Michal Yoles-Frenkel1, Oksana Cohen2, Rohini Bansal3, Noa Horesh4, Yoram Ben-Shaul5. 1. Department of Medical Neurobiology, The Faculty of Medicine, The Hebrew University of Jerusalem, POB 12272, 9112102 Jerusalem, Israel. Electronic address: michal.yoles@mail.huji.ac.il. 2. Department of Medical Neurobiology, The Faculty of Medicine, The Hebrew University of Jerusalem, POB 12272, 9112102 Jerusalem, Israel. Electronic address: oksana.cohen@mail.huji.ac.il. 3. Department of Medical Neurobiology, The Faculty of Medicine, The Hebrew University of Jerusalem, POB 12272, 9112102 Jerusalem, Israel. Electronic address: bansalr@ekmd.huji.ac.il. 4. Department of Medical Neurobiology, The Faculty of Medicine, The Hebrew University of Jerusalem, POB 12272, 9112102 Jerusalem, Israel. Electronic address: noa.rosenthal1@mail.huji.ac.il. 5. Department of Medical Neurobiology, The Faculty of Medicine, The Hebrew University of Jerusalem, POB 12272, 9112102 Jerusalem, Israel. Electronic address: yoramb@ekmd.huji.ac.il.
Abstract
BACKGROUND: Achieving controlled stimulus delivery is a major challenge in the physiological analysis of the vomeronasal system (VNS). NEW METHOD: We provide a comprehensive description of a setup allowing controlled stimulus delivery into the vomeronasal organ (VNO) of anesthetized mice. VNO suction is achieved via electrical stimulation of the sympathetic nerve trunk (SNT) using cuff electrodes, followed by flushing of the nasal cavity. Successful application of this methodology depends on several aspects including the surgical preparation, fabrication of cuff electrodes, experimental setup modifications, and the stimulus delivery and flushing. Here, we describe all these aspects in sufficient detail to allow other researchers to readily adopt it. We also present a custom written MATLAB based software with a graphical user interface that controls all aspects of the actual experiment, including trial sequencing, hardware control, and data logging. RESULTS: The method allows measurement of stimulus evoked sensory responses in brain regions that receive vomeronasal inputs. An experienced investigator can complete the entire surgical procedure within thirty minutes. COMPARISON WITH EXISTING METHODS: This is the only approach that allows repeated and controlled stimulus delivery to the intact VNO, employing the natural mode of stimulus uptake. The approach is economical with respect to stimuli, requiring stimulus volumes as low as 1-2μl. CONCLUSIONS: This comprehensive description will allow other investigators to adapt this setup to their own experimental needs and can thus promote our physiological understanding of this fascinating chemosensory system. With minor changes it can also be adapted for other rodent species.
BACKGROUND: Achieving controlled stimulus delivery is a major challenge in the physiological analysis of the vomeronasal system (VNS). NEW METHOD: We provide a comprehensive description of a setup allowing controlled stimulus delivery into the vomeronasal organ (VNO) of anesthetized mice. VNO suction is achieved via electrical stimulation of the sympathetic nerve trunk (SNT) using cuff electrodes, followed by flushing of the nasal cavity. Successful application of this methodology depends on several aspects including the surgical preparation, fabrication of cuff electrodes, experimental setup modifications, and the stimulus delivery and flushing. Here, we describe all these aspects in sufficient detail to allow other researchers to readily adopt it. We also present a custom written MATLAB based software with a graphical user interface that controls all aspects of the actual experiment, including trial sequencing, hardware control, and data logging. RESULTS: The method allows measurement of stimulus evoked sensory responses in brain regions that receive vomeronasal inputs. An experienced investigator can complete the entire surgical procedure within thirty minutes. COMPARISON WITH EXISTING METHODS: This is the only approach that allows repeated and controlled stimulus delivery to the intact VNO, employing the natural mode of stimulus uptake. The approach is economical with respect to stimuli, requiring stimulus volumes as low as 1-2μl. CONCLUSIONS: This comprehensive description will allow other investigators to adapt this setup to their own experimental needs and can thus promote our physiological understanding of this fascinating chemosensory system. With minor changes it can also be adapted for other rodent species.
Authors: Rohini Bansal; Maximilian Nagel; Romana Stopkova; Yizhak Sofer; Tali Kimchi; Pavel Stopka; Marc Spehr; Yoram Ben-Shaul Journal: BMC Biol Date: 2021-06-28 Impact factor: 7.431