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Dive into the research topics where Bonita L. Funk is active.

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Featured researches published by Bonita L. Funk.


Circulation | 1999

Subtype Specific Regulation of Human Vascular α1-Adrenergic Receptors by Vessel Bed and Age

Xiaowen L. Rudner; Dan E. Berkowitz; John V. Booth; Bonita L. Funk; Kelli L. Cozart; Elizabeth B. D'amico; Habib E. El-Moalem; Stella O. Page; Charlene D. Richardson; Bradford Winters; Leo Marucci; Debra A. Schwinn

Background—α1-adrenergic receptors (α1ARs) regulate blood pressure, regional vascular resistance, and venous capacitance; the exact subtype (α1a, α1b, α1 d) mediating these effects is unknown and varies with species studied. In order to understand mechanisms underlying cardiovascular responses to acute stress and chronic catecholamine exposure (as seen with aging), we tested two hypotheses: (1) human α1AR subtype expression differs with vascular bed, and (2) age influences human vascular α1AR subtype expression. Methods and Results—Five hundred vessels from 384 patients were examined for α1AR subtype distribution at mRNA and protein levels (RNase protection assays, ligand binding, contraction assays). Overall vessel α1AR density is 16±2.3fmol/mg total protein. α1aAR predominates in arteries at mRNA (P<0.001) and protein (P<0.05) levels; all 3 subtypes are present in veins. Furthermore, α1AR mRNA subtype expression varies with vessel bed (α1a higher in splanchnic versus central arteries, P<0.05); competiti...


Anesthesiology | 1998

Acute depression of myocardial β-adrenergic receptor signaling during cardiopulmonary bypass. Impairment of the adenylyl cyclase moiety

John V. Booth; Kevin P. Landolfo; Lynn C. Chesnut; Elliott Bennett-Guerrero; Mark A. Gerhardt; Darryl M. Atwell; Habib E. El-Moalem; Mark Stafford Smith; Bonita L. Funk; Cynthia M. Kuhn; Madan M. Kwatra; Debra A. Schwinn

BACKGROUND Previously the authors showed that myocardial beta-adrenergic (betaAR) function is reduced after cardiopulmonary bypass (CPB) in a canine model Whether CPB results in similar effects on betaAR function in adult humans is not known. Therefore the current study tested two hypotheses: (1) That myocardial betaAR signaling is reduced in adult humans after CPB, and (2) that administration of long-term preoperative betaAR antagonists prevents this process. METHODS After they gave informed consent, 52 patients undergoing aortocoronary surgery were enrolled. Atrial biopsies were obtained before CPB and immediately before discontinuation of CPB. Plasma catecholamine concentrations, myocardial betaAR density, and functional responsiveness (basal, isoproterenol, zinterol, sodium fluoride, and manganese-stimulated adenylyl cyclase activity) were assessed. RESULTS Catecholamine levels increased significantly during CPB (P < 0.005). Myocardial betaAR adenylyl cyclase coupling decreased during CPB, as evidenced by a 21% decrease in isoproterenol-stimulated adenylyl cyclase activity (750 [430] pmol cyclic adenosine monophosphate per milligram total protein 15 min before CPB compared with 540 [390] at the end of CPB, P = 0.0062, medians [interquartile range]) despite constant betaAR density. Differential activation along the betaAR signal transduction cascade localized the defect to the adenylyl cyclase moiety. Administration of long-term preoperative betaAR antagonists did not prevent acute CPB-induced myocardial betaAR dysfunction. CONCLUSIONS These data indicate that the myocardial adenylyl cyclase response to betaAR agonists decreases acutely in adults during aortocoronary surgery requiring CPB, regardless of whether long-term preoperative betaAR antagonists are administered. The mechanism underlying acute betaAR dysfunction appears to be direct impairment of the adenylyl cyclase moiety. Similar increases in manganese-stimulated activity before and at the end of CPB show preserved adenylyl cyclase catalytic activity, suggesting that other mechanisms (such as decreased protein levels or altered isoform expression or function) may be responsible for decreased adenylyl cyclase function.


Journal of Alzheimer's Disease | 2016

The Effect of Propofol Versus Isoflurane Anesthesia on Human Cerebrospinal Fluid Markers of Alzheimer's Disease: Results of a Randomized Trial

Miles Berger; Jacob W. Nadler; Allan H. Friedman; David L. McDonagh; Ellen R. Bennett; Mary Cooter; Wenjing Qi; Daniel T. Laskowitz; Vikram Ponnusamy; Mark F. Newman; Leslie M. Shaw; David S. Warner; Joseph P. Mathew; Michael L. James; Senthil Radhakrishnan; James H. Carter; Shivanandan Lad; Ali R. Zomorodi; John H. Sampson; Takanori Fukushima; Owoicho Adogwa; Karen Clemmons; Carlos Conde; Omowunmi Olaleye; Naraida Balajonda; Jhoanna Aquino; Bonita L. Funk; Yi-Ju Li; William D. White

BACKGROUND Preclinical studies have found differential effects of isoflurane and propofol on the Alzheimers disease (AD)-associated markers tau, phosphorylated tau (p-tau) and amyloid-β (Aβ). OBJECTIVE We asked whether isoflurane and propofol have differential effects on the tau/Aβ ratio (the primary outcome), and individual AD biomarkers. We also examined whether genetic/intraoperative factors influenced perioperative changes in AD biomarkers. METHODS Patients undergoing neurosurgical/otolaryngology procedures requiring lumbar cerebrospinal fluid (CSF) drain placement were prospectively randomized to receive isoflurane (n = 21) or propofol (n = 18) for anesthetic maintenance. We measured perioperative CSF sample AD markers, performed genotyping assays, and examined intraoperative data from the electronic anesthesia record. A repeated measures ANOVA was used to examine changes in AD markers by anesthetic type over time. RESULTS The CSF tau/Aβ ratio did not differ between isoflurane- versus propofol-treated patients (p = 1.000). CSF tau/Aβ ratio and tau levels increased 10 and 24 h after drain placement (p = 2.002×10-6 and p = 1.985×10-6, respectively), mean CSF p-tau levels decreased (p = 0.005), and Aβ levels did not change (p = 0.152). There was no interaction between anesthetic treatment and time for any of these biomarkers. None of the examined genetic polymorphisms, including ApoE4, were associated with tau increase (n = 9 polymorphisms, p > 0.05 for all associations). CONCLUSION Neurosurgery/otolaryngology procedures are associated with an increase in the CSF tau/Aβ ratio, and this increase was not influenced by anesthetic type. The increased CSF tau/Aβ ratio was largely driven by increases in tau levels. Future work should determine the functional/prognostic significance of these perioperative CSF tau elevations.


Anesthesia & Analgesia | 2002

Serum creatinine patterns in coronary bypass surgery patients with and without postoperative cognitive dysfunction

Madhav Swaminathan; Brian J. McCreath; Barbara Phillips-Bute; Mark F. Newman; Joseph P. Mathew; Peter K. Smith; James A. Blumenthal; Mark Stafford-Smith; Hilary P. Grocott; Steven E. Hill; J. G. Reves; Debra A. Schwinn; David S. Warner; Malissa Harris; Jerry Kirchner; Brenda S. Mickley; Mandy Barnes; Elizabeth H. Carver; Bonita L. Funk; E. D. Derilus; Jason Hawkins; Terri Moore; Chonna Campbell; Amanda Cheek; Tanya Kagarise; Tori Latiker; Erich Lauff; Melanie Tirronen; Regina DeLacy; William Hansley

Renal dysfunction is common after coronary artery bypass graft (CABG) surgery. We have previously shown that CABG procedures complicated by stroke have a threefold greater peak serum creatinine level relative to uncomplicated surgery. However, postoperative creatinine patterns for procedures complicated by cognitive dysfunction are unknown. Therefore, we tested the hypothesis that postoperative cognitive dysfunction is associated with acute perioperative renal injury after CABG surgery. Data were prospectively gathered for 282 elective CABG surgery patients. Psychometric tests were performed at baseline and 6 wk after surgery. Cognitive dysfunction was defined both as a dichotomous variable (cognitive deficit [CD]) and as a continuous variable (cognitive index). Forty percent of patients had CD at 6 wk. However, the association between peak percentage change in postoperative creatinine and CD (parameter estimate = −0.41;P = 0.91) or cognitive index (parameter estimate = −1.29;P = 0.46) was not significant. These data indicate that postcardiac surgery cognitive dysfunction, unlike stroke, is not associated with major increases in postoperative renal dysfunction.


Anesthesiology | 1998

Acute depression of myocardial beta-adrenergic receptor signaling during cardiopulmonary bypass: impairment of the adenylyl cyclase moiety. Duke Heart Center Perioperative Desensitization Group.

John V. Booth; Kevin P. Landolfo; Lynn C. Chesnut; Elliott Bennett-Guerrero; Mark A. Gerhardt; Darryl M. Atwell; Habib E. El-Moalem; Mark Stafford Smith; Bonita L. Funk; Cynthia M. Kuhn; Madan M. Kwatra; Debra A. Schwinn


Anesthesia & Analgesia | 2004

Metoprolol and Coronary Artery Bypass Grafting Surgery: Does Intraoperative Metoprolol Attenuate Acute -Adrenergic Receptor Desensitization During Cardiac Surgery?

John V. Booth; Erin E. Ward; Kelly C. Colgan; Bonita L. Funk; Habib E. El-Moalem; Michael P. Smith; Carmelo A. Milano; Peter K. Smith; Mark F. Newman; Debra A. Schwinn


Circulation | 1998

Acute myocardial beta-adrenergic receptor dysfunction after cardiopulmonary bypass in patients with cardiac valve disease. Duke Heart Center Perioperative Desensitization Group.

Mark A. Gerhardt; John V. Booth; Lynn C. Chesnut; Bonita L. Funk; Habib E. El-Moalem; Madan M. Kwatra; Debra A. Schwinn


Circulation | 1998

Acute myocardial β-adrenergic receptor dysfunction after cardiopulmonary bypass in patients with cardiac valve disease

Mark A. Gerhardt; John V. Booth; Lynn C. Chesnut; Bonita L. Funk; Habib E. El-Moalem; Madan M. Kwatra; Debra A. Schwinn


Anesthesia & Analgesia | 1999

PERIOPERATIVE RENAL DYSFUNCTION IN CARDIAC SURGICAL PATIENTS beta ADRENERGIC RECEPTOR BLOCKADE DOES NOT INFLUENCE

C Garduno; Barbara Phillips-Bute; Bonita L. Funk; Debra A. Schwinn; M Stafford Smith


Anesthesiology | 1998

Acute Depression of Myocardial [Greek small letter beta]-Adrenergic Receptor Signaling during Cardiopulmonary Bypass: Impairment of the Adenylyl Cyclase Moiety

John V. Booth; Kevin P. Landolfo; Lynn C. Chesnut; Elliott Bennett-Guerrero; Mark A. Gerhardt; Darryl M. Atwell; Habib E. El-Moalem; Mark Stafford Smith; Bonita L. Funk; Cynthia M. Kuhn; Madan M. Kwatra; Debra A. Schwinn

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Mark A. Gerhardt

Medical University of South Carolina

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