The basic symptoms of major depressive disorder are depressed mood and loss of interest or pleasure [1] . However, the complex pathogenesis of this severe affective disorder is still not clear. Various factors such as biogenic amine deficiency, genetic, environmental, immunologic and endocrine factors, as well as neurogenesis have been considered as mechanisms that provide explanations for the pathophysiology of depression [2] [3] .

In 2010 I proposed the “syncytiopathy hypothesis of depression” [4] . It has been hypothesized “that disorders in the astrocytic syncytium (network) may represent a main component of the pathophysiology of depression, called syncytiopathy. If the expression of connexin proteins (building gap junctions in the astrocytic syncytium) is downregulated, a compensatory upregulation of astrocytic receptors may occur leading to an overproduction of these. Such an excess of astrocytic receptors exerts an imbalance of synaptic neurotransmission, because of a relative lack of neurotransmitters for the occupancy of astrocytic receptors so that neurotransmission is protracted. This delay of information processing may be responsible for the main symptoms of depression [4] .

Significantly, the biophysical interpretation of these imbalances of synaptic information processing [5] opens a new perspective of depressive behavior as follows: If the astrocytic receptors coding the expected sensations from the environment outnumber the number of neurotransmitters that code the environmental sensations, then the overexpression of astrocytic receptors connotes over expectation in the sense of unrealizable expectations. The unrealizability of expectations is caused by the prolonged processing of sensory information that frustrates the full comprehension of the expected event, since it cannot be grasped in time. Moreover, expectation frustration affects memory. This cyclic mechanism of imbalanced synaptic information processing may exert the self-frustration of expectation responsible for cognitive dysfunctions in major depressive disorder.

The study starts with a model of a balanced tripartite synapse and the astroglial syncytium. Then the operation loops between the memory-based model of reality and the expected external reality running in tripartite synapses and their networks are outlined. Next, from a formal description of the logic of balance between expectation variables and sensation values a system state of over-expectation is deduced. On this background the novel pathophysiological model of self-frustration of expectations in major depression is discussed.

A tripartite synapse is composed of the presynapse and the postsynapse as the neuronal components and the astrocyte with its network (syncytium) as the glial component [6] . Figure 1 outlines a model of a balanced tripartite synapse [7] [8] . Neurotransmitters (NT) occupy astrocytic receptors (acr) and postsynaptic receptors (por) released from the presynapse (double-headed arrows designate activation and reuptake). The activation of acr by NT activates calcium ions (Ca²⁺) that interact with the glial syncytium (depicted as lattice). Activated Ca²⁺

causes the production of gliotransmitters (GT) that occupy extrasynaptic receptors (esr) and in parallel exert a feedback to presynaptic receptors (psr). The balance of receptors and transmitter substances enables a normal synaptic information processing.

The biological structure suggested focuses on gap junctions between astrocytes, the main glial cell type together with oligodendrocytes and microglia. Gap junctions provide a structural link through which single cells are coupled to form a functional network, called syncytium, with communication dynamics that cannot be effected by individual cells. Gap junctions of an astroglial syncytium are composed of connexin proteins forming gap junction channels by various hemichannels [9] . While astrocytes are interconnected with their neighbors via gap junctions, the interactions of astrocytes with neurons occur mainly in tripartite synapses [6] .

Figure 2 shows a diagram of an astroglial syncytium. Six astrocytes (Ac₁, …, Ac₆) are completely interconnected via fifteen gap junctions (gj). Each astrocyte contacts neuronal synapses (not shown) forming tripartite synapses. The simple diagram refers to the basic components and their interconnections in the astroglial syncytium. Frequently activated gap junctions (downward arrows) generate a plaque. An example of a plaque formation is given between the Ac₃-Ac₄-Ac₅-Ac₃-loop. This loop becomes embodied in a gap junction plaque that consists of a hierarchical loop structure (cycles) [10] .

Based on my model of glial-neuronal interactions [7] [8] [10] [11] the role of gap junctions in memory formation can be interpreted in the following: gap junctions register already generated cyclic pathways in the astroglial syncytium. Depending on feedback from the neuronal network to the glial syncytium based on feasible expectations with regard to environmental information, gap junctions could strengthen their structure embodying a memory mechanism. In this case we have a double memory function of gap junctions: a local embodiment of memories and a pathway memory determined by gap junctions [10] . This double memory function of gap junction plaques may work as expectations expressed in the receptor pattern of astrocytes experienced in synaptic neuroglial interactions and realized in the neuronal networks via sensory-motor activation in the environment [5] [12] [13] .

If the amount of neurotransmitters exactly corresponds to the amount of expressed astrocytic receptors, a balance between the glial and neuronal network is generated and gliotransmitters released occupy presynaptic receptors that exert a feedback mechanism. The comparison between expected internal and measured external signals provides updated feedback to the glial syncytium that modifies the information flow through the neuronal network [5] .

The formalism of the logic of balance was introduced by the German-American philosopher Gotthard Guenther [14] . The proposition is that the operations of a living system are balanced if the number of variables (n) and the number of values (m) is equal. If the values outnumber the variables (m > n), then the system is overbalanced. Inversely, if the variables outnumber the values (n > m), then the system is underbalanced.

Figure 3 shows the formalism of balance between glial receptors (acr) as expectation variables (n) and neurotransmitters (NT) representing sensation values (m). The balanced system states are designated as pairs of equal numbers in squares (diagonal). The overbalanced states are listed below the diagonal, and the underbalanced states above. Here the expectation variables outnumber the sensation values representing a system state of over-expectation (embodied by overexpressed astrocytic receptors).

Figure 4 depicts a diagram of an incomplete astroglial syncytium that may cause memory impairment in depression. A complete astroglial syncytium is outlined (a). If the expression of connexins is downregulated (downward arrows), then the structure of the network is incomplete, since the number of gap junctions is reduced (dotted squares). Such a “leaky” network may be responsible for memory impairment in depression (b).

Of note, this was the first hypothesis that the downregulation of connexins in the astroglial syncytium is responsible for the pathophysiology, especially for memory impairment of major depressive disorder [4] [15] . Since then this hypothesis has been supported by various experimental investigations. Nagy and colleagues [16] found a widespread astrocytic connexin gene repression in depressed suicides, possibly mediated through epigenetic mechanisms. Similarly, aberrant expression of astrocytic connexins Cx30 and Cx43 in the medial prefrontal cortex and hippocampus significantly affects brain region-specific neuronal activity responsible for depressive-like behavior in mice [17] . Moreover, deletion of glial connexins and loss of gap junction communication result in a loss of short-term spatial memory [18] . Basically, disrupting astroglial coupling impairs spatial learning and memory [19] .

Figure 5 depicts the basic effects on synaptic information transmission if the expression of connexins in the astroglial syncytium is downregulated, and compensated by the upregulation of astrocytic receptors (acr) as follows: overexpressed

astrocytic receptors cannot be activated by neurotransmitters (NT) in real time. This leads to diminished calcium Ca²⁺ concentration and production of gliotransmitters (GT) in the astrocyte causing protracted negative feedback on presynaptic receptors (psr) and extrasynaptic receptors (esr), so that information processing is delayed. Similarly, the synaptic activation of the astroglial syncytium is protracted and the propagation of calcium waves (Ca²⁺) is slowed down (see Figure 5). This could explain symptoms of retardation of thinking, concentration, and motor behavior [4] .

Basically, most of the typical receptors for neurotransmitters have been identified on the astrocytic membrane. Individual astroglial cells express as many as five different receptor systems linked to Ca²⁺ mobilization [20] . Dependant on the pattern of astrocytic receptors, synaptic information processing may be qualitatively modified [7] .

There is some evidence that receptors on astrocytes are upregulated. In animal models of chronic stress adenosine A_2A receptors are upregulated. This A_2A receptor overexpression may explain the depressive signs found in aging, chronic stress, and Alzheimer’s disease [21] . Similarly, the expression of A_2A receptors was upregulated in the cortex of rats in which early febrile seizures induced depressive-like behavior [22] . Importantly, inhibition of adenosine A_2A receptors by pharmacological and gene knockout methods exerts an anti-depressive-like effect [23] .

Figure 6 shows the elementary cycle of self-frustration in major depression. As discussed above, in the pathophysiological model proposed memory impairment is caused by the downregulation of the expression of connexins or connexin deficits. It is further suggested that the downregulation of connexins may be compensated by the upregulation of astroglial receptors. Since astrocytic receptors coding the expected sensations from the environment outnumber the amount of neurotransmitters that code the environmental sensations, the overexpression of astrocytic receptors connotes overexpectations. This leads to a protracted processing of sensory information that frustrates the full comprehension of the expected event, since it cannot be grasped in time. In addition, expectation frustration stresses the syncytium aggravating memory impairment. Here we deal with a cyclic pathophysiological mechanism of major depression that causes self-frustration of expectations. Significantly this mechanism is explanatory for cognitive dysfunctions in depression, as slowing down processing speed, deficits in attentions and working memory [24] .

In a psychological perspective it is suggested that patients with major depression suffer from dysfunctional expectations which are maintained despite experiences contrary to the expectations. Two mechanisms may be responsible for the maintenance of expectations: The experience in the expectation-violating situation may be considered an exception or the credibility of the information is called into question. Basically, the self-concept associated with future expectations may also play a key role in expectation maintenance [25] . Here we speak of the narcissistic personality structure of persons inclined to depression [26] .

Decisively, the model of self-frustration of expectations in major depression is based on imbalances in tripartite synapses and the glial networks along with the pathophysiological mechanism of connexin underexpression with a compensatory astrocytic receptors overexpression [4] . Fundamentally, the interpretation of astrocytic receptors as expectation variables is based on the quantum physical model of the Cognitive Action Theory of W. Baer [27] . The original syncytiopathy hypothesis of major depression is meanwhile experimentally supported what the underexpression or deficits of connexins concerns, but the overexpression of astrocytic receptors awaits experimental support, especially in humans.

My work on depression research focuses on synaptic imbalances in tripartite synapses and the glial network (syncytium). The present study represents a further elaboration of the syncytiopathy hypothesis of depression [4] . Based on a new biophysical interpretation of astrocytic receptors as expectation variables it can be shown that the prolonged sensory information processing frustrates the full comprehension of sensory events, since they cannot be grasped in real time. Crucially, this mechanism of self-frustration of expectations is explanatory for cognitive deficits in major depression as slowing down processing speed, deficits in attentions and working memory. Admittedly, in depression astrocytes undergo morphological alterations (astrocyte atrophy) in various brain regions [28] [29] . However, experimental findings depend on the stage or course of illness [30] . The main message of the present study is that patients with major depression are unable to fully acknowledge the existence of an intended event.

This study is dedicated to my personal doctor Gerda Weiss. I am grateful to Christian Streili for designing the figures and the table, and especially Marie Motil for preparing the final version of the paper.

The author declares no conflicts of interest regarding the publication of this paper.

Mitterauer, B.J. (2023) Self-Frustration of Expectations in Major Depressive Disorder: The Syncytiopathy Hypothesis of Depression Revisited. Advances in Bioscience and Biotechnology, 14, 534-544. https://doi.org/10.4236/abb.2023.1412037