Urethral obstruction in patients with BPO is frequently explained by exaggerated α₁-adrenergic prostate smooth muscle contraction and by prostate growth [Figure 1].[12] Both may cause bladder outlet obstruction (BOO), resulting in obstructive storage symptoms.[12] Accordingly, α₁-adrenoceptors and prostate growth are important targets for therapy of LUTS in patients with BPO.[3] In patients with OAB, irritative symptoms are caused by spontaneous, uncontrolled phasic contractions of bladder smooth muscle (detrusor overactivity, DO) [Figure 1].[4] Therefore, prevention of detrusor contraction and decreasing smooth muscle tone in the bladder is an important strategy for medical treatment of these symptoms.[4] It is now well known that relationships between LUTS, their etiology, and organ-specific context are highly variable.[5] It has been proposed that the causal relationship between BOO, maximum flow rate (Qmax), and symptom scores may be lower as previously assumed.[6]

Three subtypes of α₁-adrenoceptors are known from the lower urinary tract, designated as α_1A, α_1B, and α_1D.[78] In the human prostate, the α_1A subtype covers around 70% of the total α1-adrenoceptors population and is responsible for smooth muscle contraction.[78] Prostatic expression of α_1B-adrenoceptors is most likely confined to the glandular epithelium, while α_1D is expressed by intraprostatic blood vessels.[9] α₁-adrenoceptors in the prostate and elsewhere may occur in two phenotypes, designated as α_1A and α_1L, both belonging to the α_1A subtype.[1011] Although both are products of the same gene (Adra1A), factors deciding whether Adra1A mRNA is translated as α_1A or α_1L are still unknown.[11] It has been proposed that interaction with the binding partner CRELD1α (cysteine-rich epidermal growth factor-like domain 1α) may confer the unique pharmacological profile of α_1L to α_1A-adrenoceptors.[11] Both phenotypes show distinct pharmacological properties. A key difference is their affinity to the non-selective α₁-adrenoceptor antagonist prazosin, which is high for α_1A, but low for α_1L.[11] α_1A-adrenoceptors may also occur in the bladder, where they mediate smooth muscle contraction in the human trigonum and bladder base.[710] In animal models, the subtype distribution of α₁-adrenoceptors in the lower urinary tract may differ.[7]

It is widely accepted that beneficial effects of α-blockers in patients with obstructive LUTS are explained by smooth muscle relaxation in the prostate.[1278] In addition, it is now clear that mechanisms besides prostate smooth muscle relaxation are involved in therapeutic effects of α₁-blockers.[12] These may include actions on the bladder microcirculation, and α₁-adrenoceptors in the urothelium, in afferent nerves, or in bladder smooth muscle.[12] In fact, α₁-blockers may improve symptoms in women, in men without BPO, or in animal models, where a prostate-dependent contribution can be excluded.[8131415]

While α₁-adrenoceptors in the lower urinary tract were intensively studied at expression level, their intracellular signaling or posttranslational regulation attracted less attention.[7] Following receptor stimulation, activation of intracellular signaling cascades via receptor-associated heterotrimeric G proteins leads to contraction of prostate smooth muscle [Figure 2].[1] Activation of phospholipase C (PLC) causes formation of inositol-1,4,5-trisphosphate (IP₃) and diacylglycerol (DAG), leading to activation of myosin light chain (MLC) kinase by calcium-dependent mechanisms, and to deactivation of MLC phosphatase via protein kinase C (PKC) [Figure 2].[1] Result is an increased MLC phosphorylation, being the prerequisite for smooth muscle contraction.[1] In parallel to PLC, the monomeric GTPase RhoA is activated by G proteins.[16] RhoA activates Rho kinase, which subsequently leads to contraction by MLC phosphatase inhibition [Figure 2].[16]

Besides contraction, α₁-adrenergic Rho kinase activation in the prostate has been linked to proliferation of prostate cells and therefore to prostate growth [Figure 2].[17] In fact, an involvement of α₁-adrenoceptors in prostate growth and hyperplasia has been repeatedly suggested.[181920] However, α₁-blockers do not reduce prostate volume.[2122] Recent evidence from experimental studies unequivocally proved the existence of signal transduction by prostate α₁-adrenoceptors, which is not involved in contraction. This may be termed as “non-motoric” signaling, and comprises a panel of pathways including mitogen-activated protein kinases, Akt, and transcription factors, which are all activated by α₁-adrenoceptors in the human prostate [Figure 2].[23242526]

Different α₁-adrenoceptor antagonists (“α-blocker”) are routinely applied for treatment of obstructive symptoms.[27] Although their subtype selectivity may differ, their efficacy is similar in appropriate doses.[1027] Application of α₁-blockers still represents a gold standard for medical therapy of BPO.[27] The recent approval of silodosin in the USA and Europe reflects a high interest for α₁-blockers with improved subtype selectivity and efficacy.[102829] Before the introduction of silodosin, tamsulosin had the highest α_1A-selectivity and was the most prescribed of all available α₁-blockers.[1030] Naftopidil, which is available for therapy of obstructive symptoms in India, blocks α_1D-adrenoceptors in addition to α_1A and has a comparable efficacy to tamsulosin.[3132]

α₁-blockers cause rapid amelioration of mild to moderate symptoms, which frequently persists for several years.[3212227] However, they do not prevent the progression of benign prostate hyperplasia (BPH), as the rate of acute urinary retention, the need for invasive therapy, or serum PSA levels are not reduced by α₁-blockers.[212227] Together, this leads to application of combination therapies (α₁-blockers with 5α-reductase inhibitors) or non-medical, ablative therapies in many patients, if effects from α₁-blockers are insufficient.[27] Despite the marked improvement of symptoms by α₁-blockers, their efficacy is in fact limited. Symptom scores may be reduced 30-50% by α₁-blockers, while placebos may cause an improvement of 10-34%.[32733] Similarly, α₁-blockers enhance maximum flow rate (Qmax) by 15-40%, while increases up to 27% were observed by treatment with placebos.[32733] This points to non-adrenergic mediators of contraction, contributing to prostate smooth muscle tone in parallel to α₁-adrenoceptors. Indeed, thromboxane A2 (TXA2) induces smooth muscle contraction in the human prostate, by activation of TXA2 receptors [Figure 2].[34] Finally, the contribution of further mediators cannot be excluded.

Prostate growth in BPH depends on testosterone.[3536] Testosterone is metabolized to dihydrotestosterone (DHT) by 5α-reductases (5-AR).[3536] In the prostate, 5-AR-2 is the prevailing isoform, being located to stromal and basal cells.[3536] DHT has a 4-5 fold higher affinity for androgen receptors as testosterone.[3536] Consequently, inhibition of 5-AR by 5-AR inhibitors (5-ARI) abolishes prostate growth and reduces prostate size.[327] Therapy with 5-ARIs is applied to prevent the progression of BPH.[327] While finasteride selectively inhibits 5-AR-2, dutasteride inhibits both isoforms (5-AR-1, -2).[37] Beneficial effects of 5-ARIs become apparent 3-6 month after continuous application. Finasteride and dutasteride may reduce LUTS by 30% and prostate volume by 25%.[32737]

In rats, reduction of prostate volume can be obtained by treatment with the luteinizing hormone-releasing hormone antagonist, cetrorelix.[38] Cetrorelix is available for anti-cancer treatment. However, approval for therapy of LUTS and BPH (as a benign disease) appears unlikely, due to the inappropriate balance of benefits and side effects.

In the lower urinary tract, muscarinic receptors are of outstanding importance for smooth muscle contraction in the bladder detrusor, while their relevance for smooth muscle tone in the prostate or urethra is minor.[39] Prevailing subtypes in the human detrusor are M2 and M3, which account for 70% and 20% of the total muscarinic receptor population.[39] Contraction of detrusor smooth muscle is primarily mediated by M3 receptors.[439] Muscarinic receptors are activated by acetylcholine, released from parasympathetic nerves.[439] In addition to smooth muscle cells, muscarinic receptors in the bladder are found in the urothelium and in presynaptic nerve terminals, the latter being involved in the regulation of neurotransmitter release.[439] Interestingly, the intracellular mechanisms leading to smooth muscle contraction by muscarinic receptors in the detrusor strongly resemble those used by α₁-adrenoceptors in the prostate, as they involve IP₃/Ca²⁺, DAG/PKC, and Rho kinase.[4]

Muscarinic antagonists are routinely applied for the treatment of storage symptoms in patients with OAB.[439] Several antagonists are available, despite different affinities and subtype selectivities. Nevertheless, side effects and efficacy are similar between all substances. Although application of antimuscarinics represents the gold standard of medical OAB therapy, the efficacy may not be fully satisfactory.[4] In fact, patients adherence to the therapy is quite low: Up to 45% or more patients discontinue the therapy, due to the perception that the medication is not working.[40]

Combinations with muscarinic antagonists may be effective in patients, where monotherapy with 5-AR or α₁-blockers is insufficient. Despite initial concerns that such combinations may induce urinary retention, the combination of tolterodine with dutasteride may be effective and safe in patients with OAB and symptoms secondary to BPH.[41] Similarly, combinations of antimuscarinics with α₁-blockers have been recently addressed by clinical studies.[27]

Phosphodiesterases hydrolyze the cyclic nucleotides, cGMP and cAMP, which both mediate smooth muscle relaxation in the lower urinary tract and other organs.[42] In the prostate, cGMP is synthesized by guanylyl cyclases, which are activated by nitric oxide (NO) released by neuronal NO synthase (nNOS) as a neurotransmitter, or by inducible NOS (iNOS) from macrophages.[43] Inhibitors for the cGMP-specific PDE5 were introduced in the 90's, for the treatment of erectile dysfunction (ED). PDE5 inhibition causes accumulation of cGMP in smooth muscle cells, promoting cGMP-mediated relaxation.[42] While PDE5 inhibitors are now available for treatment of LUTS in patients with BPH, cAMP-specific PDE4 is currently under preclinical investigation.[44]

The PDE5 inhibitor tadalafil has been approved very recently for treatment of obstructive symptoms in patients with BPH in the USA and Europe.[2745] The advantage of tadalafil to other PDE5 inhibitors may be its extended half-life, allowing a once-daily application for treatment of LUTS.[45] The efficacy of tadalafil is comparable to that of α₁-blockers.[46] In contrast to most other medical options for LUTS treatment, high attention has to be paid to possible contraindications, excluding the application of PDE5 inhibitors.[27] Patients receiving nitrates, potassium channel openers, nicroandil, or the α₁-blockers doxazosin or terazosin cannot be treated with PDE5 inhibitors, due to high risks of dangerous interactions.[27] Further contraindications are unstable angina pectoris, recent myocardial infarction (<3 mo) or stroke (<6 mo), myocardial insufficiency, hypotension, poorly controlled blood pressure, hepatic or renal insufficiency, and anterior ischemic optic neuropathy with sudden loss of vision after previous use of PDE5 inhibitors.[27]

The antidiuretic hormone, arginine vasopressin (AVP), is a key regulator of body water homeostasis and in the control of urine production.[47] AVP promotes water reabsorption and decreases water as well as total urine volume.[47] It is released to compensate dehydrated conditions, resulting in water reasorption and formation of a concentrated, low volume urine.[47] In parallel, AVP induces moderate vasoconstriction and elevation of blood pressure by activation of AVP receptor 1 (V1), to counteract hypovolemic states.[47]

The vasopressin receptor 2 (V2)-selective agonist, desmopressin, is available for the treatment of nocturia secondary to nocturnal polyuria in adult patients.[27] Desmopressin reduces the overall number of nocturnal voids and prolongs the periods of undisturbed sleep.[27] Nevertheless, it is rarely used for treatment of nocturia in adults. According to the role of AVP for urine homeostasis, desmopressin has been considered for the treatment of OAB.[47] Urodynamic actions were addressed by two clinical studies, with promising results.[47] Nevertheless, this did not proceed to clinical application.

Preclinical studies revealed several targets, which were related to promising results in experimental models. Some of them were recently transferred into clinical stages of examination and may await approval for clinical application in LUTS therapy.

In the human lower urinary tract, β₂- and β₃-adrenoceptors induce smooth muscle relaxtion, while the function and expression of β₁-adrenoceptors are of minor importance.[748] In addition to smooth muscle cells, β-adrenoceptos in the lower urinary tract may be present in the urothelium and in afferent nerves.[748] In the bladder, β-adrenoceptors enhance urine storage, while their function in the prostate or urethra is less understood.[748] β₃-adrenoceptors cover > 95% of the total β-adrenoceptor mRNA pool in the human bladder and induce detrusor relaxation.[48] In the human prostate, β₂ is the prevailing subtype at protein level; in fact, β-adrenergic activation inhibits α1-adrenergic prostate smooth muscle contraction via β₂-adrenoceptors.[48]

With regard to clinical application, β₃-adrenoceptors in the bladder attracted large attention. Following randomized clinical studies, mirabegron, a β₃-adrenergic agonist, has now been approved for the treatment of OAB in Europe, Japan, and the USA.[49505152] Nevertheless, long-term experiences with mirabegron during clinical application are still missing.[53] Although proof-of-concept studies with two other agonists, solabegron and ritobegron, yielded promising results, these agonists did not proceed to clinical application to date.[53]

The endocannabinoid system and transient receptor potential (TRP) channels have been recognized as important regulators of smooth muscle tone in the lower urinary tract.[5455] Cannabinoid receptors, TRPA, and TRPV cooperatively mediate smooth muscle relaxation in the prostate, urethra, and bladder.[5455] In this process, mechano-afferent signals cause activation of the cannabinoid receptor 2 (CB2) and TRP channels on sensory neurons, leading to the release of NO and cyclooxygenase activation by neurons, which finally results in postsynaptic smooth muscle relaxation [Figure 3].[55] In contrast to animal models, where CB1 strongly inhibits bladder smooth muscle contraction, endocannabinoid effects in the human lower urinary tract are prevailingly mediated by CB2.[5456]

While cannabinoid receptors and TRP channels have been intensively studied in vitro and in animal models, evidence for urodynamic effects in patients is still rare.[5657585960] Accumulation of endocannabinoids by inhibition of their degradation has been proposed as a new strategy for improvement of LUTS.[61] Endocannabinoid degradation is promoted by fatty acid amide hydrolase (FAAH).[61] In rats, FAAH inhibition by oleoyl ethyl amide (OetA) caused urodynamic alterations, which may improve symptoms in OAB.[61] In proof of concept studies, intravesical application of the vanilloid TRPV agonist capsaicin or resiniferatoxin increased bladder capacity and decreased urge incontinence in patients with neurogenic and non-neurogenic DO.[62] Clinical studies focused on the application of cannabinoids for the treatment of bladder dysfunction in multiple sclerosis (MS).[54] However, results were divergent and are not easy to discriminate from placebo effects in MS.[54]

Type A botulinum toxins (BTX-A), in particular onabotulinumtoxin A (BoNT-ONA, “botox”), has been investigated for use in the lower urinary tract. While intraprostatic injection is still controversially discussed and effects on obstructive symptoms may be limited,[6364] its application in the bladder is now an established therapy of DO.[65] In the USA and Europe, BoNT-ONA is used for second-line treatment of neurogenic DO, as an alternative for anticholinergic therapy.[6566] Approval for therapy of idiopathic DO may follow soon, as clinical trials provided encouraging results.[656768]

The botulinum neurotoxins (type A to G) are proteins secreted by strains of Clostridium botulinum.[69] They disrupt neurotransmission at neuromuscular junctions by inhibition of presynaptic acetylcholine release.[69] In this process, BTX-A prevents complex formation of synaptic vesicles (containing acetylcholine) with synaptobrevin and syntaxin.[69] Under normal conditions, this is required for the transport of vesicles to the membrane, and subsequent neurotransmitter release.[69] Inhibition of this mechanism accounts for the beneficial effects of BoNT-ONA in DO, as detrusor contraction is explained by equipment of smooth muscle cells with muscarinic receptors, and parasympathetic cholinergic innervation.

Preclinical studies with the vitamin D receptor agonist, BXL628 (elocalcitol), provided promising results and have been moved into the clinical testing stage. BXL628 prevents proliferation and contraction of smooth muscle cells in the bladder and the prostate, which is thought to be mediated by inhibition of the RhoA/Rho kinase pathway.[707172] In a placebo-controlled phase II study in 119 patients with BPH (prostate volume >40 ml), application of BXL628 for 12 weeks caused a significant effect on prostate growth.[73] However, this was not paralleled by significant effects on Qmax, which may be related to the short treatment period.[73] The effects on storage symptoms were studied in another trial performed in 257 women with OAB due to idiopathic DO, who received BXL628 for 4 weeks.[74] In this study, treatment with elocalcitol significantly reduced the episodes of incontinence and significantly improved the Patient's Perception of Bladder Condition score (PPBC), while effects on other parameters were lacking.[74] The primary end point, a change in bladder volume at the first involuntary detrusor contraction, was not achieved.[74] Thus, a clinical progress in LUTS treatment by vitamin D-dependent therapies appears unlikely.

For most of the described pharmacologic agents with urodynamic effects in vivo, direct effects on smooth muscle cells are well established. These are exerted by receptors on the cell membrane (adrenoceptors, cholinergic receptors) or by intracellular enzymes (PDEs, 5-AR). Numerous studies demonstrated that peripheral mechanisms are of relevance for urodynamic effects as well. Evidence for a contribution of neuronal α₁-adrenoceptors in the central and peripheral nervous system to urodynamic effects of α₁-blockers was provided quite early by several investigators.[8] More recently, it has been demonstrated by intrathecal application that peripheral effects and actions in the spinal cord may contribute to urodynamic effects of muscarinic antagonists, PDE5 inhibitors, and β₃-agonists.[757677] Less surprising, but noteworthy was the finding that urodynamic alterations induced by FAAH inhibitors can be observed following an intrathecal application.[78]