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c-Maf is required for the development of dorsal horn laminae III/IV neurons and mechanoreceptive DRG axon projections.
Hu J, Huang T, Li T, Guo Z, Cheng L (2012) c-Maf is required for the development of dorsal horn laminae III/IV neurons and mechanoreceptive DRG axon projections. J Neurosci 32(16):5362-5373. doi: 10.1523/JNEUROSCI.6239-11.2012 PMID: 22514301
Summary: The molecular mechanisms responsible for development of laminae III/IV neurons are not yet well understood. In this work the authors investigated the role of c-Maf, a basic leucine-zipper transcription factor from the AP-1 superfamily. Anti-TrkA (Cat. #AB-N03: 1:100) was used for immunohistochemistry.
Related Products: trkA Rabbit Polyclonal (Cat. #AB-N03)
Arcuate kisspeptin/neurokinin b/dynorphin (KNDy) neurons mediate the estrogen suppression of gonadotropin secretion and body weight.
Mittelman-Smith MA, Williams H, Krajewski-Hall SJ, Lai J, Ciofi P, McMullen NT, Rance NE ( 2012 ) Arcuate kisspeptin/neurokinin b/dynorphin (KNDy) neurons mediate the estrogen suppression of gonadotropin secretion and body weight. Endocrinology 153(6):2800-2812 . doi: 10.1210/en.2012-1045
Related Products: NKB-SAP (Cat. #IT-63), Blank-SAP (Cat. #IT-21)
Intrinsic voltage dynamics govern the diversity of spontaneous firing profiles in basal forebrain noncholinergic neurons.
Ovsepian SV, Dolly JO, Zaborszky L (2012) Intrinsic voltage dynamics govern the diversity of spontaneous firing profiles in basal forebrain noncholinergic neurons. J Neurophysiol 108(2):406-418. doi: 10.1152/jn.00642.2011 PMID: 22496531
Summary: The voltage modulation functions of the basal forebrain have commonly been associated with cholinergic cells. More recent work has suggested that noncholinergic cells have an influence on this type of neuronal activity. The authors labeled cholinergic neurons by injecting 0.8-1.6 μg of Cy3-192-IgG (Cat. #FL-01) into the lateral ventricles of rats. Patch-clamp recordings were taken from brain slices of these animals under various blockade conditions. The results demonstrate that neuropeptide Y receptors as well as ions such as Ca2+ and K+ are important for regenerative firing in basal forebrain cholinergic neurons.
Related Products: 192-IgG Mouse Monoclonal, Cy3-labeled (Cat. #AB-N43FL3)
Sudden death and myocardial lesions after damage to catecholamine neurons of the nucleus tractus solitarii in rat.
Talman WT, Dragon DN, Jones SY, Moore SA, Lin LH (2012) Sudden death and myocardial lesions after damage to catecholamine neurons of the nucleus tractus solitarii in rat. Cell Mol Neurobiol 32(7):1119-1126. doi: 10.1007/s10571-012-9835-1
Summary: Previous work has shown that elimination of neurons expressing the neurokinin-1 receptor (NK1r) from the nucleus tractus solitarii (NTS) causes various circulatory system dysfunctions, often leading to sudden death. The authors injected the brainstem of rats with 42 ng anti-DBH-SAP (Cat. #IT-03). to eliminate catecholaminergic neurons in the NTS that express tyrosine hydroxylase. This elimination had similar cardiac and cardiovascular effects to the elimination of NK1r-expressing neurons.
Related Products: Anti-DBH-SAP (Cat. #IT-03)
Featured Article: Use of a novel saporin conjugate (NK3-SAP) to study the function of neurokinin 3 receptor (NK3r)-expressing kisspeptin/neurokinin B/dynorphin (KNDy) neurons in the rat arcuate nucleus
Rance NE, Mittelman-Smith MA, Krajewski-Hall SJ (2012) Featured Article: Use of a novel saporin conjugate (NK3-SAP) to study the function of neurokinin 3 receptor (NK3r)-expressing kisspeptin/neurokinin B/dynorphin (KNDy) neurons in the rat arcuate nucleus. Targeting Trends 13(2)
Related Products: NKB-SAP (Cat. #IT-63), Blank-SAP (Cat. #IT-21)
Read the featured article in Targeting Trends.
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Analgesia targeting IB4-positive neurons in cancer-induced mechanical hypersensitivity.
Ye Y, Dang D, Viet CT, Dolan JC, Schmidt BL (2012) Analgesia targeting IB4-positive neurons in cancer-induced mechanical hypersensitivity. J Pain 13(6):524-531. doi: 10.1016/j.jpain.2012.01.006
Summary: DOR (δ opioid receptor) agonists produce minimal side effects and do not lead to tolerance, making them potential alternatives to the widely used μ opioid receptor agonists. Utilizing the fact that DOR’s are expressed by IB4-positive neurons, the authors injected the subarachnoid space between the L4 and L5 vertebrae of rats with 2.4 μg of IB4-SAP (Cat. #IT-10). 3 μg of saporin (Cat. #PR-01) was used as a control. The results indicate that pharmacological agents targeting IB4-positive neurons may have use in cancer pain treatment.
Related Products: IB4-SAP (Cat. #IT-10), Saporin (Cat. #PR-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)
TrkA gene ablation in basal forebrain results in dysfunction of the cholinergic circuitry.
Sanchez-Ortiz E, Yui D, Song D, Li Y, Rubenstein JL, Reichardt LF, Parada LF (2012) TrkA gene ablation in basal forebrain results in dysfunction of the cholinergic circuitry. J Neurosci 32(12):4065-4079. doi: 10.1523/JNEUROSCI.6314-11.2012 PMID: 22442072
Summary: The authors created a conditional trkA knockout mouse line. Anti-trkA (Cat. #AB-N03) was used for immunohistochemistry (1:1000) and western blots (1:4000). The data demonstrate the importance of trkA in the establishment of basal forebrain cholinergic circuitry, and choline acetyltransferase expression.
Related Products: trkA Rabbit Polyclonal (Cat. #AB-N03)
Collateral damage and compensatory changes after injection of a toxin targeting neurons with the neurokinin-1 receptor in the nucleus tractus solitarii of rat.
Lin LH, Nitschke Dragon D, Talman WT (2012) Collateral damage and compensatory changes after injection of a toxin targeting neurons with the neurokinin-1 receptor in the nucleus tractus solitarii of rat. J Chem Neuroanat 43(2):141-148. doi: 10.1016/j.jchemneu.2012.02.001
Summary: Loss of substance P receptor (SPR)-expressing neurons in the nucleus tractus solitarii (NTS) results in reduced baroreflex strength and unstable arterial pressure. The neuronal population expressing the SPR also expresses several other types of receptors – such as N-methyl-D-aspartate (NMDA), and aalpha-amino-3-hydroxy-5-methyl-4-isoxazoleproprionic (AMPA) receptors. The authors administered 9 ng of SSP-SAP (Cat. #IT-11) into the NTS and looked for differences in the expression of NMDA and AMPA receptors, as well as several different transporters and neuronal markers. he data suggest that the pathological effects of SSP-SAP lesions result from disruption of other neurotransmission systems than those using the SPR.
Related Products: SSP-SAP (Cat. #IT-11)
CXB-909 attenuates cognitive deficits in the mu-p-75 saporin mouse model of Alzheimer’s disease.
Lowrance S, Matchynski J, Rossignol J, Dekorver N, Sandstrom M, Dunbar G (2012) CXB-909 attenuates cognitive deficits in the mu-p-75 saporin mouse model of Alzheimer’s disease. Neuroscience & Medicine 3(1):65-68. doi: 10.4236/nm.2012.31010
Summary: CXB-909 is a small molecule NGF amplifier that has been shown to enhance neurite outgrowth in various neuronal cell lines. This type of molecule has potential therapeutic use in disorders such as Alzheimer’s disease. In this work the authors lesioned cholinergic cells in the basal forebrain of mice with bilateral 0.8 μg intracerebroventricular injections of mup75-SAP (Cat. #IT-16). Lesioned animals performed significantly worse than controls in a water maze task. Lesioned animals subsequently treated with CXB-909 displayed improved performance, indicating that CXB-909 can attenuate memory deficits caused by loss of cholinergic input.
Related Products: mu p75-SAP (Cat. #IT-16)
