Agmatine may act as a neurotransmitter or neuromodulator. Behaviorally, agmatine exerts antidepressant-like effects. The enzyme agmatinase degrades and thereby inactivates agmatine. The gene coding for human agmatinase is located on chromosome 1p36, a gene locus which has been linked to bipolar disorder and major depression. However, the enzyme has not yet been studied in detail in the context of neuropsychiatric diseases. We analyzed agmatinase protein expression in postmortem hippocampi of individuals with affective disorders. Agmatinase protein was detected in a subset of interneurons in the hippocampus and other brain regions. In depressive patients the number and the numerical density of agmatinase-immunopositive cell bodies was strongly elevated in all regions under study (i.e. hippocampus, habenula, insular cortex and temporal cortex). Agmatine is naturally produced by the breakdown of arginine. The cellular uptake of L-arginine and other cationic amino acids (such as L-lysine and L-ornithine) is mainly mediated by cationic amino acid transporter (CAT) proteins. In patients with mood disorder there was a circumscribed decrease in the numerical density of hCAT1 immunoreactive neurons in the CA2 region of the hippocampus.

The glutamate hypothesis of schizophrenia based on the observations that administration of drugs that block N-methyl-D-aspartate (NMDA) glutamate receptors could induce schizophrenia-like symptoms. There are several evidences linking abnormal glutamatergic transmission to cognitive, negative, and positive symptoms of schizophrenia and the glutamatergic system is now a major focus for the development of new compounds in schizophrenia. The polyamines are omnipresent aliphatic molecules comprising putrescine, spermidine, spermine and agmatine. The polyamines and their biosynthetic enzymes are found throughout the body, including the central nervous system (CNS), where they display specific regional distributions in the CNS. The polyamines have an important role in the modulation of cell growth and on cell membrane functions. It was hypothesized that schizophrenia may be related to a general abnormality in neuronal membranes. Agmatine, a polyamine, selectively blocks the NMDA subclass of glutamate receptors in rat hippocampal neurons. There are also several evidences indicate that a relationship between polyamines and etiopathogenesis of schizophrenia. In this review, a new approach for understanding schizophrenia via NMDA receptors and their interaction with agmatine which is a biological active polyamine transmitter in brain is proposed.

Polyamines, including spermidine, spermine, and agmatine, serve several brain-specific functions. Polyamine transport mechanisms may account for the redistribution of these organic cations, which may also be synaptically released as neuromodulators or neurotransmitters, in the brain. Therefore, the localization of polyamine pathway enzymes, in addition to the localization and functional investigation of the polyamines itself, provides valuable insights regarding the identification of cell- and region-specific roles for polyamines, notably in the context of mental disorders and neurodegenerative diseases. Identified neuronal circuits are subject to physiological and pharmacological investigations. With this respect, we electrophysiologically studied the cerebellar cortex and the medial habenula, showing a prominent synaptic expression of spermidine synthase and agmatinase, respectively. In both areas, the relevant polyamines clearly influence the electrical activity. The medial habenula may be involved with the aetiology of major depressive disorder. In this context, the expression of agmatinase in other brain areas, e.g. the paraventricular thalamic nucleus, possibly also involved with depression, is discussed.

Blood injury injection phobia (BII) involves an intense fear of situations, in which an individual is directly or indirectly exposed to blood, injections or viewing injuries, along with a tendency to avoid these situations. BII phobia is highly prevalent in females as compared to males. It is virtually the only specific phobia and the only anxiety disorder, in which fainting occurs. Although fainting is much distressed to the BII phobic individuals, but it may have developed in the humans at the time when they needed it much as a survival mechanism. In this article we discuss how in the humans there may have developed the trait of BII phobia in the ancestors, including the variation in the symptoms among sexes. There are not studies which specifically examine the syncope related brain differences among genders. But there are other well defined studies which highlight marked differences among male and female brains. Considering this we also review some recent breakthrough discoveries showing differences in the brain of males and females at gene expression level which leads to the variation in brain and behaviour related problems among genders. There is an exigent need to understand the brain behavioral problems through multiple perspectives.

Rabies is a tropical zoonotic disease, transmitted to human being by carnivorous animals. Majority of human rabies cases were reported from Asia and African countries. India recorded more deaths from rabies than any other country in the world. There is no effective treatment for rabies; it can only be prevented by vaccination. It needs multiple levels of interventions at human and animal level. World Health Organization’s target is to eliminate the disease by 2020 in endemic South-East Asian countries which include India. Key challenges in control of rabies in India are lack of intersectoral coordination, weak surveillance system on rabies, inadequate rabies research and lack of sustainability. To conclude, breaking the rabies cycle in a sustained manner is necessary to eliminate rabies from this part of the world.

Autism is a childhood neurodevelopmental disorder that affects 1–2 in 100 children, according to recent data on the broad array of autism spectrum disorders. It is a neurodevelopmental disorder, genetic and environmental factors playing role in autism. Molecular and mechanistic basis of autism started to be enlightened. As a genetic basis of disease, glutamate gene mechanisms supposed to develop a new method for diagnosing and treatment of autism. Aim of this mini-review is to gain a general knowledge about genetic and environmental reasons of autism.

The future of neuroscience needs an innovative outlook on the study of brain by scientists coming from various disciplines and traditions. The field of Mind, Brain, and Education (MBE) is a meeting point for researchers and scientists in psychology, biology, and education. Unlike the one-way information sharing from psychology to education as in educational psychology or from neuroscience to education as in educational neuroscience, MBE is credited with its two-way flow of information between the three fields. The transdisciplinary initiatives between neuroscience, psychology, and education, as in the case of MBE, offer an increased optimism not only for the treatment of biological and neurological diseases but also for the realization of optimal outcomes in effective learning and positive development.

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