1996
DOI: 10.1007/bf00168760
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Chronic (?)-isoprenaline infusion down-regulates ?1- and ?2-adrenoceptors but does not transregulate muscarinic cholinoceptors in rat heart

Abstract: Regulation of beta-adrenoceptor (beta-ar) subtypes and transregulation of muscarinic cholinoceptors (mAchr) was examined in regions of rat heart after chronic infusion of (-)-isoprenaline (450 micrograms/kg per hour) for 14 days. Following (-)-isoprenaline infusion systolic blood pressure was reduced for 10 days but then gradually returned to control levels, whereas heart rate was increased for 7 days before declining to a level significantly above control. Heart weight to body weight ratio was increased in (-… Show more

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Cited by 17 publications
(22 citation statements)
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References 36 publications
(44 reference statements)
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“…However, compared with the experiment situation, where the mice get only one injection of NE, mice living in the cold have a continuous flow of NE stimulating BAT and are therefore capable of producing enough heat to survive the cold. One would speculate that a prolonged exposure to cold (which increases sympathetic outflow) would decrease ␤ 1 -AR levels since continued stimulation of ␤ 1 -ARs in the rat heart results in loss of ␤ 1 -AR numbers and desensitization of the ␤ 1 -AR and also adenylate cyclase pathway (29,31). However, we show in BAT (Fig.…”
Section: Discussioncontrasting
confidence: 52%
“…However, compared with the experiment situation, where the mice get only one injection of NE, mice living in the cold have a continuous flow of NE stimulating BAT and are therefore capable of producing enough heat to survive the cold. One would speculate that a prolonged exposure to cold (which increases sympathetic outflow) would decrease ␤ 1 -AR levels since continued stimulation of ␤ 1 -ARs in the rat heart results in loss of ␤ 1 -AR numbers and desensitization of the ␤ 1 -AR and also adenylate cyclase pathway (29,31). However, we show in BAT (Fig.…”
Section: Discussioncontrasting
confidence: 52%
“…Indeed, a reduced heart rate deceleration in response to stimulation of arterial baroreceptors or cardiac chemoreceptors was found in ISO-induced cardiac hypertrophy [70,155]. On the other hand, acetylcholine-induced cardioinhibitory effects as assessed ex vivo were enhanced following chronic ISO administration [35, 155,156]. Taken together, these findings suggest that a reduction of parasympatheticallymediated cardiac effects following chronic ISO administration is related to an impaired integrative function of the brain stem rather than reduced responsiveness of the myocardium to acetylcholine.…”
Section: Basal Cardiac Systolic Functionmentioning
confidence: 99%
“…Ventricle stiffness, inferred from the gradient of the diastolic performance curve, appears to be unchanged by CA, and therefore decreases in developed pressure/RPP are likely to be a consequence of reduced acto-myosin cross-links for increased length sarcomeres. This will preserve stroke volume at the expense of greater residual volume in the ventricle but result in reduced force development; hence, a diminished RPP:CA led to a reduced developed pressure that was only partially recovered by -adrenergic stimulation (dobutamine), suggesting a down-regulation of adrenoreceptor reserve (Cheng and Hauton, 2008) through prolonged catecholamine exposure (Benjamin et al, 1989;Matthews et al, 1996). The poor developed pressure, however, is in contrast to the elevated MABP seen in vivo, suggesting that intrinsic weakness of the myocardium is compensated for physiologically in situ.…”
Section: Intrinsic Vs Extrinsic Factors Responsible For Camentioning
confidence: 99%