targeted-toxins

Emanuel AJ, Ritter S (2010) Hindbrain catecholamine neurons modulate the growth hormone but not the feeding response to ghrelin. Endocrinology 151(7):3237-3246. doi: 10.1210/en.2010-0219

Summary: In this work the authors investigated the role of hindbrain catecholamine neurons in the response to a gastrointestinal peptide, ghrelin. Rats received 42 ng injections of anti-DBH-SAP (Cat. #IT-03) into the paraventricular nucleus of the hypothalamus. Saporin (Cat. #PR-01) was used as a control. Lesioned animals had a prolonged growth hormone (GH) response to ghrelin administration as compared to controls, but the feeding response was unchanged. The results indicate that ghrelin or GH may be involved with a negative feedback response controlling GH levels.

Related Products: Anti-DBH-SAP (Cat. #IT-03), Saporin (Cat. #PR-01)

Coradazzi M, Gulino R, Garozzo S, Leanza G (2010) Selective lesion of the developing central noradrenergic system: Short- and long-term effects and reinnervation by noradrenergic-rich tissue grafts. J Neurochem 114(3):761-771. doi: 10.1111/j.1471-4159.2010.06800.x

Summary: The authors removed noradrenergic neurons in the locus coeruleus/subcoeruleus complex of neonatal rats with 0.25-1.0 µg bilateral injections of anti-DBH-SAP (Cat. #IT-03). No damage was seen in dopaminergic, adrenergic, serotonergic, or cholinergic neurons after this treatment. Rats receiving fetal locus coeruleus tissue implants showed significant post-lesion recovery suggesting that this model can be used to investigate compensatory reinnervation and functional recovery in the central nervous system.

Related Products: Anti-DBH-SAP (Cat. #IT-03)

Klinkenberg I, Blokland A (2010) The validity of scopolamine as a pharmacological model for cognitive impairment: A review of animal behavioral studies. Neurosci Biobehav Rev 34(8):1307-1350. doi: 10.1016/j.neubiorev.2010.04.001 PMID: 20398692

Objective: To provide an overview is given of the effects of scopolamine on animal behavior.

Summary: The most important and influential articles over the past 40 years are included in the present review. The cholinergic hypothesis of memory function as originally put forward by Bartus et al. (1982) has undergone a revision after several lesion studies were performed which used the highly specific cholinergic toxin 192 IgG-SAP (Wiley et al., 1995).

Related Products: 192-IgG-SAP (Cat. #IT-01)

See Also:

• Chudasama Y et al. Cholinergic modulation of visual attention and working memory: Dissociable effects of basal forebrain 192-IgG-saporin lesions and intraprefrontal infusions of scopolamine. Learn Mem 11(1):78-86, 2004.
• Wiley RG et al. Destruction of the cholinergic basal forebrain using immunotoxin to rat NGF receptor: modeling the cholinergic degeneration of Alzheimer’s disease. J Neurol Sci 128:157-166, 1995.
• Wiley RG et al. Immunolesioning: Selective destruction of neurons using immunotoxin to rat NGF receptor. Brain Res 562:149-153, 1991.
• Wrenn CC et al. The behavioral functions of the cholinergic basal forebrain: lessons from 192 IgG-saporin. Int J Dev Neurosci 16(7-8):595-602, 1998.
• Wenk GL The nucleus basalis magnocellularis cholinergic system: one hundred years of progress. Neurobiol Learn Mem 67(2):85-95, 1997.
• Baxter MG et al. Intact spatial learning in both young and aged rats following selective removal of hippocampal cholinergic input. Behav Neurosci 110:460-467, 1996.
• Baxter MG et al. Intact spatial learning in both young and aged rats following selective removal of hippocampal cholinergic input. Behav Neurosci 110:460-467, 1996.
• Baxter MG et al. Disruption of decrements in conditioned stimulus processing by selective removal of hippocampal cholinergic input. J Neurosci 17:5230-5236, 1997.
• Chiba AA et al. Selective removal of cholinergic neurons in the basal forebrain alters cued target detection. Neuroreport 10(14):3119-3123, 1999.
• McGaughy J et al. Effects of chlordiazepoxide and scopolamine, but not aging, on the detection and identification of conditional visual stimuli. J Gerontol A Biol Sci Med Sci 50(2):B90-B96, 1995.
• McGaughy J et al. Crossmodal divided attention in rats: effects of chlordiazepoxide and scopolamine. Psychopharmacology (Berl) 115(1-2):213-220, 1994.
• Torres EM et al. Behavioral, histochemical and biochemical consequences of selective immunolesions in discrete regions of the basal forebrain cholinergic system. Neuroscience 63:95-122, 1994.
• Voytko ML Cognitive functions of the basal forebrain cholinergic system in monkeys: memory or attention?. Behav Brain Res 75(1-2):13-25, 1996.

Marques-Lopes J, Pinho D, Albino-Teixeira A, Tavares I (2010) The hyperalgesic effects induced by the injection of angiotensin II into the caudal ventrolateral medulla are mediated by the pontine A(5) noradrenergic cell group. Brain Res 1325:41-52. doi: 10.1016/j.brainres.2010.02.043

Summary: Injection of angiotensin II into the caudal ventrolateral medulla (CVLM) has been shown to induce angiotensin type 1 receptor-mediated hyperalgesia. Here the authors lesioned the pontine A5 cell group with anti-DBH-SAP (Cat. #IT-03) to evaluate the role of these neurons in this model. Rats received a 1.1 µg injection of anti-DBH-SAP into the CVLM. Behavioral responses indicate that loss of noradrenergic neurons in the CVLM partially prevented angiotensin II-induced hyperalgesia.

Related Products: Anti-DBH-SAP (Cat. #IT-03)

Vianna DM, Carrive P (2010) Cardiovascular and behavioural responses to conditioned fear and restraint are not affected by retrograde lesions of A5 and C1 bulbospinal neurons. Neuroscience 166:1210-1218. doi: 10.1016/j.neuroscience.2010.01.039

Summary: To investigate the role of A5 neurons in some forms of psychological stress the authors injected 22 or 44 ng of anti-DBH-SAP (Cat. #IT-03) into the spinal cord of rats. Mouse IgG-SAP (Cat. #IT-18) was used as a control. The data shows that A5 presympathetic neurons are not essential for the expression of the tachycardic and pressor responses to conditioned fear and restraint.

Related Products: Anti-DBH-SAP (Cat. #IT-03), Mouse IgG-SAP (Cat. #IT-18)

Dailey MJ, Bartness TJ (2010) Arcuate nucleus destruction does not block food deprivation-induced increases in food foraging and hoarding. Brain Res 1323:94-108. doi: 10.1016/j.brainres.2010.01.078

Summary: While some aspects of food intake are understood, mechanisms controlling hoarding of food have not been identified. This work investigates the role of NPY in the arcuate nucleus (Arc) in hoarding. Siberian hamsters received 48 ng injections of NPY-SAP (Cat. #IT-28) into the Arc; blank-SAP (Cat. #IT-21) was used as a control. In lesioned animals food deprivation-induced hoarding was increased 100%, but baseline foraging and food hoarding was unchanged.

Related Products: NPY-SAP (Cat. #IT-28), Blank-SAP (Cat. #IT-21)

Gulino R, Perciavalle V, Gulisano M (2010) Expression of cell fate determinants and plastic changes after neurotoxic lesion of adult mice spinal cord by cholera toxin-B saporin. Eur J Neurosci 31(8):1423-1434. doi: 10.1111/j.1460-9568.2010.07170.x

Summary: Sonic hedgehog, Notch-1, and Numb are proteins known to be involved in the function of stem cells. Understanding of how they might work in adults may provide methods to improve recovery from spinal cord injury. In this work the authors injected 3 µg of CTB-SAP (Cat. #IT-14) into the medial and lateral gastrocnemius muscles of mice. Analysis of protein levels following motoneuron depletion gives some insight into the molecular framework of nerve injury.

Related Products: CTB-SAP (Cat. #IT-14)

Read the featured article in Targeting Trends.

Larsson M, Broman J (2011) Synaptic plasticity and pain: role of ionotropic glutamate receptors. Neuroscientist 17(3):256-73. doi: 10.1177/1073858409349913

Summary: This review discusses the role of glutaminergic sensory synapses in pain hypersensitivity caused by tissue or nerve injury. The focus is on the roles of ionotrophic glutamate receptors, and how they are involved in dorsal horn synaptic plasticity. The role of substance P in such mechanisms is briefly discussed, as elucidated by the use of SP-SAP (Cat. #IT-07).

Related Products: SP-SAP (Cat. #IT-07)

De Bartolo P, Cutuli D, Ricceri L, Gelfo F, Foti F, Laricchiuta D, Scattoni ML, Calamandrei G, Petrosini L (2010) Does age matter? Behavioral and neuro-anatomical effects of neonatal and adult basal forebrain cholinergic lesions. J Alzheimers Dis 20:207-227. doi: 10.3233/JAD-2010-1355 PMID: 20164586

Summary: The authors characterized the differences caused by age on the effect of cholinergic lesions of the basal forebrain. Seven-day-old rats received 210 ng bilateral intracerebroventricular injections of 192-IgG-SAP (Cat. #IT-01). Eighty-day-old rats received 4 µg bilateral intracerebroventricular injections of 192-IgG-SP. Both experimental groups displayed similar behavior, indicating that development of a depleted cholinergic system yields similar results to cholinergic dysfunction in adulthood.

Related Products: 192-IgG-SAP (Cat. #IT-01)

Nag N, Baxter MG, Berger-Sweeney JE (2009) Efficacy of a murine-p75-saporin immunotoxin for selective lesions of basal forebrain cholinergic neurons in mice. Neurosci Lett 452:247-251. doi: 10.1016/j.neulet.2009.01.006

Summary: The authors tested a new version of mu p75-SAP (Cat. #IT-16) in mice. Mice received bilateral injections of 0.65 or 1.3 µg of immunotoxin into each lateral ventricle. Both amounts produced a complete loss of cholinergic neurons in the medial septum, while a dose-dependent loss of cholinergic neurons was seen in the nucleus basalis magnocellularis.

Related Products: mu p75-SAP (Cat. #IT-16)