Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3145
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Synaptic connections among neurons are critical for information processing and memory storage in the brain, making them hotspots for neuropathologies. Understanding the physiology of synapses, therefore, may facilitate the development of therapeutic approaches. However, synapses are micrometer-sized functional structures involved in many neuronal processes, where the challenge is deciphering differential signaling in presynaptic and postsynaptic compartments of relatively intact microcircuits. Here we developed a method combining two-photon laser microsurgery with compartment-specific electrophysiological activation and readout to improve the specificity with which neuronal signaling is detected. After finding a connection, femtosecond laser pulses are used to sever the presynaptic axon from the cell body with micrometer precision. This microdissection method is effective to a depth of at least 100 µm. The initial segment of the isolated axon is extracellularly stimulated and activated to release neurotransmitters, as detected via a recipient whole-cell neuron, which is being recorded. This methodology is an alternative to axonal patch-clamp recordings, which are short-lasting and difficult. Together with pharmacology and genetic manipulation, our approach allows the interrogation of compartmentalized signaling in intact synapses. The total time of laser exposure is a few seconds and the microsurgery takes 5-10 min, which enables the interrogation of multiple synapses within an experiment. Our protocol provides a tool to investigate compartment-specific signaling in relatively intact brain tissue, enabling a more comprehensive understanding of neuronal synapses.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1038/s41596-024-01125-5 | DOI Listing |
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