82 research outputs found

    Developing a new resetting tool for controlling rats

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    A resetting toxin device (the “Spitfire”) has been designed that delivers a toxic paste to a rat’s ventral surface when it passes through a tunnel. The rat grooms off the paste and ingests the toxin. The system was assessed in cage trials and one field trial. The purpose of the cage trials was to investigate whether a range of toxins can be delivered by the Spitfire to rats (Rattus rattus and R. norvegicus), namely 0.55% sodium fluoroacetate (1080), 0.2% brodifacoum, 15% cholecalciferol, and 12.5% zinc phosphide. The trials with 1080, brodifacoum, and zinc phosphide were successful with > 85% of rats ingesting lethal doses. The trials with cholecalciferol were less successful with only 58% of rats dying. A one-month pilot field trial was undertaken using 1080 in the Spitfires. There was a knockdown in rat (and stoat Mustela erminea) abundance, establishing proof of concept for the Spitfire delivery system with this toxin. The long-term, effective control of introduced rats will require a range of toxins with different modes of action. The Spitfire could be a useful additional control tool for rats and is currently being re-engineered to be made more reliable

    The landscape of potential health benefits of carotenoids as natural supportive therapeutics in protecting against Coronavirus infection

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    The Coronavirus Disease-2019 (COVID-19) pandemic urges researching possibilities for prevention and management of the effects of the virus. Carotenoids are natural phytochemicals of anti-oxidant, anti-inflammatory and immunomodulatory properties and may exert potential in aiding in combatting the pandemic. This review presents the direct and indirect evidence of the health benefits of carotenoids and derivatives based on in vitro and in vivo studies, human clinical trials and epidemiological studies and proposes possible mechanisms of action via which carotenoids may have the capacity to protect against COVID-19 effects. The current evidence provides a rationale for considering carotenoids as natural supportive nutrients via antioxidant activities, including scavenging lipid-soluble radicals, reducing hypoxia-associated superoxide by activating antioxidant enzymes, or suppressing enzymes that produce reactive oxygen species (ROS). Carotenoids may regulate COVID-19 induced over-production of pro-inflammatory cytokines, chemokines, pro-inflammatory enzymes and adhesion molecules by nuclear factor kappa B (NF-κB), renin-angiotensin-aldosterone system (RAS) and interleukins-6- Janus kinase-signal transducer and activator of transcription (IL-6-JAK/STAT) pathways and suppress the polarization of pro-inflammatory M1 macrophage. Moreover, carotenoids may modulate the peroxisome proliferator-activated receptors γ by acting as agonists to alleviate COVID-19 symptoms. They also may potentially block the cellular receptor of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), human angiotensin-converting enzyme 2 (ACE2). These activities may reduce the severity of COVID-19 and flu-like diseases. Thus, carotenoid supplementation may aid in combatting the pandemic, as well as seasonal flu. However, further in vitro, in vivo and in particular long-term clinical trials in COVID-19 patients are needed to evaluate this hypothesis

    Separation, characterisation and biological evaluation of the individual isomers of the rat selective toxicant norbormide – isolated using a chemical derivatization strategy

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    Norbormide [5-(α-hydroxy-α-2-pyridylbenzyl)-7-(α-2-pyridylbenzylidene)-5-norbornene-2,3-dicarboximide] (NRB, 1), an existing but infrequently used rodenticide, is known to be uniquely toxic to rats but relatively harmless to other rodents/mammals. However, as an acute vasoactive, NRB has a rapid onset of action, often leading to sub-lethal uptake/bait shyness. Recently, it was brought to our attention that baits containing two independently sourced batches of NRB (which differed noticeably in their stereochemical composition) displayed markedly different palatability/efficacy profiles in rats. Accordingly, with a view to independently evaluating the individual isomers of NRB in rats by means of a palatability and efficacy bait trial, this research describes the isolation of the individual isomers of endo-NRB (Y, V, W and U) from the parent mixture, by means of a chemical derivatization strategy

    Investigation of tutin, a naturally-occurring plant toxin, as a novel, culturally-acceptable rodenticide in New Zealand

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    He nui nga mātauranga a te Māori (Ngai Tūhoe) e pā ana ki nga momo hua tāokeoke (Toxins) etaea ana te whakarite hei rauemi tāwai i ngā riha kīrearea, pērā anō ki nga whiu takarangi o te tāoke 1080. I whakamātauhia e matou i nga ira tāoke o roto o te hua Tutu, ki rō taiwhanga pūtaiao. Mā te wero atu ki tētahi kiore (Norway Rat) i hua mai ngā mohiotanga o te nui me te momo o ngā tāokeoke kei roto i tēnei miro Māori, me te āhua o tēnei tāoke kia mau-rohā tonu tōna tuku whakahemo (Humaneness). Kei tua o te 55 mg kg⁻¹neke atu, te ine i tūtuki pai ai nga tāhawahawatanga o te miro Tutu, ā, e mau-roha tonu ana te kōhurutanga o te r iha. Ko te whakatau kia kawea atu tēnei kaupapa ki nga ahurewa rangahau e taea ai te waihanga i tētahi mōunu tāokeoke, kia whakamātauria ki rō ngāhere. Hei tāpiritanga ki tēnei, he roa rawa te wā e pakari ai te whanaketanga mai o tētahi tākoe e rerekē ana ki te 1080, anō nei, mā ngā kawenga o te mātauranga Māori ki tēnei take e whanake tika ai te kaupapa nei. New Zealand has many introduced mammalian species that are managed as pests of conservation and/or economic importance, including four rodent species. Vertebrate pesticides are the most important rodent management tool, largely dominated by anticoagulants such as brodifacoum, and by the metabolic disruptor, Compound 1080. There has been considerable opposition to these pesticides, primarily based on concerns about environmental persistence and non-target effects; Maori have been particularly vocal in opposition. Maori have place-based knowledge about naturally-occurring plant toxins that could be used as culturally-acceptable alternatives to existing rodenticides. In the context of the research presented here, the term ‘culturally-acceptable’ refers to new pest control options that have been co-designed with Matauranga Maori experts that inherently include Maori ways of thinking, being, and acting. Tuhoe researchers in our study wanted to pursue the most promising natural toxic compound found in native plants as a suitable alternative to current vertebrate pesticides. Therefore, we undertook an oral gavage trial to assess the toxicity of tutin, the toxin active in tutu (Coriaria arborea), to the Norway rat, (Rattus norvegicus). Tutin was toxic to this species at a dose of 55 mg kg⁻¹, with a quick, humane death compared to other existing rodenticides. At a dose rate of 55 mg kg⁻¹, all animals of both sexes died within an hour, and once neurological poisoning symptoms commenced these animals were unconscious within 5-10 minutes. We conclude it is warranted to take the next logical research step, which is to prove whether this dose rate would be technically attainable in the field. Although for now New Zealand remains reliant on 1080 and anti-coagulants for mammalian pest control, efforts should continue to develop more targeted toxins and delivery systems. We recommend incorporating Matauranga Maori to identify alternative control tools that could lead to more culturally acceptable pest control

    Human malarial disease: a consequence of inflammatory cytokine release

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    Malaria causes an acute systemic human disease that bears many similarities, both clinically and mechanistically, to those caused by bacteria, rickettsia, and viruses. Over the past few decades, a literature has emerged that argues for most of the pathology seen in all of these infectious diseases being explained by activation of the inflammatory system, with the balance between the pro and anti-inflammatory cytokines being tipped towards the onset of systemic inflammation. Although not often expressed in energy terms, there is, when reduced to biochemical essentials, wide agreement that infection with falciparum malaria is often fatal because mitochondria are unable to generate enough ATP to maintain normal cellular function. Most, however, would contend that this largely occurs because sequestered parasitized red cells prevent sufficient oxygen getting to where it is needed. This review considers the evidence that an equally or more important way ATP deficency arises in malaria, as well as these other infectious diseases, is an inability of mitochondria, through the effects of inflammatory cytokines on their function, to utilise available oxygen. This activity of these cytokines, plus their capacity to control the pathways through which oxygen supply to mitochondria are restricted (particularly through directing sequestration and driving anaemia), combine to make falciparum malaria primarily an inflammatory cytokine-driven disease

    The Acute Toxicity of Cholecalciferol to the European Rabbit, Oryctolagus Cuniculus.

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    Connections between rodenticides and drugs: a review of natural compounds with ecological, biocidal and medical applications

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    Natural products have inspired over 60% of today’s drugs and biocides, including rodenticides, with examples such as warfarin, fluoroacetate and cholecalciferol. Fluoroacetate is a toxic component of poisonous plants found in Australia, Africa, South America and India and is thought to deter herbivores. Together with other rodenticides it has medical applications. In relation to its use for the control of unwanted introduced animals in New Zealand, research has focused on mode of action, sub-lethal effects, welfare, reducing its risk to non-target species, and fate in the environment following use in baits. Less attention has been placed on its role in nature. In this paper the natural occurrence of bioactives that have stimulated the development of rodenticides are reviewed and links between biocidal and medical applications are explored

    Primary poisoning risk for encapsulated sodium nitrite, a new tool for pest control

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    Acute toxicity of sodium nitrite (NaNO₂) was assessed in chickens (Gallus gallus domesticus) and domestic mallard ducks (Anas platyrhynchos domestica) by oral gavage and in free-feeding trials with chickens, domestic mallard ducks, pigeons (Columba livia f. domestica), budgerigars (Melopsittacus undulates) and wētā (Family: Rhaphidophoridae). Free-feeding trials involved the presentation of toxic paste and pellet baits containing encapsulated NaNO₂ developed for the control of common brushtail possums (Trichosurus vulpecula) and feral pigs (Sus scrofa). The oral gavage LD₅₀ value for NaNO₂ in solution was approximately 68.50 mg/kg (95% CI 55.00–80.00 mg/kg) for both chickens and ducks. In feeding trials, six out of 12 chickens consumed toxic paste bait and four of these birds consumed a lethal dose. When chickens consumed toxic paste bait, the LD₅₀ value was approximately 254.6 mg/kg (95% CI 249.1–260.2 mg/kg). Of the other three species of birds presented with toxic baits only one duck consumed a lethal dose of paste bait. There was no evidence of wētā feeding on toxic baits
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