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The medial diencephalon, in particular the mammillary bodies and anterior thalamic nuclei, has long been linked to memory and amnesia. The mammillary bodies provide a dense input into the anterior thalamic nuclei, via the mammillothalamic tract. In both animal models, and in patients, lesions of the mammillary bodies, mammillothalamic tract and anterior thalamic nuclei all produce severe impairments in temporal and contextual memory, yet it is uncertain why these regions are critical. Mounting evidence from electrophysiological and neural imaging studies suggests that mammillothalamic projections exercise considerable distal influence over thalamo-cortical and hippocampo-cortical interactions. Here, we outline how damage to the mammillary body-anterior thalamic axis, in both patients and animal models, disrupts behavioural performance on tasks that relate to contextual ("where") and temporal ("when") processing. Focusing on the medial mammillary nuclei as a possible 'theta-generator' (through their interconnections with the ventral tegmental nucleus of Gudden) we discuss how the mammillary body-anterior thalamic pathway may contribute to the mechanisms via which the hippocampus and neocortex encode representations of experience.
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http://dx.doi.org/10.1016/j.neubiorev.2020.11.031 | DOI Listing |
Introduction: Advances in neonatology, neonatal surgery, and extracorporeal membrane oxygenation (ECMO) have improved the prognosis of congenital diaphragmatic hernia (CDH). However, CDH survivors are at considerable risk of long-term neurological morbidity. Magnetic resonance imaging (MRI) abnormalities are reported in up to 84% of CDH-survivors but have only been rarely compared with neurodevelopmental outcomes.
View Article and Find Full Text PDFChildren (Basel)
July 2025
Medical Imaging Department, Perth Children's Hospital, Nedlands, Perth 6009, Australia.
Acute necrotising encephalopathy (ANE) is a rare and severe type of encephalopathy with bilateral symmetrical brain lesions, often following a viral prodrome. ANE type 1 (ANE1) is a disease subtype with a predisposing mutation in the gene encoding RAN binding protein 2 (). We report a case of a 3-year-old girl with clinical symptoms of ANE and brain MRI findings suggesting ANE1, which was subsequently confirmed by genetic analysis.
View Article and Find Full Text PDFJ Med Imaging Radiat Oncol
August 2025
Perth Children's Hospital, Nedlands, Western Australia, Australia.
Background: Hypothalamic hamartoma (HH) is a rare congenital malformation that can significantly disrupt patient quality of life and typically presents with either central precocious puberty or gelastic seizures.
Objective: We seek to add to the current literature through a retrospective review of all cases of HH seen at our paediatric tertiary centre over the previous two decades. We also sought to test the novel hypothesis that lesions located closer to or contacting the infundibulum were more likely to present with central precocious puberty (CPP).
Clin Neurol Neurosurg
October 2025
Department of Neurology, National Neuroscience Institute (Singapore General Hospital Campus), Singapore. Electronic address:
Immune checkpoint inhibitors have revolutionized the treatment of many cancers since their introduction in the early 2010s. Consequently, immune checkpoint inhibitor-induced encephalitis (ICI-iE) is increasingly reported in scientific literature, but its diagnosis can be challenging due to the non-specific clinico-radiological features. Herein, we report the case of an elderly man with metastatic renal cell carcinoma, who developed ICI-iE slightly over a year into his pembrolizumab treatment.
View Article and Find Full Text PDFJ Neurophysiol
September 2025
Department of Chemical Physiology and Biochemistry, Oregon Health and Science University, Portland, Oregon, United States.
There are over seven million people in the United States living with Alzheimer's disease (AD), and two-thirds of these patients are postmenopausal women. In addition to neurodegenerative changes within the cortex and hippocampus, there are pronounced pathological changes in the mammillary bodies (MBs), which are thought to play a role in the development of AD. Currently, we documented in 5XFAD female mice that there was an early onset of Aβ immunostaining extracellularly that coincided with increased staining of vesicular glutamate transporter2 (vGlut2) intracellularly in medial MB neurons.
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