Page 653 - Veterinary Toxicology, Basic and Clinical Principles, 3rd Edition
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618 SECTION | VIII Rodenticides




  VetBooks.ir  RED SQUILL                                       ingest a product containing scilliroside, because they are
                                                                  Scilliroside has an emetic property; thus, if rodents
             Introduction
                                                                incapable of vomiting, they develop glycoside intoxica-
             Red squill, which is also known as sea onion, is obtained  tion and pulmonary edema. However, it has rarely been
             in the powder form from the plant Urginea maritima. The  associated with toxicity in humans because humans are
             plant is native to the Mediterranean region. It resembles  capable of vomiting and exhibit poor GI absorption.
             an onion, and its bulb extracts and dried powders have
             been used for the control of rodents since the 13th cen-  Toxicokinetics
             tury. Although red squill has many alkaloids, scilliroside
             is the most toxic, and provides rodenticidal activity. It has  Scilliroside is inefficiently absorbed from the GI tract. Its
             the chemical formula C 32 H 44 O 12 and a molecular weight  metabolism is not well-studied, although the unmetabo-
             of 620.7. Its structural formula is shown in Fig. 47.4. The  lized scilliroside is rapidly excreted in the urine.
             compound is sparingly soluble in water and thermostable.
             Scilliroside is formulated in the powder form (Dethdiet)
             and liquid extract (Rodine), and it has many other names,  Mechanism of Action
             including Sea squill, Scilla maritima, Silmurin, Silmine,
                                                                Red squill bulbs contain many glycosides, but scilliroside
             Sea onion, and Squill. It was demonstrated long ago by
                                                                is the major component that has a rodenticidal property.
             Winton (1927b) that only red squill, not white squill, has
                                                                The compound is cardiotoxic, similar to digitalis; i.e.,
             rodenticide activity. The red squill is mixed in baits and
                                                                injection of scilliroside induces cardiac impulse condition
             applied at a 10% concentration and mixed with meat,
                                                                and arrhythmias. In very early experiments, red squill pre-
             fish, and cereals (Thomson, 1991 1992).
                                                                parations administered to rats induced convulsions and
                                                                paralysis (Winton, 1927a). Female rats succumb to red
                                                                squill at half the dose that is required to kill males.
             Background
             Red squill bulbs were an ancient source of rodenticide  Toxicity
             products replaced later by warfarin and other modern anti-
             coagulant rodenticides. Because rats have developed  The red squill plant (mainly the bulb) contains scilliroside,
             resistance to such products, there is renewed interest in  a highly toxic bufadienolide glycoside. It adversely affects
             the red squill. Studies suggest that the white squill drug is  cardiovascular and CNSs, causing convulsions and death.
             used as a diuretic, stimulant, and expectorant, whereas the  The oral LD 50 of scilliroside is 0.7 mg/kg in male rats,
             red squill is used mostly as a rat poison. Many glycosides  0.43 mg/kg in female rats, and 0.35 mg/kg in mice. Studies
             and aglycones have been isolated from the red squill bulb.  found that pigs and cats survived doses of 16 mg/kg and
             Krenn et al. (1994) and Pascual-Villalobos (2002) isolated  fowls survived 400 mg/kg (Worthing, 1983). It is classified
             five different bufadienolides as pure substances (proscil-  as class I—i.e., a highly toxic chemical.
             laridin A, scillaren A, scilliroside, gammabufotalin, and  Red squill contains several compounds that have emetic
             scillirosidin). Scilliroside is the most toxic bufadienolide  properties. Due to poor GI absorption and decreased
             glycoside (Verbiscar et al., 1986a,b).             potency, red squill has seldom been associated with toxic-
                                                                ity in humans, dogs, cats, and pigeons. However, rats and
                                                                mice are unable to vomit, and they die within a few hours
                                                                after ingesting a lethal dose of scilliroside.
                                                                  In toxic doses, red squill produces inflammation of the
                                                                GI and genitourinary tracts, manifested by nausea, vomit-
                                                                ing, abdominal pain, and purging. Other signs of poisoning
                                                                include convulsions, hypothermia, enfeebled circulation,
                                                                blurred vision and, sometimes, death. Convulsions are seen
                                                                in humans, and they have also been observed in rats.
                                                                Higher doses of red squill can cause serious heart rhythm
                                                                alterations, resulting in death. Farm animals require large
                                                                quantities for intoxication. There are field cases in which
                                                                dogs, cats, and pigs have been poisoned. Signs of poison-
                                                                ing include vomiting, ataxia, and hyperesthesia, followed
                                                                by paralysis, depression, or convulsions. Cardiac arrest
             FIGURE 47.4 Structural formula of scilliroside.    occurs due to bradycardia and cardiac arrhythmias.
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