ArticleThe Journal of physiology2005
Interactions between histamine and bradykinin in stimulation of ischaemically sensitive cardiac afferents in felines.
Article in The Journal of physiology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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13 citing papers in PubMed, 25 citations in OpenAlex.
- Fundamental hemodynamic mechanisms mediating the response to myocardial ischemia in conscious paraplegic mice: cardiac output versus peripheral resistance.Physiological reports · 2017Article
- Low esophageal mucosal blood flow in patients with nutcracker esophagus.American journal of physiology. Gastrointestinal and liver physiology · 2016Article
- Electroacupuncture Ameliorates the Coronary Occlusion Related Tachycardia and Hypotension in Acute Rat Myocardial Ischemia Model: Potential Role of Hippocampus.Evidence-based complementary and alternative medicine : eCAM · 2015Article
- Cardiac contractility modulation increases action potential duration dispersion and decreases ventricular fibrillation threshold via β1-adrenoceptor activation in the crystalloid perfused normal rabbit heart.International journal of cardiology · 2014Article
- Esophageal wall blood perfusion during contraction and transient lower esophageal sphincter relaxation in humans.American journal of physiology. Gastrointestinal and liver physiology · 2012Article
- Ionotropic glutamate receptors in the external lateral parabrachial nucleus participate in processing cardiac sympathoexcitatory reflexes.American journal of physiology. Heart and circulatory physiology · 2012Article
- Cardiac spinal deafferentation reduces the susceptibility to sustained ventricular tachycardia in conscious rats.American journal of physiology. Regulatory, integrative and comparative physiology · 2011Article
- A new function for ATP: activating cardiac sympathetic afferents during myocardial ischemia.American journal of physiology. Heart and circulatory physiology · 2010Article
- Endogenous endothelin stimulates cardiac sympathetic afferents during ischaemia.The Journal of physiology · 2010Article
- Bradykinin and thromboxane A2 reciprocally interact to synergistically stimulate cardiac spinal afferents during myocardial ischemia.American journal of physiology. Heart and circulatory physiology · 2010Article
- Myocardial ischemia-mediated excitatory reflexes: a new function for thromboxane A2?American journal of physiology. Heart and circulatory physiology · 2008Article
- Undiscovered role of endogenous thromboxane A2 in activation of cardiac sympathetic afferents during ischaemia.The Journal of physiology · 2008Article
- Interactions between histamine and bradykinin in stimulation of ischaemically sensitive cardiac afferents in felines.The Journal of physiology · 2005Article
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2 authors at 1 institution in 1 country.
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Abstract
Cardiac spinal afferents are activated during myocardial ischaemia. Our previous studies have shown that during ischaemia, histamine and bradykinin (BK) stimulate cardiac spinal afferents. Because the two mediators are released together during ischaemia, the present study examined the interactions between these two mediators with respect to their influence on ischaemically sensitive cardiac afferents. Single-unit cardiac afferent activity was recorded from the left sympathetic chain or rami communicantes (T(2)-T(5)) in anaesthetized cats. Fifty-five ischaemically sensitive cardiac afferents (conduction velocity (CV) = 0.2-5.6 m s(-1), 8 Adelta- and 47 C-fibres) were identified. Administration of histamine (10 microg kg(-1)) and BK (1 microg) in combination into the left atrium (LA) caused an additive response in 16 afferents compared with administration of either BK or histamine alone (2.62 +/- 0.39 versus 1.67 +/- 0.20 versus 1.24 +/- 0.23 impulses s(-1) (imp s(-1)), BK + histamine versus BK versus histamine). To further evaluate interactions between these mediators, we observed that injection of histamine (10 microg kg(-1), LA) 4 min after the administration of BK (1 microg, LA) induced a significantly larger cardiac afferent response than the response to histamine before BK (1.24 +/- 0.23 versus 1.96 +/- 0.39 imp s(-1), before versus after, n = 10). In contrast, six other afferents responded reproducibly to repeated injections of histamine (10 microg kg(-1), LA) in the absence of BK. BK sensitization of the afferent response to histamine lasted for less than 10 min. Cyclooxygenase blockade with indomethacin (5 mg kg(-1), i.v.) abolished BK sensitization of the response to histamine (1.09 +/- 0.11 versus 1.11 +/- 0.10 imp s(-1), n = 10). Conversely, the response of most (7/9) cardiac afferents to repeat application of BK (1 microg, LA) 4 min after histamine (10 microg kg(-1), LA) was attenuated compared with the BK response before histamine (1.84 +/- 0.25 versus 1.31 +/- 0.18 imp s(-1), before versus after, P < 0.05). Repeat BK (1 microg, LA) induced a consistent response in five other afferents in the absence of histamine. Thus, BK interacts with histamine, and together they cause a larger response than either one alone. BK sensitizes cardiac afferents responding to histamine in a time-dependent fashion, and the BK sensitization effect is dependent on an intact cyclooxygenase pathway. Conversely, histamine reduces the response of most afferents to BK.
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