Abstract
Abamectin (MK-0936) is a natural fermentation product of Streptomyces avermitilis. Ivermectin (MK-0933) is a synthetic derivative of abamectin. The chemical structure of abamectin differs from ivermectin only in the bond between carbons 22 and 23; abamectin has a double bond where ivermectin has a single bond and additional hydrogens on C-22 and C-23 (Figure 6.1). Both compounds are a mixture of homologous products with B1a and B1b components. The B1b component differs chemically from the B1a component by only 1 methylene (CH2) unit at the 26-carbon position: the ethyl group (C2H5) is a methyl group (CH3) in the B1b form. Abamectin and ivermectin are defined as containing a minimum of 80% B1a, and a maximum of 20% B1b components. Studies in our laboratories have clearly demonstrated that the individual components have very similar biological and toxicological properties and, for all practical purposes, can be considered equivalent.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Amano Y (1967) Changes of the levels of blood glucose during pregnancy in the rat. Jap. J. Pharmacol. 17:105–114
Ames BN, McCann J, Yamasaki E (1975) Methods for detecting carcinogens and mutagens with the Salmonella/mammalian microsome mutagenicity test. Mutat. Res. 31:347–364
Betz L, Goldstein GN (1981) Developmental changes in metabolism and transport properties of capillaries isolated from rat brain. J. Physiol. 312:365–376
Bohr V, Mollgard K (1974) Tight junctions in human fetal choroid plexus visualized by freeze-etching. Brain Res. 81:314–318
Brent RL (1986) Definition of a teratogen and the relationship of teratogenicity to carcinogenicity. Teratol. 34:359–360
Campbell WC, Benz GW (1984) Ivermectin: a review of efficacy and safety. J. Vet. Pharm. & Therap. 7:1–16
Chiu SH, Sestokas E, Taub R, Buhs RP, Green M, Sestokas R, Vandenheuval WJ, Arison BH, Jacob TA (1986) Metabolic disposition of ivermectin in tissues of cattle, sheep, and rats. Drug Me tab. & Dispos. 14:590–600
Clive D, Flamm W, Machesko M, Bernheim J (1972) A mutational assay system using the thymidine binase locus in mouse lymphoma cells. Mutat. Res. 16:77–87
Clive D, Spector JASF (1975) Laboratory procedure for assessing specific locus mutations at the TK locus in cultured L5178Y mouse lymphoma cells. Mutat. Res. 31:17–29
Cooper JR (1982) Amino acids. In Cooper JR, Bloom FR, Roth RH (eds), The Biochemical Basis of Neuropharmacology, 4th ed., Oxford University Press, p 250
Cutler SJ, Ederer F (1958) Maximum utilization of the life table method in analyzing survival. J. Chron. Dis. 8:699–712
Greene BM, Taylor HR, Cupp EW, Murphy RP, White AT, Aziz MA, Schulz-Key H, D’Anna SA, Newland HS, Goldschmidt LP, Auer C, Hanson AP, Freeman SV, Reber EW, Williams PN (1985) Comparison of ivermectin and diethylcarbamazine in the treatment of onchocerciasis. New Eng. J. Med. 313:133–138
Harter HL (1957) Error rates and sample sizes for range tests in multiple comparisons. Biometrics 13:511–36
Khera KS (1984) Maternal Toxicity—A possible factor in fetal malformation in mice. Teratol. 29:411–416
Mantel N (1963) Chi-square tests with one degree of freedom; extensions of the Mantel-Haenszel procedure. J. Am. Stat. Assoc. 58:690–700
Mantel N (1980) Assessing laboratory evidence for neoplastic activity. Biometrics 36:381–99
Mantel N, Ciminera J (1979) Use of log-rank scores in the analysis of litter- matched data on time to tumor appearance. Cane. Res. 39:4308–4315
Mantel N, Tukey JW, Ciminera JL, Heyse, JF (1982) Tumorigenicity assays, including use of the jackknife. Biomet. J. 24:579–596
Peto R (1974) Guidelines on the analysis of tumor rates and death rates in experimental animals. Brit. J. Cane. 29:101–105
Peto R, Pike MC, Day NE, Gray RC, Lee PN, Parish S, Peto J, Richards S, Wahrendorf J (1980) Guidelines for simple, sensitive significance tests for carcinogenic effects in long term animal experiments. In International Association for Research on Cancer Monographs, Supplement 2, Lyon, France, pp. 365–367
Robson DS (1959) A simplified method for constructing orthogonal polynomials when independent variable is unequally spaced. Biometrics 15:187–191
Saunders NR (1977) Ontogeny of the blood-brain barrier. Exper. Eye Res. (Suppl.), pp 523–550
Scow RO, Chernick SS, Brinley MS (1964) Hyperlipemia and ketosis in the pregnant rat. Am. J. Physiol. 206:796–804
Setlow RB, Carrier WL (1964) The disappearance of thymine dimers from DNA: An error correcting mechanism. Proc. Natl. Acad. Sci. USA 51:226–231
Tukey JW, Ciminera JL, Heyse JF (1985) Testing the statistical certainty of a response to increasing doses of a drug. Biometrics 41:295–301
Wester RC, Maibach HI (1975) Percutaneous absorption in the rhesus monkey compared to man. Toxicol. & App. Pharm. 32:394–398
Wester RC, Maibach HI (1983) Cutaneous pharmacokinetics. 10 steps to percutaneous absorption. Drug Metab. Rev. 14(2): 169–205
Wilkins RJ, Hart RW (1973) Preferential DNA repair in human cells. Nature 247:35–36
Williams GM, Laspia MF, Dunkel, VC (1982) Reliability of the hepatocyte primary culture/DNA repair test in testing coded carcinogens and non- carcinogens. Mutat. Res. 97:359–370
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1989 Springer-Verlag New York Inc.
About this chapter
Cite this chapter
Lankas, G.R., Gordon, L.R. (1989). Toxicology. In: Campbell, W.C. (eds) Ivermectin and Abamectin. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-3626-9_6
Download citation
DOI: https://doi.org/10.1007/978-1-4612-3626-9_6
Publisher Name: Springer, New York, NY
Print ISBN: 978-1-4612-8184-9
Online ISBN: 978-1-4612-3626-9
eBook Packages: Springer Book Archive