TY - JOUR
T1 - Inactivation of baroafferents leads to loss of barosensitivity without changes in nerve morphology
AU - Stevens, M. F.
AU - Novotny, G. E.
AU - Lipfert, P.
PY - 1998
Y1 - 1998
N2 - Baroreceptors are stretch-sensitive mechanoreceptors, which are silenced by preventing distension of the receptor zone. Does chronic inactivation of these peripheral afferents alter their function or morphology? Compound action potentials and morphometry of carotid sinus nerves of 10 rabbits were investigated. The baroafferents were inactivated by embedding the pressure-released carotid sinus into silicon gel. The success of this procedure was validated by the absence of spike activity of the sinus nerve during normal and elevated systemic blood pressure. The contralateral vessels of the same animals were sham-operated and also embedded into silicon, but without prevention of wall movements. After 5, 7, 14 or 28 days the nerves were functionally reinvestigated before and after release of the sinus wall. Afterwards, the morphology of the nerve cross-sections was analysed by morphometry of electron micrographs. Baroafferents did not regain spike activity during immobilisation of the sinus wall. After release of the carotid sinus wall only nerves inactivated for five days regained their pulse synchronous baroreceptor discharge. Following seven days of inactivation, baroreceptor discharge could be elicited by maximal pressure elevation in only one of three nerves. At any time later, the baroreceptor response to arterial pressure changes was lost completely. The activity of the control nerves was preserved after 28 days. No obvious differences in fibre size and myelin thickness were observed between inactivated and control nerves. Inactivation of baroafferents for more than one week leads to a loss of pressure-dependent spike activity. Since morphology did not differ between inactivated and control nerves, it is suggested that changes of baroreceptor endings are responsible for this loss of function
AB - Baroreceptors are stretch-sensitive mechanoreceptors, which are silenced by preventing distension of the receptor zone. Does chronic inactivation of these peripheral afferents alter their function or morphology? Compound action potentials and morphometry of carotid sinus nerves of 10 rabbits were investigated. The baroafferents were inactivated by embedding the pressure-released carotid sinus into silicon gel. The success of this procedure was validated by the absence of spike activity of the sinus nerve during normal and elevated systemic blood pressure. The contralateral vessels of the same animals were sham-operated and also embedded into silicon, but without prevention of wall movements. After 5, 7, 14 or 28 days the nerves were functionally reinvestigated before and after release of the sinus wall. Afterwards, the morphology of the nerve cross-sections was analysed by morphometry of electron micrographs. Baroafferents did not regain spike activity during immobilisation of the sinus wall. After release of the carotid sinus wall only nerves inactivated for five days regained their pulse synchronous baroreceptor discharge. Following seven days of inactivation, baroreceptor discharge could be elicited by maximal pressure elevation in only one of three nerves. At any time later, the baroreceptor response to arterial pressure changes was lost completely. The activity of the control nerves was preserved after 28 days. No obvious differences in fibre size and myelin thickness were observed between inactivated and control nerves. Inactivation of baroafferents for more than one week leads to a loss of pressure-dependent spike activity. Since morphology did not differ between inactivated and control nerves, it is suggested that changes of baroreceptor endings are responsible for this loss of function
U2 - https://doi.org/10.1016/S0165-1838(97)00118-5
DO - https://doi.org/10.1016/S0165-1838(97)00118-5
M3 - Article
C2 - 9626938
SN - 0165-1838
VL - 68
SP - 125
EP - 134
JO - Journal of the Autonomic Nervous System
JF - Journal of the Autonomic Nervous System
IS - 3
ER -