BETA-ESCIN 1 24-METHYLENE-CYCLOARTANOL 2 3,3'-DIMETHYLELLAGIC-ACID 1 3,4-DIMETHOXYTOLUENE 2 3,4-METHYLENE-DIOXYCINNAMIC-ACID-BORNYL-ESTER 1 3,4-SECOTRITERPENE-ACID-20-EPI-KOETJAPIC-ACID
    [Show full text]
  • Dr. Duke's Phytochemical and Ethnobotanical Databases List of Chemicals for Epilepsy
    Dr. Duke's Phytochemical and Ethnobotanical Databases List of Chemicals for Epilepsy Chemical Activity Count (+)-ALPHA-VINIFERIN 1 (+)-BORNYL-ISOVALERATE 1 (+)-CATECHIN 3 (+)-EUDESMA-4(14),7(11)-DIENE-3-ONE 1 (+)-HERNANDEZINE 1 (+)-ISOCORYDINE 1 (+)-PSEUDOEPHEDRINE 1 (+)-SYRINGARESINOL-DI-O-BETA-D-GLUCOSIDE 1 (+)-T-CADINOL 1 (-)-16,17-DIHYDROXY-16BETA-KAURAN-19-OIC 1 (-)-ALPHA-BISABOLOL 2 (-)-ANABASINE 1 (-)-APOGLAZIOVINE 1 (-)-BETONICINE 1 (-)-BORNYL-CAFFEATE 1 (-)-BORNYL-FERULATE 1 (-)-BORNYL-P-COUMARATE 1 (-)-DICENTRINE 2 (-)-EPIAFZELECHIN 1 (-)-EPICATECHIN 1 (-)-EPIGALLOCATECHIN-GALLATE 1 (1'S)-1'-ACETOXYCHAVICOL-ACETATE 1 (15:1)-CARDANOL 1 (E)-4-(3',4'-DIMETHOXYPHENYL)-BUT-3-EN-OL 1 1,7-BIS-(4-HYDROXYPHENYL)-1,4,6-HEPTATRIEN-3-ONE 1 1,8-CINEOLE 4 10-ACETOXY-8-HYDROXY-9-ISOBUTYLOXY-6-METHOXYTHYMOL 1 Chemical Activity Count 10-DEHYDROGINGERDIONE 1 10-GINGERDIONE 1 11-HYDROXY-DELTA-8-THC 1 11-HYDROXY-DELTA-9-THC 1 13',II8-BIAPIGENIN 1 13-OXYINGENOL-ESTER 1 16,17-DIHYDROXY-16BETA-KAURAN-19-OIC 1 16-EPIMETHUENINE 1 16-HYDROXYINGENOL-ESTER 1 2'-O-GLYCOSYLVITEXIN 1 2-BETA,3BETA-27-TRIHYDROXYOLEAN-12-ENE-23,28-DICARBOXYLIC-ACID 1 2-METHYLBUT-3-ENE-2-OL 2 20-DEOXYINGENOL-ESTER 1 22BETA-ESCIN 1 24-METHYLENE-CYCLOARTANOL 1 3,3'-DIMETHYLELLAGIC-ACID 1 3,4-DIMETHOXYTOLUENE 1 3,4-METHYLENE-DIOXYCINNAMIC-ACID-BORNYL-ESTER 2 3,4-SECOTRITERPENE-ACID-20-EPI-KOETJAPIC-ACID 1 3-ACETYLACONITINE 1 3-ACETYLNERBOWDINE 1 3-BETA-HYDROXY-2,3-DIHYDROWITHANOLIDE-F 1 3-HYDROXY-FLAVONE 1 3-N-BUTYL-PHTHALIDE 3 3-O-ACETYLOLEANOLIC-ACID 1 3-OXO-11-ALPHA-HYDROXYOLEAN-12-ENE-30-OIC-ACID
    [Show full text]
  • Anti-Inflammatory Activity of Phenylpropanoids and Phytoquinoids from Illicium Species in RBL-2H3 Cells
    Anti-Inflammatory Activity of mediate phase and the latter is released in the late phase of type I allergic reactions [9], [10]. Phenylpropanoids and Phytoquinoids from Illicium Species in RBL-2H3 Cells This study was conducted to investigate the anti-inflammatory activity of the compounds isolated from Illicium species on mast Takuya Matsui1,2, Chihiro Ito1, Masataka Itoigawa3, Tadashi Okada2, cells. We analyzed the effect of six phenylpropanoids (1±6) and Hiroshi Furukawa1 six phytoquinoids (7±12), isolated from three Illicium species (Fig.1), on histamine release and TNF-a production and/or secre- tion from A23187-stimulated rat basophilic leukemia RBL-2H3 Abstract cells. Two phenylpropanoids, 1-allyl-3,5-dimethoxy-4-(3-methyl-but- Among the compounds tested, phenylpropanoids 4 and 6 and 2-enyloxy)benzene (4) and 4-allyl-2,6-dimethoxy-3-(3-methyl- phytoquinoids 7 and 8 at a concentration of 50 mM markedly in- 2-butenyl)phenol (6), and two phytoquinoids, 4R-(±)-illicinone- hibited histamine release from RBL-2H3 cells (96.9 2.9%, 84.3 Letter A(7) and 2S,4R-(±)-illicinone-B (8), isolated from plants of the 4.1%, 99.4 1.0% and 98.3 1.9% inhibition, respectively), Illicium species significantly inhibited histamine release from whereas the inhibition rate of the standard reference epigalloca- rat basophilic leukemia (RBL-2H3) cells stimulated with thechin gallate (EGCG) was 28.6 6.0% (Fig. 2A). These com- A23187. Furthermore, these compounds caused a decline in pounds showed a dose-dependent inhibitory effect in the con- TNF-a levels in culture supernatants of RBL-2H3 cells following centration range of 1±50 mM on histamine release without ap- treatment with A23187.
    [Show full text]
  • Supplementary Materials: Metabolomics and Cheminformatics Analysis of Antifungal Function of Plant Metabolites
    Metabolites 2016, 6, 31: S1 of S15 Supplementary Materials: Metabolomics and Cheminformatics Analysis of Antifungal Function of Plant Metabolites Miroslava Cuperlovic-Culf, NandhaKishore Rajagopalan, Dan Tulpan and Michele C. Loewen List of resistance related metabolites obtained from referenced publications with their plant origin. Pubchem (CID) Metabolite Synonim Plant Origin Reference 179 3-hydroxy-2-butanone - Chickpea volatiles Cruz, 2012 445154 Resveratrol - General resistance Lattanzio, 2006 199 Agmatine - Wheat Gunnaiah, 2012 243 Benzoic acid - Wheat Hamzehzarghani, 2005 264 Butanoic acid - Wheat Hamzehzarghani, thesis 273 Cadaverine 1,5-Diaminopentane Wheat Hamzehzarghani, PhD 311 Citric acid - Barley Bollina, 2010 323 Coumarin - barley Chamarthi, 2014 338 p-hydroxybenzoic acid salicylic acid Wheat Gunnaiah, 2012 370 5-O-β-glucoside of gentisic acid, gallic acid gallic acid Wheat Boutigny, 2010 Hamzehzarghani, PhD; 424 Aspartic acid - Wheat; Barley Bollina, 2010 441 β-D-glucopyranosyl-sinapic acid beta-Hydroxybutyric acid Wheat Gunnaiah, 2012 469 2-Aminoadipic acid - Barley Bollina, 2010 674 dimethylamine - Chickpea volatiles Cruz, 2012 750 Glycine - Wheat Hamzehzarghani, PhD 753 Glycerol - barley Bollina, 2011 754 glycerol-3-phosphate - signaling molecule Dempsey, 2012 760 Glyoxylate/Oxaloacetiec acid - Wheat (Sumai-3) Gunnaiah, 2014 801 auxin - hormon Petti, 2012 802 Indole-3-acetate - wheat Gunnaiah, PhD 811 2-methylenesuccinic acid Itaconic acid Wheat Gunnaiah, PhD 847 Methionine sulfoxide - Barley Bollina, 2011 Systemic acquired
    [Show full text]
  • PROPERTIES of R-AMINOBUTYRIC ACID ACTIVATED CHLORIDE CHANNELS in MAMMALIAN NEURONES by Claire Fiona Newland a Thesis Subm Itted
    PROPERTIES OF r-AMINOBUTYRIC ACID ACTIVATED CHLORIDE CHANNELS IN MAMMALIAN NEURONES b y Claire Fiona Newland A Thesis submitted for the degree of Doctor of Philosophy at the University of London. Department of Pharmacology University College London Supervisors: Dr. S. G. Cull-Candy & Prof. D. Colquhoun, FRS. 1990 1 ProQuest Number: 10609808 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a com plete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. uest ProQuest 10609808 Published by ProQuest LLC(2017). Copyright of the Dissertation is held by the Author. All rights reserved. This work is protected against unauthorized copying under Title 17, United States C ode Microform Edition © ProQuest LLC. ProQuest LLC. 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, Ml 48106- 1346 ABSTRACT GABA a receptor-channels in dissociated rat sympathetic ganglion neurones have been studied by conventional patch clamp techniques, with both whole-cell and outside-out patch configurations* T hese GABA a receptor-channels are shown to be pharmacologically similar to those of mammalian central neurones, being inhibited by bicuculline, picrotoxin, picrotoxinin and penicillin, and potentiated by pentobarbitone. Furthermore, peripheral GABAA-channels resemble central ones in their cur rent-voltage relationship (whole-cell and Bingle-channel) and in the voltage-dependence of their kinetic properties (noise an aly sis). The mechanism of action of the well established GABA a antagonist, picrotoxin, has been further investigated in these neurones.
    [Show full text]
  • (12) Patent Application Publication (10) Pub. No.: US 2009/0269772 A1 Califano Et Al
    US 20090269772A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2009/0269772 A1 Califano et al. (43) Pub. Date: Oct. 29, 2009 (54) SYSTEMS AND METHODS FOR Publication Classification IDENTIFYING COMBINATIONS OF (51) Int. Cl. COMPOUNDS OF THERAPEUTIC INTEREST CI2O I/68 (2006.01) CI2O 1/02 (2006.01) (76) Inventors: Andrea Califano, New York, NY G06N 5/02 (2006.01) (US); Riccardo Dalla-Favera, New (52) U.S. Cl. ........... 435/6: 435/29: 706/54; 707/E17.014 York, NY (US); Owen A. (57) ABSTRACT O'Connor, New York, NY (US) Systems, methods, and apparatus for searching for a combi nation of compounds of therapeutic interest are provided. Correspondence Address: Cell-based assays are performed, each cell-based assay JONES DAY exposing a different sample of cells to a different compound 222 EAST 41ST ST in a plurality of compounds. From the cell-based assays, a NEW YORK, NY 10017 (US) Subset of the tested compounds is selected. For each respec tive compound in the Subset, a molecular abundance profile from cells exposed to the respective compound is measured. (21) Appl. No.: 12/432,579 Targets of transcription factors and post-translational modu lators of transcription factor activity are inferred from the (22) Filed: Apr. 29, 2009 molecular abundance profile data using information theoretic measures. This data is used to construct an interaction net Related U.S. Application Data work. Variances in edges in the interaction network are used to determine the drug activity profile of compounds in the (60) Provisional application No. 61/048.875, filed on Apr.
    [Show full text]
  • Natural Agents Affecting Excitatory and Inhibitory Neurotransmission: Adenosine Receptor Antagonism: Caffeine (Coffea Spp/C
    Natural Agents Affecting Excitatory and Inhibitory Neurotransmission: Adenosine receptor antagonism: ● Caffeine (Coffea spp/Coffee) Primary GABA inhibition: ● Anisatin (Japanese star anise/Illicium anisatum) ○ non-competitive GABA (channel) inhibition 1’2 ● Bicuculline (Dicentra cucullaria/Dutchman's breeches) ○ competitive inhibition GABA site ○ (and probably non-competitive via allosteric change) 3 ● Cicuta maculata (Water Hemlock) & Cicuta Virosa (Cowbane or Northern Water Hemlock) ○ Cicutoxin- GABA +/- inhibition potassium channels 4’5 ○ Virol A: non-competitive with GABA binding site, but does produce competitive GABA channel (chloride) inhibition ■ structurally similar to cicutoxin 6 ● Colchicine (Colchicum autumnale/autumn crocus) ○ competitive antagonist 7 ● Oenanthe fistulosa (Water Dropwort) [Toxin] ○ probably competitive inhibition of GABA Chloride channel (dose dependent blockade) ○ structure similar to cicutoxin ○ from island of Sardinia; ? glycine antagonism- risus sardonicus 8 ● Picrotoxin (Anamirta cocculus/Fishberries) ○ non-competitive inhibition 9 1 Rietjens IM, Martena MJ, Boersma MG, et al. Molecular mechanisms of toxicity of important food-borne phytotoxins. Molecular mechanisms of toxicity of important food-borne phytotoxins. Mol Nutr Food Res. 2005 Feb;49(2):131-58. PMID: 15635687 2 Perret C, Tabin R, Marcoz JP et al. [Apparent life-threatening event in infants: think about star anise intoxication!]. [Article in French] Arch Pediatr. 2011 Jul;18(7):750-3. doi: 10.1016/j.arcped.2011.03.024. 3 Ueno S, Bracamontes J, Zorumski C, et al. Bicuculline and gabazine are allosteric inhibitors of channel opening of the GABAA receptor. J Neurosci. 1997 Jan 15;17(2):625-34.PMID: 8987785 4 Schep LJ, Slaughter RJ, Becket G, Beasley DM. Poisoning due to water hemlock. Clin Toxicol (Phila). 2009 Apr;47(4):270-8.
    [Show full text]
  • Pediculus Humanus
    Studies into the insecticidai activity and mode of action of monoterpenoid constituents of essentiai oiis against the human iouse, Pediculus humanus. A thesis presented by Caroline Mary Priestley For the degree of Doctor of Philosophy Centre for Pharmacognosy and Phytotherapy, Department of Pharmaceutical and Biological Chemistry, The School of Pharmacy, Faculty of Medicine, University of London. 2002 Abstract The incidence of head lice, 'Pediculus humanus capitis^ in the West is increasing, with insecticide resistance the likely cause. Previous studies have explored the utility of essential oils, and some of their constituent monoterpenoids, in the treatment of head lice. This investigation examines the relative short-term toxicity of a range of different monoterpenoid structures on adult clothing lice, Pediculus humanus corporis, and their eggs; a structure-activity series was generated for the adults, and partially for eggs. The most effective monoterpenoid against adult Hce was (+)-terpinen-4-ol, with monocyclic compounds containing a single O-atom having the highest activities. Furthermore, there appear to be important differences between the relative potencies of monoterpenoids on lice and eggs, as nerolidol was particularly effective against eggs but completely ineffective against adult lice. To investigate the insecticidal mechanism of action of monterpenoids, various pediculicidal structures were screened for activity on an insect ionotropic GABA receptor, composed of the Drosophila melanogaster svhum t RDL^^, expressed in Xenopus oocytes. Thymol, eugenol and carvacrol potentiated GABA responses at this receptor, and possessed agonist activity at high concentrations. This is the first documentation of monoterpenoid bioactivity at an isolated insect receptor known to be representative of an in vivo insecticidal target.
    [Show full text]
  • Novel Modulation of Adenylyl Cyclase Type 2 Jason Michael Conley Purdue University
    Purdue University Purdue e-Pubs Open Access Dissertations Theses and Dissertations Fall 2013 Novel Modulation of Adenylyl Cyclase Type 2 Jason Michael Conley Purdue University Follow this and additional works at: https://docs.lib.purdue.edu/open_access_dissertations Part of the Medicinal-Pharmaceutical Chemistry Commons Recommended Citation Conley, Jason Michael, "Novel Modulation of Adenylyl Cyclase Type 2" (2013). Open Access Dissertations. 211. https://docs.lib.purdue.edu/open_access_dissertations/211 This document has been made available through Purdue e-Pubs, a service of the Purdue University Libraries. Please contact [email protected] for additional information. Graduate School ETD Form 9 (Revised 12/07) PURDUE UNIVERSITY GRADUATE SCHOOL Thesis/Dissertation Acceptance This is to certify that the thesis/dissertation prepared By Jason Michael Conley Entitled NOVEL MODULATION OF ADENYLYL CYCLASE TYPE 2 Doctor of Philosophy For the degree of Is approved by the final examining committee: Val Watts Chair Gregory Hockerman Ryan Drenan Donald Ready To the best of my knowledge and as understood by the student in the Research Integrity and Copyright Disclaimer (Graduate School Form 20), this thesis/dissertation adheres to the provisions of Purdue University’s “Policy on Integrity in Research” and the use of copyrighted material. Approved by Major Professor(s): ____________________________________Val Watts ____________________________________ Approved by: Jean-Christophe Rochet 08/16/2013 Head of the Graduate Program Date i NOVEL MODULATION OF ADENYLYL CYCLASE TYPE 2 A Dissertation Submitted to the Faculty of Purdue University by Jason Michael Conley In Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy December 2013 Purdue University West Lafayette, Indiana ii For my parents iii ACKNOWLEDGEMENTS I am very grateful for the mentorship of Dr.
    [Show full text]