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Control of sleep and wakefulness.
Brown RE, Basheer R, McKenna JT, Strecker RE, McCarley RW (2012) Control of sleep and wakefulness. Physiol Rev 92(3):1087-1187 . doi: 10.1152/physrev.00032.2011
Summary: This review summarizes mechanisms in the brain that control sleep and wakefulness. Areas discussed include wakefulness promoting systems, non-REM sleep and REM sleep definitions, the function of each kind of sleep, and dysfunction that occurs as a result of sleep disruption. Several targeted conjugates are mentioned, such as 192-IgG-SAP (Cat. #IT-01), anti-DBH-SAP (Cat. #IT-03), and orexin-SAP (Cat. #IT-20). The review summarizes the use of these products to better understand sleep networks.
Related Products: 192-IgG-SAP (Cat. #IT-01), Anti-DBH-SAP (Cat. #IT-03), Orexin-B-SAP (Cat. #IT-20)
Vestibular stimulation enhances hippocampal long-term potentiation via activation of cholinergic septohippocampal cells.
Tai SK, Leung LS (2012) Vestibular stimulation enhances hippocampal long-term potentiation via activation of cholinergic septohippocampal cells. Behav Brain Res 232(1):174-182. doi: 10.1016/j.bbr.2012.04.013
Summary: It is known that vestibular stimulation induces acetylcholine release in the hippocampus. The authors hypothesized that this stimulation enhances long-term potentiation (LTP) in CA1 and depends on the activation of septohippocampal cholinergic neurons. Rats received 105-ng bilateral infusions of 192-IgG-SAP (Cat. #IT-01) into the medial septum. The data suggest that LTP enhancement during vestibular stimulation is mediated by cholinergic septohippocampal cells.
Related Products: 192-IgG-SAP (Cat. #IT-01)
Neonatal cholinergic lesion alters the acoustic structure of infant rat vocalization but not the early cognitive development.
Kruger HS, Hanganu-Opatz IL (2013) Neonatal cholinergic lesion alters the acoustic structure of infant rat vocalization but not the early cognitive development. Dev Psychobiol 55(3):294-308. doi: 10.1002/dev.21029
Summary: The architecture of the cerebral cortex is dependent on cholinergic innervations for proper maturation and network assembly. The authors administered 0.1 μg of 192-IgG-SAP (Cat. #IT-01) to each lateral ventricle of rats on the day of birth. Although the resulting cholinergic depletion did not affect the general development of the rats during the first two weeks of life, infant ultrasonic vocalization was significantly affected. The altered vocalization did not affect maternal care of the pup, suggesting that previous results recording behavioral deficits in the pups after basal forebrain lesions were due to cholinergic depletion rather than altered mother-pup interaction.
Related Products: 192-IgG-SAP (Cat. #IT-01)
Selective cholinergic depletion in medial septum leads to impaired long term potentiation and glutamatergic synaptic currents in the hippocampus.
Kanju PM, Parameshwaran K, Sims-Robinson C, Uthayathas S, Josephson EM, Rajakumar N, Dhanasekaran M, Suppiramaniam V (2012) Selective cholinergic depletion in medial septum leads to impaired long term potentiation and glutamatergic synaptic currents in the hippocampus. PLoS One 7(2):e31073. doi: 10.1371/journal.pone.0031073
Summary: Long term potentiation (LTP) is dependent on excitatory neurotransmission in the hippocampus, which plays a major role in learning and memory. The authors examine whether cholinergic lesions in the medial septum result in LTP alteration or affect synaptic glutamate receptor subtypes. After bilateral administration of 192-IgG-SAP (Cat. #IT-01, 50 ng per injection) into the medial septum of rats, hippocampal slices were made and the LTP of the slices was measured. The data show modulation of medial septal LTP and hippocampal glutaminergic currents by cholinergic afferents.
Related Products: 192-IgG-SAP (Cat. #IT-01)
Recognition of novel objects and their location in rats with selective cholinergic lesion of the medial septum.
Cai L, Gibbs RB, Johnson DA (2012) Recognition of novel objects and their location in rats with selective cholinergic lesion of the medial septum. Neurosci Lett 506(2):261-265. doi: 10.1016/j.neulet.2011.11.019
Summary: This work examined object recognition and object location recognition as specific components of memory. Rats received 0.22 μg of 192-IgG-SAP (Cat. #IT-01) infused into the medial septum followed by testing in novel object recognition (NOR) and object location recognition (OLR) models. Substantial decreases in choline acetyltransferase activity in the hippocampus and frontal cortex produced no difference in NOR but caused a significant impairment in OLR – highlighting the role that septo-hippocampal cholinergic projections play in OLR.
Related Products: 192-IgG-SAP (Cat. #IT-01), Mouse IgG-SAP (Cat. #IT-18)
Subplate neurons promote spindle bursts and thalamocortical patterning in the neonatal rat somatosensory cortex.
Tolner EA, Sheikh A, Yukin AY, Kaila K, Kanold PO (2012) Subplate neurons promote spindle bursts and thalamocortical patterning in the neonatal rat somatosensory cortex. J Neurosci 32(2):692-702. doi: 10.1523/JNEUROSCI.1538-11.2012
Summary: Immature cortices in both human and rat have spontaneous activity associated with the maturation of cortical synapses and neuronal circuits. In order to investigate what cells are controlling these events the authors administered 400 ng of 192-IgG-SAP (Cat. #IT-01) to the S1 cortex hindlimb/forelimb area of rats. mu p75-SAP (Cat. #IT-16) and mouse-IgG-SAP (Cat. #IT-18) were used as controls. This lesion eliminates subplate neurons which results in a significant loss of evoked spindle burst activity.
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Featured Article: Motivation’s modulation of attention through the mesolimbic-corticopetal cholinergic circuitry
St Peters M, Sarter M (2012) Featured Article: Motivation’s modulation of attention through the mesolimbic-corticopetal cholinergic circuitry. Targeting Trends 13(1)
Related Products: 192-IgG-SAP (Cat. #IT-01), Mouse IgG-SAP (Cat. #IT-18)
Read the featured article in Targeting Trends.
See Also:
Cholinergic control in developing prefrontal-hippocampal networks.
Janiesch PC, Kruger HS, Poschel B, Hanganu-Opatz IL (2011) Cholinergic control in developing prefrontal-hippocampal networks. J Neurosci 31(49):17955-17970. doi: 10.1523/JNEUROSCI.2644-11.2011
Summary: In this work the authors examined the role of acetylcholine in the maturation of cognitive processing due to oscillatory rhythms entraining neuronal networks. Rats received 50 ng of 192-IgG-SAP (Cat. #IT-01) into each lateral ventricle, or 25 ng directly into the medial septum. Among other results, cholinergic input was shown to reach the prefrontal cortex toward the end of the first postnatal week, initially targeting GABAergic neurons. Reduction of this activity by lesioning cholinergic neurons may cause global diminishment of neocortical activity.
Related Products: 192-IgG-SAP (Cat. #IT-01), Mouse IgG-SAP (Cat. #IT-18)
Impaired visual search in rats reveals cholinergic contributions to feature binding in visuospatial attention.
Botly LC, De Rosa E (2012) Impaired visual search in rats reveals cholinergic contributions to feature binding in visuospatial attention. Cereb Cortex 22(10):2441-2453. doi: 10.1093/cercor/bhr331
Summary: Previous work established the role of acetylcholine from the nucleus basalis magnocellularis in attentional processing and visuospatial attention. In order to investigate the necessity of cortical cholinergic input for support of feature binding in visuospatial attention the authors administered bilateral intraparenchymal injections of 192-IgG-SAP (Cat. #IT-01, 4 injections, 40 ng per injection). Lesioned animals took longer to locate targets during type-specific search trials, demonstrating that cholinergic input influences feature binding during visuospatial attention tasks.
Related Products: 192-IgG-SAP (Cat. #IT-01), Mouse IgG-SAP (Cat. #IT-18)
The effects of basal forebrain cholinergic neuron on novel object recognition
Lee J, Jeong D, Chang J (2011) The effects of basal forebrain cholinergic neuron on novel object recognition. Neuroscience 2011 Abstracts 878.10. Society for Neuroscience, Washington, DC.
Summary: Medial septum and basal nucleus areas of the basal forebrain project cholinergic neurons to the frontal cortex and the Hippocampus.And degeneration of the cholinergic basal forebrain neurons is a common feature of Alzheimer’s disease (AD) has been correlated with cognitive decline. This research was studied to verify the effects of cholinergic neuron in basal forebrain to the role of the hippocampus and the frontal cortex on recognition through recognition test and immunohistochemistry after damaging cholinergic neuron of the basal forebrain by intraventricular injection of 192 IgG-saporin. 192 IgG-saporin of 8ul (0.63ug/ul) was injected to the bilateral lateral ventricle of rats. After 2 weeks, novel object recognition (NOR) test was conducted to elucidate damage of cholinergic neuron. In the NOR test, rats are exposed to two identical objects for 15 minutes in empty plastic box (60cmx60cmx30cm). After 3 hours, they are reintroduced to the same object and a new novel object for 10 minutes. This procedure was repeated for 4 days After completing the behavioral experiment, the ChAT of cholinergic neuron in the basal forebrain was ascertained to confirm with immunohistochemistry if cholinergic neuron was damaged. In NOR test, the lesion group with 192 IgG-saporin showed 10% lower novel object preference than normal group. However, this rate is not that significant value enough to elucidate behavioral difference between normal group and lesion group. In immunohistochemistry, the number of cholinergic neuron was remarkably decreased in basal forebrain. According to both of the NOR test and Immunohistochemistry in the condition under lesion, Cholingergic input to hippocampus and frontal cortex from basal forebrain affects recognition somewhat, however the effect is not so essential.
Related Products: 192-IgG-SAP (Cat. #IT-01)