INTRATHECAL CAPSAICIN ENHANCES ONE-KIDNEY RENAL WRAP HYPERTENSION IN THE RAT

被引:13
作者
BURG, M
ZAHM, DS
KNUEPFER, MM
机构
[1] ST LOUIS UNIV, SCH MED, DEPT PHARMACOL & PHYSIOL SCI, ST LOUIS, MO 63104 USA
[2] ST LOUIS UNIV, SCH MED, DEPT ANAT & NEUROBIOL, ST LOUIS, MO 63104 USA
来源
JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM | 1994年 / 50卷 / 02期
关键词
CAPSAICIN; ONE-KIDNEY RENAL WRAP; DEOXYCORTICOSTERONE ACETATE SALT; SPINAL CORD; SUBSTANCE P; CALCITONIN GENE-RELATED PEPTIDE; AFFERENT RENAL NERVE;
D O I
10.1016/0165-1838(94)90009-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Afferent renal nerves (ARN) have been implicated in the development of one-kidney renal wrap (1K-WRAP) hypertension. The role of renal nerves in desoxycorticosterone acetate-salt (DOCA) hypertension, a low-renin model of hypertension, is controversial. The present study was designed to determine if spinal substance P (SP) and/or calcitonin gene-related peptide (CGRP) in ARN affects the development of 1K-WRAP or DOCA hypertension in adult rats. Selective long-term partial depletion of spinal SP and CGRP within small primary afferent nerve fibers including unmyelinated ARN was achieved by intrathecal administration of capsaicin. After capsaicin treatment, 1K-WRAP hypertension was induced by removing the right kidney and wrapping the left kidney with a figure-8 ligature. In a second group of rats, DOCA hypertension was induced by subcutaneous application of desoxycorticos-terone pellets after unilateral nephrectomy. Systolic arterial pressure was monitored for 8 weeks by tail cuff plethysmography after which direct blood pressure measurement was performed followed by immunohistochemistry. Intrathecal capsaicin administration had no significant effect on SP-ir and CGRP-ir of ARN soma located within thoracic dorsal root ganglia whereas immunoreactivity against these peptides was reduced by one third to one half in the dorsal horn, indicating effective long-term spinal depletion of these neuropeptides. Intrathecal capsaicin enhanced the development of 1K-WRAP hypertension, since arterial pressure was greater in the treated group. In contrast, DOCA hypertension was unaffected by capsaicin pretreatment. Considering the neurotoxic action of capsaicin for SP-ir and CGRP-ir unmyelinated primary afferent neurons, we hypothesize that spinal SP, CGRP and/or related peptides existing in ARN and other capsaicin-sensitive unmyelinated primary afferent neurons in the lower thoracic spinal cord may ameliorate 1K-WRAP hypertension, but not DOCA hypertension.
引用
收藏
页码:189 / 199
页数:11
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