Review
Copyright ©The Author(s) 2021.
World J Diabetes. Jul 15, 2021; 12(7): 954-974
Published online Jul 15, 2021. doi: 10.4239/wjd.v12.i7.954
Table 1 Ejaculatory behavior in diabetic animals
Ref.
Animal model
Effects observed on ejaculatory function
Type of treatment and response
Sach et al[31], 1982STZ-induced diabetic ratsNo sexual performance difference between diabetic and control rats.
Clark[32], 1995STZ-induced diabetic ratsNo sexual performance difference between diabetic and control rats.
Scarano et al[33], 2006STZ-induced diabetic ratsNo sexual performance differences in EL after 15 d.
Steger et al[34], 1990STZ-induced diabetic ratsProlonged EL (DE or AE)Delayed insulin replacement (4 wk) cannot prevent ejaculatory dysfunction.
Murray et al[35], 1992 Diabetic BB/WOR ratsProlonged EL (DE or AE) after 28 wk
McVary et al[36], 1997Diabetic BB/WOR ratsProlonged EL (DE or AE) after 40 wk, reduced number of ejaculations.
No differences regarding serum testosterone, FSH, and LH.
Ebiko et al[37], 2006STZ-induced diabetic ratsDeteriorated spontaneous seminal emission after 5 wk.Early insulin replacement can prevent ejaculatory dysfunction.
In 15 and 30 wk, occurrence of SSE was almost completely suppressed.
Yonezawa et al[38], 2009Streptozotocin (STZ)-induced diabetic ratsDeteriorated spontaneous seminal emission after 5 wk.Early insulin replacement can prevent ejaculatory dysfunction. Once dysfunction occurs, insulin cannot restore it.
Decreased ejaculated semen and decreased seminal vesicle fluid.
Suresh et al[39], 2012STZ-induced diabetic ratsProlonged EL suggesting DE. -Low serum testosterone.Mucuna pruriens showed recovery of EL.
De et al[40], 2016STZ-induced diabetic ratsProlonged EL suggesting DE. -Low serum testosterone.l-Norvaline (arginase inhibitor) reduced EL.
Shi et al[41], 2017STZ-induced diabetic ratsProlonged EL suggesting DE.Lycium barbarum polysaccharide reduced EL.
Li et al[42], 2019STZ-induced diabetic ratsProlonged EL at 62 d suggesting DE. No effect of vitexin (herb) on EL.
Lert-Amornpat et al[43], 2016STZ-induced diabetic ratsLack of copulatory behavior suggesting AE.Kaempferia parviflora (herb) showed recovery of EL.
Fernández-Collazo et al[44], 1970Rats with subtotal pancreatectomyThey did not AE.
Hassan et al[45], 1993STZ-induced diabetic ratsRats exhibited AE in diabetics. -Low serum testosterone.Sabeluzole treatment was beneficial to correct dysfunction.
Pontes et al[46], 2011STZ-induced diabetic ratsLack of the sperms ejaculated into the uterus. -Low serum testosterone.Testosterone supplement did not restore ejaculatory function.
Ghaheri et al[47], 2018 STZ-induced diabetic ratsShorten EL after 28 d suggesting PE.Stevia Bertoni extract improved EL.
Minaz et al[48], 2019STZ-induced diabetic ratsShorten EL after 8 wk suggesting PE. -Low serum testosterone.Inhibition of soluble epoxide hydrolase prolonged EL.
Table 2 Possible pathophysiological mechanisms underlying ejaculatory dysfunctions in diabetes mellitus (animal studies)
Ref.
Postulated mechanisms
Possible ejaculatory dysfunction
McVary et al[36], Yagihashi et al[49]Pathologic changes in the nerve supply of seminal tract due to accumulation of AGE increased ROS (sympathetic neuropathy)Prolongation of EL
Tomlinson et al[50], Longhurst et al[51]Decreased number of synapses in thoracic gangliaReduction of the numbers of ejaculations
Kaschube et al[52], Kamata et al[53]Axonopathy in postganglionic sympathetic fibersDisturbed the emission phase
Güneş et al[54], Tsounapi et al[55]Neuropathic changes in hypogastric nerve and motor pudendal nerve fibersDisruption of the ejection phase
Tomlinson et al[50], Longhurst et al[51], Kaschube et al[52], Kamata et al[53], Güneş et al[54]Hypersensitivity (supersensitivity) of seminal tract smooth muscles to exogenous noradrenalineReduction of EL
Sakai et al[56], Sakai et al[57]Hyperactivity of Ca channels in smooth musclesReduction of EL
Ebiko et al[37], Yonezawa et al[38]Yagihashi et al[49], Torimoto et al[60] Sympathetic neuropathy and external urethral sphincter relaxation dysfunctionDisruption of bladder neck closure
Disruption of AE
Sandrini et al[61], Abraham et al[62]Changes in serotonergic transmissionReduction or prolongation of EL
Seethalakshmi et al[71], Wolfe et al[72]Impaired hypothalamic or pituitary signalingDecreased sexual performance
Oksanen et al[73], Sudha et al[74]Deficiency of gonadotropic hormones or blockade of their actionsDecreased sexual performance
Ballester et al[75], Neirijnck et al[76]Decrease in number and function of Leydig cellsDecreased sexual performance
Neirijnck et al[76]Defective testicular steroidogenesisDecreased sexual performance
Kühn-Velten et al[64], Anderson et al[65], Ricci et al[66], Murray et al[67], Cameron et al[68], Ohta et al[69], Nakane et al[70]Reduced serum levels of LH and testosterone (T)Decreased sexual performance
McVary et al[36], Minaz et al[48], Steger et al[85], Al-Roujayee et al[86], Kashif et al[87]Reduced libidoDecreased sexual performance, decreased mount frequency, and reduced EL
Hassan et al[45], Steger et al[77]Reduced reproductive organ weightExact Effects on ejaculation still unknown
Table 3 Possible pathophysiological mechanisms underlying ejaculatory dysfunctions in diabetes mellitus (human studies)
Ref.
Possible cause
Outcome
Premature ejaculation
Culha et al[88]Anxiety Among PE patients with DM, 15% had anxiety
Culha et al[88], Khan et al[89]DepressionAmong PE patients with DM, 16.9% had depression
Depression score Significantly higher among diabetic-related PE patients
Khan et al[89], Malavige et al[90]Genetic and racial factorsLong tri-nucleotide repeats of the androgen receptor are related to the lowest IELT (PE)
Asian men reported higher diabetic PE than European counterparts
El-Sakka[91]Diabetic condition, duration of MD > 10 yr of diabetes were 2.7 times as likely to report diabetic-related PE
Poor glycemic controlPoor glycemic control were 9.6 times as likely to report PE
El-Sakka[91], Majzoub et al[92]Having diabetic-related -erectile dysfunction (ED) and Cardiovascular diseasesSignificant association between PE and cardiovascular diseases
Malavige et al[93], Malavige et al[90]ED showed a significantly higher incidence of PE
Olamoyegun et al[94]ED was strongly associated with PE odds ratio = 4.4
El-Sakka[91]Having diabetic –related neuropathyIt is not associated with PE
Khan et al[89]Total serum testosteroneSignificantly higher among type 2 diabetic-related PE patients
Owiredu et al[95]It correlates negatively with short IELT among type 2 DM
Bellastella et al[96]No significant difference in type 1 diabetes
Delayed ejaculation and anejaculation
Corona et al[97]DepressionSevere depressive symptoms are associated with ejaculatory problems in DM
Ellenberg et al[25] , La Vignera et al[27] , Dinulovic et al[98]Progressive autonomic neuropathy of the sympathetic nervesDenervation leads to weak or loss of VD and SV peristaltic movements
Dunsmuir et al[99], Condorelli et al[100]Abnormal inflammatory responses lead to alteration of the VD and SV peristaltic movements
La Vignera et al[101] , Pop-Busui et al[102]Delayed /poor emission
Absent emission
Haddad et al[26], Culver et al[103]Calcification of vas deferens and seminal vesiclesLoss of their ability to contract as the smooth muscle is replaced by fibrotic, calcified tissue
Tsuno et al[104]Delayed/poor emission
Hylmarova et al[29] , Corona et al[81]HypogonadismNo association between serum testosterone levels and ejaculation time in men self-reporting DE including diabetic patients
Paduch et al[82], Gianatti et al[105]
Morgentaler et al[106]T replacement is not associated with improvement in DE or AE
Burke et al[107], Corona et al[108]Low sexual desireDM is significantly associated with low sexual desire
Corona et al[109]DE and AE are associated with low sexual desire
Retrograde ejaculation
Klebanow et al[110]Diabetic neuropathy (T10-L3)Intact vasal and seminal vesicle contraction but incomplete simultaneous bladder neck closure leads to partial RE
Greene et al[111]Intact vasal and seminal vesicle contraction and simultaneous complete lack of bladder neck closure leads to complete RE
Koyanagi[112]External urethral sphincter relaxation dysfunction (triple parasympathetic-sympathetic-somatic innervation)Lack of active external urethral sphincter relaxation leads to disruption of antegrade ejaculation
Cao et al[113]
Table 4 Assessment steps in the evaluation of diabetes mellitus-related ejaculatory dysfunctions
History
Asking about the period from vaginal intromission to ejaculation (intravaginal ejaculatory latency time).
Is the patient unable to advance his ejaculatory response?
Is the patient or his partner distressed or bothered by the situation?
Is the symptom occurring since the first sexual experience or occurring after a period of normal ejaculatory performance?
Onset and duration of the symptom.
Is the symptom occurring on every/almost every attempt and with every partner?
Presence or absence of premonitory ejaculatory sensation.
The duration of thrusting before the suspension of intercourse.
Reasons for delay of intercourse (e.g., fatigue, loss of erection, a sense of ejaculatory futility, or partner request).
Presence of post-coital self- or partner-assisted masturbation.
Psychogenic anejaculation/anorgasmia can be suspected when there is a history of nocturnal emission.
Patient's ability to get an erection, relax, sustain, and heighten sexual arousal.
Exclude anorgasmia by asking about lack of orgasm.
Whether orgasm is present but there is a lack of external ejaculation that may indicate retrograde ejaculate.
Feeling before ejaculation/orgasm: The inadequate combination of “friction and fantasy” may exacerbate DE.
Intercourse frequency.
Presence of other sexual dysfunctions such as ED (ability to initiate or maintain an erection), low libido.
Other symptoms of hypogonadism (such as lack of energy, depressed mood).
Masturbation habits
The life events/circumstances related to the complaint.
Sexual communication abilities.
Paraphilic inclinations/interests (may be related to DE and anejaculation).
Cultural or religious beliefs (if any).
History of a psychiatric disorder (may be the etiologic factor).
History of previous treatment for this symptom.
History of neurologic disorders, spinal cord injury, medical diseases, trauma, abdominal/pelvic operations, drug intake, or pelvic radiotherapy.
History of pelvic or testicular pain (may indicate inflammation).
History of dysuria, burning micturition, or any urinary symptom (indicate inflammation).
Clinical examination
Signs of diabetic complications and co-morbidities.
Signs of hypogonadism.
Rule out systemic disorders that contribute to ejaculation dysfunction as neurological impairment, endocrine/ urological diseases.
Examination for secondary sexual characteristics, penile and testicular abnormalities.
Examination of the epididymis, and vas deferens on each side.
PR examination to determine the prostate size, anal sphincter tone, and quality of the bulbocavernosus reflex.
The cremasteric reflex: measures intact L1-2 spinal segments, also mediating emission and psychogenic erection.
Perineal reflexes (bulbocavernosus and anal reflex) mediated by sacral segments, also mediating reflex erection (for intact S2–4 pathway).
Examination of pinprick and temperature sensations in the saddle area (perineal) and glans penis for healthy sacral cord segments.
Inability to feel testicular squeeze: measures the integrity of T11 to T12 spinal nerves via the sympathetic nervous system.
Examination of lower abdominal cutaneous reflex: measures intact Th11-12.
Penile biothesiometry.
Investigations
Blood levels of glucose, HbA1c, serum testosterone, thyrotropin, and prolactin to exclude other endocrine disorders.
Post-masturbation first-void urine if we suspect retrograde ejaculation to search for spermatozoa and fructose content to confirm retrograde ejaculate
Microbiological examination of expressed prostatic secretion and urine to verify or exclude associated genital infections.
Urine cytology to exclude bladder cancer
Serum prostate-specific antigen to exclude prostate cancer
Neurophysiologic investigations (bulbocavernosus evoked response and dorsal nerve somatosensory evoked-potentials): If there is clinical evidence of neurologic lesions. These tests are little used in clinical practice and usually do not affect management.
Trans-rectal ultrasound examination if we suspect ejaculatory duct obstruction, prostatic or seminal vesicle abnormalities or stones.
CT or MRI scans to assess pelvic anatomy if we suspect major pelvic lesions.
Table 5 Studies involving medical treatment for reversal of diabetic retrograde ejaculation
Ref.
Dosage
Ejaculation after
n
No. of successes
Ejaculate volume (ml)
Sperm count (106/m)
Sperm motility (%)
Brompheniramine
Andaloro et al[152]16 mg/d p.o.12 h11UnclearUnclearUnclear
Budd[153]16 mg/d p.o.3 d11UnclearUnclearUnclear
Chlorpheniramine + phenylpropanalamine
Stewart et al[154]50 mg/d p.o.Unclear114.5NormalNormal
Ephedrine
Gilja et al[155]50 mg/d p.o.4 wk173UnclearUnclearUnclear
Arafa et al[156]120 mg twice/d14 d2311UnclearUnclearUnclear
Shoshany et al[157]60 mg/6 h the day before test + 2 doses on test day At the test641.5Unclear17.8
Imipramine
Brooks et al[158]75 mg/d p.o.1 wk2231.7233
Okada et al[159]25-150 mg/dUnclear73UnclearUnclearUnclear
Gilja et al[155]75 mg/d p.o.4 wk142UnclearUnclearUnclear
Eppel et al[160]50 mg/d p.o.5 d3382050
Arafa et al[156]50 mg/d p.o14 d2310UnclearUnclearUnclear
Imramine + pseudoepherine
Arafa et al[156]50 + 120 mg/d14 d2316UnclearUnclearUnclear
Amoxapine
Hibi et al[161]50 mg/d1 mo110.221353
Table 6 Semen parameters of studies recovering sperms from alkalized urine in diabetic premature ejaculation patients
Ref.
Medium installed
Post-masturbatory retrieval
No. of patients
Total sperm count (106)
Total sperm motility (%)
Pregnancies
Brassesco et al[163]NaHCO3 4 gVoiding391283
Templeton et al[162]NaHCO3Voiding1Unclear2–210
Shangold et al[164]NaHCO3 1.6 gVoiding130–24005