Effects of graded muscle contractions on spinal cord substance P release, arterial blood pressure, and heart rate.

The release of substance P (SP)-like immunoreactivity (SP-LI) in the dorsal horn of the spinal cord and the cardiovascular changes to both high-tension (HT) and low-tension (LT) contractions were determined using alpha-chloralose-anesthetized cats. Over a 10-minute period, seven contractions (HT or LT) were induced. Each contraction was 20 seconds in duration and was followed by an 80-second quiescent period. The tension-time index (TTI) for the HT contractions was 2751 +/- 348 kg.s (mean +/- SD), which was greater than the TTI of 813 +/- 167 kg.s for the LT contractions. The HT contractions caused a greater release of SP-LI than the LT contractions: SP-LI increased from 0.18 +/- 0.02 to 0.32 +/- 0.03 fmol/100 microL and from 0.18 +/- 0.02 to 0.25 +/- 0.04 fmol/100 microL for the two types of contractions, respectively. Concomitant with this greater SP-LI release, HT contractions caused larger increases in mean arterial pressure (34 +/- 16 versus 11 +/- 4 mm Hg) and heart rate (18 +/- 7 versus 8 +/- 4 beats per minute) than did the LT contractions. These changes in SP-LI, mean arterial pressure, and heart rate were virtually abolished when the contractions were repeated after sectioning the L-5-S-2 dorsal and ventral roots or when the electrical stimulation of the ventral roots was repeated after muscle paralysis with gallamine triethiodide. These results demonstrate that contraction-evoked SP-LI release in the dorsal horn is related to the developed tension. Furthermore, these data provide additional support for the hypothesis that the release of SP from the central terminations of muscle afferents plays a role in mediating the cardiovascular responses to static contraction of skeletal muscle.

[1]  J. Hill,et al.  Attenuation of reflex pressor and ventilatory responses to static contraction by an NK-1 receptor antagonist. , 1992, Journal of applied physiology.

[2]  J. Mitchell,et al.  Effect of spinal microinjections of an antagonist to substance P or somatostatin on the exercise pressor reflex. , 1992, Circulation research.

[3]  C. Williams,et al.  Sustained isometric contraction of skeletal muscle results in release of immunoreactive neurokinins in the spinal cord of the anaesthetized cat , 1991, Neuroscience Letters.

[4]  K. Matsukawa,et al.  Multiplicity of the afferent pathways mediating the exercise pressor reflex , 1991, Brain Research.

[5]  H. Benveniste,et al.  Microdialysis—Theory and application , 1990, Progress in Neurobiology.

[6]  J. Mitchell,et al.  Reflex responses of renal nerve activity during isometric muscle contraction in cats. , 1990, The American journal of physiology.

[7]  P. Mantyh,et al.  Diversity in mammalian tachykinin peptidergic neurons: multiple peptides, receptors, and regulatory mechanisms 1 , 1990, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[8]  J. Mitchell,et al.  J.B. Wolffe memorial lecture. Neural control of the circulation during exercise. , 1990, Medicine and science in sports and exercise.

[9]  R. Victor,et al.  Stimulation of Renal Sympathetic Activity by Static Contraction: Evidence for Mechanoreceptor‐Induced ReflexesFrom Skeletal Muscle , 1989, Circulation research.

[10]  A. Craig,et al.  Spinal and supraspinal terminations of primary afferent fibers from the gastrocnemius-soleus muscle in the cat , 1988, Neuroscience.

[11]  V. Go,et al.  Release of substance P from the cat spinal cord. , 1987, The Journal of physiology.

[12]  U. Ungerstedt,et al.  In vivo release of substance P in cat dorsal horn studied with microdialysis , 1987, Neuroscience Letters.

[13]  G. Iwamoto,et al.  Immunoneutralization of substance P attenuates the reflex pressor response to muscular contraction , 1986, Brain Research.

[14]  I. Kanazawa,et al.  Regional distribution of substance P, neurokinin α and neurokinin β in rat spinal cord, nerve roots and dorsal root ganglia, and the effects of dorsal root section or spinal transection , 1985, Brain Research.

[15]  J. Mitchell,et al.  Pressor reflex evoked by muscular contraction: contributions by neuraxis levels. , 1985, Journal of applied physiology.

[16]  G. Iwamoto,et al.  Peripheral factors influencing expression of pressor reflex evoked by muscular contraction. , 1985, Journal of applied physiology.

[17]  G. Kozlowski,et al.  Attenuation of the reflex pressor response to muscular contraction by a substance P antagonist. , 1985, Brain research.

[18]  S. Mense,et al.  Responses in muscle afferent fibres of slow conduction velocity to contractions and ischaemia in the cat. , 1983, The Journal of physiology.

[19]  J. Mitchell,et al.  Effects of static muscular contraction on impulse activity of groups III and IV afferents in cats. , 1983, Journal of applied physiology: respiratory, environmental and exercise physiology.

[20]  M. Randić,et al.  The actions of neuropeptides on dorsal horn neurons in the rat spinal cord slice preparation: an intracellular study , 1982, Brain Research.

[21]  R. Schmidt,et al.  Muscle receptors with fine afferent fibers which may evoke circulatory reflexes. , 1981, Circulation research.

[22]  F. Kao,et al.  Central projections from ergoreceptors (C fibers) in muscle involved in cardiopulmonary responses to static exercise. , 1981, Circulation research.

[23]  W. S. Ring,et al.  Regional Myocardial Blood Flow during Exercise in Dogs with Chronic Left Ventricular Hypertrophy , 1981, Circulation research.

[24]  S. Vatner,et al.  Reduction of Maximal Coronary Vasodilator Capacity in Conscious Dogs with Severe Right Ventricular Hypertrophy , 1981, Circulation research.

[25]  A. Iggo,et al.  The substantia gelatinosa of the spinal cord: a critical review. , 1980, Brain : a journal of neurology.

[26]  J. Fleiss,et al.  Some Statistical Methods Useful in Circulation Research , 1980, Circulation research.

[27]  E. Perl,et al.  Reexamination of the dorsal root projection to the spinal dorsal horn including observations on the differential termination of coarse and fine fibers , 1979, The Journal of comparative neurology.

[28]  I. Tulloch,et al.  Effects of substance P on neurones in the dorsal horn of the spinal cord of the cat , 1979, Brain Research.

[29]  D. Reis,et al.  Ultrastructural localization of substance P in neurons of rat spinal cord. , 1977, Brain research.

[30]  T. Hökfelt,et al.  Experimental immunohistochemical studies on the localization and distribution of substance P in cat primary sensory neurons , 1975, Brain Research.

[31]  D. McCloskey,et al.  Reflex cardiovascular and respiratory responses originating in exercising muscle , 1972, The Journal of physiology.

[32]  S M Hilton,et al.  The reflex nature of the pressor response to muscular exercise , 1971, The Journal of physiology.

[33]  E. Braunwald,et al.  Hemodynamic determinants of oxygen consumption of the heart with special reference to the tension-time index. , 1957, The American journal of physiology.

[34]  J. Mitchell,et al.  Substance P release in the spinal cord during the exercise pressor reflex in anaesthetized cats. , 1993, The Journal of physiology.

[35]  W. Willis,et al.  Sensory Mechanisms of the Spinal Cord , 1991, Springer US.

[36]  P F Morrison,et al.  Steady-state theory for quantitative microdialysis of solutes and water in vivo and in vitro. , 1990, Life sciences.

[37]  K. Kendrick Use of microdialysis in neuroendocrinology. , 1989, Methods in enzymology.

[38]  C. Lamotte Organization of Dorsal Horn Neurotransmitter Systems , 1986 .

[39]  J. Mitchell,et al.  The exercise pressor reflex: its cardiovascular effects, afferent mechanisms, and central pathways. , 1983, Annual review of physiology.

[40]  J. Perez-Gonzalez Factors determining the blood pressure responses to isometric exercise. , 1981, Circulation research.