β-caryophyllene improves sexual performance via modulation of crucial enzymes relevant to erectile dysfunction in rats

被引:0
作者
Stephen A. Adefegha
Ganiyu Oboh
Elijah O. Olopade
机构
[1] Federal University of Technology,Functional Foods and Nutraceuticals Unit, Department of Biochemistry
来源
Toxicological Research | 2021年 / 37卷
关键词
β-caryophyllene; Sildenafil citrate; Paroxetine; Enzymes; Erectile dysfunction;
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学科分类号
摘要
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.
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页码:249 / 260
页数:11
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  • [1] Biri TH(2003)Cavernosal tissue nitrite, nitrate, malondialdehyde and glutathione levels in diabetic and non-diabetic erectile dysfunction Int J Androl 26 250-254
  • [2] Onaran M(2005)Physiology of penile erection and pathophysiology of erectile dysfunction Urol Clin North Am 32 379-395
  • [3] Dean RC(2003)Endothelial dysfunction in erectile dysfunction: role of the endothelium in erectile physiology and disease J Androl 24 S17-S37
  • [4] Lue TF(2017)A novel experimental model of erectile dysfunction in rats with heart failure using volume overload PLoS ONE 12 0187083-397
  • [5] Bivalacqua TJ(2006)Antidepressants and sexual dysfunction Acta Psychiatr Scand 114 384-94
  • [6] Usta MF(1992)Nitric oxide as a mediator of relaxation of the corpus cavernosum in response to nonadrenergic, noncholinergic neurotransmission, New England J Med Surg Collat Branches Sci 326 90-685
  • [7] Champion HC(2007)Determination of adenosine effects and adenosine receptors in murine corpus cavernosum J Pharm Exp Ther 322 678-591
  • [8] Silva FH(2008)Effect of caffeine on erectile function via up-regulating cavernous cyclic guanosine monophosphate in diabetic rats J Androl 29 586-419
  • [9] Veiga FJR(2013)Phosphodiesterase-5 (PDE5) inhibitors in the management of erectile dysfunction Pharm Therap 38 407-431
  • [10] Mora AG(1998)Endogenous neurotransmitters mediating penile erection Br J Urol 81 424-3564