Selective immunotoxic lesions of basal forebrain cholinergic cells: Effects on learning and memory in rats.

Cholinergic hypofunction impairs memory acquisition possibly through hippocampal Arc and BDNF downregulation

Gil-Bea, F. J., Solas, M., Mateos, L., Winblad, B. G., Ramírez, M. J., & Cedazo-Mı́nguez, Á. (2010) · Hippocampus · doi:10.1002/hipo.20812 · Cited by 54

The septohippocampal cholinergic system and spatial working memory in the Morris water maze

Frielingsdorf, H., Thal, L. J., & Pizzo, D. P. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.10.008 · Cited by 54

Association of basal forebrain volumes and cognition in normal aging

Wolf, D. G. F., Grothe, M. J., Fischer, F. U., Heinsen, H., Kilimann, I., Teipel, S. J., & Fellgiebel, A. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.11.002 · Cited by 53

Transplanted Bone Marrow Mesenchymal Stem Cells Improve Memory in Rat Models of Alzheimer's Disease

Babaei, P., Tehrani, B. S., & Alizadeh, A. (2012) · Stem Cells International · doi:10.1155/2012/369417 · Cited by 54

Cholinergic and noncholinergic septal neurons modulate strategy selection in spatial learning

Cahill, J. F. X., & Baxter, M. G. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01807.x · Cited by 54

Hilar neuropeptide Y interneuron loss in the aged rat hippocampal formation

Cadiacio, C. L., Milner, T. A., Gallagher, M., & Pierce, J. P. (2003) · Experimental Neurology · doi:10.1016/s0014-4886(03)00126-2 · Cited by 53

Individual differences in neurocognitive aging of the medial temporal lobe

Gallagher, M., Colantuoni, C., Eichenbaum, H., Haberman, R. P., Rapp, P. R., Tanila, H., & Wilson, I. A. (2006) · AGE · doi:10.1007/s11357-006-9017-5 · Cited by 57

Blockade of GABA(B) receptors completely reverses age-related learning impairment

LaSarge, C. L., Bañuelos, C., Mayse, J. D., & Bizon, J. L. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.08.055 · Cited by 52

Neurosteroids and cholinergic systems: implications for sleep and cognitive processes and potential role of age-related changes

George, O., Vallée, M., Moal, M. L., & Mayo, W. (2006) · Psychopharmacology · doi:10.1007/s00213-005-0254-6 · Cited by 52

MRI-based volumetric measurement of the substantia innominata in amnestic MCI and mild AD

George, S., Mufson, E. J., Leurgans, S. E., Shah, R. C., Ferrari, C., & deToledo‐Morrell, L. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.11.006 · Cited by 49

Visual acuity in the water maze: sensitivity to muscarinic receptor blockade in rats and mice

Robinson, L., Harbaran, D., & Riedel, G. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.001 · Cited by 51

Recognition memory in rats—III. Neurochemical substrates

Steckler, T., Sahgal, A., Aggleton, J. P., & Drinkenburg, W. H. I. M. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00062-2 · Cited by 51

Noncholinergic Lesions of the Medial Septum Impair Sequential Learning of Different Spatial Locations

Dwyer, T. A., Servatius, R. J., & Pang, K. C. H. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4189-06.2007 · Cited by 50

The Role of the Central Cholinergic Projections in Cognition: Implications of the Effects of Scopolamine on Discrimination Learning by Monkeys

Harder, J. A., Baker, H. F., & Ridley, R. M. (1998) · Brain Research Bulletin · doi:10.1016/s0361-9230(97)00381-x · Cited by 49

Donepezil treatment restores the ability of estradiol to enhance cognitive performance in aged rats: Evidence for the cholinergic basis of the critical period hypothesis

Gibbs, R. B., Mauk, R., Nelson, D. A., & Johnson, D. A. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.03.003 · Cited by 48

Septal cholinergic neurons suppress seizure development in hippocampal kindling in rats: comparison with noradrenergic neurons

Ferencz, I., Leanza, G., Nanobashvili, A., Kokaia, Z., Kokaia, M., & Lindvall, O. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00499-1 · Cited by 47

Combined 192 IgG-saporin and 5,7-dihydroxytryptamine lesions in the male rat brain

Lehmann, O., Jeltsch‐David, H., Lazarus, C., et al. (2002) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(02)00752-9 · Cited by 48

Toward a conceptualization of retrohippocampal contributions to learning and memory

Bucci, D. J., & Robinson, S. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.05.007 · Cited by 48

Selective lesion of septal cholinergic neurons in rats impairs acquisition of a delayed matching to position T-maze task by delaying the shift from a response to a place strategy

Fitz, N. F., Gibbs, R. B., & Johnson, D. A. (2008) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2008.08.016 · Cited by 47

Cholinergic Deafferentation of the Neocortex Using 192 IgG-Saporin Impairs Feature Binding In Rats

Botly, L. C. P., & Rosa, E. D. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0654-09.2009 · Cited by 44

Lipid mapping of the rat brain for models of disease

Martínez‐Gardeazabal, J., Román, E. G. D. S., Moreno‐Rodríguez, M., Llorente‐Ovejero, A., Manuel, I., & Rodríguez‐Puertas, R. (2017) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2017.02.011 · Cited by 45

Regulation of Cognitive Processing by Hippocampal Cholinergic Tone

Al‐Onaizi, M., Parfitt, G. M., Kolisnyk, B., Law, C. S. H., Guzmán, M. S., Barros, D. M., Leung, L.-W. S., Prado, M. A. M., & Prado, V. F. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv349 · Cited by 46

Differential effects of 192IgG-saporin and NMDA-induced lesions into the basal forebrain on cholinergic activity and taste aversion memory formation

Gutiérrez, H., Gutiérrez, R., Silva-Gandarias, R., Estrada, J., Miranda, M. I., & Bermúdez‐Rattoni, F. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01519-x · Cited by 44

Selective lesion of the cholinergic basal forebrain causes a loss of cortical neuropeptide Y and somatostatin neurons

Zhang, Z.-J., Lappi, D. A., Wrenn, C. C., Milner, T. A., & Wiley, R. G. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00484-3 · Cited by 44

Brain-derived neurotrophic factor/neurotrophin-4 receptor TrkB is localized on ganglion cells and dopaminergic amacrine cells in the vertebrate retina

Cellerino, A., & Köhler, K. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970915)386:1 · Cited by 149

Modulation of cholinergic functions by serotonin and possible implications in memory: General data and focus on 5-HT1A receptors of the medial septum

Jeltsch‐David, H., Koenig, J., & Cassel, J. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.02.037 · Cited by 43

Age-related changes in rostral basal forebrain cholinergic and GABAergic projection neurons: relationship with spatial impairment

Bañuelos, C., LaSarge, C. L., McQuail, J. A., Hartman, J. J., Gilbert, R. J., Ormerod, B. K., & Bizon, J. L. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2012.06.013 · Cited by 48

Selective lesions of the nucleus basalis magnocellularis impair cognitive flexibility.

Cabrera, S. M., Chavez, C. M., Corley, S. R., Kitto, M. R., & Butt, A. E. (2006) · Behavioral Neuroscience · doi:10.1037/0735-7044.120.2.298 · Cited by 42

Medial septum lesions disrupt exploratory trip organization: Evidence for septohippocampal involvement in dead reckoning

Martin, M. M., Horn, K. L., Kusman, K. J., & Wallace, D. G. (2006) · Physiology & Behavior · doi:10.1016/j.physbeh.2006.10.007 · Cited by 41

Cholinergic Signaling Dynamics and Cognitive Control of Attention

Parikh, V., & Bangasser, D. A. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_133 · Cited by 43

Selective immunolesions of CH4 cholinergic neurons do not disrupt spatial memory in rats

Galani, R., Lehmann, O., Bolmont, T., Aloy, E. M., Bertrand, F., Lazarus, C., Jeltsch‐David, H., & Cassel, J. (2002) · Physiology & Behavior · doi:10.1016/s0031-9384(02)00674-1 · Cited by 41

Septal Lesions Impair the Acquisition of a Cued Place Navigation Task: Attentional or Memory Deficit?

Brandner, C., & Schenk, F. (1998) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1997.3814 · Cited by 41

The role of the septo-hippocampal cholinergic projection in T-maze rewarded alternation

Kirby, B. P., & Rawlins, J. N. P. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(03)00005-6 · Cited by 40

Crossed unilateral lesions of the medial forebrain bundle and either inferior temporal or frontal cortex impair object–reward association learning in Rhesus monkeys

Easton, A., & Gaffan, D. (2001) · Neuropsychologia · doi:10.1016/s0028-3932(00)00098-1 · Cited by 40

Insights Into the Role of the Cholinergic Component of the Septohippocampal Pathway: What Have We Learned from Experimental Lesion Studies?

Hörtnagl, H., & Hellweg, R. (1997) · Brain Research Bulletin · doi:10.1016/s0361-9230(97)00005-1 · Cited by 40

Extensive Lesions of Cholinergic Basal Forebrain Neurons Do Not Impair Spatial Working Memory

Vuckovich, J. A., Semel, M. E., & Baxter, M. G. (2004) · Learning & Memory · doi:10.1101/lm.63504 · Cited by 39

Water maze versus radial maze: differential performance of rats in a spatial delayed match-to-position task and response to scopolamine

Ormerod, B. K., & Beninger, R. J. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00316-3 · Cited by 39

Cholinergic Neurons and Networks Revisited

Butcher, L. L., & Woolf, N. J. (2004) · Elsevier eBooks · doi:10.1016/b978-012547638-6/50036-5 · Cited by 41

Environmental enrichment mitigates the effects of basal forebrain lesions on cognitive flexibility

Bartolo, P. D., Leggio, M. G., Mandolesi, L., Foti, F., Gelfo, F., Ferlazzo, F., & Petrosini, L. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.03.069 · Cited by 37

Intraseptal infusion of the cholinergic agonist carbachol impairs delayed‐non‐match‐to‐sample radial arm maze performance in the rat

Bunce, J. G., Sabolek, H. R., & Chrobak, J. J. (2004) · Hippocampus · doi:10.1002/hipo.10200 · Cited by 38

Decreased glucocorticoid receptor mRNA and dysfunction of HPA axis in rats after removal of the cholinergic innervation to hippocampus.

Han, J., Bizon, J. L., Chun, H., Maus, C. E., & Gallagher, M. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02191.x · Cited by 37

Cholinergic receptor blockade in prefrontal cortex and lesions of the nucleus basalis: implications for allocentric and egocentric spatial memory in rats

Nieto-Escámez, F. A., Sánchez-Santed, F., & de Bruin, J. P. C. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00458-2 · Cited by 37

Cholinergic lesions produce task-selective effects on delayed matching to position and configural association learning related to response pattern and strategy

Gibbs, R. B., & Johnson, D. A. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.03.007 · Cited by 36

Effects of hippocampal cholinergic deafferentation on learning strategy selection in a visible platform version of the water maze

Bizon, J. L., Han, J., Hudon, C., & Gallagher, M. (2003) · Hippocampus · doi:10.1002/hipo.10113 · Cited by 38

Cholinergic immunolesions by 192IgG‐saporin—a useful tool to simulate pathogenic aspects of alzheimer's disease

Roßner, S. (1997) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(97)00035-x · Cited by 36

Selective Lesioning of the Cholinergic Septo-Hippocampal Pathway Does Not Disrupt Spatial Short-Term Memory: A Comparison With the Effects of Fimbria-Fornix Lesions.

Winters, B. D., & Dunnett, S. B. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.3.546 · Cited by 37

Central cholinergic depletion induced by 192 IgG-Saporin alleviates the sedative effects of propofol in rats

Pain, L., Jeltsch‐David, H., Lehmann, O., Lazarus, C., Laalou, F.-Z., & Cassel, J. (2000) · British Journal of Anaesthesia · doi:10.1093/bja/85.6.869 · Cited by 34

Inhibitory effect of Thymus vulgaris extract on memory impairment induced by scopolamine in rat

Rabiei, Z., Mokhtari, S., Asgharzade, S., Gholami-Arjenaki, M., Rahnama, S., & Rafieian‐Kopaei, M. (2015) · Asian Pacific Journal of Tropical Biomedicine · doi:10.1016/j.apjtb.2015.07.006 · Cited by 34

A Comparison of Dopaminergic and Cholinergic Populations Reveals Unique Contributions of VTA Dopamine Neurons to Short-Term Memory

Choi, J. Y., Jang, H. J., Ornelas, S., Fleming, W., Fürth, D., Au, J., Bandi, A., Engel, E. A., & Witten, I. B. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108492 · Cited by 29

Effects of cholinergic lesions produced by infusions of 192 IgG-saporin on glucocorticoid receptor mRNA expression in hippocampus and medial prefrontal cortex of the rat

Helm, K., Han, J., & Gallagher, M. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00487-6 · Cited by 32

Cell Assemblies of the Basal Forebrain

Tingley, D., Alexander, A. S., Quinn, L. K., Chiba, A. A., & Nitz, D. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4432-14.2015 · Cited by 34

Basal forebrain neurons suppress amygdala kindling via cortical but not hippocampal cholinergic projections in rats

Ferencz, I., Leanza, G., Nanobashvili, A., Kokaia, M., & Lindvall, O. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00077.x · Cited by 31

Comparison of perirhinal cortex ablation and crossed unilateral lesions of the medial forebrain bundle from the inferior temporal cortex in the rhesus monkey: Effects on learning and retrieval.

Easton, A., & Gaffan, D. (2000) · Behavioral Neuroscience · doi:10.1037/0735-7044.114.6.1041 · Cited by 31

Task-phase-specific dynamics of basal forebrain neuronal ensembles

Tingley, D., Alexander, A. S., Kolbu, S., de Sa, V. R., Chiba, A. A., & Nitz, D. A. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00174 · Cited by 32

Transverse Patterning Reveals a Dissociation of Simple and Configural Association Learning Abilities in Rats with 192 IgG-Saporin Lesions of the Nucleus Basalis Magnocellularis

Butt, A. E., & Bowman, T. D. (2002) · Neurobiology of Learning and Memory · doi:10.1006/nlme.2001.4013 · Cited by 30

Anticholinergic effects in frogs in a Morris water maze analog

Bilbo, S. D., Day, L. B., & Wilczynski, W. (2000) · Physiology & Behavior · doi:10.1016/s0031-9384(99)00251-6 · Cited by 29

Emergence of spatial impairment in rats following specific cholinergic depletion of the medial septum combined with chronic stress

Craig, L. A., Hong, N. S., Kopp, J., & McDonald, R. J. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06179.x · Cited by 29

Memory enhancing activity of Lawsonia inermis Linn. leaves against scopolamine induced memory impairment in Swiss albino mice

Rajesh, V., Riju, T., Sellamuthu, V., & Babu, G. (2017) · Oriental Pharmacy and Experimental Medicine · doi:10.1007/s13596-017-0268-8 · Cited by 28

Scopolamine Induces Deficits in Spontaneous Object-Location Recognition and Fear-Learning in Marmoset Monkeys

Melamed, J., de Jesus, F. M., Maior, R. S., & Barros, M. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00395 · Cited by 25

The forebrain medial septal region and nociception

Ang, S. T., Ariffin, M. Z., & Khanna, S. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.07.017 · Cited by 31

Environment‐spatial conditional learning in rats with selective lesions of medial septal cholinergic neurons

Janisiewicz, A. M., Jackson, O., Firoz, E. F., & Baxter, M. G. (2004) · Hippocampus · doi:10.1002/hipo.10175 · Cited by 28

192 IgG-saporin lesions to the nucleus basalis magnocellularis (nBM) disrupt acquisition of learning set formation

Bailey, A. M., Rudisill, M. L., Hoof, E. J., & Loving, M. L. (2003) · Brain Research · doi:10.1016/s0006-8993(03)02294-7 · Cited by 26

Single-cell RT-PCR detects shifts in mRNA expression profiles of basal forebrain neurons during aging

Han, S., McCool, B. A., Murchison, D. A., et al. (2002) · Molecular Brain Research · doi:10.1016/s0169-328x(01)00322-9 · Cited by 27

Animal models of memory impairment

The American Association for Research into Nervous and Mental Diseases, & Gallagher, M. (1997) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1997.0153 · Cited by 27

Simple and configural association learning in rats with bilateral quisqualic acid lesions of the nucleus basalis magnocellularis

Butt, A. E., & Hodge, G. K. (1997) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)00062-4 · Cited by 25

Cholinergic depletion of the medial septum followed by phase shifting does not impair memory or rest–activity rhythms measured under standard light/dark conditions in rats

Craig, L. A., Hong, N. S., Kopp, J., & McDonald, R. J. (2008) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2008.10.013 · Cited by 27

SK-PC-B70M from Pulsatilla koreana improves scopolamine-induced impairments of memory consolidation and spatial working memory

Han, C.-K., Park, Y. H., Jin, D., Hwang, Y. K., Oh, K.-B., & Han, J. (2007) · Brain Research · doi:10.1016/j.brainres.2007.09.084 · Cited by 25

Differential changes in rat cholinergic parameters subsequent to immunotoxic lesion of the basal forebrain nuclei

Waite, J. J., & Chen, A. D. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02968-7 · Cited by 25

Dexibuprofen (S(+)-isomer ibuprofen) reduces microglial activation and impairments of spatial working memory induced by chronic lipopolysaccharide infusion

Jin, D., Sung, J., Hwang, Y. K., Kwon, K. J., Han, S., Min, S. S., & Han, J. (2008) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2008.01.016 · Cited by 25

Habituation to stress and dexamethasone suppression in rats with selective basal forebrain cholinergic lesions

Helm, K. A., Ziegler, D. R., & Gallagher, M. (2004) · Hippocampus · doi:10.1002/hipo.10203 · Cited by 24

Isolation and cultivation of mesenchymal stem cells from iliac crest bone marrow for further cartilage defect management.

Lubis, A. M. T., Sandhow, L., Lubis, V. K., Noor, A., Gumay, F., Merlina, M., Yang, W., Kusnadi, Y., Lorensia, V., Sandra, F., et al. (2011) · PubMed · Cited by 25

Memory Changes during Normal Aging

Barnes, C. A. (1998) · Elsevier eBooks · doi:10.1016/b978-012475655-7/50008-3 · Cited by 26

Evaluation of Muscarinic M2 Receptor Sites in Basal Forebrain and Brainstem Cholinergic Systems of Behaviorally Characterized Young and Aged Long-Evans Rats

Gill, T. M., & Gallagher, M. (1998) · Neurobiology of Aging · doi:10.1016/s0197-4580(98)00048-7 · Cited by 24

Basal Forebrain Mediates Motivational Recruitment of Attention by Reward-Associated Cues

Tashakori-Sabzevar, F., & Ward, R. D. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00786 · Cited by 23

Selective Cholinergic Depletion in Medial Septum Leads to Impaired Long Term Potentiation and Glutamatergic Synaptic Currents in the Hippocampus

Kanju, P. M., Parameshwaran, K., Sims‐Robinson, C., Uthayathas, S., Josephson, E. M., Rajakumar, N., Dhanasekaran, M., & Suppiramaniam, V. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031073 · Cited by 28

Intraseptal infusion of oxotremorine impairs memory in a delayed-non-match-to-sample radial maze task

Bunce, J. G., Sabolek, H. R., & Chrobak, J. J. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00462-7 · Cited by 23

Ibotenic acid lesions of the medial septum retard delay eyeblink conditioning in rabbits (Oryctolagus cuniculus).

Allen, M. T., Padilla, Y., & Gluck, M. A. (2002) · Behavioral Neuroscience · doi:10.1037/0735-7044.116.4.733 · Cited by 22

Potential roles of cholinergic modulation in the neural coding of location and movement speed

Dannenberg, H., Hinman, J. R., & Hasselmo, M. E. (2016) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2016.09.002 · Cited by 22

Selective lesion of medial septal cholinergic neurons followed by a mini-stroke impairs spatial learning in rats

Craig, L. A., Hong, N. S., Kopp, J., & McDonald, R. J. (2008) · Experimental Brain Research · doi:10.1007/s00221-008-1592-5 · Cited by 21

Muscarinic receptor-mediated activation of nitric oxide synthase

Wotta, D. R., & El‐Fakahany, E. E. (1997) · Drug Development Research · doi:10.1002/(sici)1098-2299(199702)40:2 · Cited by 10

N-methyl-d-aspartate receptors in the medial septal area have a role in spatial and emotional learning in the rat

Elvander-Tottie, E., Eriksson, T., Sandin, J., & Ögren, S. O. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.07.043 · Cited by 22

Impaired object-location learning and recognition memory but enhanced sustained attention in M2 muscarinic receptor-deficient mice

Romberg, C., Bartko, S. J., Wess, J., Saksida, L. M., & Bussey, T. J. (2018) · Psychopharmacology · doi:10.1007/s00213-018-5065-7 · Cited by 20

Role of central cholinergic receptor sub-types in spatial working memory: a five-arm maze task in mice provides evidence for a functional role of nicotinic receptors in mediating trace access processes

Maviel, T., & Durkin, T. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00403-2 · Cited by 20

Place cells of aged rats in two visually identical compartments

Wilson, I. A., Ikonen, S., Gurevicius, K., McMahan, R. W., Gallagher, M., Eichenbaum, H., & Tanila, H. (2004) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2004.09.006 · Cited by 20

Visuospatial Abilities

Lalonde, R. (1997) · International review of neurobiology · doi:10.1016/s0074-7742(08)60352-9 · Cited by 20

Efficacy of a murine-p75-saporin immunotoxin for selective lesions of basal forebrain cholinergic neurons in mice

Nag, N., Baxter, M. G., & Berger-Sweeney, J. E. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.01.006 · Cited by 19

Characterization of age-related changes in synaptic transmission onto F344 rat basal forebrain cholinergic neurons using a reduced synaptic preparation

Griffith, W. H., DuBois, D. W., Fincher, A. S., Peebles, K. A., Bizon, J. L., & Murchison, D. A. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00129.2013 · Cited by 19

Transfer Effects and Conditional Learning in Rats With Selective Lesions of Medial Septal/Diagonal Band Cholinergic Neurons.

Janisewicz, A. M., & Baxter, M. G. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.6.1342 · Cited by 19

Enhanced learning by posttrial injection of H1-but not H2-histaminergic antagonists into the nucleus basalis magnocellularis region.

Privou, C., Li, J.-S., Hasenöhrl, R., & Huston, J. (1999) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1998.3885 · Cited by 19

The recombinant C-terminal fragment of tetanus toxin protects against cholinotoxicity by intraseptal injection of β-amyloid peptide (25–35) in rats

Patricio-Martínez, A., Mendieta, L., Martínez, I., Aguilera, J., & Limón, I. D. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.11.066 · Cited by 18

Effect of Placenta-Derived Mesenchymal Stem Cells in a Dementia Rat Model via Microglial Mediation: a Comparison between Stem Cell Transplant Methods

Cho, J. S., Lee, J., Jeong, D. U., Kim, H. W., Chang, W. S., Moon, J., & Chang, J. W. (2018) · Yonsei Medical Journal · doi:10.3349/ymj.2018.59.3.406 · Cited by 18

Vestibular stimulation enhances hippocampal long-term potentiation via activation of cholinergic septohippocampal cells

Tai, S. K., & Leung, L.-W. S. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.04.013 · Cited by 18

Hippocampal N-methyl-d-aspartate and kainate binding in response to entorhinal cortex aspiration or 192 IgG-saporin lesions of the basal forebrain

Nicolle, M. M., Shivers, A., Gill, T. M., et al. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00519-2 · Cited by 18

Lesions of the rat nucleus basalis magnocellularis disrupt appetitive-to-aversive transfer learning

Butt, A. E., Schultz, J. A., Arnold, L. L., Garman, E., George, C. L., & Garraghty, P. E. (2003) · Integrative Psychological and Behavioral Science · doi:10.1007/bf02688857 · Cited by 18

Impairments in negative patterning, but not simple discrimination learning, in rats with 192 IgG-saporin lesions of the nucleus basalis magnocellularis.

Butt, A. E., Noble, M. M., Rogers, J. L., et al. (2002) · Behavioral Neuroscience · doi:10.1037/0735-7044.116.2.241 · Cited by 18

Saporin as a Commercial Reagent: Its Uses and Unexpected Impacts in the Biological Sciences—Tools from the Plant Kingdom

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Editorial

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