TY - JOUR
T1 - Capsaicin pretreatment attenuates chronic hypoxic pulmonary hypertension
AU - Lai, Y. L.
AU - Chen, C. F.
AU - Chien, C. T.
AU - Shiao, H. L.
AU - Thacker, A. A.
AU - Zhang, H. Q.
N1 - Funding Information:
The authorsth ankt het echnicaal ssistancoef Mr. M.J. Ma and Ms. Y.-J. Su. The help of Dr. H.-H. Tai for settingu p enzymeim munoassaayn dt hep ro-vidingo f Dr. J.-S. Hong for antiserumof substance P are also gratefullya cknowledgeTdh. e work was supportedb y the NationalS cienceC ouncilof the Republico f China (NSC82-0412-B-002-011).
PY - 1995/2
Y1 - 1995/2
N2 - Capsaicin pretreatment was used to deplete tachykinins in order to study the role of tachykinins in chronic hypoxia-induced pulmonary hypertension. Forty three young Wistar rats weighing 235 ± 4 g were randomly divided into four groups: control (n = 10); capsaicin pretreatment (n = 10); intermittent chronic hypoxia (n = 10); and capsaicin pretreatment + intermittent chronic hypoxia (n = 13). Control animals breathed room air. Rats in the capsaicin pretreatment groups were given capsaicin via subcutaneous injection over a three-day period. Hypobaric hypoxia was intermittently applied by placing animals into a hypobaric chamber with a barometric pressure of 380 Torr for two weeks. In the capsaicin pretreatment + intermittent chronic hypoxia group, rats were exposed to intermittent hypoxia for two weeks immediately after the last dose of capsaicin. Subsequently, pulmonary vascular function, as well as substance P (a tachykinin) level and neutral endopeptidase (NEP, the major degradation enzyme for tachykinins) activity in the lungs were measured. Chronic hypoxia caused significant increases in pulmonary artery pressure, right ventricle/(left ventricle + septum) weight ratio, hematocrit, and lung substance P level, as well as a significant decrease in lung NEP activity. All these chronic hypoxia-induced changes were significantly lessened by capsaicin pretreatment. Capsaicin pretreatment alone did not induce any significant alteration in vascular function. These results suggest that the chronic hypoxia causes an increase in lung tachykinin levels which, in turn, enhance the development of pulmonary hypertension.
AB - Capsaicin pretreatment was used to deplete tachykinins in order to study the role of tachykinins in chronic hypoxia-induced pulmonary hypertension. Forty three young Wistar rats weighing 235 ± 4 g were randomly divided into four groups: control (n = 10); capsaicin pretreatment (n = 10); intermittent chronic hypoxia (n = 10); and capsaicin pretreatment + intermittent chronic hypoxia (n = 13). Control animals breathed room air. Rats in the capsaicin pretreatment groups were given capsaicin via subcutaneous injection over a three-day period. Hypobaric hypoxia was intermittently applied by placing animals into a hypobaric chamber with a barometric pressure of 380 Torr for two weeks. In the capsaicin pretreatment + intermittent chronic hypoxia group, rats were exposed to intermittent hypoxia for two weeks immediately after the last dose of capsaicin. Subsequently, pulmonary vascular function, as well as substance P (a tachykinin) level and neutral endopeptidase (NEP, the major degradation enzyme for tachykinins) activity in the lungs were measured. Chronic hypoxia caused significant increases in pulmonary artery pressure, right ventricle/(left ventricle + septum) weight ratio, hematocrit, and lung substance P level, as well as a significant decrease in lung NEP activity. All these chronic hypoxia-induced changes were significantly lessened by capsaicin pretreatment. Capsaicin pretreatment alone did not induce any significant alteration in vascular function. These results suggest that the chronic hypoxia causes an increase in lung tachykinin levels which, in turn, enhance the development of pulmonary hypertension.
KW - Hypertension, pulmonary
KW - Hypoxia, pulmonary hypertension
KW - Mammals, rat
KW - Mediators, substance P, tachy-kinins
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U2 - 10.1016/0034-5687(94)00098-K
DO - 10.1016/0034-5687(94)00098-K
M3 - Article
C2 - 7539934
AN - SCOPUS:0028819594
SN - 0034-5687
VL - 99
SP - 283
EP - 289
JO - Respiration Physiology
JF - Respiration Physiology
IS - 2
ER -