Matyanga Celia M J, Morse Gene D, Gundidza Mazuru, Ndawana Billy, Reid Andrew, Chitsike Inam, Nhachi Charles F B
Department of Clinical Pharmacology, College of Health Sciences, University of Zimbabwe, Harare, Zimbabwe.
Center for Integrated Global Biomedical Sciences; School of Pharmacy and Pharmaceutical Sciences, University at Buffalo, Buffalo, New York, United States.
J Herb Med. 2021 Apr;26. doi: 10.1016/j.hermed.2021.100427. Epub 2021 Jan 8.
African potato () is used against HIV to enhance immune-function, although no studies have evaluated its use in HIV infected individuals on combination antiretroviral therapy. The study aimed to evaluate the acute effects of orally administered hypoxoside, a constituent of African potato, on the hepatic and renal function in HIV infected individuals on tenofovir disoproxil fumarate/ lamivudine/ efavirenz regimen.
This was an open-label, two-period, fixed-sequence, pre-post test study, pilot design. Ethical approval was obtained from Medical Research Council of Zimbabwe (MRCZ A/2045) and Medicines Control Authority of Zimbabwe (MCAZ CT134/2016). Blood samples were collected before and after administration of African potato tablets. Tablets were administered orally once daily at 15mg/ kg hypoxoside for 10 days. Hepatic function tests (ALT, AST, ALP, GGT, albumin, total/ direct bilirubin); renal function tests (eGFR, blood urea nitrogen, creatinine), serum electrolytes (sodium, potassium, chloride) were assayed. STATA was used for statistical analysis.
Twenty-six participants were enrolled (85% female). Median age (range) was 43 (28-52) years. Most had overweight Body Mass Index (46%) and were married (54%). No statistical difference was noted during hypoxoside for AST/ ALT/ ALP/ GGT/ albumin/ bilirubin. There were no changes in creatinine/ eGFR/ electrolytes. A mean significant increase in total protein (p=0.04) and decrease in blood urea nitrogen (p=0.04) were noted.
Short-term exposure to hypoxoside from African potato appeared safe and was not associated with clinically significant changes in hepatic, renal function tests/electrolytes. There is further need to evaluate extent of systemic exposure during long-term use in a larger population.
非洲土豆( )被用于对抗艾滋病毒以增强免疫功能,尽管尚无研究评估其在接受联合抗逆转录病毒治疗的艾滋病毒感染者中的应用。本研究旨在评估口服非洲土豆的成分次黄苷对接受富马酸替诺福韦二吡呋酯/拉米夫定/依非韦伦方案治疗的艾滋病毒感染者肝脏和肾脏功能的急性影响。
这是一项开放标签、两阶段、固定序列、前后测试的先导性研究。获得了津巴布韦医学研究理事会(MRCZ A/2045)和津巴布韦药品管理局(MCAZ CT134/2016)的伦理批准。在服用非洲土豆片剂前后采集血样。片剂以每天15mg/kg次黄苷的剂量口服给药,持续10天。检测肝功能指标(谷丙转氨酶、谷草转氨酶、碱性磷酸酶、γ-谷氨酰转肽酶、白蛋白、总胆红素/直接胆红素);肾功能指标(估算肾小球滤过率、血尿素氮、肌酐),血清电解质(钠、钾、氯)。使用STATA进行统计分析。
招募了26名参与者(85%为女性)。中位年龄(范围)为43(28 - 52)岁。大多数人体重指数超重(46%)且已婚(54%)。在服用次黄苷期间,谷丙转氨酶/谷草转氨酶/碱性磷酸酶/γ-谷氨酰转肽酶/白蛋白/胆红素方面未发现统计学差异。肌酐/估算肾小球滤过率/电解质无变化。总蛋白平均显著增加(p = 0.04),血尿素氮降低(p = 0.04)。
短期接触非洲土豆中的次黄苷似乎是安全的,且与肝脏、肾脏功能测试/电解质的临床显著变化无关。进一步需要在更大规模人群中评估长期使用期间的全身暴露程度。