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Featured researches published by Tina Hines.


Circulation Research | 1994

Responses of neurons in the nucleus tractus solitarius to stimulation of heart and lung receptors in the rat.

Tina Hines; Glenn M. Toney; Steven W. Mifflin

To characterize central integration of reflex responses to stimulation of mechanically and chemically sensitive receptors in the heart and lung, male rats (350 to 425 g) were anesthetized (pentobarbital, 50 mg/kg IP) and paralyzed (gallamine triethiodide, 25 mg/kg IV) and then they underwent bilateral sinoaortic denervation. Extracellular activity of neurons in the nucleus tractus solitarius (NTS) was recorded in response to bolus intra-atrial saline (50, 100, 200, or 300 microL) or phenylbiguanide (PBG, 16 micrograms/kg in 100 microL) administered in random sequence. Changes in mean arterial pressure (MAP), mean right atrial pressure, and right atrial systolic pressure (RASP) were measured as correlates of stimulus intensity, and heart rate (HR) and renal sympathetic nerve activity (RSNA) were used to assess efferent reflex effects of cardiac and pulmonary receptor stimulation. NTS neurons with possible afferent input from stretch and chemically sensitive receptors were identified by an excitatory evoked response to electrical stimulation of the ipsilateral vagus nerve (1 Hz, 500 microA, 1-millisecond duration). Thirty-eight vagus nerve-evoked NTS units with onset latencies of 25.3 +/- 0.9 milliseconds displayed excitatory or inhibitory responses to saline or PBG injections or to both interventions. Saline administration elicited volume-dependent transient increases in MAP and RASP, which were followed by reflex decreases in MAP, HR, and RSNA. PBG injections also evoked hypotension, bradycardia, and sympathoinhibition.(ABSTRACT TRUNCATED AT 250 WORDS)


American Journal of Obstetrics and Gynecology | 1997

Nitric oxide mediation of cardiac receptor reflex responses in the pregnant rat

Tina Hines; Steven W. Mifflin

OBJECTIVES Our purpose was to determine the contribution of centrally released nitric oxide to baseline sympathetic tone and reflex cardiovascular responses to cardiac stretch in the pregnant rat. STUDY DESIGN Baseline blood pressure and renal sympathetic nerve activity and reflex changes in these variables in response to intraatrial saline solution injections were measured in anesthetized pregnant (n = 24) and virgin (n = 27) rats before and after bilateral microinjection of L-nitroarginine methyl ester (0.01 to 1 micromol) into the dorsal medulla. Data were analyzed with use of nonparametric analysis of variance. RESULTS L-Nitroarginine methyl ester microinjection altered basal blood pressure and sympathetic nerve activity (p < 0.05) in virgin but not pregnant rats. L-Nitroarginine methyl ester significantly and equivalently attenuated the reflex sympathoinhibitory and depressor responses to cardiac stretch for 40 minutes in pregnant and virgin animals. CONCLUSION Central nitric oxide does not modulate basal sympathetic tone in the pregnant rat but is released in the medulla in response to cardiac stretch and plays a role in reflex cardiovascular responses similar to that in virgin rats.


American Journal of Obstetrics and Gynecology | 1994

Effect of autonomic blockade on pressor responses to vasopressin in pregnant rats

Tina Hines; Marshall D. Lindheimer; William M. Barron

OBJECTIVE We tested the hypothesis that gestational changes in reflex neural control of the heart and vasculature contribute to altered cardiovascular responses to vasopressin during pregnancy. STUDY DESIGN Changes in mean arterial pressure, cardiac output, total peripheral resistance, and heart rate were measured in response to constant infusion of arginine vasopressin (0.15 to 2.5 mU/kg/min) in conscious pregnant and virgin rats (n = 9) with total autonomic blockade plus restoration of baseline hemodynamics by norepinephrine infusion. RESULTS Resting cardiac output was 40% higher and total peripheral resistance 30% lower in pregnant animals (p < 0.01). Constant infusion of arginine vasopressin evoked equivalent changes in mean arterial pressure in both groups, but the respective contributions of cardiac output and total peripheral resistance to mean arterial pressure differed between groups. Cardiac output was unchanged and the increase in total peripheral resistance was significantly blunted in pregnant vs virgin rats during arginine vasopressin infusion. Control data in nonblocked revealed similar pressor responses to arginine vasopressin in gravid compared with virgin rats but no differences in the contributions of cardiac output and total peripheral resistance to the change in mean arterial pressure. CONCLUSION These findings suggest that neural modulation of arginine vasopressin-induced hypertension is altered during pregnancy and are consistent with a reduction in intrinsic vascular sensitivity to arginine vasopressin during gestation.


American Journal of Physiology-regulatory Integrative and Comparative Physiology | 2000

Baroreceptor afferent discharge in the pregnant rat

Tina Hines


American Journal of Physiology-regulatory Integrative and Comparative Physiology | 2000

Pregnancy alters cardiac receptor afferent discharge in rats

Tina Hines; Tracy M. Hodgson


Journal of Nursing Education | 1999

Directed case studies in baccalaureate nursing anatomy and physiology.

Marianne Woody; Susan Albrecht; Tina Hines; Tracy M. Hodgson


American Journal of Physiology-regulatory Integrative and Comparative Physiology | 1993

Total autonomic blockade eliminates the attenuated pressor response to angiotensin II in pregnant rats

Tina Hines; Marshall D. Lindheimer; W. M. Barron


American Journal of Physiology-regulatory Integrative and Comparative Physiology | 2000

Effect of cardiac receptor stimulation on renal vascular resistance in the pregnant rat

Tina Hines; William A. Herzer


Archive | 2011

What Does the Brain Know About Blood Pressure During Pregnancy

Tina Hines


Archive | 2011

Does Increased Blood Volume “Stretch” the Heart During Pregnancy?

Tina Hines

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Steven W. Mifflin

University of Texas Health Science Center at San Antonio

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Glenn M. Toney

University of Texas Health Science Center at San Antonio

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Marianne Woody

University of Pittsburgh

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