Sis of mini IPSC decay phase (Clampfit 10, Molecular Devices) was based

Sis of mini IPSC decay phase (Clampfit 10, Molecular Devices) was based on the following 478-01-3 site criteria: (1) Sermorelin manufacturer single events only (i.e., no multiple events), (2) events having stable baselines 15 ms before the rise, and (3) smooth transition from 0 current to peak amplitude [,20 deviation in d(pA)/dt) during rise]. Aligned GABAergic synaptic currents were averaged and the decays were fit by a double-exponential function. Glutamatergic synaptic currents were fit by a single-exponential function.ImmunocytochemistryFOS staining was prepared from Chat -tauGFP mice at postnatal age 2 months 61 week. Animals were deeply anaesthetized with a mixture of Ketamine and Xylazine and perfused transcardially with 10 ml of cold 1xPBS followed by 25 ml of 4 paraformaldehyde (PFA). Brains were immediately removed, postfixed in 4 PFA at 4uC overnight, cryoprotected in a 30 (w/w) sucrose solution at 4uC for 3 days, frozen in Tissue-Tek (Sakura), and stored at 280uC. The complete rostral to caudal extension of the DMH from Bregma level 21.5 to 22.4 was cut in 30 mm coronal sections with a Cryostat. Sections were mounted on slides, washed with 1xPBS, permeabilized with 0.2 Triton X100 and blocked with 5 normal donkey serum for 2 h at room temperature. Slides were then incubated in primary rabbit antibody to c-fos (1:750, Abcam, ab7963) for 48 h at 4uC, followed by washing and 1 h of incubation with an Alexa-594 conjugated secondary donkey antibody (1:500) at room temperature. Labeled probes were cover slipped with DAPI-Fluoromount-G (Southern Biotech). Positive controls for the c-fos protocol were provided by examination of regions of high neuronal activity (e.g. olfactory bulb). Images were TA02 site acquired using the Olympus Spinning Disk Confocal microscope (DSU; Olympus). The DAPI signal was used to confirm that immunodetection of c-fos was exclusively present in cell nuclei. Chat+ neurons of complete 30 mm sectioned DMH sets were counted as expressing positive c-fos immunoreactivity. The observer was blind to the experimental condition of each individual mouse. Biocytin filling was performed by recording from Chat+ neurons in the DMH with a K-Gluconate intracellular solution as described above, additionally containing 0.4 (w/w) Biocytin. P7C3 slices were processed with standard staining procedures. In brief, following the termination of recordings the 200 mm thick slices were submerged in 4 PFA/1xPBS for 1 week at 4uC, washed in 1xPBS, permeabilized with 1 Triton for 30 minutes at room temperature, and then incubated with Alexa 594 conjugated streptdavidin (1:1000, Molecular Probes) for 4 h at room temperature. After washing labeled probes were cover-slipped with Fluoromount G (Southern Biotech) and images acquired withMaterials and Methods AnimalsAll mouse care and experimental procedures were approved by the Institutional Animal Care Research Advisory Committee of Stony Brook University. The BAC transgenic ?Chat eGFP line was the generous gift of Dr. Sukimar Vijayaraghavan [22].Slice PreparationTransverse brain slices were prepared at postnatal age 2 months 61 week. Animals were anesthetized with a mixture of ketamine and xylazine. After decapitation, the brain was transferred into a sucrose-based solution bubbled with 95 O2/5 CO2 and maintained at ,4uC. This solution contained the following (in mM): 248 sucrose, 2 KCl, 1 MgCl2, 1.25 KH2PO4, 26 NaHCO3, 1 sodium pyruvate, and 10 glucose. Transverse coronal brain slices (200 mm) were prepared using a Vibratome (L.Sis of mini IPSC decay phase (Clampfit 10, Molecular Devices) was based on the following criteria: (1) single events only (i.e., no multiple events), (2) events having stable baselines 15 ms before the rise, and (3) smooth transition from 0 current to peak amplitude [,20 deviation in d(pA)/dt) during rise]. Aligned GABAergic synaptic currents were averaged and the decays were fit by a double-exponential function. Glutamatergic synaptic currents were fit by a single-exponential function.ImmunocytochemistryFOS staining was prepared from Chat -tauGFP mice at postnatal age 2 months 61 week. Animals were deeply anaesthetized with a mixture of Ketamine and Xylazine and perfused transcardially with 10 ml of cold 1xPBS followed by 25 ml of 4 paraformaldehyde (PFA). Brains were immediately removed, postfixed in 4 PFA at 4uC overnight, cryoprotected in a 30 (w/w) sucrose solution at 4uC for 3 days, frozen in Tissue-Tek (Sakura), and stored at 280uC. The complete rostral to caudal extension of the DMH from Bregma level 21.5 to 22.4 was cut in 30 mm coronal sections with a Cryostat. Sections were mounted on slides, washed with 1xPBS, permeabilized with 0.2 Triton X100 and blocked with 5 normal donkey serum for 2 h at room temperature. Slides were then incubated in primary rabbit antibody to c-fos (1:750, Abcam, ab7963) for 48 h at 4uC, followed by washing and 1 h of incubation with an Alexa-594 conjugated secondary donkey antibody (1:500) at room temperature. Labeled probes were cover slipped with DAPI-Fluoromount-G (Southern Biotech). Positive controls for the c-fos protocol were provided by examination of regions of high neuronal activity (e.g. olfactory bulb). Images were acquired using the Olympus Spinning Disk Confocal microscope (DSU; Olympus). The DAPI signal was used to confirm that immunodetection of c-fos was exclusively present in cell nuclei. Chat+ neurons of complete 30 mm sectioned DMH sets were counted as expressing positive c-fos immunoreactivity. The observer was blind to the experimental condition of each individual mouse. Biocytin filling was performed by recording from Chat+ neurons in the DMH with a K-Gluconate intracellular solution as described above, additionally containing 0.4 (w/w) Biocytin. Slices were processed with standard staining procedures. In brief, following the termination of recordings the 200 mm thick slices were submerged in 4 PFA/1xPBS for 1 week at 4uC, washed in 1xPBS, permeabilized with 1 Triton for 30 minutes at room temperature, and then incubated with Alexa 594 conjugated streptdavidin (1:1000, Molecular Probes) for 4 h at room temperature. After washing labeled probes were cover-slipped with Fluoromount G (Southern Biotech) and images acquired withMaterials and Methods AnimalsAll mouse care and experimental procedures were approved by the Institutional Animal Care Research Advisory Committee of Stony Brook University. The BAC transgenic ?Chat eGFP line was the generous gift of Dr. Sukimar Vijayaraghavan [22].Slice PreparationTransverse brain slices were prepared at postnatal age 2 months 61 week. Animals were anesthetized with a mixture of ketamine and xylazine. After decapitation, the brain was transferred into a sucrose-based solution bubbled with 95 O2/5 CO2 and maintained at ,4uC. This solution contained the following (in mM): 248 sucrose, 2 KCl, 1 MgCl2, 1.25 KH2PO4, 26 NaHCO3, 1 sodium pyruvate, and 10 glucose. Transverse coronal brain slices (200 mm) were prepared using a Vibratome (L.Sis of mini IPSC decay phase (Clampfit 10, Molecular Devices) was based on the following criteria: (1) single events only (i.e., no multiple events), (2) events having stable baselines 15 ms before the rise, and (3) smooth transition from 0 current to peak amplitude [,20 deviation in d(pA)/dt) during rise]. Aligned GABAergic synaptic currents were averaged and the decays were fit by a double-exponential function. Glutamatergic synaptic currents were fit by a single-exponential function.ImmunocytochemistryFOS staining was prepared from Chat -tauGFP mice at postnatal age 2 months 61 week. Animals were deeply anaesthetized with a mixture of Ketamine and Xylazine and perfused transcardially with 10 ml of cold 1xPBS followed by 25 ml of 4 paraformaldehyde (PFA). Brains were immediately removed, postfixed in 4 PFA at 4uC overnight, cryoprotected in a 30 (w/w) sucrose solution at 4uC for 3 days, frozen in Tissue-Tek (Sakura), and stored at 280uC. The complete rostral to caudal extension of the DMH from Bregma level 21.5 to 22.4 was cut in 30 mm coronal sections with a Cryostat. Sections were mounted on slides, washed with 1xPBS, permeabilized with 0.2 Triton X100 and blocked with 5 normal donkey serum for 2 h at room temperature. Slides were then incubated in primary rabbit antibody to c-fos (1:750, Abcam, ab7963) for 48 h at 4uC, followed by washing and 1 h of incubation with an Alexa-594 conjugated secondary donkey antibody (1:500) at room temperature. Labeled probes were cover slipped with DAPI-Fluoromount-G (Southern Biotech). Positive controls for the c-fos protocol were provided by examination of regions of high neuronal activity (e.g. olfactory bulb). Images were acquired using the Olympus Spinning Disk Confocal microscope (DSU; Olympus). The DAPI signal was used to confirm that immunodetection of c-fos was exclusively present in cell nuclei. Chat+ neurons of complete 30 mm sectioned DMH sets were counted as expressing positive c-fos immunoreactivity. The observer was blind to the experimental condition of each individual mouse. Biocytin filling was performed by recording from Chat+ neurons in the DMH with a K-Gluconate intracellular solution as described above, additionally containing 0.4 (w/w) Biocytin. Slices were processed with standard staining procedures. In brief, following the termination of recordings the 200 mm thick slices were submerged in 4 PFA/1xPBS for 1 week at 4uC, washed in 1xPBS, permeabilized with 1 Triton for 30 minutes at room temperature, and then incubated with Alexa 594 conjugated streptdavidin (1:1000, Molecular Probes) for 4 h at room temperature. After washing labeled probes were cover-slipped with Fluoromount G (Southern Biotech) and images acquired withMaterials and Methods AnimalsAll mouse care and experimental procedures were approved by the Institutional Animal Care Research Advisory Committee of Stony Brook University. The BAC transgenic ?Chat eGFP line was the generous gift of Dr. Sukimar Vijayaraghavan [22].Slice PreparationTransverse brain slices were prepared at postnatal age 2 months 61 week. Animals were anesthetized with a mixture of ketamine and xylazine. After decapitation, the brain was transferred into a sucrose-based solution bubbled with 95 O2/5 CO2 and maintained at ,4uC. This solution contained the following (in mM): 248 sucrose, 2 KCl, 1 MgCl2, 1.25 KH2PO4, 26 NaHCO3, 1 sodium pyruvate, and 10 glucose. Transverse coronal brain slices (200 mm) were prepared using a Vibratome (L.Sis of mini IPSC decay phase (Clampfit 10, Molecular Devices) was based on the following criteria: (1) single events only (i.e., no multiple events), (2) events having stable baselines 15 ms before the rise, and (3) smooth transition from 0 current to peak amplitude [,20 deviation in d(pA)/dt) during rise]. Aligned GABAergic synaptic currents were averaged and the decays were fit by a double-exponential function. Glutamatergic synaptic currents were fit by a single-exponential function.ImmunocytochemistryFOS staining was prepared from Chat -tauGFP mice at postnatal age 2 months 61 week. Animals were deeply anaesthetized with a mixture of Ketamine and Xylazine and perfused transcardially with 10 ml of cold 1xPBS followed by 25 ml of 4 paraformaldehyde (PFA). Brains were immediately removed, postfixed in 4 PFA at 4uC overnight, cryoprotected in a 30 (w/w) sucrose solution at 4uC for 3 days, frozen in Tissue-Tek (Sakura), and stored at 280uC. The complete rostral to caudal extension of the DMH from Bregma level 21.5 to 22.4 was cut in 30 mm coronal sections with a Cryostat. Sections were mounted on slides, washed with 1xPBS, permeabilized with 0.2 Triton X100 and blocked with 5 normal donkey serum for 2 h at room temperature. Slides were then incubated in primary rabbit antibody to c-fos (1:750, Abcam, ab7963) for 48 h at 4uC, followed by washing and 1 h of incubation with an Alexa-594 conjugated secondary donkey antibody (1:500) at room temperature. Labeled probes were cover slipped with DAPI-Fluoromount-G (Southern Biotech). Positive controls for the c-fos protocol were provided by examination of regions of high neuronal activity (e.g. olfactory bulb). Images were acquired using the Olympus Spinning Disk Confocal microscope (DSU; Olympus). The DAPI signal was used to confirm that immunodetection of c-fos was exclusively present in cell nuclei. Chat+ neurons of complete 30 mm sectioned DMH sets were counted as expressing positive c-fos immunoreactivity. The observer was blind to the experimental condition of each individual mouse. Biocytin filling was performed by recording from Chat+ neurons in the DMH with a K-Gluconate intracellular solution as described above, additionally containing 0.4 (w/w) Biocytin. Slices were processed with standard staining procedures. In brief, following the termination of recordings the 200 mm thick slices were submerged in 4 PFA/1xPBS for 1 week at 4uC, washed in 1xPBS, permeabilized with 1 Triton for 30 minutes at room temperature, and then incubated with Alexa 594 conjugated streptdavidin (1:1000, Molecular Probes) for 4 h at room temperature. After washing labeled probes were cover-slipped with Fluoromount G (Southern Biotech) and images acquired withMaterials and Methods AnimalsAll mouse care and experimental procedures were approved by the Institutional Animal Care Research Advisory Committee of Stony Brook University. The BAC transgenic ?Chat eGFP line was the generous gift of Dr. Sukimar Vijayaraghavan [22].Slice PreparationTransverse brain slices were prepared at postnatal age 2 months 61 week. Animals were anesthetized with a mixture of ketamine and xylazine. After decapitation, the brain was transferred into a sucrose-based solution bubbled with 95 O2/5 CO2 and maintained at ,4uC. This solution contained the following (in mM): 248 sucrose, 2 KCl, 1 MgCl2, 1.25 KH2PO4, 26 NaHCO3, 1 sodium pyruvate, and 10 glucose. Transverse coronal brain slices (200 mm) were prepared using a Vibratome (L.