about
Recording sympathetic nerve activity chronically in rats: surgery techniques, assessment of nerve activity, and quantificationNeurogenic and sympathoexcitatory actions of NaCl in hypertension.Chronic high-sodium diet intake after weaning lead to neurogenic hypertension in adult Wistar rats.Osmoregulatory thirst in mice lacking the transient receptor potential vanilloid type 1 (TRPV1) and/or type 4 (TRPV4) receptor.Glucocorticoids attenuate the central sympathoexcitatory actions of insulin.Dietary salt intake exaggerates sympathetic reflexes and increases blood pressure variability in normotensive ratsGlutamate receptors in the hypothalamic paraventricular nucleus contribute to insulin-induced sympathoexcitationHealthy older humans exhibit augmented carotid-cardiac baroreflex sensitivity with aspirin during muscle mechanoreflex and metaboreflex activation.Arcuate nucleus injection of an anti-insulin affibody prevents the sympathetic response to insulinDREADD-induced activation of subfornical organ neurons stimulates thirst and salt appetite.Cerebrospinal Fluid Hypernatremia Elevates Sympathetic Nerve Activity and Blood Pressure via the Rostral Ventrolateral Medulla.Increased dietary salt intake enhances the exercise pressor reflex.Blood pressure responses to dietary sodium: Association with autonomic cardiovascular function in normotensive adults.Hypothalamic Signaling in Body Fluid Homeostasis and Hypertension.NaCl and osmolarity produce different responses in organum vasculosum of the lamina terminalis neurons, sympathetic nerve activity and blood pressure.Recent Advances in Neurogenic Hypertension: Dietary Salt, Obesity, and Inflammation.High fat diet attenuates glucose-dependent facilitation of 5-HT3 -mediated responses in rat gastric vagal afferents.Hypernatremia-induced vasopressin secretion is not altered in TRPV1-/- rats.The hypothalamic paraventricular nucleus may not be at the heart of sympathetic outflow.Airway obstruction produces widespread sympathoexcitation: role of hypoxia, carotid chemoreceptors, and NTS neurotransmission.Organum Vasculosum of the Lamina Terminalis Detects NaCl to Elevate Sympathetic Nerve Activity and Blood Pressure.The influence of acute elevations in plasma osmolality and serum sodium on sympathetic outflow and blood pressure responses to exercise.Peripheral venous distension elicits a blood pressure raising reflex in young and middle-aged adults.Urinary K promotes irritative voiding symptoms and pain in the face of urothelial barrier dysfunctionAlterations in dietary sodium intake affect cardiovagal baroreflex sensitivityIntegration of Hypernatremia and Angiotensin II by the Organum Vasculosum of the Lamina Terminalis Regulates ThirstShort-term water deprivation does not increase blood pressure variability or impair neurovascular function in healthy young adultsReducing Dietary Sodium to 1000 mg per Day Reduces Neurovascular Transduction Without Stimulating Sympathetic OutflowWater deprivation does not augment sympathetic or pressor responses to sciatic afferent nerve stimulation in rats or to static exercise in humansMissing pieces of the Piezo1/Piezo2 baroreceptor hypothesis: an autonomic perspectiveRenal sensory nerves increase sympathetic nerve activity and blood pressure in 2-kidney 1-clip hypertensive mice
P50
Q30557837-D9AC9C4A-7CB7-48CD-B7D3-8F9C2C9D3145Q33598143-AF7B5DC0-3D09-4071-B74C-1DA748379A24Q33916160-49227EC2-4AEF-4B44-AA36-8531DD92B67CQ34439996-64B943E0-53E1-4838-B348-C17AACDF4380Q34519152-F86168DA-EC31-4018-BD92-266092936B66Q34711079-3E7EB081-82FF-4EB3-9196-274482A4F5D1Q35138449-69C4B0BC-0F56-402A-8C7E-4C112DDF0316Q36244479-D4B06CF0-2B37-4695-9679-A9CFF66E40DDQ36923773-A12CFE9D-6E1E-4008-A87F-02453D628B66Q37098032-CF47FE7B-282F-4579-BAB7-3BB7A63E6B1FQ37342413-AC6E1A09-8D63-4DBB-8B2D-DE62232ED337Q37575883-8C6AABFA-3280-4F29-9ADC-A5FFAFA6F6EAQ38627609-483F42BD-9C8C-466E-8FB8-AAA2884507C7Q38681396-F37822A9-9B9D-4CFA-B066-1EB6198E7F6EQ38693069-5FDED716-1D70-46B9-929D-6AE41118EBDDQ39455507-8D57266B-AF8A-4101-8F33-E5693FEFC2E5Q40443079-CFD8BD7A-B7D4-462F-92A0-6CE9FB435EBAQ42028810-257C6002-7C89-4341-8A55-A0E661FF189FQ45677252-BAB96617-7E09-4CF4-9E0F-48A87EFC6B4EQ47638488-6C7F6C40-19B6-41FE-B501-B67CCFC4835AQ48414032-4E2B5047-4CFE-4D23-B7CC-414FAD7C0FBCQ50092301-0E2291ED-40CA-47CE-B01A-0090D664CB2FQ53127896-DAF88A15-CB22-4CB3-A0F5-2109A87F81DAQ64087055-496D9BD4-8837-40EB-AB22-8A1ED9471655Q89289794-6B37E5A9-1492-4F19-BAF0-6264FF1BB232Q89474112-81273B47-E419-45DB-BF0B-AB79B8CD9CB5Q90741876-BFE8E5ED-27A2-4228-AC94-D23C7CCBE152Q91128168-8D998DFF-97BC-4F27-9400-067E70076E85Q91881637-B39FBC20-6238-4645-B947-C8126EB86952Q91957090-14084A64-71DF-4E41-BEB7-6908B41AE41FQ92038683-EE9CA149-C219-496A-9A8A-5843DCDEF997
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Sean D Stocker
@ast
Sean D Stocker
@en
Sean D Stocker
@es
Sean D Stocker
@nl
type
label
Sean D Stocker
@ast
Sean D Stocker
@en
Sean D Stocker
@es
Sean D Stocker
@nl
prefLabel
Sean D Stocker
@ast
Sean D Stocker
@en
Sean D Stocker
@es
Sean D Stocker
@nl
P106
P31
P496
0000-0001-6317-6300