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Suicide Transport and Immunolesioning
Wiley RG, Lappi DA (1994) Suicide Transport and Immunolesioning. R.G. Landes, Houston.
This book is available in many university libraries and can also be purchased here
192 IgG-saporin: I. Specific lethality for cholinergic neurons in the basal forebrain of the rat.
Book AA, Wiley RG, Schweitzer JB (1994) 192 IgG-saporin: I. Specific lethality for cholinergic neurons in the basal forebrain of the rat. J Neuropathol Exp Neurol 53:95-102. doi: 10.1097/00005072-199401000-00012
Related Products: 192-IgG-SAP (Cat. #IT-01)
Differential effects of suicide transport lesions of the striatonigral or striatopallidal pathways on subsets of striatal neurons.
Roberts RC, Harrison MB, Francis SMN, Wiley RG (1993) Differential effects of suicide transport lesions of the striatonigral or striatopallidal pathways on subsets of striatal neurons. Exp Neurol 124:242-252. doi: 10.1006/exnr.1993.1194
Related Products: OX7-SAP (Cat. #IT-02)
Dose-related effects of 192 IgG-saporin on basal forebrain cholinergic neurons: Biochemical, immunocytochemical and behavioral studies on neonatal and adult rats.
Leanza G, Nilsson O, Wiley RG, Bjorklund A (1993) Dose-related effects of 192 IgG-saporin on basal forebrain cholinergic neurons: Biochemical, immunocytochemical and behavioral studies on neonatal and adult rats. Neuroscience 1993 Abstracts 771.12.
Summary: Highly selective and efficient depletions of the NGF receptor-positive cholinergic neurons in the basal forebrain, associated with profound behavioral changes, have been reported after treatment with 192 IgG-saporin, a recently introduced immunotoxin. In the present study, the effects of different doses of the toxin conjugate were compared following bilateral injections in the lateral ventricles of infant (2-3 days post-natal, 0.2 to 0.8 µg dose-range) and adult rats (1.25 to 10 µg dose-range). Five to eight weeks post-injection, dose-related behavioral effects of the lesion were evaluated in water maze, passive avoidance and locomotor activity tests, followed by biochemical and histologic analyses performed on tissue specimens. In the adult rats, the immunotoxin produced severe dose-dependent cognitive deficits in water maze task performance and passive avoidance retention that correlated with decline in choline acetyltransferase (ChAT) activity in neocortical and hippocampal areas (up to 95% reduction) and depletion of NGF receptor-positive neurons in the septal-diagonal band area and nucleus basalis (>95%). Similar dose-related patterns of ChAT activity reduction and neuronal loss throughout the basal forebrain were seen in rats neonatałly injected with the immunotoxin. ChAT levels in other regions such as brainstem, cerebellum or the spinal cord were found largely unaffected in both adult and neonatałly lesioned rats. The present results confirm 192 IgG-saporin as a powerful tool to induce specific and robust cholinergic lesions either during development or adulthood and emphasize the crucial role of the forebrain cholinergic system in cognitive functions.
Related Products: 192-IgG-SAP (Cat. #IT-01)
Noradrenergic lesioning using anti-DBH immunotoxin
Picklo MJ, Wiley RG, Lappi DA, Robertson D (1993) Noradrenergic lesioning using anti-DBH immunotoxin. Neuroscience 1993 Abstracts 771.10. Society for Neuroscience, Washington, DC.
Summary: Current methods of lesioning noradrenergic neurons have significant drawbacks due either to incompleteness, partial specificity, or reversibility. We sought to determine if an immunotoxin to dopamine ß-hydroxylase (DBH) would efficiently destroy noradrenergic neurons in vivo. The MAB3O8 monoclonal antibody to bovine DBH was obtained from Chemicon International (Temecula, CA). Antibody was disulfide coupled to the ribosome inactivating protein, saporin, using SPDP. The resulting immunotoxin was injected into anesthetized adult, male Sprague-Dawley rats. Injection sites in individual animals were the submandibular gland (3.1-12.5 µg), intravenous (6-31 µg), and intraventricular (1.8-4.8 µg). Three days after systemic injections, rats were reanesthetized and transcardially perfused with aldehyde fixative. Frozen sections of peripheral ganglia were processed for Nissi staining. In sections from sympathetic ganglia, most neurons showed severe chromatolysis characteristic of the cytotoxic effect of immunotoxins containing saporin. Sensory ganglia showed small numbers of similarly poisoned neurons. Eleven days after intraventricular injections, rats were sacrificed and brain sections stained either with cresyl violet (N¡ssl) or for tyrosine hydroxylase (TH) using indirect immunoperoxidase technique. Nissi staining of the locus coeruleus showed a decrease in the numbers of neurons as was confirmed by staining for TH. Dopaminergic neurons in the midbrain appeared unaffected as did catecholaminergic neurons in the caudal brainstem. We conclude that anti-DBH-saporin efficiently destroys noradrenergic neurons in the CNS and PNS. This immunotoxin may be a valuable lesioning tool with greater selectivity than has been previously available.
Related Products: Anti-DBH-SAP (Cat. #IT-03)
Synthesis and receptor binding analysis of dermorphin hepta-, hexa- and pentapeptides.
Attila M, Salvadori S, Balboni G, Bryant SD, Lazarus LH (1993) Synthesis and receptor binding analysis of dermorphin hepta-, hexa- and pentapeptides. Int J Pept Prot Res 42:550-559. doi: 10.1111/j.1399-3011.1993.tb00363.x
Related Products: Dermorphin-SAP / MOR-SAP (Cat. #IT-12)
Biphasic effect of the mitotoxin bFGF-saporin on bovine lens epithelial cell growth: effect of cell density and extracellular matrix.
David T, Tassin J, Lappi DA, Baird A, Courtois Y (1992) Biphasic effect of the mitotoxin bFGF-saporin on bovine lens epithelial cell growth: effect of cell density and extracellular matrix. J Cell Physiol 153:483-490. doi: 10.1002/jcp.1041530307
Related Products: FGF-SAP (Cat. #IT-38)
Spatial learning impairments in rats with selective immunolesion of the forebrain cholinergic system.
Nilsson OG, Leanza G, Rosenblad C, Lappi DA, Wiley RG, Bjorklund A (1992) Spatial learning impairments in rats with selective immunolesion of the forebrain cholinergic system. NeuroReports 3:1005-1008. doi: 10.1097/00001756-199211000-00015 PMID: 1482757
Objective: To study the impact of depletion of NGF receptor-positive neurons.
Summary: 192-IgG-SAP (Cat. IT-01) is a neurotoxin that targets specific cholinergic neurons in the rat brain. When injected, it leads to severe and long-lasting impairment in spatial learning. This is associated with a significant reduction in choline acetyltransferase activity (ChAT) in the hippocampus and cortex, while other cholinergic neuron systems remain largely unaffected.
Usage: 4.7 micrograms of 192-IgG-SAP, in 7 microliters, injected into the right lateral ventricle of rats.
Related Products: 192-IgG-SAP (Cat. #IT-01)
Specificity of 192 IgG-saporin for NGF receptor-positive cholinergic basal forebrain neurons in the rat.
Book AA, Wiley RG, Schweitzer JB (1992) Specificity of 192 IgG-saporin for NGF receptor-positive cholinergic basal forebrain neurons in the rat. Brain Res 590:350-355. doi: 10.1016/0006-8993(92)91121-t
Related Products: 192-IgG-SAP (Cat. #IT-01)
Soluble and membrane-bound forms of dopamine b-hydroxylase are encoded by the same mRNA.
Lewis EJ, Asnani LP (1992) Soluble and membrane-bound forms of dopamine b-hydroxylase are encoded by the same mRNA. J Biol Chem 267:494-500. doi: 10.1016/S0021-9258(18)48522-5
Related Products: Anti-DBH-SAP (Cat. #IT-03)
