Adefegha Stephen A, Oboh Ganiyu, Olopade Elijah O
Functional Foods and Nutraceuticals Unit, Department of Biochemistry, Federal University of Technology, P.M.B. 704, Akure, 340001 Nigeria.
Toxicol Res. 2020 Aug 20;37(2):249-260. doi: 10.1007/s43188-020-00061-2. eCollection 2021 Apr.
This study sought to investigate the effect of β-caryophyllene (BCP) on sexual performance, crucial enzymes linked to erectile function as well as lipid peroxidation in the penile tissue of paroxetine (PD)-induced rats. Animals were randomly divided into ten groups of five animals each: normal control (NC), BCP (10 mg/kg), BCP (20 mg/kg), sildenafil citrate (SD) (20 mg/kg), BCP + SD (20 mg/kg), PD (20 mg/kg), PD + BCP (10 mg/kg), PD + BCP (20 mg/kg), PD + SD (20 mg/kg) and PD + BCP (20 mg/kg) + SD (20 mg/kg). Oral administration of 20 mg/kg body weight of PD for the first 7 days was done while treatment with BCP and SD were performed between 8 and 14 days prior to euthanasia. The sexual performance study revealed that PD caused erectile dysfuction. Elevated activities of phosphodiesterase-5' (PDE-5'), arginase, adenosine deaminase (ADA), acetylcholinesterase (AChE) and angiotensin-I converting enzyme (ACE) as well as lipid peroxidation level were observed in PD-induced rats when compared to the NC group. However, treatment with sildenafil and/ or β-Caryophyllene significantly reduced the activities of AChE, PDE-5', arginase, ADA, and ACE in penile tissues of PD-induced rats. In addition, co-administration of β-caryophyllene and sildenafil citrate showed better modulatory effects. Thus, β-caryophyllene could represent a potential nutraceutical in the management of erectile dysfunction.
本研究旨在探讨β-石竹烯(BCP)对帕罗西汀(PD)诱导的大鼠阴茎组织中性功能、与勃起功能相关的关键酶以及脂质过氧化的影响。动物被随机分为十组,每组五只:正常对照组(NC)、BCP(10毫克/千克)、BCP(20毫克/千克)、枸橼酸西地那非(SD)(20毫克/千克)、BCP + SD(20毫克/千克)、PD(20毫克/千克)、PD + BCP(10毫克/千克)、PD + BCP(20毫克/千克)、PD + SD(20毫克/千克)和PD + BCP(20毫克/千克)+ SD(20毫克/千克)。在最初7天口服给予体重20毫克/千克的PD,而在安乐死之前的第8至14天用BCP和SD进行治疗。性功能研究表明,PD导致勃起功能障碍。与NC组相比,在PD诱导的大鼠中观察到磷酸二酯酶-5'(PDE-5')、精氨酸酶、腺苷脱氨酶(ADA)、乙酰胆碱酯酶(AChE)和血管紧张素-I转换酶(ACE)的活性升高以及脂质过氧化水平升高。然而,用西地那非和/或β-石竹烯治疗可显著降低PD诱导的大鼠阴茎组织中AChE、PDE-5'、精氨酸酶、ADA和ACE的活性。此外,β-石竹烯和枸橼酸西地那非联合给药显示出更好的调节作用。因此,β-石竹烯可能是治疗勃起功能障碍的一种潜在营养保健品。