Pedro Corral

Mr. Pedro Corral

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Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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5 October 2020 in Nutrients
Verified
Journal Article
Open access
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TBTengfei Bian
Tengfei Bian
PCPedro Corral
Pedro Corral
YWYuzhi Wang
Yuzhi Wang
JBJordy Botello
Jordy Botello
RKRick Kingston
Rick Kingston
CXCheng-Guo Xing
Cheng-Guo Xing
Kava beverages are typically prepared from the root of Piper methysticum. They have been consumed among Pacific Islanders for centuries. Kava extract preparations were once used as herbal drugs to treat anxiety in Europe. Kava is also marketed as a dietary supplement in the U.S. and is gaining popularity as a recreational drink in Western countries. Recent studies suggest that kava and its key phytochemicals have anti-inflammatory and anticancer effects, in addition to the well-documented neurological benefits. While its beneficial effects are widely recognized, rare hepatotoxicity had been associated with use of certain kava preparations, but there are no validations nor consistent mechanisms. Major challenges lie in the diversity of kava products and the lack of standardization, which has produced an unmet need for quality initiatives. This review aims to provide the scientific community and consumers, as well as regulatory agencies, with a broad overview on kava use and its related research. We first provide a historical background for its different uses and then discuss the current state of the research, including its chemical composition, possible mechanisms of action, and its therapeutic potential in treating inflammatory and neurological conditions, as well as cancer. We then discuss the challenges associated with kava use and research, focusing on the need for the detailed characterization of kava components and associated risks such as its reported hepatotoxicity. Lastly, given its growing popularity in clinical and recreational use, we emphasize the urgent need for quality control and quality assurance of kava products, pharmacokinetics, absorption, distribution, metabolism, excretion, and foundational pharmacology. These are essential in order to inform research into the molecular targets, cellular mechanisms, and creative use of early stage human clinical trials for designer kava modalities to inform and guide the design and execution of future randomized placebo controlled trials to maximize kava’s clinical efficacy and to minimize its risks.

11 June 2020 in Chemical Research in Toxicology
Verified
Journal Article
Closed access
QHQi Hu
Qi Hu
PCPedro Corral
Pedro Corral
SNSreekanth C. Narayanapillai
Sreekanth C. Narayanapillai
PLPablo Leitzman
Pablo Leitzman
PUPramod Upadhyaya
Pramod Upadhyaya
CXCheng-Guo Xing
Cheng-Guo Xing

11 November 2019 in Planta Medica
Verified
Journal Article
Closed access
PDF file
JBJordy F. Botello
Jordy F. Botello
PCPedro Corral
Pedro Corral
TBTengfei Bian
Tengfei Bian
CXCheng-Guo Xing
Cheng-Guo Xing
Kava, the extract of the roots of Piper methysticum, has been traditionally consumed in the South Pacific islands for its natural relaxing property. Epidemiological data suggests that kava consumption may reduce human cancer risk, and in vitro and in vivo models suggest chemopreventive potential against carcinogen-induced tumorigenesis. Therefore, knowledge about its molecular mechanisms and responsible ingredient(s) for these beneficial properties will better guide kavaʼs use for the management of these disorders. Psychological stress typically results in increased production of stress hormones, such as norepinephrine (NE), which activate adrenergic receptors (ARs). Psychological stress has also been associated with increased cancer incidence and poor clinical outcomes in cancer patients. Mechanistically, binding of NE to ARs induces intracellular calcium influx, which activates downstream signaling pathways involved in both stress and cancer development. In this study, we characterized the effect of kava and its components, 3 fractions and 6 major kavalactones, on NE-induced intracellular calcium influx in H1299, a human non-small cell lung carcinoma cell line. Results show that kava extract effectively inhibits NE-mediated intracellular calcium influx in H1299 cells, potentially through antagonizing β-AR signaling. This inhibitory activity is recapitulated by the major kavalactones in kava. Among the 6 major kavalactones, DHK demonstrated the best potency. Taken together, our study suggests a novel mechanism through which kava and its ingredients potentially offer the anxiolytic and cancer-preventive activity.

1 January 2020 in Bioorganic & Medicinal Chemistry Letters
Verified
Journal Article
Closed access
PCPedro Corral
Pedro Corral
JBJordy F. Botello
Jordy F. Botello
CXCheng-Guo Xing
Cheng-Guo Xing